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<front>
<journal-meta>
<journal-id journal-id-type="pmc">JPM</journal-id>
<journal-id journal-id-type="nlm-ta">JPM</journal-id>
<journal-id journal-id-type="publisher-id">JPM</journal-id>
<journal-title-group>
<journal-title>Journal of Polymer Materials</journal-title>
</journal-title-group>
<issn pub-type="epub">0976-3449</issn>
<issn pub-type="ppub">0973-8622</issn>
<publisher>
<publisher-name>Tech Science Press</publisher-name>
<publisher-loc>USA</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">59156</article-id>
<article-id pub-id-type="doi">10.32604/jpm.2024.059156</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Review</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Recent Advancements in Nanocomposites-Based Antibiofilm Food Packaging</article-title>
<alt-title alt-title-type="left-running-head">Recent Advancements in Nanocomposites-Based Antibiofilm Food Packaging</alt-title>
<alt-title alt-title-type="right-running-head">Recent Advancements in Nanocomposites-Based Antibiofilm Food Packaging</alt-title>
</title-group>
<contrib-group>
<contrib id="author-1" contrib-type="author">
<name name-style="western"><surname>Padhan</surname><given-names>Bandana</given-names>
</name><xref ref-type="aff" rid="aff-1">1</xref><xref ref-type="fn" rid="fn1"><sup>#</sup></xref></contrib>
<contrib id="author-2" contrib-type="author">
<name name-style="western"><surname>Patel</surname><given-names>Rajkumar</given-names>
</name><xref ref-type="aff" rid="aff-2">2</xref><xref ref-type="fn" rid="fn1"><sup>#</sup></xref></contrib>
<contrib id="author-3" contrib-type="author">
<name name-style="western"><surname>Bhowmik</surname><given-names>Priyanka</given-names>
</name><xref ref-type="aff" rid="aff-3">3</xref></contrib>
<contrib id="author-4" contrib-type="author">
<name name-style="western"><surname>Roy</surname><given-names>Ananya</given-names>
</name><xref ref-type="aff" rid="aff-1">1</xref></contrib>
<contrib id="author-5" contrib-type="author" corresp="yes">
<name name-style="western"><surname>Das</surname><given-names>Joyjyoti</given-names>
</name><xref ref-type="aff" rid="aff-1">1</xref><email>jjd0007@gmail.com</email></contrib>
<contrib id="author-6" contrib-type="author">
<name name-style="western"><surname>Yu</surname><given-names>Yong</given-names>
</name><xref ref-type="aff" rid="aff-4">4</xref><xref ref-type="aff" rid="aff-5">5</xref></contrib>
<contrib id="author-7" contrib-type="author" corresp="yes">
<name name-style="western"><surname>Patel</surname><given-names>Madhumita</given-names>
</name><xref ref-type="aff" rid="aff-6">6</xref><email>madhurk29@gmail.com</email></contrib>
<aff id="aff-1"><label>1</label><institution>Department of Biotechnology, School of Life Science and Biotechnology, Adamas University</institution>, <addr-line>Kolkata, 700 126, West Bengal</addr-line>, <country>India</country></aff>
<aff id="aff-2"><label>2</label><institution>Integrated Science and Engineering Division (ISED), Underwood International College, Yonsei University</institution>, <addr-line>Incheon, 21983, Republic</addr-line> <country>of Korea</country></aff>
<aff id="aff-3"><label>3</label><institution>Department of Biological Sciences, School of Life Science and Biotechnology, Adamas University</institution>, <addr-line>Kolkata</addr-line>, <country>700</country> <addr-line>126, West Bengal</addr-line>, <country>India</country></aff>
<aff id="aff-4"><label>4</label><institution>Key Laboratory of Equipment and Informatization in Environment Controlled Agriculture, Ministry of Agriculture</institution>, <addr-line>Hangzhou, 310058</addr-line>, <country>China</country></aff>
<aff id="aff-5"><label>5</label><institution>College of Biosystems Engineering and Food Science, Zhejiang University</institution>, <addr-line>Hangzhou, 310058</addr-line>, <country>China</country></aff>
<aff id="aff-6"><label>6</label><institution>Department of Chemistry and Nanoscience, Ewha Womans University</institution>, <addr-line>Seodaemun-gu, Seoul, 03760, Republic</addr-line> <country>of Korea</country></aff>
</contrib-group>
<author-notes>
<corresp id="cor1"><label>&#x002A;</label>Corresponding Authors: Joyjyoti Das. Email: <email>jjd0007@gmail.com</email>; Madhumita Patel. Email: <email>madhurk29@gmail.com</email></corresp>
<fn id="fn1">
<p><sup>#</sup>Contributed equally to this paper</p>
</fn>
</author-notes>
<pub-date date-type="collection" publication-format="electronic">
<year>2025</year></pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>11</day>
<month>07</month>
<year>2025</year></pub-date>
<volume>42</volume>
<issue>2</issue>
<fpage>411</fpage>
<lpage>433</lpage>
<history>
<date date-type="received">
<day>29</day>
<month>9</month>
<year>2024</year>
</date>
<date date-type="accepted">
<day>20</day>
<month>11</month>
<year>2024</year>
</date>
</history>
<permissions>
<copyright-statement>&#x00A9; 2025 The Authors.</copyright-statement>
<copyright-year>2025</copyright-year>
<copyright-holder>Published by Tech Science Press.</copyright-holder>
<license xlink:href="https://creativecommons.org/licenses/by/4.0/">
<license-p>This work is licensed under a <ext-link ext-link-type="uri" xlink:type="simple" xlink:href="https://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution 4.0 International License</ext-link>, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
</license>
</permissions>
<self-uri content-type="pdf" xlink:href="TSP_JPM_59156.pdf"></self-uri>
<abstract>
<p>The food industry prioritizes food safety throughout the entire production process. This involves closely monitoring and evaluating all potential sources of biological or chemical contamination, starting from entering raw materials into the production chain and continuing to the final product. Biofilms on food surfaces or containers can harbor dangerous pathogens, such as <italic>Listeria monocytogenes</italic>. Therefore, it is essential to continuously manage microbial contamination on food contact surfaces to prevent foodborne infections. Recently, there has been increasing interest in using nanomaterials as surface coatings with antimicrobial properties in the food industry, especially since traditional disinfectants or antibiotics may contribute to developing resistance. However, the use of antibiofilm materials for long-term food storage remains underexplored, and there is a notable lack of focused reviews on nanomaterial-based antibiofilm coatings specifically for long-term food preservation. This review aims to consolidate recently reported nanoparticle-based antibiofilm food packaging materials. We discuss the effectiveness of various metal and metal oxide nanoparticles and biopolymer nanocomposites in combating biofilms. Additionally, we highlight the growing importance of biodegradable nanocomposite materials for antibiofilm food packaging. Furthermore, we explore the mechanisms of action, processing methods, and safety aspects of these nanomaterials being developed for food packaging applications.</p>
</abstract>
<kwd-group kwd-group-type="author">
<kwd>Antibiofilm</kwd>
<kwd>metal nanoparticles</kwd>
<kwd>metal oxide nanoparticle</kwd>
<kwd>biopolymer nanocomposites</kwd>
<kwd>food packaging</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<sec id="s1">
<label>1</label>
<title>Introduction</title>
<p>Food packaging is crucial in safeguarding food from spoilage and preserving its quality and shelf life. However, traditional packaging materials, primarily derived from petrochemicals, can have adverse effects on both human well-being and the environment [<xref ref-type="bibr" rid="ref-1">1</xref>,<xref ref-type="bibr" rid="ref-2">2</xref>]. Biobased packaging materials offer a promising solution to replace petrochemical-based packaging. These materials, derived from sustainable sources like plants, possess desirable properties for food packaging applications [<xref ref-type="bibr" rid="ref-3">3</xref>]. Nanomaterials, including nanoparticles and nanocomposites, are also being investigated for their potential applications in food packaging. These materials can enhance mechanical properties, improve barrier performance, and provide antimicrobial benefits. For instance, nanocomposites based on biobased polymers reinforced with nanoparticles can offer improved protection against oxygen and moisture, thereby extending the freshness and durability of processed food. Based on their objectives and functional requirements, food packaging can be categorized as passive packaging (for maintaining thermal stability and mechanical strength), active packaging (utilizing antimicrobial compounds, oxygen or free radical scavengers), intelligent or smart packaging (incorporating time-temperature and gas indicators), and sustainable or green packaging, which addresses environmental pollution concerns [<xref ref-type="bibr" rid="ref-4">4</xref>,<xref ref-type="bibr" rid="ref-5">5</xref>].</p>
<p>Biofilms are communities of bacteria that adhere to surfaces. They are not simply collections of individual bacteria, but rather complex populations with diverse gene expression profiles that contribute to their ecological success [<xref ref-type="bibr" rid="ref-6">6</xref>,<xref ref-type="bibr" rid="ref-7">7</xref>]. Biofilm formation relies on quorum sensing, a process of intercellular communication. During biofilm formation, individual cells aggregate on a surface and attach to extracellular polymeric substances (EPS). Bacterial biofilms make bacteria resistant to many antibiotics because the drugs cannot penetrate the biofilm structure [<xref ref-type="bibr" rid="ref-8">8</xref>]. As a result, biofilms are implicated in numerous bacterial diseases. Biofilm formation on medical devices such as implants, catheters, and dialysis equipment can be particularly problematic in hospital settings. Nanotechnology can be utilized to encapsulate or deliver quorum sensing inhibitors that disrupt the signaling pathways involved in biofilm formation, thereby preventing microorganisms from coordinating the formation of biofilms. Furthermore, nanotechnology-based biosensors integrated into food packaging can detect the presence and growth of biofilms [<xref ref-type="bibr" rid="ref-9">9</xref>].</p>
<p>In recent years, there has been a growing interest in the unique physicochemical properties of nanocomposites with antimicrobial properties in food packaging. Many review reports have primarily focused on the use of functional biopolymer-based nanocomposites [<xref ref-type="bibr" rid="ref-10">10</xref>], inorganic nanoparticles [<xref ref-type="bibr" rid="ref-11">11</xref>], and metal oxides [<xref ref-type="bibr" rid="ref-12">12</xref>] in food packaging. Recently, Qi et al. investigated the application of composite nanomaterials in addressing biofilm formation in the medical industry. They discussed the potential effectiveness of organic, inorganic, and organic&#x2013;inorganic hybrid nanocomposites in traditional antibiofilm treatments as well as innovative phototherapy methods [<xref ref-type="bibr" rid="ref-13">13</xref>]. Jamwal et al. investigated the potential risks of using nanomaterials in food packaging while underscoring the necessity for continued advancements in this area [<xref ref-type="bibr" rid="ref-14">14</xref>]. Mishra et al. concentrated on biopolymer blends, biodegradable bio-nanocomposite materials, and the synthesis and characterization techniques currently employed in smart food packaging [<xref ref-type="bibr" rid="ref-15">15</xref>]. Their study highlighted the challenges hindering the widespread adoption of biopolymer nanocomposites and explored future opportunities for developing sustainable and innovative food packaging solutions. Similarly, Brandelli explored the role of nanotechnology in food packaging, particularly the use of nanostructured materials to produce packaging with antimicrobial properties [<xref ref-type="bibr" rid="ref-16">16</xref>]. The study emphasized how nanostructures can serve as carriers for natural antimicrobials, showcasing recent research demonstrating their potential to enhance food safety and extend shelf life. While several reports have been published, there is a lack of information on using nanocomposites to combat biofilm-forming microbes in food packaging applications.</p>
<p>In this review, we discuss the importance of nanotechnology-based approaches. We thoroughly discuss the effectiveness of nanoparticles made from silver, selenium, and metal oxides as antibiofilm agents. Finally, it highlights the growing popularity of biopolymer nanocomposites as antibiofilm materials for food packaging. By summarizing the application of each composite in different food systems, this review provides valuable information to food scientists for the development of innovative food packaging materials.</p>
</sec>
<sec id="s2">
<label>2</label>
<title>Strategies for Controlling Biofilm in the Food Industry</title>
<p>The food industry faces major challenges from biofilm-forming microorganisms, which not only spoil food and cause foodborne illnesses but also show high antibiotic resistance and harbor virulent factors [<xref ref-type="bibr" rid="ref-17">17</xref>]. This section describes the various strategies adopted by the food industry to control biofilm development. To combat foodborne illnesses, it is essential to prevent biofilm formation by regularly cleaning surfaces with strong chemical disinfectants like hypochlorites, quaternary ammonium compounds, peroxides, aldehydes, and phenols [<xref ref-type="bibr" rid="ref-18">18</xref>]. Additionally, the industry must adopt strategies to regulate microbial signaling pathways, disrupt mature biofilms using bacteriophages, and apply anti-quorum sensing (QS) compounds, matrix-degrading enzymes, and diguanylate cyclase inhibitors as antibiofilm agents. Anti-QS agents, such as those limiting N-acyl homoserine lactones (AHLs), are particularly effective. Moreover, eco-friendly antibiofilm coatings, nanotechnology, disinfectants, surfactants, essential oils, and non-thermal plasma are necessary to prevent biofilm formation. Addressing drug resistance and reducing excessive antibiotic use are crucial to combat persistent biofilms [<xref ref-type="bibr" rid="ref-19">19</xref>] (<xref ref-type="fig" rid="fig-7">Scheme 1</xref>). While conventional biofilm control strategies have several intrinsic limitations, nanotechnology-empowered strategies for food preservation have started taking center stage in recent times due to their myriad benefits. These have been discussed at length in the subsequent section.</p>
<fig id="fig-7">
<label>Scheme 1</label>
<caption>
<title>Biofilm control strategies employed in the food industry</title>
</caption>
<graphic mimetype="image" mime-subtype="tif" xlink:href="JPM_59156-SC01.tif"/>
</fig>
<sec id="s2_1">
<label>2.1</label>
<title>Nanotechnology to Manage Biofilm Formation</title>
<p>Researchers have been exploring the use of nanotechnology to combat bacterial infections caused by biofilms. Nanoparticles have shown great promise in fighting these infections, and research in this field is rapidly growing. These nanoparticles possess antimicrobial properties, effectively preventing the growth of biofilm-forming microorganisms. They can be integrated into packaging materials or applied as surface coatings to prevent biofilm formation actively. Biosensors can detect specific biofilm-related molecules, providing real-time feedback, allowing for actions such as alerting consumers or signaling the need for package replacement. Nanoscale surface modifications offer a viable approach to deter biofilm adhesion on food packaging by altering surface properties, making them less conducive to microorganism adhesion. Examples include nanostructured coatings, nanotextured surfaces, or hydrophilic/hydrophobic patterning, which repel biofilm-forming microorganisms [<xref ref-type="bibr" rid="ref-20">20</xref>]. Furthermore, nanocarriers can deliver biofilm-inhibiting agents or antimicrobial compounds directly to packaging surfaces, providing sustained antimicrobial effects and preventing biofilm formation over time [<xref ref-type="bibr" rid="ref-21">21</xref>]. The antimicrobial effectiveness of metal ions supported on nanostructures stems from their small size and high surface area, allowing enhanced interaction with bacteria. Their action is linked to reactive oxygen species production, causing DNA damage and oxidative stress in cells. Bacterial polysaccharides attract metal cations through electrostatic attraction, leading to changes in cell membrane structure and permeability. Metal ions on nanostructures can impair protein function through protein carbonylation, causing cellular damage. Additionally, metal oxides and ions disrupt DNA replication and cell division, impacting bacterial signal transduction (<xref ref-type="fig" rid="fig-8">Scheme 2</xref>) [<xref ref-type="bibr" rid="ref-22">22</xref>]. Certain nanoparticles such as silver, selenium, metal oxide, and biopolymeric nanomaterials improve the treatment efficacy. The following subsections describe the different categories of antibiofilm nanomaterials and their merits and limitations.</p>
<fig id="fig-8">
<label>Scheme 2</label>
<caption>
<title>Mechanism of action of nanomaterials used for food packaging</title>
</caption>
<graphic mimetype="image" mime-subtype="tif" xlink:href="JPM_59156-SC02.tif"/>
</fig>
<sec id="s2_1_1">
<label>2.1.1</label>
<title>Silver Nanoparticles against Biofilm</title>
<p>Silver nanoparticles (AgNPs) possess strong antimicrobial properties against various microbes, including those commonly found in biofilms [<xref ref-type="bibr" rid="ref-23">23</xref>]. Incorporating AgNPs into food packaging materials such as films or coatings can help prevent biofilm formation and reduce bacterial growth [<xref ref-type="bibr" rid="ref-24">24</xref>]. AgNPs disrupt bacterial adhesion and growth, inhibiting biofilm formation and maintaining the safety and quality of packaged food products [<xref ref-type="bibr" rid="ref-23">23</xref>]. The use of AgNPs against biofilm-forming microorganisms is outlined in <xref ref-type="table" rid="table-1">Table 1</xref>.</p>
<table-wrap id="table-1">
<label>Table 1</label>
<caption>
<title>Application of silver nanoparticles for antibiofilm food packaging</title>
</caption>
<table frame="hsides">
<colgroup>
<col align="left"/>
<col align="left"/>
<col align="left"/>
<col align="left"/>
<col align="left"/>
<col align="left" />
</colgroup>
<thead>
<tr>
<th>Composite</th>
<th>Incorporation level</th>
<th>Antimicrobial capacity</th>
<th>Other physical properties</th>
<th>Limitations</th>
<th>References</th>
</tr>
</thead>
<tbody>
<tr>
<td>Chitosan and AgNPs</td>
<td>AgNPs 0.075&#x2013;75 mg L<sup>&#x2212;1</sup></td>
<td>The biofilm mass was not removed, but its metabolic activity was reduced by at least 80%.</td>
<td>&#x2013;&#x2013;&#x2013;</td>
<td>Biofilm growth was only prevented by nanoparticles when the greatest doses were used.</td>
<td>[<xref ref-type="bibr" rid="ref-23">23</xref>]</td>
</tr>
<tr>
<td>Stainless steel surface with silver</td>
<td>The AISI 304 stainless steel with an Ag film of 2-inch diameter and 99.9% purity</td>
<td>Decreased Gram-positive and Gram-negative bacterial loads. The cathodic sputtering has shown to be successful in lowering the adherent microbial load.</td>
<td>&#x2013;&#x2013;&#x2013;</td>
<td>The functionalized sample showed small increase in roughness.</td>
<td>[<xref ref-type="bibr" rid="ref-24">24</xref>]</td>
</tr>
<tr>
<td>Alumina discs functionalized with biogenic AgNPs</td>
<td>Alumina discs, 17 mg/mL of AgNO<sub>3</sub>, and 20 mg/mL of a phytoextract solution</td>
<td>The fungal isolate showed a decrease of over 90%, while both Gram-positive and Gram-negative bacteria showed a decrease of over 99.9% in CFU mL<sup>&#x2212;1</sup>.</td>
<td>Improved hydrophobicity.</td>
<td>Roughness was observed on the surface of the functionalized samples.</td>
<td>[<xref ref-type="bibr" rid="ref-26">26</xref>]</td>
</tr>
<tr>
<td>IONPURE IPL incorporated LDPE films</td>
<td>Ag_50&#x2014;LDPE film with 2% of IONPURE IPL (0.036% silver) incorporation</td>
<td></td>
<td>&#x2013;&#x2013;&#x2013;</td>
<td>No antibacterial effects against <italic>A. flavus</italic> and <italic>E. coli</italic></td>
<td>[<xref ref-type="bibr" rid="ref-28">28</xref>]</td>
</tr>
<tr>
<td>Ethyl lauroyl arginate (LAE<sup>&#x00AE;</sup>) incorporated biofilms</td>
<td>LAE_50&#x2014;INZEA F19 biofilm with 6% LAE incorporation</td>
<td><italic>S.enterica</italic> growth decreased.</td>
<td>&#x2013;&#x2013;&#x2013;</td>
<td><italic>Aspergillus flavus</italic> was not affected</td>
<td>[<xref ref-type="bibr" rid="ref-28">28</xref>]</td>
</tr>
<tr>
<td>Ethyl lauroyl arginate (LAE<sup>&#x00AE;</sup>) incorporated polystyrene pads</td>
<td>LAE<sup>&#x00AE;</sup>&#x2014;30 mg/mL for spraying and 22 mg/L for total immersion</td>
<td>Reduction in <italic>P. putida</italic> growth by 99.99%.</td>
<td>&#x2013;&#x2013;&#x2013;</td>
<td>&#x2013;&#x2013;&#x2013;</td>
<td>[<xref ref-type="bibr" rid="ref-28">28</xref>]</td>
</tr>
<tr>
<td>Silver zeolite</td>
<td>Silver zeolite coated stainless sheets in 0.01 M AgNO<sub>3</sub></td>
<td>Reduced bacterial adhesion of <italic>E. coli</italic> O157:H7 and <italic>L. innocua</italic> Seeliger.</td>
<td>&#x2013;&#x2013;&#x2013;</td>
<td>&#x2013;&#x2013;&#x2013;</td>
<td>[<xref ref-type="bibr" rid="ref-27">27</xref>]</td>
</tr>
<tr>
<td>Ag-NPs and ZnO-NPs</td>
<td>Ag-NPs (400, 500, 650, 850 ppm), ZnO-NPs(400, 500, 650, 850 ppm)</td>
<td>At a concentration of 850 ppm, AgNPs along with 400 ppm ZnONPs exhibited good antibacterial efficiency against <italic>E. coli</italic> (5.80 log CFU/cm<sup>2</sup>) and <italic>S. aureus</italic>. At concentrations of 500 ppm, AgNPs prevented biofilm formation of <italic>L. monocytogenes</italic> under humid growth conditions.</td>
<td>&#x2013;&#x2013;&#x2013;</td>
<td>Optimization of the long-term durability of surfaces with antibacterial qualities is needed.</td>
<td>[<xref ref-type="bibr" rid="ref-25">25</xref>]</td>
</tr>
<tr>
<td>Surface-functionalize stainless steel and polyethylene with AgNPs</td>
<td>PE (20 &#x00D7; 20 &#x00D7; 1 mm) and SS AISI 304 (10 &#x00D7; 10 &#x00D7; 1 mm) are functionalized with AGNP</td>
<td>Reduce bacterial adhesion, reduce the occurrence of biofilms.</td>
<td>The solid-liquid contact has increased hydrophobicity.</td>
<td>&#x2013;&#x2013;&#x2013;</td>
<td>[<xref ref-type="bibr" rid="ref-33">33</xref>]</td>
</tr>
<tr>
<td>PBAT contain CNCs</td>
<td>PBAT (5 g) and CNC (1.5 wt%) based nanocomposites</td>
<td>Decrease biofilm formation of <italic>E. coli</italic> on nanocomposites (antibacterial properties).</td>
<td>Improved in thermal and mechanical properties.</td>
<td>&#x2013;&#x2013;&#x2013;</td>
<td>[<xref ref-type="bibr" rid="ref-29">29</xref>]</td>
</tr>
<tr>
<td>PDMS coatings with AgNPs</td>
<td>AgNO<sub>3</sub> at 0.18 wt% and carboxymethylcellulose at 0.4 wt%</td>
<td>The film eliminated planktonic cells and prevented biofilm formation of <italic>S. aureus</italic> and <italic>E. coli</italic>.</td>
<td>Increased surface irregularity and hydrophobicity.</td>
<td>&#x2013;&#x2013;&#x2013;</td>
<td>[<xref ref-type="bibr" rid="ref-30">30</xref>]</td>
</tr>
</tbody>
</table>
<table-wrap-foot><fn><p><bold>Abbreviations:</bold> AgNPs: Silver nanoparticles; PDMS: Poly(dimethyl siloxane); PBAT: Polybutylenes adipate-co-terephthalate; CNC: Nanocrystals; LAE: Ethyl lauroyl arginate; ZnO-NPs: Zinc oxide nanoparticles.</p></fn></table-wrap-foot>
</table-wrap>
<p>A combination of AgNPs, gold nanoparticles (AuNPs), and chitosan has been shown to exhibit antibacterial characteristics, effectively inhibiting biofilm formation and reducing bacterial metabolic activity. Chitosan prevented biofilm development at concentrations ranging from 0.31 to 5 mg/ml, while nanoparticles combined with chitosan significantly reduced metabolic activity by at least 80%. The disruption of bacterial membranes by chitosan and AgNPs causes leakage of internal components from planktonic cells, further inhibiting microbial growth [<xref ref-type="bibr" rid="ref-23">23</xref>]. Additionally, combining zinc oxide nanoparticles (ZnONPs) with AgNPs on polyester surfaces has shown significant efficacy in preventing biofilm formation by harmful bacteria such as <italic>Escherichia coli</italic> (<italic>E. coli)</italic> and <italic>Staphylococcus aureus (S. aureus)</italic>. These nanoparticles also inhibit biofilms causing <italic>Listeria monocytogenes</italic> (<italic>L. monocytogenes</italic>). A combination of 850 ppm AgNPs and 400 ppm ZnONPs has demonstrated strong antibacterial effects, reducing <italic>E. coli</italic> CFU/cm<sup>2</sup> levels by 5.80 log and <italic>S. aureus</italic> by 4.11 log. In humid conditions, AgNPs at 500 ppm effectively prevent biofilm formation by <italic>L. monocytogenes</italic> [<xref ref-type="bibr" rid="ref-25">25</xref>].</p>
<p>Furthermore, functionalized stainless-steel surfaces with silver coupons exhibit lower counts of adherent <italic>S. aureus</italic> cells compared to <italic>E. coli</italic>. Cathodic sputtering of silver onto stainless steel lowers the microbial load on surfaces, with silver ions from the coating reducing both Gram-negative and Gram-positive bacteria. This highlights the potential use of silver-functionalized surfaces in the food industry to reduce microbial adhesion and biofilm formation [<xref ref-type="bibr" rid="ref-24">24</xref>]. Alumina discs coated with biogenic AgNPs show enhanced hydrophobicity and a significant reduction in microbial adhesion over 99.9% for both Gram-negative and Gram-positive bacteria, and over 90% for fungal isolates. These surfaces offer antibacterial properties, inhibit biofilm formation, and maintain biocompatibility with Caco-2 and HaCaT cell lines [<xref ref-type="bibr" rid="ref-26">26</xref>].</p>
<p>A study by Griffith et al. examined the antimicrobial effectiveness of silver zeolite coatings in minimizing contamination. Silver zeolite effectively prevents biofilm formation caused by common foodborne pathogens such as <italic>Listeria innocua</italic> (<italic>L. innocua</italic>) Seeliger and <italic>E. coli</italic> O157:H7. At a concentration of 0.3% w/v, silver zeolite inhibited <italic>L. innocua</italic> growth for up to 8 h. Its effectiveness against <italic>E. coli</italic> depended on dosage, showing reduced bacterial numbers after 4 h. This suggests silver zeolite&#x2019;s potential as a coating material to enhance food safety and prevent microbial contamination on food-contact [<xref ref-type="bibr" rid="ref-27">27</xref>].</p>
<p>In a study conducted by [<xref ref-type="bibr" rid="ref-28">28</xref>], the antibacterial activity of two novel active films with silver, as IONPURE IPL, and ethyl lauroyl arginate (LAE&#x00AE;) respectively was assessed. One of these films was fabricated by incorporating silver in a low-density polyethylene (LDPE) matrix while the other was fabricated using an LAE&#x00AE; incorporated biofilm material INZEA F19. While silver incorporated LDPE films showed no antibacterial activity against E. coli and Aspergillus flavus, LAE&#x00AE; incorporated INZEA F19 reduced the growth of Salmonella enterica (S. enterica) but did not inhibit the growth of Aspergillus flavus. Interestingly, a 99.99% reduction in growth of Pseudomonas putida was observed when active polystyrene (PS) pads incorporated with LAE&#x00AE; were used. Notably, LAE&#x00AE; retained its antibacterial action against S. enterica even after thermal treatment at 180&#x00B0;C for 6 and 15 min (<xref ref-type="fig" rid="fig-1">Fig. 1</xref>) [<xref ref-type="bibr" rid="ref-28">28</xref>].</p>
<fig id="fig-1">
<label>Figure 1</label>
<caption>
<title>Diagrammatic illustration of silver incorporation and ethyl lauroyl arginate in different matrices [<xref ref-type="bibr" rid="ref-28">28</xref>]</title>
</caption>
<graphic mimetype="image" mime-subtype="tif" xlink:href="JPM_59156-fig-1.tif"/>
</fig>
<p>The effects of AgNP-functionalized stainless-steel surfaces on biofilm formation and bacterial adhesion were thoroughly examined. Thin silver film coatings on polybutylene adipate-co-terephthalate (PBAT) and cellulose nanocrystal (CNC) nanocomposites showed improved crystallinity, ranging from 51% to 56%. These nanocomposites, created by solution casting with varying CNC concentrations (0.8, 1.5, and 2.3 wt%) and coated with silver thin films using magnetron sputtering, led to a significant 56% reduction in <italic>E. coli</italic>-induced biofilm, indicating potential use in food packaging [<xref ref-type="bibr" rid="ref-29">29</xref>]. Similarly, a poly (dimethyl siloxane) (PDMS) coating with AgNPs demonstrated remarkable antimicrobial activity, showing a 22-fold increase in effectiveness against <italic>E. coli</italic> and <italic>S. aureus</italic> compared to untreated PDMS. This was achieved using the solution blow spraying (SBS) technique to deposit AgNPs on partly crosslinked PDMS [<xref ref-type="bibr" rid="ref-30">30</xref>].</p>
<p>Additionally, the modification of a poly(butylene succinate-co-terephthalate) (PBST) matrix with Magnesium oxide (MgO)/AgNPs created PBST/MgO/Ag nanocomposite films. These films not only enhanced the mechanical, thermal, and barrier properties of the matrix but also exhibited excellent antibacterial activity against <italic>S. aureus</italic>, <italic>E. coli</italic>, and <italic>Salmonella paratyphi</italic> [<xref ref-type="bibr" rid="ref-31">31</xref>]. Furthermore, a study developed an antimicrobial polymer blend with immobilized fine silver nanophases (&#x007E;25 nm), showing exceptional efficiency in inhibiting foodborne pathogens such as <italic>S. aureus</italic> and <italic>S. enteri</italic>ca. The biomaterial showed exceptional efficiency in inhibiting the mentioned pathogens, making it a promising biodegradable food packaging material [<xref ref-type="bibr" rid="ref-32">32</xref>].</p>
</sec>
<sec id="s2_1_2">
<label>2.1.2</label>
<title>Selenium Nanoparticles against Biofilm</title>
<p>Nanostructures made of silver, copper, zinc, titanium, and selenium have shown potential in the field of food safety and technology, despite potential hazards associated with some of them [<xref ref-type="bibr" rid="ref-34">34</xref>,<xref ref-type="bibr" rid="ref-35">35</xref>]. <xref ref-type="table" rid="table-2">Table 2</xref> presents the use of selenium nanoparticles (SeNPs) as antibiofilm food packaging materials. Selenium plays a role in thyroid hormone metabolism, cellular redox state regulation, and protection against reactive oxygen species. SeNPs were synthesized using the cell-free supernatant of <italic>Bacillus licheniformis</italic>, which was isolated from food wastes. Six foodborne pathogens, including <italic>Enterococcus faecalis</italic>, <italic>Bacillus cereus, E. coli</italic> O157:H7, <italic>S. aureus, Salmonella enteritidis</italic>, and <italic>S. Typhimurium</italic>, were found to be susceptible to the antibiofilm and antimicrobial properties of biosynthesized selenium nanoparticles with a diameter range of 10&#x2013;50 nm [<xref ref-type="bibr" rid="ref-35">35</xref>]. The SeNPs showed a minimum inhibitory concentration (MIC90) of 25 mg/mL against all tested bacteria, effectively inhibiting their growth. Additionally, the SeNPs displayed antibiofilm activity at a concentration of 20 mg/mL against all examined bacteria, except <italic>B. cereus</italic>. Furthermore, the established biofilms were removed at concentrations of 75 mg/mL, and the SeNPs did not exhibit any toxicity to <italic>Artemia larvae</italic> [<xref ref-type="bibr" rid="ref-35">35</xref>]. Ullah et al. [<xref ref-type="bibr" rid="ref-21">21</xref>] conducted a study using SeNPs produced by <italic>Bacillus subtilis</italic>, and their antibacterial activity was assessed using the agar overlay technique. The results demonstrated that the SeNPs exhibited similar antibacterial effects against <italic>Pseudomonas aeruginosa, Salmonella typhi</italic>, and <italic>S. aureus</italic> at concentrations of 150 and 200 &#x03BC;g/mL. Notably, the SeNPs caused breakdown of the bacterial cell membrane in both <italic>S. aureus</italic> and <italic>P. aeruginosa</italic>. Significant anti-biofilm activity was observed at 700 &#x03BC;g/mL concentration against pathogenic strains capable of forming biofilms by SeNPs. The SeNPs dispersed biofilms of <italic>P. aeruginosa</italic> (85.7%), <italic>S. typhi</italic> (89.6%), and <italic>S. aureus</italic> (78.3%) within a time span of 15 min [<xref ref-type="bibr" rid="ref-21">21</xref>].</p>
<table-wrap id="table-2">
<label>Table 2</label>
<caption>
<title>Application of selenium nanoparticles for antibiofilm food packaging</title>
</caption>
<table frame="hsides">
<colgroup>
<col align="left"/>
<col align="left"/>
<col align="left"/>
<col align="left"/>
<col align="left"/>
<col align="left" />
</colgroup>
<thead>
<tr>
<th>Composite</th>
<th>Incorporation level</th>
<th>Antimicrobial capacity</th>
<th>Other physical properties</th>
<th>Limitations</th>
<th>References</th>
</tr>
</thead>
<tbody>
<tr>
<td rowspan="2">Biosynthesize SeNPs by <italic>B. licheniformis</italic></td>
<td rowspan="2">The antibiofilm concentration was 20 mg/mL, but MIC90 of SeNPs was<break/> 25 mg/mL</td>
<td rowspan="2">Inhibited the growth of <italic>B.cereus, S. aureus, E. coli</italic>, <italic>E. faecalis, S. typhi</italic>, and <italic>S. enteritidis</italic></td>
<td rowspan="2">&#x2013;&#x2013;&#x2013;&#x2013;</td>
<td>Do not removed the established biofilm up to 50 mg/mL.</td>
<td rowspan="2">[<xref ref-type="bibr" rid="ref-35">35</xref>]</td>
</tr>
<tr>
<td>No toxicity on <italic>Artemia</italic> larvae by SeNPs upto 100 mg/mL</td>
</tr>
<tr>
<td><italic>Bacillus subtilis</italic> BSN313 generated SeNPs</td>
<td>150&#x2013;200&#x2009;&#x00B5;g/mL of SeNPs</td>
<td>Inhibited biofilm formation</td>
<td>&#x2013;&#x2013;&#x2013;&#x2013;</td>
<td>&#x2013;&#x2013;&#x2013;</td>
<td>[<xref ref-type="bibr" rid="ref-21">21</xref>]</td>
</tr>
</tbody>
</table>
<table-wrap-foot><fn><p><bold>Abbreviations:</bold> SeNPs: Selenium nanoparticles; MIC: Minimum inhibitory concentration.</p></fn></table-wrap-foot>
</table-wrap>
</sec>
<sec id="s2_1_3">
<label>2.1.3</label>
<title>Metal Oxide Nanoparticles against Biofilm</title>
<p>Metal oxide nanoparticles have been extensively studied for their potential in food packaging, particularly for their ability to combat microbial biofilms. Nanoparticles such as silver oxide, titanium dioxide (TiO<sub>2</sub>), and zinc oxide (ZnO) offer strong antibacterial properties that help prevent microbial contamination [<xref ref-type="bibr" rid="ref-36">36</xref>]. When integrated into packaging, these nanoparticles release metal ions or generate reactive oxygen species (ROS) upon exposure to moisture or light, effectively inhibiting bacteria, fungi, and other microorganisms. Silver oxide nanoparticles, for instance, release silver ions (Ag<sup>&#x002B;</sup>) that interact with microbial cells, disrupting their functions and preventing growth. Similarly, TiO<sub>2</sub> nanoparticles generate ROS, such as hydroxyl radicals, which damage microbial cell membranes [<xref ref-type="bibr" rid="ref-20">20</xref>,<xref ref-type="bibr" rid="ref-36">36</xref>].</p>
<p>Another approach to food packaging involves using metal oxide coatings to enhance antibacterial properties. A notable method includes the use of a nano-CuO coating on copper foil (Cu(CuO)), which produces reactive chlorine species (RCS) <italic>in situ</italic>, suppressing biofilms and killing bacteria on contact. This approach successfully treats bacteria like <italic>S. aureus</italic> and <italic>E. coli</italic> by employing heterogeneous Fenton chemistry to generate ROS, damaging bacterial cells. The concentration of H<sub>2</sub>O<sub>2</sub> and Cl<sup>&#x2013;</sup> in the environment also influences bacterial growth. Furthermore, the NO<sub>2</sub>-Cu-Fenton system has shown enhanced performance in eliminating biofilms and killing bacteria, proving particularly effective against <italic>E. coli</italic> and <italic>S. aureus</italic> in food and water [<xref ref-type="bibr" rid="ref-37">37</xref>]. Moreover, a blend film consisting of pullulan/collagen/ZnO nanoparticles has been found to be effective against <italic>A. niger</italic> and has shown potential as an edible food packaging material due to its water solubility [<xref ref-type="bibr" rid="ref-38">38</xref>]. Another antibacterial composite such as PAL@ZnO, created by incorporating natural palygorskite (PAL) nanorods into a chitosan/gelatin (CS/GL) matrix. This material enhances mechanical strength, water resistance, and thermal stability, while effectively combating <italic>E. coli</italic> and <italic>S. aureus</italic> [<xref ref-type="bibr" rid="ref-39">39</xref>]. Furthermore, anthocyanins extracted from purple potatoes or roselle were used to modify a chitosan/polyvinyl alcohol/nano-ZnO (CPZ) based film, which displayed strong antibacterial activity against <italic>S. aureus</italic> and <italic>E. coli</italic>, while also being capable of monitoring the spoilage status of packaged shrimp through changes in pH caused by microbial spoilage [<xref ref-type="bibr" rid="ref-40">40</xref>]. Additionally, antimicrobial nanocomposites containing ZnO-NPs with gelatin and tragacanth significantly inhibited bacteria such as <italic>S. aureus</italic> and <italic>E. coli</italic>, while enhancing the mechanical properties of the packaging [<xref ref-type="bibr" rid="ref-41">41</xref>]. The zinc sulfide nanoparticles (ZnS NPs) also possess antibiofilm activity and, like ZnO NPs, have potential applications in the food industry. Both ZnO and ZnS NPs were equally effective in killing bacteria, with <italic>S. aureus</italic> being more susceptible compared to <italic>P. aeruginosa</italic> and <italic>Klebsiella oxytoca</italic> [<xref ref-type="bibr" rid="ref-42">42</xref>].</p>
<p>Nanocomposite films composed of bovine gelatin and magnetic iron oxide (MIO) nanoparticles (5&#x2013;20% w/w) have significantly improved mechanical and barrier properties, with optimal performance observed at a 10% concentration. Notably, the 20% MIO nanocomposites exhibited the highest antimicrobial activity against <italic>E. coli</italic> (7.1 mm) and <italic>S. aureus</italic> (8.22 mm). These gelatin/MIO films were further evaluated for their potential to extend the shelf life of grapes, underscoring their suitability as biodegradable packaging materials [<xref ref-type="bibr" rid="ref-43">43</xref>]. Liu et al. reported that soluble soybean polysaccharide composite films incorporating 5 wt% nano zinc oxide and 10 wt% tea tree essential oil exhibited enhanced water vapor barrier properties, thermal stability, and UV protection. Although there was no change in tensile strength and elongation, light transmittance at 600 nm decreased from 85.5% to 10.1%. These films demonstrated a DPPH radical scavenging activity of 67.7% and exhibited strong antibacterial effects against <italic>E. coli</italic> and <italic>S. aureus</italic>, indicating their promising potential for active packaging applications [<xref ref-type="bibr" rid="ref-44">44</xref>]. Additionally, an active packaging biofilm developed from biodegradable poly(butylene adipate-co-terephthalate) (PBAT), combined with 2% copper oxide nanoparticles (CuO-NPs) and varying amounts of enzymatically prepared nanocellulose fibers, showed enhanced thermal stability, improved mechanical strength, and robust antimicrobial activity against both Gram-positive and Gram-negative bacteria, as well as unicellular and filamentous fungi [<xref ref-type="bibr" rid="ref-45">45</xref>].</p>
<p>Purohit et al. examined the antimicrobial effects of nanoceria-infused chitosan-based biopolymer films for food packaging, finding significant antimicrobial activity against <italic>E. coli</italic> and <italic>L. monocytogenes</italic>, particularly under visible light. This antimicrobial effect is attributed to nanoceria&#x2019;s ability to alternate between oxidation states (Ce<sup>3&#x002B;</sup> and Ce<sup>4&#x002B;</sup>), which enhances its photocatalytic properties [<xref ref-type="bibr" rid="ref-46">46</xref>]. In a related study, Osman et al. explored hydroxypropyl-methyl cellulose (HPMC) films that incorporated Al<sub>2</sub>O<sub>3</sub> and SiO<sub>2</sub> nanoparticles (NPs) to target foodborne pathogens such as <italic>Bacillus cereus</italic>, <italic>S. aureus</italic>, and <italic>S. Typhimurium</italic> on chicken fillets. The nanoparticles, approximately 80 nm in size and applied at a concentration of 80 ppm, exhibited substantial antimicrobial efficacy, reducing microbial loads by 2&#x2013;3 log<sub>10</sub> CFU/cm&#x00B2; over 15 days of refrigerated storage [<xref ref-type="bibr" rid="ref-47">47</xref>]. Additionally, Momtaz et al. developed gelatin/chitosan (GEL/CS) nanocomposite films enhanced with nickel oxide nanoparticles (NiO NPs) for active food packaging. The inclusion of optimized concentrations of NiO NPs significantly improved the films&#x2019; mechanical, barrier, and thermal properties, with tensile strength increasing from 23.83 MPa (without NPs) to 30.13 MPa with the addition of 1% NiO NPs. These films demonstrated strong antibacterial activity against the Gram-positive bacterium <italic>S. aureus</italic> compared to the Gram-negative bacterium <italic>E. coli</italic>. Toxicity assessments further revealed that the films were non-toxic to fibroblast cells, achieving a survival rate exceeding 88% [<xref ref-type="bibr" rid="ref-48">48</xref>].</p>
<p>The development of new materials and coatings continues to push the boundaries of food packaging technology. For example, a photocatalyst called graphitic carbon nitride (g-C<sub>3</sub>N<sub>4</sub>) has been studied for its potential to prevent and remove biofilms. Unlike TiO<sub>2</sub>, which requires ultraviolet light, g-C<sub>3</sub>N<sub>4</sub> harnesses visible light. When exposed to white LEDs, it effectively disrupts biofilm formation, progressing from the surface to the core, facilitated by ROS diffusion [<xref ref-type="bibr" rid="ref-20">20</xref>].</p>
<p>Another study explored silver-graphene-TiO<sub>2</sub> nanocomposites for controlling the growth of <italic>Campylobacter jejuni</italic>. These nanocomposites induced leakage of proteins and DNA from bacterial cells, reduced bacterial motility and hydrophobicity, and significantly inhibited biofilm formation. Importantly, these synthesized nanoparticles were confirmed as non-cytotoxic to human cells [<xref ref-type="bibr" rid="ref-49">49</xref>]. According to the research findings, Similarly, nanocomposites combining silver, ZnO, reduced graphene oxide (rGO), and polyethylene glycol (PEG) showed robust anti-biofilm activity. the biofilm formation of <italic>Saureus</italic> and <italic>P. aeruginosa</italic> bacteria was robustly inhibited due to the pronounced anti-biofilm effects of AZGP nanocomposites. The AZGP nanocomposite, containing 0.05 M silver nitrate and a dosage of 31.25 &#x03BC;g/mL, inhibited around 95% of biofilm formation while maintaining antimicrobial activity for up to 90 days (<xref ref-type="fig" rid="fig-2">Fig. 2</xref>) [<xref ref-type="bibr" rid="ref-50">50</xref>].</p>
<fig id="fig-2">
<label>Figure 2</label>
<caption>
<title>Illustration of the production process of silver-incorporated ZnO-rGO-PEG (AZGP) nanocomposite [<xref ref-type="bibr" rid="ref-50">50</xref>]</title>
</caption>
<graphic mimetype="image" mime-subtype="tif" xlink:href="JPM_59156-fig-2.tif"/>
</fig>
<p>Silica nanoparticles (SNPs), a type of metal oxide nanoparticle, are effective in mitigating biofilms due to their high surface-to-volume ratio, which enhances interactions with microbial cells and biofilm matrices. In food packaging, SNPs can prevent microbial attachment and growth, disrupt biofilm structures, and exhibit antimicrobial activity by damaging microbial cell membranes, inhibiting biofilm formation [<xref ref-type="bibr" rid="ref-34">34</xref>].</p>
<p>One promising application involves SNPs encapsulating basil oil, incorporated into chitosan films. These basil oil@SiNPs films demonstrated antimicrobial inhibition against both Gram-positive and Gram-negative bacteria, as well as pathogenic yeast. While they increased the water contact angle and activation energy, they decreased water vapor permeability but increased oxygen permeability [<xref ref-type="bibr" rid="ref-51">51</xref>]. SNPs are also utilized as delivery platforms for biocidal agents in anti-biofilm research. When grafted onto polyethylene, polystyrene, and polyvinyl chloride surfaces, SNPs increased surface nanoroughness while maintaining mechanical properties. These grafted surfaces significantly reduced the adhesion of Gram-positive <italic>B. licheniformis</italic> or Gram-negative bacteria <italic>P. aeruginosa</italic>. This method offers a durable anti-biofouling solution for biomedical devices, food, water treatment systems, and industrial applications (<xref ref-type="fig" rid="fig-3">Fig. 3</xref>) [<xref ref-type="bibr" rid="ref-34">34</xref>].</p>
<fig id="fig-3">
<label>Figure 3</label>
<caption>
<title>Illustration depicting the incorporation of biocidal agents on nanosilica into anti-biofouling polymers [<xref ref-type="bibr" rid="ref-34">34</xref>]</title>
</caption>
<graphic mimetype="image" mime-subtype="tif" xlink:href="JPM_59156-fig-3.tif"/>
</fig>
<p>Moreover, a study demonstrated that stainless-steel surfaces coated with silica nanoparticles (SNPs) modified with polyethyleneimine (PEI) and polytetrafluoroethylene (PTFE) nanoparticles in an electroless nickel coating exhibited antimicrobial and nonfouling properties. These coatings reduced <italic>L. monocytogenes</italic> populations by over 5 log and decreased biofilm formation by more than 2 log. The coatings also inhibited exopolysaccharide production, lowering the risk of cross-contamination, nosocomial infections, and foodborne diseases (<xref ref-type="fig" rid="fig-4">Fig. 4</xref>) [<xref ref-type="bibr" rid="ref-52">52</xref>]. Some recent studies outlined the application of various metal oxides conjugated films to mitigate microbial biofilm, as presented in <xref ref-type="table" rid="table-3">Table 3</xref>.</p>
<fig id="fig-4">
<label>Figure 4</label>
<caption>
<title>Illustration depicting the bactericidal properties of Ni-PTFE-SiNP &#x002B;-modified coatings (A) and the synthesis process of SiO<sub>2</sub>@PEI NPs (B) [<xref ref-type="bibr" rid="ref-52">52</xref>]</title>
</caption>
<graphic mimetype="image" mime-subtype="tif" xlink:href="JPM_59156-fig-4a.tif"/>
<graphic mimetype="image" mime-subtype="tif" xlink:href="JPM_59156-fig-4b.tif"/>
</fig><table-wrap id="table-3">
<label>Table 3</label>
<caption>
<title>Application of various metal oxides for antibiofilm food packaging</title>
</caption>
<table frame="hsides">
<colgroup>
<col align="left"/>
<col align="left"/>
<col align="left"/>
<col align="left"/>
<col align="left"/>
<col align="left" />
</colgroup>
<thead>
<tr>
<th>Composite</th>
<th>Incorporation level</th>
<th>Antimicrobial capacity</th>
<th>Other physical properties</th>
<th>Limitations</th>
<th>References</th>
</tr>
</thead>
<tbody>
<tr>
<td>Nano-CuO onto copper foil</td>
<td>Copper foil coated with nano-CuO for making Cu(CuO) film</td>
<td>Killed planktonic bacteria and suppress the biofilm production of <italic>S. aureus</italic> and <italic>E. coli</italic></td>
<td>&#x2013;&#x2013;&#x2013;</td>
<td>&#x2013;&#x2013;&#x2013;</td>
<td>[<xref ref-type="bibr" rid="ref-53">53</xref>]</td>
</tr>
<tr>
<td>Nano-CuO</td>
<td>NO<sub arrange="stack">2</sub><sup arrange="stack">&#x2013;</sup>&#x2013;Cu-Fenton, the combination of NO<sub arrange="stack">2</sub><sup arrange="stack">&#x2013;</sup> &#x002B; H<sub>2</sub>O<sub>2</sub></td>
<td>Disrupt biofilms with varied maturity and planktonic-bacteria killing of <italic>P. aeruginosa</italic>. RNS (reactive nitrogen species) act as disinfectants</td>
<td>&#x2013;&#x2013;&#x2013;</td>
<td>Limiting mass transfer is a significant constraint</td>
<td>[<xref ref-type="bibr" rid="ref-37">37</xref>]</td>
</tr>
<tr>
<td>Silver-graphene-TiO<sub>2</sub> nanocomposites</td>
<td>Silver-Graphene-TiO<sub>2</sub> Composite: 200 mg Ag/TiO<sub>2</sub></td>
<td>Reduced cell growth caused by DNA and protein leaks from <italic>C. jejuni</italic> cells. Decreased motility, hydrophobicity, autoaggregation as well as biofilm formation inhibition</td>
<td>Biocompatible to human cell lines</td>
<td>&#x2013;&#x2013;&#x2013;</td>
<td>[<xref ref-type="bibr" rid="ref-49">49</xref>]</td>
</tr>
<tr>
<td>Graphitic carbon nitride (g-C<sub>3</sub>N<sub>4</sub>)</td>
<td>g-C<sub>3</sub>N<sub>4</sub>(MCB0.07), melamine, cyanuric acid, and barbituric acid (2:1.93:0.07 g)</td>
<td>Removes the extracellular polymeric substances (EPS) and PIA within <italic>S. epidermidis</italic> Biofilm</td>
<td>Increased stiffness</td>
<td>&#x2013;&#x2013;&#x2013;</td>
<td>[<xref ref-type="bibr" rid="ref-20">20</xref>]</td>
</tr>
<tr>
<td>Nanocomposites of Ag-ZnO-reduced graphene oxide (rGO)-PEG (AZGP)</td>
<td>Silver nitrate (up to 0.1 M)</td>
<td>Kills <italic>S. aureus</italic> and <italic>P. aeruginosa</italic> cells and has antibiofilm action</td>
<td>Enhanced tensile strength</td>
<td>&#x2013;&#x2013;&#x2013;&#x2013;</td>
<td>[<xref ref-type="bibr" rid="ref-50">50</xref>]</td>
</tr>
<tr>
<td>SiO<sub>2</sub>@PEI-functionalized SNPs in Ni-PTFE SiNP &#x002B; Coating</td>
<td>SiO<sub>2</sub>@PEI NPs (0.20 gL<sup>&#x2212;1</sup></td>
<td>Prevention of bacteria growth &#x0026; Biocidal agents. The coatings apparently inhibit the production of exopoly- saccharide by the adhered cells</td>
<td>Hydrophobicity and low-surface-energy properties</td>
<td>&#x2013;&#x2013;&#x2013;</td>
<td>[<xref ref-type="bibr" rid="ref-52">52</xref>]</td>
</tr>
<tr>
<td>Monodispersed SNPs</td>
<td>Polymer (PE, PVC, or PS) films<break/> (4 &#x00D7; 2 cm)</td>
<td>Reduced the bacterial adhesion, Gram positive <italic>B. licheniformis</italic> or Gram-negative <italic>P. aeruginosa</italic></td>
<td>&#x2013;&#x2013;&#x2013;</td>
<td>Decrease the bacterial adhesion but no notable killing effect. Rise in nanoroughness by 1.6&#x2212;2.7 times</td>
<td>[<xref ref-type="bibr" rid="ref-34">34</xref>]</td>
</tr>
<tr>
<td>Hydroxypropyl-methyl cellulose</td>
<td>Al&#x2082;O&#x2083; and SiO&#x2082; nanoparticles (NPs) of 80 nm in size</td>
<td>Antimicrobial activity against <italic>B. cereus</italic>, <italic>S. aureus</italic>, and <italic>S. Typhimurium</italic></td>
<td>&#x2013;&#x2013;&#x2013;</td>
<td>&#x2013;&#x2013;&#x2013;</td>
<td>[<xref ref-type="bibr" rid="ref-47">47</xref>]</td>
</tr>
<tr>
<td>Gelatin/chitosan</td>
<td>Nickel oxide nanoparticles (NiO NPs) of 1%</td>
<td>Antibacterial activity against Gram-positive <italic>S. aureus</italic> compared to Gram-negative <italic>E. coli</italic></td>
<td>Enhanced the mechanical, barrier, and thermal properties of the films, with tensile strength</td>
<td>&#x2013;&#x2013;&#x2013;</td>
<td>[<xref ref-type="bibr" rid="ref-48">48</xref>]</td>
</tr>
</tbody>
</table>
<table-wrap-foot><fn><p><bold>Abbreviations:</bold> g-C<sub>3</sub>N<sub>4</sub>: Graphitic carbon nitride; rGO: Reduced graphene oxide; PEG: Polyethylene glycol; SNPs: Silica nanoparticles; PEI: Polyethyleneimine; PTFE: Polytetrafluoroethylene; PEG: Polyethylene glycol.</p></fn></table-wrap-foot>
</table-wrap>
</sec>
<sec id="s2_1_4">
<label>2.1.4</label>
<title>Biopolymeric Nanomaterials against Biofilm</title>
<p>Food packaging materials must meet specific criteria, with antimicrobial and antibiofilm packaging gaining importance. Eco-friendly, bio-derived polymers are increasingly replacing petroleum-based products. These biobased polymers include natural polymers (cellulose, chitin), synthetic polymers (polyhydroxy alkanoates [PHA], poly(glycolic acid) [PGA]), and biobased nanocomposites, which combine a biopolymer matrix with nanoparticles for enhanced antimicrobial properties [<xref ref-type="bibr" rid="ref-54">54</xref>,<xref ref-type="bibr" rid="ref-55">55</xref>]. Nanoparticles made from biopolymers and biosurfactants have also gained interest as they can be produced without harmful chemicals [<xref ref-type="bibr" rid="ref-9">9</xref>]. These materials are used in films, coatings, and emulsions, serving as active components to maintain food quality and safety [<xref ref-type="bibr" rid="ref-56">56</xref>,<xref ref-type="bibr" rid="ref-57">57</xref>]. Exopolysaccharides (EPS), polyhydroxy alkanoates (PHA), polylactic acid (PLA), starch, lignin, and protein-based polymers like collagen, gelatin, and gluten are currently under scrutiny for their potential as food packaging agents [<xref ref-type="bibr" rid="ref-58">58</xref>].</p>
<p>The effectiveness of various natural antimicrobial chemicals, such as citric acid, curcumin, calcium lactate, erythorbic acid, hop extract, garlic extract, and nisin, has been evaluated as food additives and in packaging materials. These agents were tested for their antibacterial and anti-biofilm properties against bacteria such as <italic>L. monocytogenes</italic>, <italic>S. aureus</italic>, and <italic>E. coli</italic>. It was found that garlic extract, erythorbic acid, and citric acid were the most effective in inhibiting bacteria. Moreover, combining two additives resulted in better efficacy, and mixtures of all these showed higher efficiency in inhibiting bacteria [<xref ref-type="bibr" rid="ref-59">59</xref>]. PEG-decorated GO Nanosheets have been demonstrated to enhance the efficiency of chitosan biopolymer, providing better thermal and mechanical stability as well as antibacterial properties [<xref ref-type="bibr" rid="ref-60">60</xref>]. Chitosan nanoparticles (CNPs) have also shown promise in preventing biofilm formation. CNPs at a concentration of 1500 &#x03BC;g/mL effectively suppressed biofilm formation by <italic>P. aeruginosa, S. aureus</italic>, and <italic>C. albicans</italic> by 91.83%, 55.47%, and 66.4%, respectively [<xref ref-type="bibr" rid="ref-61">61</xref>].</p>
<p>A recent study demonstrated the effectiveness of poly-L-aspartic acid nanoparticles with essential oil in combating <italic>S. aureus</italic> biofilm contamination on food-contact surfaces. This approach shows promise for applications in the food industry. The study confirmed the effectiveness of PASP in damaging <italic>S. aureus</italic> biofilms by impacting metabolic activity, bacterial adhesion, and extracellular polymeric substances. PASP was particularly effective in reducing the production of extracellular DNA (eDNA) by 49.4%. Additionally, nanoparticles containing essential oil (EO@PASP/HACCNPs) exhibited enhanced permeation and dispersion effects on biofilms, resulting in long-lasting anti-biofilm activity. When tested on a 72-h-old biofilm, EO@PASP/HACCNPs reduced the population of <italic>S. aureus</italic> by 0.63 log CFU/mL compared to the use of EO alone [<xref ref-type="bibr" rid="ref-62">62</xref>].</p>
<p>The use of nanocomposites in food packaging can help prevent the formation of biofilms on food. These nanocomposite biofilms are also useful in managing plastic waste and combating infectious diseases. For instance, Reference [<xref ref-type="bibr" rid="ref-22">22</xref>] demonstrated that electrospun fiber-based biofilms can act as a barrier against infectious microorganisms. By incorporating polylactic acid microfibers with active agents, nanocomposite biofilms with antimicrobial properties can be developed. The study revealed that acetylated cellulose nanofibers, with diameters of about 83 nm, and microfibrillar structures with diameters ranging from 1.7 to 2.4 &#x00B5;m, exhibited favorable characteristics for this purpose. Moreover, these nanocomposite biofilms demonstrated antibacterial activity against <italic>S. typhimurium</italic> and <italic>S. aureus</italic> [<xref ref-type="bibr" rid="ref-22">22</xref>]. In another study by Sun et al. it was found that starch-lignin nanoparticles composite films exhibited impressive tensile strength and elastic modulus, surpassing pure starch film. Additionally, lignin nanoparticles improved the thermal stability of the composite films and enhanced UV protection, reduced oxygen permeation, and scavenged DPPH free radicals, thus delaying the oxidation of soybean oil. Furthermore, bionanocomposites can effectively trap antimicrobial bioactive compounds [<xref ref-type="bibr" rid="ref-63">63</xref>]. Bionanocomposites are capable of trapping antimicrobial bioactive compounds which is a significant advantage. In a study by Cacciatore et al., it was demonstrated that carvacrol encapsulated into nanoliposomes and polymeric Eudragit<sup>&#x00AE;</sup> nanocapsules significantly reduced the presence of bacteria such as <italic>S. aureus, L. monocytogenes, E. coli</italic>, and <italic>Salmonella</italic> spp. on stainless steel surfaces. The encapsulated carvacrol displayed regulated release and a subdued scent, making it a desirable option for food applications [<xref ref-type="bibr" rid="ref-64">64</xref>]. The application of electrospun biodegradable polymers in biomedical and food industries was explored by Rumbo et al. as well. Their study revealed that electrospun polycaprolactone (PCL) microfibrous mesh could become colonized by pathogenic bacteria. However, it was suggested that functionalizing PCL meshes with antimicrobial compounds can make them effective food packaging materials, preventing bacterial adherence and biofilm development (<xref ref-type="fig" rid="fig-5">Fig. 5</xref>) [<xref ref-type="bibr" rid="ref-65">65</xref>].</p>
<fig id="fig-5">
<label>Figure 5</label>
<caption>
<title>Schematic illustration of colonization of pathogenic bacterial strains on electrospun polycaprolactone fibres [<xref ref-type="bibr" rid="ref-65">65</xref>]</title>
</caption>
<graphic mimetype="image" mime-subtype="tif" xlink:href="JPM_59156-fig-5.tif"/>
</fig>
<p>The research conducted by [<xref ref-type="bibr" rid="ref-66">66</xref>] revealed that composite films made of ethyl cellulose and polydimethylsiloxane, and containing small amounts of clove essential oil, exhibited antibacterial properties against <italic>E. coli</italic>, <italic>S. aureus</italic>, and <italic>P. aeruginosa</italic>. The clove essential oil was found to enhance the hydrophobicity of the composite material, which comprised 20 wt% PDMS and 80 wt% ethyl cellulose. According to the study, the presence of clove essential oil on the composites seemed to inhibit the growth of biofilms [<xref ref-type="bibr" rid="ref-66">66</xref>]. Additionally, Reference [<xref ref-type="bibr" rid="ref-9">9</xref>] developed antibacterial nanoparticles by combining chitosan with the biosurfactant rhamnolipid. The addition of rhamnolipid reduced the size and polydispersity index of chitosan nanoparticles, leading to a higher positive surface charge and increased stability of chitosan/rhamnolipid nanoparticles (C/RL-NPs). These nanoparticles demonstrated antimicrobial activity against both planktonic bacteria and biofilms of <italic>Staphylococcus</italic> strains. Furthermore, moderate concentrations of NPs effectively eliminated both <italic>S. aureus</italic> and <italic>Staphylococcus epidermidis</italic> biofilms (<xref ref-type="fig" rid="fig-6">Fig. 6</xref>) [<xref ref-type="bibr" rid="ref-9">9</xref>].</p>
<fig id="fig-6">
<label>Figure 6</label>
<caption>
<title>Schematic representation of rhamnolipid and chitosan nanoparticles and their antimicrobial properties [<xref ref-type="bibr" rid="ref-9">9</xref>]</title>
</caption>
<graphic mimetype="image" mime-subtype="tif" xlink:href="JPM_59156-fig-6.tif"/>
</fig>
<p>Antimicrobial packaging incorporates antimicrobial compounds into the packaging material to inhibit the growth of microorganisms [<xref ref-type="bibr" rid="ref-67">67</xref>]. This type of packaging not only helps prevent foodborne epidemics but also extends the shelf life and maintains the quality of food products. Starch-based materials, like chitosan, are commonly used as antibacterial agents against various microbes, and chitosan has been effectively applied as an edible coating with strong antibacterial properties [<xref ref-type="bibr" rid="ref-68">68</xref>]. Bio-nanocomposite materials, including chitosan and starch, play a critical role in food packaging due to their superior barrier qualities, which enhance food stability [<xref ref-type="bibr" rid="ref-17">17</xref>]. Starch is the most widely used biopolymer for food packaging. Various antimicrobial additives, such as tea tree essential oil, cinnamon essential oil, cassava starch, cellulose nanofibrils, neem, oregano, lemongrass essential oil, rosemary extract, and pomegranate peel powder, are being evaluated in combination with starch-based biopolymers as antimicrobial additives [<xref ref-type="bibr" rid="ref-69">69</xref>,<xref ref-type="bibr" rid="ref-70">70</xref>]. Furthermore, a modified antimicrobial peptide (1018K6) was bioconjugated to polyethylene terephthalate, demonstrating antibacterial and anti-biofilm capabilities against foodborne pathogens such as <italic>L. monocytogenes</italic> [<xref ref-type="bibr" rid="ref-71">71</xref>].</p>
<p>Microbial biofilm is a major concern in the food industry as it can be formed by several pathogens such as <italic>E. coli</italic>, <italic>S. enterica</italic>, <italic>Yersinia enterocolitica</italic>, <italic>C. jejuni</italic>, <italic>S. aureus</italic>, <italic>L. monocytogenes</italic>, and <italic>E. coli</italic> O157:H7 [<xref ref-type="bibr" rid="ref-72">72</xref>] These biofilms provide various advantages to the microorganisms, including forming a physical barrier against desiccation, mechanical resistance against liquid streams in food industries, and resistance to antimicrobial agents. Several methods, such as ultrasound, ultraviolet rays, magnetic fields, as well as the application of different chemicals and inhibitors, can disrupt biofilm formation and growth [<xref ref-type="bibr" rid="ref-73">73</xref>]. Studies have shown that incorporating phytochemicals like eugenol and thymol into packaging materials made of poly(lactic acid), poly(butylene succinate), and PBAT improves their antimicrobial properties against food-related pathogens like <italic>B. cereus</italic> and <italic>S. aureus</italic> [<xref ref-type="bibr" rid="ref-74">74</xref>]. Additionally, grafting CNPs with eugenol and carvacrol enhances their antimicrobial properties against <italic>E. coli</italic> and <italic>S. aureus</italic> [<xref ref-type="bibr" rid="ref-75">75</xref>]. An edible coating of nano-emulsion using carboxymethyl cellulose (CMC) and cardamom essential oil (CEO) was found to be effective against <italic>E. coli</italic> and <italic>L. monocytogenes</italic>. This coating material was also found to reduce the loss of fruit (tomato) weight significantly by maintaining firmness and reducing oxidative stress [<xref ref-type="bibr" rid="ref-76">76</xref>]. Furthermore, the use of food additives to inhibit biofilm formation on food can be a promising solution. Sodium citrate and cinnamic aldehyde have been reported to prevent the growth of biofilms of <italic>S. aureus</italic>, <italic>E. coli</italic>, and <italic>P. fluorescens</italic>. Methyl eugenol has been found to inhibit biofilm development by Gram-negative bacteria [<xref ref-type="bibr" rid="ref-77">77</xref>]. In previous research, efforts have been made to produce various biofilm-controlling packaging materials, especially through nanoparticle approaches such as metal oxide nanoparticles and AgNPs, silica composite materials, and biopolymer-based packaging films, to enhance their pharmacological properties and antimicrobial activity. The use of biopolymer-conjugated nanocomposites to combat the biofilm of various microorganisms is presented in <xref ref-type="table" rid="table-4">Table 4</xref>.</p>
<table-wrap id="table-4">
<label>Table 4</label>
<caption>
<title>Application of biopolymer nanocomposites as antibiofilm food packaging materials</title>
</caption>
<table frame="hsides">
<colgroup>
<col align="left"/>
<col align="left"/>
<col align="left"/>
<col align="left"/>
<col align="left"/>
<col align="left" />
</colgroup>
<thead>
<tr>
<th>Composite</th>
<th>Incorporation level</th>
<th>Antimicrobial capacity</th>
<th>Other physical properties</th>
<th>Limitations</th>
<th>References</th>
</tr>
</thead>
<tbody>
<tr>
<td>Nanocrystalline cellulose or cellulose nanofibers</td>
<td>Acetylated CNF in acetone and PLA in chloroform. PLA in chloroform and 2% nZH-Cu in acetone</td>
<td>The nanofiber showed antibacterial activity against <italic>S. typhi</italic> and <italic>S. aureus</italic>.</td>
<td>Increased in the elastic modulus, tensile strength, water vapor permeability.</td>
<td></td>
<td>[<xref ref-type="bibr" rid="ref-22">22</xref>]</td>
</tr>
<tr>
<td>Carvacrol incorporated into NCC and NLC</td>
<td>liposome containing Carvacrol (0.106 g)</td>
<td>Hinder the development of biofilms made by <italic>S. aureus</italic>, <italic>L. monocytogenes</italic>, <italic>E. coli</italic>, and <italic>Salmonella spp</italic>.</td>
<td>&#x2013;&#x2013;&#x2013;&#x2013;</td>
<td>&#x2013;&#x2013;&#x2013;&#x2013;</td>
<td>[<xref ref-type="bibr" rid="ref-64">64</xref>]</td>
</tr>
<tr>
<td>Electrospun polycaprolactone microfibrous mesh</td>
<td>Dimethylformamide and linear thermoplastic PCL diol polymer CAPA 6800 (12% w/v) were used to create PCL microfibre meshes</td>
<td>Antimicrobial and antibiofilm properties against <italic>S.aureus</italic>, <italic>E. coli</italic>, and <italic>P. aeruginosa</italic>.</td>
<td>Smooth hydrophilicity surface.</td>
<td>PCL meshes do not appear to affect the bacterial adhesion.</td>
<td>[<xref ref-type="bibr" rid="ref-65">65</xref>]</td>
</tr>
<tr>
<td>EC/PDMS</td>
<td>Ethyl cellulose solutions (0.1 g/mL), PDMS (0&#x2013;20 wt%), clove essential oil (80 wt%)</td>
<td>Antimicrobial activity against <italic>P.aeruginosa</italic>, <italic>S.aureus</italic>, and <italic>E.coli</italic>.</td>
<td>Increase opacity, hydrophobicity, water uptake, and water permeability, flexibility and the antioxidant capacity.</td>
<td>Without essential oil it has no antibiofilm property.</td>
<td>[<xref ref-type="bibr" rid="ref-66">66</xref>]</td>
</tr>
<tr>
<td>Rhamnolipid/<break/>Chitosan Nanoparticles (C/RL-NPs)</td>
<td>Solutions of chitosan, rhamnolipid, and TPP (0.5 mg mL<sup>&#x2212;1</sup>)</td>
<td>Antimicrobial and antibiofilm activity against <italic>S. aureus</italic>, <italic>S. epidermidis</italic>, <italic>staphi</italic>.</td>
<td>Nontoxic at concentrations at 116/150 &#x03BC;g mL<sup>&#x2212;1</sup> and below.</td>
<td>Its effect on Gram negative bacteria is very low.</td>
<td>[<xref ref-type="bibr" rid="ref-9">9</xref>]</td>
</tr>
</tbody>
</table>
<table-wrap-foot><fn><p><bold>Abbreviations:</bold> CNC: Nanocrystalline cellulose; CNF: Cellulose nanofibers; NCC: Nanocapsules; NLC: Nanoliposomes; PCL: Polycaprolactone; DMF: Dimethylformamide; C/RL-NPs: Rhamnolipid/Chitosan Nanoparticles; EC: Ethyl cellulose; PDMS: Polydimethylsiloxane; PLA: Polylactic acid.</p></fn></table-wrap-foot>
</table-wrap>
</sec>
</sec>
</sec>
<sec id="s3">
<label>3</label>
<title>Conclusion and Future Aspects</title>
<p>The food industry is searching for new food packaging films to prevent the growth of harmful microorganisms. It is easier to stop the initial stages of biofilm formation than to remove an established biofilm. ZnO and TiO<sub>2</sub> are the most commonly used metal oxide nanoparticles in active food packaging due to their antibiofilm properties. However, there are concerns about these nanoparticles migrating from the packaging into the food, which can be harmful to human health. Despite these concerns, studies have shown that incorporating certain nanoparticles can prevent biofilm formation and improve the properties of food packaging. Green synthesis methods can help make synthesized nanoparticles safer and more compatible with living tissues. Biopolymeric nanomaterials are thus creating ripples in the food packaging industry due to their compatibility with living tissues and ability to degrade naturally. By encapsulating and releasing antimicrobial agents in a controlled manner, biopolymeric nanomaterials can provide long-lasting protection against biofilm formation on food packaging surfaces. Additionally, combining biopolymers with other nanoparticles can create matrices for bioactive protection and controlled delivery. These aspects not only put forth biopolymeric nanocomposites ahead of the other types of nanomaterials but also emphasizes on the fact that biopolymeric nanocomposites rightly match all the criteria for serving as long term food preservation materials. We hope that the present review justifies the reasons for the growing popularity of this category of antibiofilm food packaging materials and will foster future research in these lines. However, rigorous testing of these coating surfaces are required to ensure their effectiveness and safety for food packaging. Nanotechnology can also integrate sensors and smart tags into food packaging to monitor parameters like temperature and humidity, ensuring food safety and quality control throughout the supply chain.</p>
</sec>
</body>
<back>
<ack>
<p>None.</p>
</ack>
<sec><title>Funding Statement</title>
<p>The authors received no specific funding for this study.</p>
</sec>
<sec><title>Author Contributions</title>
<p>All authors, including Bandana Padhan, Priyanka Bhowmik, Ananya Roy, Madhumita Patel and Joyjyoti Das contributed to the writing of the original draft of the manuscript. In addition, Bandana Padhan and Rajkumar Patel were involved in the conceptualization of the manuscript. Madhumita Patel, Rajkumar Patel, Joyjyoti Das and Yong Yu participated in the review and editing of the manuscript. All authors reviewed the results and approved the final version of the manuscript.</p>
</sec>
<sec sec-type="data-availability"><title>Availability of Data and Materials</title>
<p>Not applicable.</p>
</sec>
<sec><title>Ethics Approval</title>
<p>Not applicable.</p>
</sec>
<sec sec-type="COI-statement"><title>Conflicts of Interest</title>
<p>The authors declare no conflicts of interest to report regarding the present study.</p>
</sec>
<ref-list content-type="authoryear">
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