<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD with OASIS Tables with MathML3 v1.2d1 20130915//EN" "JATS-archive-oasis-article1.dtd"><article article-type="reciprocal-meat-conference-invited-reviews" xml:lang="en" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink"><front><journal-meta><journal-id journal-id-type="publisher-id">MMB</journal-id><journal-title-group><journal-title>Meat and Muscle Biology</journal-title></journal-title-group><issn pub-type="epub">2575-985X</issn><publisher><publisher-name>American Meat Science Association</publisher-name><publisher-loc/></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.22175/mmb.20112</article-id><article-id pub-id-type="publisher-id"/><article-categories><subj-group subj-group-type="heading"><subject>Reciprocal Meat Conference Invited Reviews</subject></subj-group></article-categories><title-group><article-title>Developments and Advances in Materials for Meats: Active Packaging, Edible Coatings, and Smart Packaging<xref ref-type="fn" rid="an1"><sup>&#x02021;</sup></xref></article-title><alt-title alt-title-type="right-running">Dittoe et al.&#x02003;&#x02003;&#x02003;Developments and advances in materials for meats</alt-title></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name><surname>Dittoe</surname><given-names>Dana K.</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author"><name><surname>O&#x02019;Bryan</surname><given-names>Corliss A.</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author"><name><surname>Legako</surname><given-names>Jerrad F.</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author"><name><surname>Olson</surname><given-names>Elena G.</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib><contrib contrib-type="author" corresp="yes"><name><surname>Ricke</surname><given-names>Steven C.</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><aff id="aff1"><label><sup>1</sup></label>Department of Animal Science, <institution>University of Wyoming</institution>, Laramie, WY 82071, USA</aff><aff id="aff2"><label><sup>2</sup></label>Department of Food Science, <institution>University of Arkansas</institution>, Fayetteville, AR 72701, USA</aff><aff id="aff3"><label><sup>3</sup></label>Department of Animal Science, <institution>Texas A&#x00026;M University</institution>, College Station, TX 77843, USA</aff><aff id="aff4"><label><sup>4</sup></label>Meat Science and Animal Biologics Discovery Program, Department of Animal and Dairy Sciences, <institution>University of Wisconsin&#x02013;Madison</institution>, Madison, WI 53706, USA</aff></contrib-group><author-notes><corresp id="cor1"><label><sup>*</sup></label>Corresponding author. Emails: <email>ddittoeuwyo.edu</email> (Dana K. Dittoe); <email>sricke@wisc.edu</email> (Steven C. Ricke)</corresp><fn id="an1"><label><sup>&#x02021;</sup></label><p>This material presented in this review was part of symposium entitled: Concurrent Technical Session VI&#x02014;Preservation, Packaging and Shelf-Life Microbial Ecology: Current Applications and Future Prospects. Reciprocal Meat Conference, St. Paul, MN, 26 June 2023.</p></fn></author-notes><pub-date date-type="epub" publication-format="electronic"><day>00</day><month>00</month><year>0000</year></pub-date><volume>9</volume><issue>1</issue><fpage>1</fpage><lpage>20</lpage><history><date date-type="received"><day>30</day><month>04</month><year>2025</year></date><date date-type="accepted"><day>11</day><month>10</month><year>2025</year></date></history><permissions><copyright-statement>&#x000A9; 2025 Dittoe, O&#x02019;Bryan, Legako, Olson, and Ricke.</copyright-statement><copyright-year>2025</copyright-year><copyright-holder>&#x000A9; 2025 Dittoe, O&#x02019;Bryan, Legako, Olson, and Ricke.</copyright-holder><license license-type="open-access"><license-p>This is an open access article distributed under the CC BY license (<ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by/4.0/">https://creativecommons.org/licenses/by/4.0/</ext-link>)</license-p></license></permissions><abstract><title>Abstract</title><p>Sufficient packaging of meats to maintain and extend shelf life is a critical focus of the industry to meet economic and environmental goals. Although traditional packaging materials have met several of the requirements for maintaining shelf life of meat products, there are still areas for potential improvement in the utility of packaging. Innovative packaging technologies such as active packaging, edible coatings, and films continue to be developed to further extend product shelf life and quality. More recent research efforts have offered opportunities to expand the functionality of packaging beyond just extending shelf life. Emerging packaging technologies include advances in nanomaterial and intelligent packaging such as packaging sensors, barcodes, radio-frequency identification tags, and indicators of time-temperature, gas, freshness, and pathogens. These technological advances provide opportunities to create &#x0201C;smart&#x0201D; packaging that delivers key information and feedback of the status of packaged meat products. The current review aims to discuss current and future directions in packaging technologies that will not only enhance microbial shelf life and quality of meat products but provide information on that product during storage.</p></abstract><kwd-group><title>Keywords:</title><kwd>meat</kwd><kwd>packaging technology</kwd><kwd>innovative packaging</kwd><kwd>edible films</kwd><kwd>sensors</kwd></kwd-group></article-meta></front><body><sec id="sec1"><title>Introduction</title><p>On a worldwide basis, plastic production continues to expand (<xref ref-type="bibr" rid="r7">Amobonye et&#x000A0;al., 2021</xref>; <xref ref-type="bibr" rid="r73">Hayat et&#x000A0;al., 2024</xref>). Plastics continue to be popular because of their versatility and durability, with nonbiodegradable plastic polymers being predominant (<xref ref-type="bibr" rid="r132">Peng et&#x000A0;al., 2022</xref>). While synthetic plastics derived from petroleum products make up the bulk of the plastics used in a wide range of applications, biological materials can be used to create biobased plastic polymers with the same properties as petroleum-based plastics; however, the end products are still not biodegradable (<xref ref-type="bibr" rid="r178">Tamoor et&#x000A0;al., 2021</xref>; <xref ref-type="bibr" rid="r89">Kim et&#x000A0;al., 2023</xref>). Regardless of their initial utilization, these polymers have 3 ultimate destinies: recycling, incineration, or discarded (<xref ref-type="bibr" rid="r95">Lear et al., 2021</xref>). Most of these plastic wastes are discarded and enter landfills or oceans, where they can persist and accumulate over extended periods (<xref ref-type="bibr" rid="r95">Lear et al., 2021</xref>; <xref ref-type="bibr" rid="r132">Peng et&#x000A0;al., 2022</xref>). While recycling is certainly practiced, recovery can still be challenging in part due to the method of disposal, resulting in the difference between waste production and recycling remaining highly imbalanced (Leng et&#x000A0;al., 2020; <xref ref-type="bibr" rid="r178">Tamoor et&#x000A0;al., 2021</xref>; <xref ref-type="bibr" rid="r153">Samadhiya et&#x000A0;al., 2022</xref>; <xref ref-type="bibr" rid="r89">Kim et&#x000A0;al., 2023</xref>). However, because these plastics are commonly petroleum-derived products, they also contribute to rising carbon dioxide levels due to emissions during incineration of plastic or disposal in landfills (<xref ref-type="bibr" rid="r170">Song et&#x000A0;al., 2021</xref>; <xref ref-type="bibr" rid="r91">Kumar et&#x000A0;al., 2022</xref>). Furthermore, upon exposure to environmental elements such as ultraviolet rays, temperature, photooxidation, biological activities, and general weathering, they can be degraded into particle sizes below 5&#x000A0;mm, becoming what is referred to as microplastics (<xref ref-type="bibr" rid="r127">Padervand et&#x000A0;al., 2020</xref>; <xref ref-type="bibr" rid="r132">Peng et&#x000A0;al., 2022</xref>).</p><p>Plastics used for food packaging account for over 36% of the packaging market because they are inexpensive, lightweight, transport easily, are considered strong, exhibit barrier properties, possess ease of manufacturing properties, and are adaptable to various package forms (<xref ref-type="bibr" rid="r95">Lear et&#x000A0;al., 2021</xref>; <xref ref-type="bibr" rid="r62">Gasti et&#x000A0;al., 2022</xref>; <xref ref-type="bibr" rid="r66">Gil and Rudy, 2023</xref>). The consumer discards synthetic plastic packaging materials, which are generally considered nondegradable and nonrenewable, leading to disposal problems with over 70% entering dumps and landfills (<xref ref-type="bibr" rid="r105">Marsh and Bugusu, 2007</xref>; <xref ref-type="bibr" rid="r66">Gil and Rudy, 2023</xref>; <xref ref-type="bibr" rid="r89">Kim et&#x000A0;al., 2023</xref>; <xref ref-type="bibr" rid="r122">Nath et&#x000A0;al., 2024</xref>). These materials break into microplastics, which fish can consume, leading to bioaccumulation and posing concerns for human health (<xref ref-type="bibr" rid="r164">Smith et&#x000A0;al., 2018</xref>). Further human concerns are linked with reports of foodborne pathogens being associated with microplastic particles and forming biofilms as part of the plastisphere microbial consortia that, in turn, can be consumed by animals and found in food (<xref ref-type="bibr" rid="r132">Peng et&#x000A0;al., 2022</xref>; <xref ref-type="bibr" rid="r181">Tavelli et&#x000A0;al., 2022</xref>). Once ingested, microplastics may also alter the gastrointestinal ecology of animals and interact with foodborne pathogens under these conditions. For example, Chatman et&#x000A0;al. (<xref ref-type="bibr" rid="r36">2024</xref>) demonstrated with an in vitro broiler cecal model that the cointroduction of microplastics and <italic>Salmonella typhimurium</italic> caused greater disruption in the cecal microbiome and metabolome than exposure to either treatment alone. Finally, direct contact of consumers with food products held in plastic packages can serve as an exposure route (<xref ref-type="bibr" rid="r181">Tavelli et&#x000A0;al., 2022</xref>).</p><p>Due to these growing environmental concerns, packaging is under scrutiny because it is a source of large amounts of plastic waste, which has led to research into efforts to remove microplastics from the environment and for the development of renewable alternatives (<xref ref-type="bibr" rid="r46">Dikky and Stevia, 2019</xref>; <xref ref-type="bibr" rid="r131">Payne et&#x000A0;al., 2019</xref>; <xref ref-type="bibr" rid="r127">Padervand et&#x000A0;al., 2020</xref>). Consequently, developing plastics that can be reusable, biodegradable, and/or recyclable as packaging materials has become much more relevant (<xref ref-type="bibr" rid="r66">Gil and Rudy, 2023</xref>). Biopolymers derived from natural products have emerged as an alternative, including polysaccharide- and protein-based polymers (<xref ref-type="bibr" rid="r129">Pal et&#x000A0;al., 2021</xref>). Some of these are derived from plants, animals, or marine sources, and other food-grade materials can be considered edible packaging materials (<xref ref-type="bibr" rid="r91">Kumar et&#x000A0;al., 2022</xref>). The following sections describe some of these natural polymers that have been examined and implemented for meat product packaging. In addition, so-called innovative packaging, which increases the functional versatility of packaging materials for meat products, will be discussed.</p></sec><sec id="sec2"><title>Biological-Based Coatings and Films</title><sec id="sec2.1"><title>Polylactic acid films</title><p>Polylactic acid (PLA) polymers are derived from lactic acid and can be created by various polymerization processes including direct condensation, azeotropic polycondensation, and lactide-based polymerization (<xref ref-type="bibr" rid="r142">Rajendran et&#x000A0;al., 2024</xref>; <xref ref-type="bibr" rid="r192">Wongphan et&#x000A0;al., 2024</xref>). The lactic acid precursor can be chemically generated or biologically produced as a common organic acid from a wide range of fermentations including food products, silage, gastrointestinal tracts of animals, and as a product of numerous probiotics and starter cultures (<xref ref-type="bibr" rid="r32">Caplice and Fitzgerald, 1999</xref>; <xref ref-type="bibr" rid="r146">Ricke et&#x000A0;al., 2013</xref>; <xref ref-type="bibr" rid="r48">Dittoe et&#x000A0;al., 2018</xref>; <xref ref-type="bibr" rid="r118">Muck et&#x000A0;al., 2018</xref>; <xref ref-type="bibr" rid="r142">Rajendran et&#x000A0;al., 2024</xref>). Given the diverse array of lactic acid producing organisms and renewable substrates for fermentation, there is no shortage of potential sources for lactic acid to generate the corresponding PLA polymer. However, large-scale commercial production can be handicapped by the generation of racemic mixtures of DL-lactate and obtaining pure L-lactate is preferred for PLA generation (<xref ref-type="bibr" rid="r142">Rajendran et&#x000A0;al., 2024</xref>).</p><p>Polylactic polymers have been used as packaging materials for a wide range of both liquid and solid foods including meat products (<xref ref-type="bibr" rid="r107">McMillin, 2017</xref>; <xref ref-type="bibr" rid="r130">Panseri et&#x000A0;al., 2018</xref>; <xref ref-type="bibr" rid="r192">Wongphan et&#x000A0;al., 2024</xref>; <xref ref-type="bibr" rid="r113">Moldovan et&#x000A0;al., 2025</xref>). They are considered optimal package film candidates for their high tensile strength and durability, along with transparency, clarity, and insolubility with air, ethanol, methanol, and aliphatic carbon (<xref ref-type="bibr" rid="r71">Halloran et&#x000A0;al., 2002</xref>; <xref ref-type="bibr" rid="r121">Nasution et&#x000A0;al., 2023</xref>). In addition, PLA as a biopolymer possesses environmental attributes such as biocompatibility and biodegradability and is compostable (<xref ref-type="bibr" rid="r12">Asadi and Mozafari, 2025</xref>; <xref ref-type="bibr" rid="r142">Rajendran et&#x000A0;al., 2024</xref>). Films made with PLA are classified as GRAS (Generally Recognized as Safe) by the US Food and Drug Administration and offer the potential for compliance with food safety regulations (<xref ref-type="bibr" rid="r130">Panseri et&#x000A0;al., 2018</xref>; <xref ref-type="bibr" rid="r12">Asadi and Mozafari, 2025</xref>). However, PLA as a flexible packaging material can suffer from brittleness at room temperature, poor thermal stability, and low water vapor barrier properties depending on the application (<xref ref-type="bibr" rid="r121">Nasution et&#x000A0;al., 2023</xref>; <xref ref-type="bibr" rid="r192">Wongphan et&#x000A0;al., 2024</xref>).</p><p>Mechanical improvements can be achieved by incorporating chemical plasticizers, but these leach out and lead to environmental problems (<xref ref-type="bibr" rid="r71">Halloran et&#x000A0;al., 2022</xref>). Biobased plasticizers such as glycerol have been used as substitutes and have been demonstrated to create PLA blends, exhibiting improved flexibility, minimal leaching, and no toxicity based on in vitro mammalian cell toxicity assays (<xref ref-type="bibr" rid="r71">Halloran et&#x000A0;al., 2022</xref>). Functional improvements have been explored combining PLA with various additives such as plant-based extracts, antimicrobial compounds, and lignocellulose waste among others for food and meat products (<xref ref-type="bibr" rid="r120">Mu&#x000F1;oz-Pabon et&#x000A0;al., 2023</xref>; <xref ref-type="bibr" rid="r12">Asadi and Mozafari, 2025</xref>). Using an agar diffusion antimicrobial assay, Mu&#x000F1;oz-Pabon et&#x000A0;al. (<xref ref-type="bibr" rid="r120">2023</xref>) demonstrated that PLA composites containing nisin, oregano, cassava bran, and coffee husks inhibited <italic>Listeria monocytogenes</italic>. When they used the corresponding composites that gave the greatest antimicrobial activity to package pork meat, the pH, texture, moisture, and pH qualities were similar to those displayed by pork products held in commercial polystyrene packaging. Further research is continuing to expand the functionality of PLA natural extract composite blends to provide antioxidant properties as well as screening antimicrobial activities against not only other bacteria but fungi as well (<xref ref-type="bibr" rid="r121">Nasution et&#x000A0;al., 2023</xref>; <xref ref-type="bibr" rid="r12">Asadi and Mozafari, 2025</xref>).</p></sec><sec id="sec2.2"><title>Edible films: cellulose and cellulose derivatives</title><p><bold>Plant-based cellulose.</bold> Cellulose polymers consist of &#x003B2; 1&#x02013;4 linked glucose monomers that, along with hydrogen linkages, possess a crystalline structure that serves as a highly structured matrix (<xref ref-type="bibr" rid="r97">Limayen and Ricke, 2012</xref>; <xref ref-type="bibr" rid="r116">Motaung, 2021</xref>). Cellulose, as a significant component of plant-cell walls, is one of the most abundant biopolymers present in nature and can be obtained from a variety of sources including wood, cotton, and food waste as well as agricultural and agronomic wastes (<xref ref-type="bibr" rid="r52">Erginkaya et&#x000A0;al., 2014</xref>; <xref ref-type="bibr" rid="r13">Asgher et&#x000A0;al., 2020</xref>; <xref ref-type="bibr" rid="r112">Mohamed et&#x000A0;al., 2020</xref>; <xref ref-type="bibr" rid="r66">Gil and Rudy, 2023</xref>; <xref ref-type="bibr" rid="r195">Yang et&#x000A0;al., 2024</xref>). Not surprisingly, the availability of cellulose, as well as being biodegradable, inexpensive, and edible, has made it attractive as a packaging material for food products (<xref ref-type="bibr" rid="r66">Gil and Rudy, 2023</xref>). In addition to cellulose polymers being biodegradable, tasteless, and odorless, they possess a high thermal tolerance and can serve as a barrier to ultraviolet rays, as well as being capable of carrying antioxidant and antimicrobial agents (<xref ref-type="bibr" rid="r52">Erginkaya et&#x000A0;al., 2014</xref>; <xref ref-type="bibr" rid="r13">Asgher et&#x000A0;al., 2020</xref>; <xref ref-type="bibr" rid="r112">Mohamed et&#x000A0;al., 2020</xref>; <xref ref-type="bibr" rid="r147">Rom&#x000E3;o et&#x000A0;al., 2022</xref>; <xref ref-type="bibr" rid="r122">Nath et&#x000A0;al., 2024</xref>). Depending on the preparation procedure, cellulose microfibrils can take on many forms, including microcrystalline, nanocrystalline, and nanofibrillated versions of the polymer microstructures (<xref ref-type="bibr" rid="r147">Rom&#x000E3;o et&#x000A0;al., 2022</xref>). Chemically altered versions of cellulose can be generated, involving a range of esters and ethers to create cellulose derivatives with methylcellulose (MC), carboxymethyl cellulose (CMC), and hydroxypropyl methylcellulose (HPMC) being the most commonly used for edible films (<xref ref-type="bibr" rid="r189">von Schantz et&#x000A0;al., 2014</xref>; <xref ref-type="bibr" rid="r81">Jiang and Ngai, 2022</xref>; <xref ref-type="bibr" rid="r147">Rom&#x000E3;o et&#x000A0;al., 2022</xref>). The resulting modified cellulose films can provide strength and transparency (<xref ref-type="bibr" rid="r2">Agustin et&#x000A0;al., 2014</xref>; <xref ref-type="bibr" rid="r69">Guzman-Puyol et&#x000A0;al., 2019</xref>). While CMC films have been shown to restrict meat protein and lipid oxidation, antioxidant properties can be generated by introducing pomegranate seed extract to MC, CMC, and HPMC films, but such additions may limit the oxygen capability of these films (<xref ref-type="bibr" rid="r124">Nemazifard et&#x000A0;al., 2017</xref>; <xref ref-type="bibr" rid="r87">Khezrian and Shahbazi, 2018</xref>). Immobilizing bioactive agents onto cellulose polymers has also exhibited antimicrobial properties (<xref ref-type="bibr" rid="r78">Irimia et&#x000A0;al., 2024</xref>).</p><p><bold>Bacterial-based cellulose.</bold> Despite the attractiveness of cellulose from plant sources, there are limitations due to the complexities associated with extraction and purification needed to retrieve a high-quality polymer that incur technical and economic scale-up hurdles for commercial applications (<xref ref-type="bibr" rid="r122">Nath et&#x000A0;al., 2024</xref>). Cellulose polymers produced by several aerobic bacteria have received interest as a possible alternative for the food industry (<xref ref-type="bibr" rid="r34">Caz&#x000F3;n and V&#x000E1;zque, 2021</xref>). Produced by cellulose synthase complexes, extracellular bacterial cellulose is an exopolysaccharide that, unlike plant cellulose, does not contain contaminants such as lignin, pectin, or hemicellulose (<xref ref-type="bibr" rid="r34">Caz&#x000F3;n and V&#x000E1;zquez, 2021</xref>; <xref ref-type="bibr" rid="r96">Li et&#x000A0;al., 2022</xref>). The resulting purity generates a product that does not require extraction or chemical purification, possesses a high degree of polymerization, and exhibits crystallinity among other properties (<xref ref-type="bibr" rid="r34">Caz&#x000F3;n and V&#x000E1;zquez, 2021</xref>; <xref ref-type="bibr" rid="r96">Li et&#x000A0;al., 2022</xref>). More optimization of bacterial cellulose production remains, including developing low-cost growth media, further identification of candidate bacterial strains, and other approaches to enhance yields and/or create new properties (<xref ref-type="bibr" rid="r49">dos Santos et&#x000A0;al., 2024</xref>). Given the advancements made in molecular biology, genetically altered bacterial strains could produce a wide range of modified cellulose polymers with potentially more properties for multifunctional packaging materials beyond the chemical approaches currently used for modifying plant-based cellulose polymers.</p></sec><sec id="sec2.3"><title>Starch edible films</title><p>Another plant-derived carbohydrate polymer that is also biodegradable, as well as economical and renewable for utilization in edible films, is starch (<xref ref-type="bibr" rid="r115">Mose and Maranga, 2011</xref>; <xref ref-type="bibr" rid="r128">Paj&#x00105;k et&#x000A0;al., 2017</xref>; <xref ref-type="bibr" rid="r170">Song et&#x000A0;al., 2021</xref>; <xref ref-type="bibr" rid="r66">Gil and Rudy, 2023</xref>). Starch sources have typically included agronomic products such as corn, potatoes, rice, and wheat, but interest has grown toward deriving starches from more nonconventional sources such as certain beans and vegetable materials (<xref ref-type="bibr" rid="r61">Garc&#x000ED;a-Guzm&#x000E1;n et&#x000A0;al., 2022</xref>; <xref ref-type="bibr" rid="r139">Putri et&#x000A0;al., 2023</xref>). While starch-based films have been extensively used in food and meat packaging due to their desirable gas barrier and organoleptic properties, they suffer from being brittle and hydrophilic and possess overall poor mechanical properties (<xref ref-type="bibr" rid="r125">Onyeaka et&#x000A0;al., 2022</xref>; <xref ref-type="bibr" rid="r66">Gil and Rudy, 2023</xref>; <xref ref-type="bibr" rid="r139">Putri et&#x000A0;al., 2023</xref>). Consequently, modifications of starch have been explored, employing either chemical or physical treatments (<xref ref-type="bibr" rid="r61">Garc&#x000ED;a-Guzm&#x000E1;n et&#x000A0;al., 2022</xref>). Physical treatments to starch polymers have involved administration of high hydrostatic pressure, ozonation, and ultrasound (<xref ref-type="bibr" rid="r61">Garc&#x000ED;a-Guzm&#x000E1;n et&#x000A0;al., 2022</xref>; <xref ref-type="bibr" rid="r90">Koshenaj and Ferrari, 2024</xref>). Chemical modifications to introduce functional groups into starch polymers have included reduction, substitution, or cross-linking (<xref ref-type="bibr" rid="r61">Garc&#x000ED;a-Guzm&#x000E1;n et&#x000A0;al., 2022</xref>). Likewise, combinations with other materials have been introduced to improve these negative characteristics (<xref ref-type="bibr" rid="r66">Gil and Rudy, 2023</xref>). For example, the incorporation of plant extracts and essential oils has been shown to improve oxygen barrier characteristics, enhance antioxidation qualities that can lead to improved shelf life, and provide antimicrobials to improve food safety (<xref ref-type="bibr" rid="r141">Radha Krishnan et&#x000A0;al., 2015</xref>; <xref ref-type="bibr" rid="r197">Y&#x00131;ld&#x00131;r&#x00131;m-Yal&#x000E7;&#x00131;n et&#x000A0;al. 2021</xref>; <xref ref-type="bibr" rid="r170">Song et&#x000A0;al., 2021</xref>; <xref ref-type="bibr" rid="r53">Erna et&#x000A0;al., 2022</xref>; <xref ref-type="bibr" rid="r61">Garc&#x000ED;a-Guzm&#x000E1;n et&#x000A0;al., 2022</xref>). In addition, merging biodegradable plastics with starch have been offered to reduce the cost of biodegradable polymers (<xref ref-type="bibr" rid="r170">Song et&#x000A0;al., 2021</xref>). It is anticipated that newer technologies such as 3-dimensional (3D) printing, electrospinning, force spinning, and others will be further developed, and the opportunities to expand the functionality of starch-based edible films and packaging will become feasible (<xref ref-type="bibr" rid="r61">Garc&#x000ED;a-Guzm&#x000E1;n et&#x000A0;al., 2022</xref>).</p></sec><sec id="sec2.4"><title>Chitosan edible films</title><p>Chitosan is a natural high-molecular weight cationic polysaccharide comprised of (1,4)-2-amino-2-deoxy-glucose that is produced by the deacetylation of chitin a polymer that occurs primarily in shrimp, crabs, and insects as well as marine diatoms and some fungi (<xref ref-type="bibr" rid="r140">Raafat and Sahl, 2009</xref>; <xref ref-type="bibr" rid="r98">Liu et&#x000A0;al., 2022</xref>). Chitosan and poly(&#x0025B;-lysine) are natural polymers that have natural antimicrobial characteristics (<xref ref-type="bibr" rid="r140">Raafat and Sahl, 2009</xref>; <xref ref-type="bibr" rid="r157">Sayed and Jardine, 2015</xref>; <xref ref-type="bibr" rid="r161">Sivakanthan, et&#x000A0;al., 2020</xref>; <xref ref-type="bibr" rid="r38">Chen et&#x000A0;al., 2023</xref>). These polymers act on bacteria&#x02019;s negatively charged cell membranes, causing intracellular leakage (<xref ref-type="bibr" rid="r156">Santos et&#x000A0;al., 2016</xref>; <xref ref-type="bibr" rid="r168">Sof&#x00131; et&#x000A0;al., 2018</xref>). These bioactive polymers can be used in composites or coatings (<xref ref-type="bibr" rid="r134">Perinelli et&#x000A0;al., 2018</xref>; <xref ref-type="bibr" rid="r190">Wang et&#x000A0;al., 2018</xref>; <xref ref-type="bibr" rid="r187">Vasile and Baican, 2021</xref>).</p><p>Chitosan films are generally made by casting, which involves dissolving and incorporating a plasticizer and an active compound and nanofiller of choice (<xref ref-type="bibr" rid="r80">Jiang et&#x000A0;al., 2023</xref>). Chitosans are an attractive alternative packaging material due to their biodegradability, nontoxicity, and renewability (<xref ref-type="bibr" rid="r80">Jiang et&#x000A0;al., 2023</xref>). Even when combined with metal oxides to form chitosan-metal oxide films, complete degradation in soil still occurs after several weeks (<xref ref-type="bibr" rid="r193">Wro&#x00144;ska et&#x000A0;al., 2023</xref>). In addition to film and coating applications, chitosans have historically received interest in various uses, from vaccine, peptide, and gene delivery systems and pharmaceuticals for tissue engineering (<xref ref-type="bibr" rid="r140">Raafat and Sahl. 2009</xref>). Chitosan has been used in food applications for enzyme stabilization, dye binding, emulsification, antioxidant, and gelling agents (<xref ref-type="bibr" rid="r1">Agull&#x000F3; et&#x000A0;al., 2003</xref>). Chitosan-based films possess the advantages of flexibility and strength and are resistant to fats, oil, and oxygen (<xref ref-type="bibr" rid="r123">Nayik et&#x000A0;al., 2015</xref>; <xref ref-type="bibr" rid="r112">Mohamed et&#x000A0;al., 2020</xref>; <xref ref-type="bibr" rid="r170">Song et&#x000A0;al., 2021</xref>). In addition to its film-forming utility, chitosan possesses a wide range of antimicrobial activities against both Gram-negative and Gram-positive bacteria, yeast, and filamentous fungi and has been demonstrated to extend shelf life in ready-to-cook meat products (<xref ref-type="bibr" rid="r58">Ferreira et&#x000A0;al., 2009</xref>; <xref ref-type="bibr" rid="r30">Campos et&#x000A0;al., 2011</xref>; <xref ref-type="bibr" rid="r5">Alem&#x000E1;n et&#x000A0;al., 2016</xref>; <xref ref-type="bibr" rid="r112">Mohamed et&#x000A0;al., 2020</xref>; <xref ref-type="bibr" rid="r80">Jiang et&#x000A0;al., 2023</xref>; <xref ref-type="bibr" rid="r9">Aresta et&#x000A0;al., 2024</xref>). Chitosan composited with essential oils or phenolic compounds have enhanced antimicrobial and antifungal activities (<xref ref-type="bibr" rid="r80">Jiang et&#x000A0;al., 2023</xref>). Phenolics included as a composite with certain phenolic compounds have been employed to improve mechanical strength (<xref ref-type="bibr" rid="r80">Jiang et&#x000A0;al., 2023</xref>).</p></sec><sec id="sec2.5"><title>Lipid edible films</title><p>Fat was used as an edible food coating in 16th-century England (<xref ref-type="bibr" rid="r93">Labuza and Contreras-Medellin, 1981</xref>). Waxes (e.g.,&#x000A0;carnauba wax, beeswax, paraffin wax) and oils (mineral oil, vegetable oil) have been commercially used as protective coatings for fresh fruits and vegetables since the beginning of the 1930s (<xref ref-type="bibr" rid="r15">Baldwin, 1994</xref>). Other lipid materials employed include lacs, fatty acids and alcohols, and acetylated glycerides (<xref ref-type="bibr" rid="r63">Ghosh et&#x000A0;al., 2021</xref>). Compared to protein and carbohydrate-based films and coatings that are hydrophilic, lipid-based materials provide a hydrophobic barrier that decreases penetration of water vapor (<xref ref-type="bibr" rid="r110">Milani and Nemati, 2022</xref>). Milani and Nemati (<xref ref-type="bibr" rid="r110">2022</xref>) describe several lipid compounds and their sources. They range from natural oils and fats to natural resins and essential oils and can originate from either animal or plant sources.</p><p>Waxes are nonpolar lipids possessing long aliphatic chains that can be derived from bees and plant sources (<xref ref-type="bibr" rid="r110">Milani and Nemati, 2022</xref>). Over the years, certain waxes have been used to encase fruits and vegetables, allowing for extended shelf life and limiting degradation over time (<xref ref-type="bibr" rid="r110">Milani and Nemati, 2022</xref>). Likewise, since the 1950s, several meat processors in the United States have applied strippable coatings of petroleum-derived microcrystalline wax on frozen meats, such as beef, veal, lamb, hamburger patties, and luncheon meats (<xref ref-type="bibr" rid="r106">McGrath, 1955</xref>). Although wax coatings are substantially more resistant to moisture transport than most other lipid or nonlipid edible coatings (<xref ref-type="bibr" rid="r158">Schultz et&#x000A0;al., 1949</xref>; <xref ref-type="bibr" rid="r94">Landmann et&#x000A0;al., 1960</xref>), wax-, fat-, and oil-based coatings have application problems (i.e., thickness and homogeneity control, greasy surface, cracking) and organoleptic problems (i.e., waxy taste, rancidity)(<xref ref-type="bibr" rid="r22">Bol&#x000ED;var-Monsalve et&#x000A0;al., 2019</xref>). Thus, pure lipids are combined with hydrocolloids such as protein, starch, cellulose, and their derivatives, providing a multicomponent system that can be applied as meat coatings (<xref ref-type="bibr" rid="r42">Cutter, 2006</xref>).</p><p>Additional beneficial functions beyond being edible may be possible with certain sources of lipid-based coatings. For example, one agronomic source of wax used for coatings is extracted from rice bran oil, either in a hard or soft form (<xref ref-type="bibr" rid="r110">Milani and Nemati, 2022</xref>). Rice bran results from milling, representing 5% to 6% of the rice kernel and comprising anywhere from 15% to 22% lipids (<xref ref-type="bibr" rid="r101">Luh, 1991</xref>; <xref ref-type="bibr" rid="r75">Henderson et&#x000A0;al., 2012</xref>; <xref ref-type="bibr" rid="r21">Bodie et&#x000A0;al., 2019</xref>). In addition, rice bran is known to exhibit prebiotic activities, and rice bran oil has been associated with health benefits such as tumor reduction (<xref ref-type="bibr" rid="r150">Ryan, 2011</xref>; <xref ref-type="bibr" rid="r75">Henderson et&#x000A0;al., 2012</xref>; <xref ref-type="bibr" rid="r21">Bodie et&#x000A0;al., 2019</xref>). Rice bran oil has received interest in several food applications due to its high nutritional quality, antioxidant activity, stabilization properties for storage, and different food colorant options based on the different pigmented rice varieties (<xref ref-type="bibr" rid="r43">Das et&#x000A0;al., 2025</xref>). Some of these characteristics associated with rice bran oil waxes would potentially qualify them as more attractive alternative wax lipid-based edible coatings for multiple food products, including meats. However, this will likely depend on whether they can be retained during extraction. Further compositional research on these waxes from other sources may reveal additional beneficial characteristics that make them more biologically active beyond just serving as edible coatings.</p></sec><sec id="sec2.6"><title>Protein edible films</title><p>Protein films are attractive because of the potential unique combinations of a wide range of amino acids that can result in various polymer structural forms and intramolecular interactions (<xref ref-type="bibr" rid="r70">Hadidi et&#x000A0;al., 2022</xref>; <xref ref-type="bibr" rid="r88">Khin et&#x000A0;al., 2024</xref>). Protein films easily lend themselves to chemical and physical manipulation and form networks for elasticity (<xref ref-type="bibr" rid="r70">Hadidi et&#x000A0;al., 2022</xref>). Sources for edible protein films can be generally categorized as originating from either plant or animal products (<xref ref-type="bibr" rid="r88">Khin et&#x000A0;al., 2024</xref>). Collagen, keratin, milk, egg, and whey have served as animal sources, while proteins from corn, wheat, and soy have been used to generate protein-based films (<xref ref-type="bibr" rid="r35">Caz&#x000F3;n et&#x000A0;al., 2017</xref>; <xref ref-type="bibr" rid="r109">Mihalca et&#x000A0;al., 2021</xref>). Plant edible protein candidates can be derived from many plant sources, including cereals, legumes, oil seeds, green leaves, and nuts (<xref ref-type="bibr" rid="r70">Hadidi et&#x000A0;al., 2022</xref>). While soy proteins were used for edible protein films early on, agricultural byproduct sources such as wheat gluten, rice bran, and corn zein have received attention as potentially sustainable edible films (<xref ref-type="bibr" rid="r138">Purewal et&#x000A0;al., 2024</xref>). In addition to the initial protein source, the types of proteins derived from these plant sources are generally categorized as either albumins, globulins, glutelins, or prolamins, which vary in their solubility (<xref ref-type="bibr" rid="r70">Hadidi et&#x000A0;al., 2022</xref>). Consequently, these differences are reflected in how these protein sources are used in packaging.</p><p>For animal products, milk proteins have been a source of films for several decades and consist primarily of casein and a lesser amount of whey (<xref ref-type="bibr" rid="r160">Shendurse et&#x000A0;al., 2018</xref>). Casein from milk was one of the early sources of edible protein films, particularly for packaging dairy products, and has the advantage of remaining stable over a wide range of temperatures, pH measurements, and salt conditions (<xref ref-type="bibr" rid="r160">Shendurse et&#x000A0;al., 2018</xref>; <xref ref-type="bibr" rid="r138">Purewal et&#x000A0;al., 2024</xref>). Whey proteins are generated as a waste byproduct after casein extraction for cheese processing. They are becoming more attractive as a protein film source because of their functional utility as a biodegradable barrier polymer and their ready availability as a surplus waste (<xref ref-type="bibr" rid="r83">Kandasamy et&#x000A0;al., 2021</xref>). Whey protein contains several fractions, but levels depend on cheese type, manufacturing process, and animal milk source, among other factors (<xref ref-type="bibr" rid="r83">Kandasamy et&#x000A0;al., 2021</xref>). Gelatins derived from the high-temperature partial acid or alkali hydrolysis of fibrous hydrophobic collagen proteins occurring in animal tissues also emerged as an attractive source for packaging due to their effectiveness as a barrier and biodegradability (<xref ref-type="bibr" rid="r173">&#x00160;uput et&#x000A0;al., 2015</xref>; <xref ref-type="bibr" rid="r99">Loo and Sarbon, 2020</xref>; <xref ref-type="bibr" rid="r102">Maciel et&#x000A0;al., 2020</xref>; <xref ref-type="bibr" rid="r138">Purewal et&#x000A0;al., 2024</xref>). Collagens occur in various organs and tissues such as cartilage, skin, lungs, tendons, and basement tissues and can compositionally vary, being homogenous in one tissue and heterogenous in another (<xref ref-type="bibr" rid="r23">Bornstein and Sage, 1980</xref>). Interest has grown in the utilization of collagen due to its availability in several animal processing operations, for example, chicken skin (<xref ref-type="bibr" rid="r99">Loo and Sarbon, 2020</xref>; <xref ref-type="bibr" rid="r144">Ricke et&#x000A0;al., 2025a</xref>). By repurposing these animal waste byproducts into useful applications such as protein films, there is an opportunity to decrease the environmental footprint of processing waste such as animal hide components that end up in landfills (<xref ref-type="bibr" rid="r104">Matinong et&#x000A0;al., 2022</xref>; <xref ref-type="bibr" rid="r175">Suurs et&#x000A0;al., 2023</xref>). However, retrieving products such as collagen from such sources will require developing large-scale economic processing methods.</p><p>Proteins have been investigated and used as sources of edible meat film for several years (<xref ref-type="bibr" rid="r37">Chen et&#x000A0;al., 2019</xref>). Protein films generally have a sound gas barrier, mechanical properties, and poor water vapor permeability (<xref ref-type="bibr" rid="r24">Bourtoom, 2008</xref>; <xref ref-type="bibr" rid="r25">Bourtoom, 2009</xref>; <xref ref-type="bibr" rid="r126">Otoni et&#x000A0;al., 2016</xref>). Protein-based edible films have been investigated for salami (<xref ref-type="bibr" rid="r114">Moreira et&#x000A0;al., 2011</xref>), chicken breast (<xref ref-type="bibr" rid="r57">Fern&#x000E1;ndez-Pan et&#x000A0;al., 2014</xref>; <xref ref-type="bibr" rid="r45">Di Giorgio et&#x000A0;al., 2019</xref>), beef (<xref ref-type="bibr" rid="r51">Emiro&#x0011F;lu et&#x000A0;al., 2010</xref>; <xref ref-type="bibr" rid="r33">Cardoso et&#x000A0;al., 2016</xref>), and pork (<xref ref-type="bibr" rid="r82">Kaewprachu et&#x000A0;al., 2015</xref>). However, protein-based films have a low resistance to mechanical stress and water diffusion and may become fragile under dried conditions (<xref ref-type="bibr" rid="r22">Bol&#x000ED;var-Monsalve et&#x000A0;al., 2019</xref>). Other drawbacks to protein-based films are their susceptibility to native enzymes present in meat. They may be susceptible to native enzymes and may cause adverse reactions in consumers allergic to certain protein fractions (<xref ref-type="bibr" rid="r155">S&#x000E1;nchez-Ortega et&#x000A0;al., 2014</xref>; <xref ref-type="bibr" rid="r60">Galus and Kadzi&#x00144;ska, 2015</xref>). In addition, protein films can suffer from low mechanical strength water barrier issues, and interactions among the protein chains may result in rigid structures and brittleness (<xref ref-type="bibr" rid="r29">Calva-Estrada et&#x000A0;al., 2019</xref>; <xref ref-type="bibr" rid="r182">Tkaczewska, 2020</xref>; <xref ref-type="bibr" rid="r138">Purewal et&#x000A0;al., 2024</xref>). However, these issues can be improved with various chemical and enzymatic modifications or by combining them with other polymers, such as plant protein blends or lipids that provide complementary characteristics to the film composite (<xref ref-type="bibr" rid="r29">Calva-Estrada et&#x000A0;al., 2019</xref>; <xref ref-type="bibr" rid="r138">Purewal et&#x000A0;al., 2024</xref>). More specifically, adding a low molecular mass, nonvolatile compound such as sugar, alcohol, as well as gelatin hydrolysates as plasticizers can improve the mechanical properties of protein films while decreasing hardness and stiffness (<xref ref-type="bibr" rid="r29">Calva-Estrada et&#x000A0;al., 2019</xref>; <xref ref-type="bibr" rid="r83">Kandasamy et&#x000A0;al., 2021</xref>; <xref ref-type="bibr" rid="r70">Hadidi et&#x000A0;al., 2022</xref>). As more of the chemistry of polymer blends becomes understood, it is anticipated that more diverse functionality can be added to these types of protein-based films and coatings.</p></sec></sec><sec id="sec3"><title>Active Packaging Strategies</title><sec id="sec3.1"><title>Antimicrobial active packaging</title><p>One version of this type of packaging is to soak pads or fill a sachet with the respective antimicrobial to be placed inside the package (<xref ref-type="bibr" rid="r126">Otoni, et&#x000A0;al., 2016</xref>). These sachets or pads may generate and release or carry and release antimicrobial ingredients of essential oils, allyl isothiocyanate, chlorine dioxide, or ethanol (<xref ref-type="bibr" rid="r126">Otoni et&#x000A0;al., 2016</xref>). The pads may be absorbent to remove liquids or gases and may be impregnated with silver, copper, or copper oxide nanoparticles (<xref ref-type="bibr" rid="r126">Otoni, et&#x000A0;al., 2016</xref>). Carbon dioxide emitters may also be placed in the packages. Carbon dioxide can act directly as an antimicrobial (<xref ref-type="bibr" rid="r55">Fang et&#x000A0;al., 2017</xref>). These sachets and pads have a few drawbacks. They may decrease productivity due to the hand placement of the sachet or pad into the package (<xref ref-type="bibr" rid="r40">Contreras et&#x000A0;al., 2018</xref>; <xref ref-type="bibr" rid="r133">Pereira de Abreu et&#x000A0;al., 2012</xref>). There is also a concern that sachets may pose a risk to consumers via disintegration, contamination, or unintentional consumption (<xref ref-type="bibr" rid="r40">Contreras et&#x000A0;al., 2018</xref>).</p><p>Antimicrobials can be incorporated into the packaging film by a method such as coextrusion of packaging films with the antimicrobials (<xref ref-type="table" rid="tab1">Table&#x000A0;1</xref>). Soysal et&#x000A0;al. (<xref ref-type="bibr" rid="r171">2015</xref>) investigated the effect of nisin, chitosan, potassium sorbate, or silver-substituted zeolite incorporated into low-density polyethylene (LDPE) on the physicochemical and microbiological quality of chicken drumsticks. The active packaging resulted in a lower level of total aerobic mesophilic bacteria, total coliform, mold, and yeast count on the product, with the chitosan-containing film being most successful in extending the shelf life and improving quality (<xref ref-type="bibr" rid="r171">Soysal et&#x000A0;al., 2015</xref>). Other methods of including antimicrobials in packaging films without affecting bioactivity are solvent compounding, electrospinning, and casting (<xref ref-type="bibr" rid="r172">Sung et&#x000A0;al., 2013</xref>). Plant extracts (e.g.,&#x000A0;rosemary extract), peptides, and nisin have been used as antimicrobial agents in active packaging systems (<xref ref-type="bibr" rid="r11">Arvanitoyannis and Stratakos, 2012</xref>). Ferrocinoa et&#x000A0;al. (<xref ref-type="bibr" rid="r59">2016</xref>) used nisin in antimicrobial packaging to retard the growth of total viable bacteria and lactic acid bacteria in refrigerated beef burgers, thus increasing the shelf life of the meat. Nanoscale silver has also been applied to fresh pork loin, inhibiting total bacterial growth (<xref ref-type="bibr" rid="r92">Kuulialaa et&#x000A0;al., 2015</xref>). Several manufacturers offer commercially available antimicrobial active packaging (<xref ref-type="bibr" rid="r55">Fang et&#x000A0;al., 2017</xref>).</p><table-wrap id="tab1"><label>Table 1.</label><caption><p>Summary of smart meat packaging technologies with respect to oxygen exposure, color stability, shelf-life extension, and associated microbial concerns.</p></caption><table frame="hsides" rules="groups"><colgroup><col align="left"/><col align="center"/><col align="center"/><col align="center"/><col align="center"/><col align="center"/></colgroup><thead><tr><th>Packaging Type</th><th align="center">Oxygen Exposure</th><th>Color Stability</th><th align="center">Shelf-Life Extension</th><th align="center">Key Microbial Concerns</th><th align="center">Notes</th></tr></thead><tbody><tr><td>Active packaging (Antiox)</td><td>Variable</td><td>Depends on film</td><td>Extended</td><td>Microbial growth inhibition</td><td>Enhanced quality with essential oils, chitosan, nisin, etc.</td></tr><tr><td>Edible films/coatings</td><td>Low to medium</td><td>Variable</td><td>Medium</td><td>Depends on film additives</td><td>Sustainable&#x02014;can deliver bioactive compounds</td></tr><tr><td>Nanotechnology packaging</td><td>Variable</td><td>Variable</td><td>Extended</td><td>Antimicrobial (e.g.,&#x000A0;AgNP)</td><td>Enhanced barrier, mechanical properties; toxicology debated</td></tr><tr><td>Intelligent packaging</td><td>N/A</td><td>N/A</td><td>Indirect</td><td>Detection of spoilage/pathogens</td><td>Includes sensors, RFID, TTI, freshness/pathogen indicators</td></tr></tbody></table><table-wrap-foot><fn><p>AgNP, silver nanoparticles; Antiox, antioxidant; N/A, not applicable; RFID, radio-frequency identification; TTI, time-temperature indicators.</p></fn></table-wrap-foot></table-wrap><p>Packaging can also be coated with a carrier of antimicrobial agents so that the agents can be released onto the surface of food through evaporation into the headspace (volatile substances) or migration into food (nonvolatile substances) through diffusion (<xref ref-type="bibr" rid="r39">Coma, 2008</xref>). The cast film method is often used with antimicrobials that cannot tolerate polymer processing temperatures or heat-sensitive antimicrobials, such as volatile chemicals (<xref ref-type="bibr" rid="r8">Appendini and Hotchkiss, 2002</xref>; <xref ref-type="bibr" rid="r50">Emamifar, 2011</xref>; <xref ref-type="bibr" rid="r172">Sung et&#x000A0;al., 2013</xref>; <xref ref-type="bibr" rid="r168">Sof&#x00131; et&#x000A0;al., 2018</xref>). Conventional coatings, including polyvinylidene chloride, polyvinyl alcohol (PVOH), and ethylene vinyl alcohol, are the most used in antimicrobial food-packaging films (<xref ref-type="bibr" rid="r86">Khaneghah et&#x000A0;al., 2018</xref>).</p></sec><sec id="sec3.2"><title>Antioxidant active packaging</title><p>High oxygen levels in meat packaging can accelerate microbial growth, lipid oxidation, changes in color and odor, and contribute to nutritional loss (<xref ref-type="bibr" rid="r67">G&#x000F3;mez-Estaca et al., 2014</xref>). Antioxidant active packaging can control the level of oxygen the product is exposed to, thus improving shelf life. Antioxidants scavenge oxygen, oxidative radical compounds, or metal ions from the food or the package headspace (<xref ref-type="bibr" rid="r107">McMillin, 2017</xref>). Antioxidant active packaging systems can be classified into 2 groups: 1) independent antioxidant devices and 2) antioxidant packaging materials (<xref ref-type="bibr" rid="r67">G&#x000F3;mez-Estaca et&#x000A0;al., 2014</xref>).</p><p>Independent devices can be sachets, pads, or labels added to conventional packaging. These devices contain oxygen scavengers, separated from meat. The most common oxygen scavengers are fine powders of iron and ferrous oxide, although ascorbic acid, sulfites, catechols, ligands, and enzymes such as glucose oxidase have also been used (<xref ref-type="bibr" rid="r26">Brody et&#x000A0;al., 2008</xref>). There are extensive reviews on the uses and applications of oxygen-scavenging packaging (<xref ref-type="bibr" rid="r27">Brody et&#x000A0;al., 2001</xref>; <xref ref-type="bibr" rid="r26">Brody et&#x000A0;al., 2008</xref>; <xref ref-type="bibr" rid="r148">Rooney, 2005</xref>; <xref ref-type="bibr" rid="r174">Suppakul et&#x000A0;al., 2003</xref>). Synthetic antioxidants such as butylated hydroxyanisole are successfully used in antioxidant packaging. However, consumers&#x02019; rejection of these synthetic compounds has resulted in a growing trend to use natural antioxidants (<xref ref-type="bibr" rid="r17">Barbosa-Pereira et&#x000A0;al., 2014</xref>; <xref ref-type="bibr" rid="r154">Sanches-Silva et&#x000A0;al., 2014</xref>; <xref ref-type="bibr" rid="r55">Fang et&#x000A0;al., 2017</xref>).</p><p>Alternative or &#x0201C;clean-label&#x0201D; additives have received considerable attention for maintaining shelf life in natural and organic ready-to-eat meats and controlling specific foodborne pathogens such as <italic>L. monocytogenes</italic> (<xref ref-type="bibr" rid="r20">Bodie et&#x000A0;al., 2023</xref>; <xref ref-type="bibr" rid="r19">Bodie et&#x000A0;al., 2024</xref>). Given their potential as food additives, it is not surprising that these alternative compounds would be attractive as packaging materials. Numerous combinations of natural antioxidants and films have been investigated. Chitosan and gelatin films with green tea extract, mango, and acerola pulps in starch films; marigold extract and barley husks in LDPE; pimento and oregano essential oils in milk protein films; palm fruit and cocoa/coffee in cassava starch films; and mustard meal in xanthan gum films have all demonstrated antioxidant capabilities (<xref ref-type="bibr" rid="r44">de Souza et&#x000A0;al., 2013</xref>). Green tea extract, oolong tea extract, and black tea extract incorporated into protein films all decreased lipid oxidation of pork wrapped in the films, with green tea extract films having the highest antioxidant activity (<xref ref-type="bibr" rid="r196">Yang et&#x000A0;al., 2016</xref>). These plant extracts and essential oils have become emphasized as an alternative to food packaging (<xref ref-type="bibr" rid="r68">Granato et&#x000A0;al., 2017</xref>; <xref ref-type="bibr" rid="r100">Lorenzo et&#x000A0;al., 2017</xref>; <xref ref-type="bibr" rid="r136">Poojary et&#x000A0;al., 2017</xref>; <xref ref-type="bibr" rid="r188">Vincekovi&#x00107; et&#x000A0;al., 2017</xref>). Essential oils often have a strong odor, so it is necessary to determine the least amount that can be used to achieve the desired effect without changing the organoleptic characteristics of the meat (<xref ref-type="bibr" rid="r201">Viuda-Martos et&#x000A0;al., 2008</xref>; <xref ref-type="bibr" rid="r159">Shen and Kamdem, 2015</xref>).</p></sec><sec id="sec3.3"><title>Health benefits</title><p>Active packaging films and coatings offer numerous benefits in support of human health and food quality. As discussed in the previous sections, opportunities to include antimicrobial compounds that restrict the proliferation of pathogenic organisms provide a public health safety attribute to package meat products. Similar approaches can also limit the growth of spoilage organisms and, in turn, the onset of spoilage and, ultimately, food waste. Incorporating active packaging is both an economic benefit to large-scale production by the food processor and extends shelf life for the retailer and the nutritive profile for consumers (<xref ref-type="bibr" rid="r185">Umaraw et&#x000A0;al., 2020</xref>; <xref ref-type="bibr" rid="r135">Petkoska et&#x000A0;al., 2021</xref>). Natural ingredients incorporated into packaging, such as herbs and spices, provide antimicrobial and/or antioxidant properties and serve as flavorings to add to sensory appeal and extend shelf life (<xref ref-type="bibr" rid="r185">Umaraw et&#x000A0;al., 2020</xref>). As more active packaging components are developed, many will likely exhibit multifunctional properties.</p><p>It is also possible more novel functions can be introduced through active packaging. Peptides and protein hydrolysates have been proposed as potential components of edible biodegradable active packaging that could extend shelf life and possess health benefits when consumed (<xref ref-type="bibr" rid="r182">Tkaczewska, 2020</xref>). Khin et&#x000A0;al. (<xref ref-type="bibr" rid="r188">2024</xref>) have suggested that bioactive compounds such as probiotics, prebiotics, and phenolic compounds could be incorporated into protein-based films and offer the means to maintain gastrointestinal health, decrease inflammation, and improve immune response. Phenolic compounds include phenolic acids, tannins, and lignans, as well as others that have been used in coating and films to improve oxidative stability and color but may also impart several health benefits such as being anticancer, anti-inflammatory, and antiallergic (Khin et&#x000A0;al., 2022). Prebiotics are nondigestible compounds that benefit the host by selecting beneficial gastrointestinal microorganisms such as <italic>Lactobacillus</italic> and <italic>Bifidobacterium</italic> (<xref ref-type="bibr" rid="r65">Gibson and Roberfroid, 1995</xref>). Initially this included only a few &#x003B2;-linked oligosaccharide polymers, such as fructooligosaccharides. Still, as a better understanding of the gastrointestinal tract microbiota through employment of molecular tools such as microbiome 16S ribosomal RNA gene sequencing is being explored, it is now becoming clear that there is greater range of prebiotic candidates including noncarbohydrate compounds (<xref ref-type="bibr" rid="r64">Gibson et&#x000A0;al., 2017</xref>; <xref ref-type="bibr" rid="r176">Swanson et&#x000A0;al., 2025</xref>). Certain prebiotic polymers can be incorporated into different films. Khin et&#x000A0;al. (2022) have proposed that including such bioactive compounds, if part of an edible film or coating, would help retain the viability of probiotic cultures in a particular food product. It is also possible that the presence of the prebiotic, these compounds could provide more direct benefits to the human gastrointestinal tract when the meat product is consumed.</p><p>Probiotics have been defined as viable organisms that, when consumed in sufficient quantities, provide health benefits to the host (<xref ref-type="bibr" rid="r76">Hill et&#x000A0;al., 2014</xref>). Probiotics have a long history in human health and are additives for animals to modulate immune function and serve as competitive exclusion cultures against foodborne pathogen colonization (<xref ref-type="bibr" rid="r176">Swanson et&#x000A0;al., 2025</xref>). Probiotics have been incorporated into certain films and coatings (Khin et&#x000A0;al., 2022). Better stability can be achieved by including a prebiotic that serves as a substrate for the probiotic as part of the coating, resulting in what is defined as a synbiotic (<xref ref-type="bibr" rid="r177">Swanson et&#x000A0;al., 2020</xref>; Khin et&#x000A0;al., 2022). More recently, postbiotics have emerged as biological additives that consist of inanimate cells and/or their components that provide a health advantage to the host (<xref ref-type="bibr" rid="r152">Salminen et&#x000A0;al., 2021</xref>). Whether such compounds could also be incorporated into packaging films and coatings remains to be determined. In general, further development of methods to retain the functionality of any of these biological agents will be needed to enhance their active components.</p></sec></sec><sec id="sec4"><title>Nanomaterial Packaging</title><p>Nanotechnology is based on creating materials on a nanometer scale. This miniaturized scale offers the opportunity to efficiently deliver multiple functionalities to meet practical and economic commercial demands (<xref ref-type="bibr" rid="r145">Ricke et&#x000A0;al., 2025b</xref>). Nanotechnology has been investigated to improve the functionality of food packaging (<xref ref-type="bibr" rid="r111">Mlalila et&#x000A0;al., 2016</xref>). Nanomaterials and edible coatings with added nanoparticles provide better preservation and quality maintenance of food products by modifying the physical and mechanical properties of packaging to improve their strength, durability, flexibility, and barrier properties (<xref ref-type="bibr" rid="r28">Bumbudsanpharoke et&#x000A0;al., 2015</xref>). Nanobased packaging material can be generally synthesized by incorporating the nanoparticles into traditional food-packaging materials or by fabricating nanocomposite multilayer packaging materials (<xref ref-type="bibr" rid="r184">Tsagkaris et&#x000A0;al., 2018</xref>). Arfat et&#x000A0;al. (<xref ref-type="bibr" rid="r10">2017</xref>) generated biocomposite films using fish skin gelatin and silver&#x02013;copper nanoparticles. These films had good mechanical strength, thermal stability, and good ultraviolet barrier properties as well as having antibacterial activity against both <italic>L. monocytogenes</italic> and <italic>S. typhimurium</italic>. Rostamzad et&#x000A0;al. (<xref ref-type="bibr" rid="r149">2016</xref>) developed a fish protein film with nanoclay and transglutaminase. The nanoclay improved the physical and mechanical properties of the film. A PLA-based film with nanoclay and nanocellulose reduced the oxygen and vapor transmission rates to 90% and 76%, respectively (<xref ref-type="bibr" rid="r183">Trifol et&#x000A0;al., 2016</xref>). Polypropylene nanocomposites incorporated with nanoclay reduced the oxygen and water vapor permeability by 22% and 33%, respectively, compared to neat polypropylene. In contrast, adding iron nanoparticles improved the oxygen and water vapor permeability by 55% and 77%, respectively, compared to neat polypropylene (<xref ref-type="bibr" rid="r85">Khalaj et&#x000A0;al., 2016</xref>). Nanoparticles can also increase the generation of reactive oxygen species that inhibit bacterial growth (<xref ref-type="bibr" rid="r162">Slavin et&#x000A0;al., 2017</xref>). Fasihnia et&#x000A0;al. (<xref ref-type="bibr" rid="r56">2018</xref>) prepared polyethylene nanocomposite films with added organoclay nanomaterials that exhibited significant activity against <italic>Staphylococcus aureus</italic> and <italic>Escherichia coli</italic>. PVOH-based films with fennel seed oil and cellulose nanoparticles improved antimicrobial and antioxidant activity (<xref ref-type="bibr" rid="r143">Ramesh and Radhakrishnan, 2019</xref>).</p><sec id="sec4.1"><title>Nanomaterials as packaging nanosensors</title><p>Nanosensors monitor the external and internal conditions of fresh and processed food products (<xref ref-type="bibr" rid="r31">Caon et&#x000A0;al., 2017</xref>). Zhai et&#x000A0;al. (<xref ref-type="bibr" rid="r199">2019</xref>) developed colorimetric hydrogen sulfide sensors made up of gellan gum-capped silver nanoparticles to indicate spoilage in chicken breast and silver carp. The sensor changes color from yellow to colorless when exposed to hydrogen sulfide. A starch-polyvinyl alcohol-based film containing zinc oxide nanoparticles is sensitive to pH and could be part of intelligent food packaging (<xref ref-type="bibr" rid="r79">Jayakumar et&#x000A0;al., 2019</xref>). A soluble soybean polysaccharide film with curcumin and silicon dioxide displayed good antibacterial activity and distinctive color changes due to changes in pH during shrimp spoilage (<xref ref-type="bibr" rid="r151">Salarbashi et&#x000A0;al., 2021</xref>).</p></sec><sec id="sec4.2"><title>Potential toxicological effects of nanoparticles</title><p>Unfortunately, some studies have indicated that nanoparticles may have toxicological effects on biological systems (<xref ref-type="bibr" rid="r47">Dimitrijevic et&#x000A0;al., 2015</xref>). The toxicity of nanoparticles depends on their type, concentration, duration of exposure, and sensitivity of the individual (<xref ref-type="bibr" rid="r47">Dimitrijevic et&#x000A0;al., 2015</xref>). Organic nanoparticles may increase bioavailability, which could lead to toxicity. Consequently, both in vivo and in vitro studies must be performed to ensure food safety (<xref ref-type="bibr" rid="r14">Ashfaq et&#x000A0;al., 2022</xref>). Numerous studies have been conducted on silver nanoparticles, which can cause neurotoxicity and genotoxicity and can deposit in the liver, kidney, testicles, and brain; however, the migration of silver nanoparticles up to this level in food is very low (<xref ref-type="bibr" rid="r3">Ahmad et&#x000A0;al., 2021</xref>). Some nanoclay has been shown to cause cytotoxicity on long-term exposure (<xref ref-type="bibr" rid="r16">Bandyopadhyay and Ray, 2019</xref>). More studies must be done on migration, toxicity, and permissible limit of nanoparticles in food packaging that come in direct contact with food. Nevertheless, nanotechnology appears to be the front runner in novel food-packaging research.</p></sec></sec><sec id="sec5"><title>Intelligent Packaging</title><p>Intelligent packaging usually refers to sensors or indicators that signal or initiate a needed change in the package environment or package (<xref ref-type="table" rid="tab2">Table&#x000A0;2</xref>). In Europe, the legal definition of &#x0201C;intelligent food contact materials and articles&#x0201D; is &#x0201C;materials and articles that monitor the condition of packaged food or the environment surrounding the food&#x0201D; (<xref ref-type="bibr" rid="r54">European Union, 2011</xref>). Yam et&#x000A0;al. (<xref ref-type="bibr" rid="r194">2005</xref>) proposed a more general definition, which is &#x0201C;a packaging system that is capable of carrying out intelligent functions (such as detecting, sensing, recording, tracing, communicating, and applying scientific logic) to facilitate decision-making to extend shelf life, enhance safety, improve quality, provide information, and warn about possible problems.&#x0201D; The devices used in intelligent packaging include barcodes, radio-frequency identification (RFID) tags, time-temperature indicators (TTI), gas indicators, freshness or microbial growth indicators, and pathogen indicators (<xref ref-type="bibr" rid="r55">Fang et&#x000A0;al., 2017</xref>).</p><table-wrap id="tab2"><label>Table 2.</label><caption><p>Summary of intelligent packaging technologies used in meat packaging, highlighting their functions and applications for monitoring quality, safety, and freshness.</p></caption><table frame="hsides" rules="groups"><colgroup><col align="left"/><col align="center"/><col align="center"/><col align="center"/></colgroup><thead><tr><th>Device Type</th><th align="center">Function</th><th align="center">Target</th><th align="center">Examples/Notes</th></tr></thead><tbody><tr><td>Barcodes/QR codes</td><td>Information display</td><td>Product tracking and consumer info</td><td>1D/2D codes; batch info, storage instructions</td></tr><tr><td>RFID tags</td><td>Real-time data collection</td><td>Traceability, inventory, cold chain</td><td>Low-frequency tags ideal for meat (high moisture)</td></tr><tr><td>TTI</td><td>Cold chain monitoring</td><td>Storage temperature history</td><td>Color change to show past temperature abuse</td></tr><tr><td>Gas indicators</td><td>Internal gas composition monitoring</td><td>O<sub>2</sub>, CO<sub>2</sub>, H<sub>2</sub>S</td><td>Color change; detects leaks, spoilage gases</td></tr><tr><td>Freshness indicators</td><td>Spoilage metabolite detection</td><td>Amines, acids, sulfides</td><td>pH-sensitive dyes; change with microbial metabolites</td></tr><tr><td>Pathogen indicators/biosensors</td><td>Pathogen detection</td><td><italic>E. coli</italic>, <italic>Salmonella</italic>, <italic>Listeria</italic></td><td>Color change, barcode disabling, antibody-based</td></tr></tbody></table><table-wrap-foot><fn><p>1D, 1-dimensional; 2D, 2-dimensional; CO<sub>2</sub>, carbon dioxide; H<sub>2</sub>S, hydrogen sulfide; O<sub>2</sub>, oxygen; QR, quick response; RFID, radio-frequency identification; TTI, time-temperature indicators.</p></fn></table-wrap-foot></table-wrap><sec id="sec5.1"><title>Barcodes</title><p>A barcode is an optical machine-readable symbol relating to the object to which it is attached. They are cheap, easy to use, and widely used (<xref ref-type="bibr" rid="r103">Manthou and Vlachopoulou, 2001</xref>). The universal product code barcode consists of a pattern of bars and spaces, representing 12 digits of data that contain limited information such as manufacturer identification number and item number (<xref ref-type="bibr" rid="r194">Yam et&#x000A0;al., 2005</xref>). Barcodes can be classified as 1-dimensional (1D) or 2-dimensional (2D). The 1D barcode is the familiar pattern of spaces and bars (<xref ref-type="bibr" rid="r119">M&#x000FC;ller and Schmid, 2019</xref>). 2D bar codes contain more information including food packing date, batch/lot number, package weight, nutritional information, cooking instructions, and the website address of the food manufacturer and are readable by smartphones. These are the familiar quick response (i.e., QR) codes (<xref ref-type="bibr" rid="r55">Fang et&#x000A0;al., 2017</xref>).</p></sec><sec id="sec5.2"><title>Radio-frequency identification tags</title><p>An RFID tag has a significantly larger data storage capacity, is noncontact, can gather real-time data out of the line of sight, and the data can penetrate nonmetallic materials (<xref ref-type="bibr" rid="r108">Mennecke and Townsend, 2005</xref>). However, RFID tags are costly compared to barcodes and require a more powerful electronic information network. Depending on the situation, RFID and barcode data carriers will likely continue to be used in the meat industry alone or in combination (<xref ref-type="bibr" rid="r194">Yam et&#x000A0;al., 2005</xref>).</p><p>An RFID tag contains a tiny transponder and antenna with a unique number. The reader emits radio waves to capture data from the RFID tag, which are then passed to a computer for analysis and decision-making (<xref ref-type="bibr" rid="r191">Want, 2004</xref>). Low-frequency tags are cheaper, use less power, and are better able to penetrate nonmetallic objects, making these the best for use with meat products, primarily if the meat itself might hide the tags. They are also ideal for close-range scanning of objects with high water content (<xref ref-type="bibr" rid="r84">Kerry et&#x000A0;al., 2006</xref>). The benefits of using RFID tags in the meat industry include traceability, inventory management, labor-saving costs, security, and promotion of quality and safety (<xref ref-type="bibr" rid="r117">Mousavi, et&#x000A0;al. 2002</xref>).</p></sec><sec id="sec5.3"><title>Time-temperature indicators</title><p>A TTI is defined as &#x0201C;a simple, inexpensive device attached to shipping containers or individual consumer packages that can show measurable, time-temperature dependent changes that reflect the full or partial temperature history of a food product&#x0201D; (<xref ref-type="bibr" rid="r180">Taoukis and Labuza, 1989</xref>). The basic operation principles of TTI are to alert processors and consumers when temperature conditions reduce quality or may result in food safety concerns (<xref ref-type="bibr" rid="r166">Smolander et&#x000A0;al., 2004</xref>; <xref ref-type="bibr" rid="r84">Kerry et&#x000A0;al., 2006</xref>; <xref ref-type="bibr" rid="r179">Taoukis and Labuza, 2003</xref>). Commercially available TTI include critical temperature indicators (show exposure above [or below] a reference temperature), partial history indicators (indicate that a product has been exposed to a temperature sufficient to cause a change in product quality or safety), and full history indicators (a continuous temperature-dependent response throughout a product&#x02019;s history) (<xref ref-type="bibr" rid="r204">Biji et al, 2015</xref>).</p></sec><sec id="sec5.4"><title>Gas indicators</title><p>After the meat is packaged, the gas composition within the package changes due to the activity of the food, the package nature, gas generation by spoilage microorganisms, or gas transmission through the packaging material or leaks (<xref ref-type="bibr" rid="r194">Yam et&#x000A0;al., 2005</xref>). Gas indicators are small devices that can be part of the package label or printed on the packaging film. Usually the gas indicator changes color to reflect the gas composition changes (<xref ref-type="bibr" rid="r55">Fang et&#x000A0;al., 2017</xref>). The most common gas indicators detect oxygen, since oxygen is the most deleterious to safety and quality because it induces oxidative rancidity, color change, and microbial spoilage. For instance, the Ageless Eye<sup>&#x000AE;</sup> oxygen indicator produced by Mitsubishi Gas Chemical Company can be inserted inside the container. When the oxygen content exceeds 0.5%, the indicator changes color from pink to blue (<xref ref-type="bibr" rid="r55">Fang et&#x000A0;al., 2017</xref>). Oxygen indicators have also been used to detect improper sealing and quality deterioration of modified atmospheric packaging in fresh beef (<xref ref-type="bibr" rid="r4">Ahvenainen et&#x000A0;al., 1997</xref>; <xref ref-type="bibr" rid="r163">Smiddy et&#x000A0;al., 2002</xref>). Carbon dioxide, water vapor, ethanol, hydrogen sulfide, and other gas indicators have also been reported (<xref ref-type="bibr" rid="r55">Fang et&#x000A0;al., 2017</xref>).</p></sec><sec id="sec5.5"><title>Freshness indicators</title><p>Freshness indicators show the actual spoilage of products (<xref ref-type="bibr" rid="r133">Pereira de Abreu et&#x000A0;al., 2012</xref>). These indicators are based on the knowledge of metabolites, specifically associated with spoilage bacteria, packaging type, and storage conditions of the meat product (<xref ref-type="bibr" rid="r55">Fang et&#x000A0;al., 2017</xref>). The major quality-indicating metabolites produced by these bacteria include glucose, organic acids (e.g.,&#x000A0;lactic acid), ethanol, volatile nitrogen compounds, biogenic amines (e.g.,&#x000A0;tyramine, cadaverine, putrescine, histamine), carbon dioxide, adenosine triphosphate degradation products, and sulfuric compounds. The presence of these compounds in the package result in a color change in the indicator (<xref ref-type="bibr" rid="r165">Smolander, 2003</xref>).</p><p>Various freshness indicators have been developed (<xref ref-type="bibr" rid="r72">Han et&#x000A0;al., 2005</xref>; <xref ref-type="bibr" rid="r84">Kerry et&#x000A0;al., 2006</xref>; <xref ref-type="bibr" rid="r165">Smolander, 2003</xref>). One of the most common freshness indicators in meat packaging is bromothymol blue pH dye, which monitors the carbon dioxide produced by microbial growth (<xref ref-type="bibr" rid="r203">Smolander et al, 1997</xref>). Other pH dyes that serve the same purpose are xylenol blue, bromocresol purple, bromocresol green, cresol red, phenol red, methyl red, and alizarin (<xref ref-type="bibr" rid="r77">Horan, 2000</xref>). Other metabolites, including sulfur dioxide, ammonium, volatile amines, and organic acids, have been used as target monitoring molecules using pH-sensitive indicators (<xref ref-type="bibr" rid="r165">Smolander, 2003</xref>). Many spoilage bacteria produce hydrogen sulfide, which is known to bind to myoglobin to produce a green pigment (sulfomyoglobin). An indicator for this has been developed that explicitly detects hydrogen sulfide even in the presence of nitrogen and carbon dioxide (<xref ref-type="bibr" rid="r167">Smolander et&#x000A0;al., 2002</xref>).</p></sec><sec id="sec5.6"><title>Pathogen indicators and biosensors</title><p>Indicators to detect pathogens directly have also been developed. These devices are biosensors that can detect, record, and transmit information on biochemical reactions specific to the pathogens (<xref ref-type="bibr" rid="r194">Yam et&#x000A0;al., 2005</xref>). These devices have a bioreceptor, an organic or biological material such as an enzyme, antigen, microorganism, hormone, or nucleic acid, that recognizes a target analyte coupled with an electrochemical, optical, or calorimetric transducer (<xref ref-type="bibr" rid="r194">Yam et&#x000A0;al., 2005</xref>). These pathogen indicators change color in the food package to warn consumers/retailers that the food must not be consumed (<xref ref-type="bibr" rid="r194">Yam et&#x000A0;al., 2005</xref>).</p><p>Foodborne pathogen detection has been a targeted area for research and commercial development. SIRA Technologies (California, USA) has a commercially available pathogen indicator called Food Sentinel System<sup>&#x02122;</sup> (SIRA Technologies, 2019). Antibodies specific to the target pathogen (e.g.,&#x000A0;<italic>Salmonella</italic> spp., <italic>E. coli</italic> O157:H7, or <italic>L. monocytogenes</italic>) are attached to a membrane that is part of the barcode. If the pathogen is present a localized dark bar forms over the barcode, making it impossible to scan the barcode. Another pathogen indicator is Toxin Guard<sup>&#x02122;</sup> developed by Toxin Alert (Ontario, Canada), which has biochemical sensors incorporating antibodies in a polyethylene-based plastic packaging. The system can detect <italic>Salmonella</italic> spp., <italic>Campylobacter</italic> spp., <italic>E. coli</italic>, and <italic>Listeria</italic> spp. (<xref ref-type="bibr" rid="r18">Bodenhamer, 2000</xref>). Yousef&#x00131; et&#x000A0;al. (<xref ref-type="bibr" rid="r198">2018</xref>) developed a transparent sensing surface that generated a fluorescent signal when encountering a specific bacterium of interest, allowing real-time monitoring without disturbing the packaged project. They accomplished this by attaching an <italic>E. coli</italic>-specific RNA-cleaving fluorogenic DNA-enzyme probe microarrays to a transparent cyclo-olefin polymer film. While initially specific to <italic>E. coli</italic>, this technology could certainly be adapted to other foodborne pathogens and eventually to indicator organisms for the onset of spoilage.</p><p>Intelligent packaging is expensive and will only be used if the technology increases sales or reduces waste (<xref ref-type="bibr" rid="r74">Heising et&#x000A0;al., 2014</xref>; <xref ref-type="bibr" rid="r186">Vanderroost, et&#x000A0;al., 2014</xref>). Although customers say they want better quality and more product information, most will not pay more for them (<xref ref-type="bibr" rid="r119">M&#x000FC;ller and Schmid, 2019</xref>). Promoting intelligent packaging to consumers to increase confidence in the safety of the systems and spelling out the benefits of intelligent packaging could increase their willingness to pay more for this packaging (<xref ref-type="bibr" rid="r169">Sohail et&#x000A0;al., 2018</xref>). However, further advances in polymer extrusion technologies are needed to accommodate introduction of these types of packaging materials (<xref ref-type="bibr" rid="r6">Alt&#x00131;parmak et&#x000A0;al., 2022</xref>; <xref ref-type="bibr" rid="r137">Prabha et&#x000A0;al., 2021</xref>; <xref ref-type="bibr" rid="r200">Zhou et&#x000A0;al., 2021</xref>). In addition, further technological developments with nanotechnology, 3D printing, and more advanced polymer composites may help decrease cost, but consumer acceptance may still be challenging.</p></sec></sec><sec id="sec6"><title>Conclusions and Future Directions</title><p>Packaging technologies for meat products continue to evolve from the more traditional plastic types of films to retain qualities such as color and freshness, as it is being realized that these types of packaging material present environmental challenges. Edible films and coatings not only offer a more environmentally friendly approach for packaging materials but also have the potential to be considerably modified. For example, the bacterial production of extracellular cellulose can avoid some of the extraction and purification requirements of the more conventional plant-based sources of cellulose. As more is understood at the molecular level of cellulose generation by these organisms, the opportunity to introduce genetic modifications that alter cellulose fibrils is possible. These modifications could create very specific types of cellulose polymers that exhibit certain functions that further accentuate the active nature of the packaging material or film to meet more targeted applications. Chitosan, lipid, and protein-based films and coatings possess several contrasting properties that can serve different roles for packaging composites. Introducing biotics such as prebiotics and probiotics into protein coatings has intriguing possibilities for delivering health benefits and extending shelf life. Equally important is the idea that some protein and lipid materials represent waste byproducts generated during meat processing that can be repurposed without requiring environmentally unfriendly disposal destinations.</p><p>Smart packaging represents tremendous possibilities for creating more interactive packaging that will provide detailed real-time information to the consumer and the retailer. There is the eventual potential for the meat product to be traced back to the animal operation (<xref ref-type="bibr" rid="r41">Crandall et&#x000A0;al., 2013</xref>). Key information could include a wide range of information such as freshness indicators, detection sensors for pathogens and spoilage organisms, early warning of chemical changes indicating the onset of spoilage, and changes in packaging conditions. Ideally, access to as much of this information as possible would be the goal. The challenge is developing noninvasive packaging systems with built-in sensors that can provide easily visualized outcomes that allow simultaneous and instant interpretation. This will require further development of packaging materials that can retain optimal packaging properties but have sufficient flexibility to be modified to become platforms for sophisticated sensor arrays. The cost of such intelligent packaging is likely still prohibitive, but, as further advancements are made in nanotechnology and composite packaging material, the economics for these packaging materials may become more favorable. However, packaging properties, such as barriers to oxygen and water vapor as well as thermal resistance, must be considered in development of packaging materials (<xref ref-type="bibr" rid="r121">Nasution et&#x000A0;al., 2023</xref>; <xref ref-type="bibr" rid="r192">Wongphan et&#x000A0;al., 2024</xref>). Likewise, improving the energy efficiency of polymer extrusion processing requires further research (<xref ref-type="bibr" rid="r202">Abeykoon et&#x000A0;al., 2021</xref>). Ultimately, the goal would be to extend the shelf life of fresh meat beyond current practices and to be able to monitor those meat products closely during storage by collecting as much information in real time as possible.</p></sec></body><back><sec id="sec7"><title>Conflict of Interest</title><p>Authors have no conflicts of interest.</p></sec><ack><title>Acknowledgments</title><p>EGO was supported by US Department of Agriculture Hatch grant under the project AAI9572.</p></ack><sec id="sec8"><title>Author Contribution</title><p>Conceptualization: DKD, JFL, and SCR; project administration: DKD, JFL, and SCR; software: EGO; supervision: DKD, JFL, and SCR; validation: DKD, CAO, JFL, EGO, and SCR; visualization: EGO; writing&#x02014;original draft: DKD, CAO, JFL, EGO, and SCR; and writing&#x02014;review and editing: DKD, CAO, JFL, EGO, and SCR.</p></sec><ref-list><title>Literature Cited</title><ref id="r202"><mixed-citation publication-type="journal"><person-group person-group-type="author"><string-name><surname>Abeykoon</surname>, <given-names>C.</given-names></string-name>, <string-name><given-names>A.</given-names> <surname>McMillan</surname></string-name>, and <string-name><given-names>B. 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