journal article·2023-11Open access

Potential and risks of nanotechnology applications in COVID-19-related strategies for pandemic control

Fatemeh Araste, Astrid Diana Bakker, Behrouz Zandieh-Doulabi

Journal of Nanoparticle Research· Volume 25· Issue 11

Abstract

Abstract The ongoing battle against viral infections highlighted so recently by the COVID-19 pandemic demonstrates the need to develop new approaches using nanotechnology in antiviral strategies. Nanoparticles have emerged as promising tools in the fight against viral outbreaks, offering various options for application such as biosensors, vaccine nanoparticles, disinfectants, and functionalized nanoparticles. In this comprehensive review, we evaluate the role of nanoparticles in pandemic control, exploring their potential applications, benefits, and associated risks. We first discuss the importance of nanotechnology in viral outbreak management, particularly in vaccine development. Although lipid nanoparticles play a crucial role in mRNA vaccines, there are concerns about their potential side effects. Although functionalization of protective face masks using metallic nanoparticles has emerged as a sustainable alternative to disposable masks, reducing waste production and enhancing virus filtration, improper disposal of such masks leads to environmental contamination and potential ecological harm. Second, we address the potential adverse effects associated with nanoparticle-based vaccines containing polyethylene glycol and other vaccine components, which trigger autoimmune diseases and alter menstrual cycles. To manage outbreaks effectively, we must minimize such potential risks and environmental impacts. Thus, when developing effective strategies for future pandemic control, it is crucial to understand the advantages and challenges associated with nanoparticle usage.
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Research context

OpenAlex topics: SARS-CoV-2 and COVID-19 Research · COVID-19 Impact on Reproduction · SARS-CoV-2 detection and testing

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (100+)

Show source-provided references
1. Kausar S, Said Khan F, Ishaq Mujeeb Ur Rehman M, Akram M, Riaz M, Rasool G, Hamid Khan A, Saleem I, Shamim S, Malik A (2021) A review: mechanism of action of antiviral drugs. Int J Immunopathol Pharmacol 35:731–738. https://doi.org/10.1177/2F2058738421100262110.1177/2F20587384211002621 ↗
2. Figueiró Longo JP, Muehlmann LA (2021) How has nanomedical innovation contributed to the COVID-19 vaccine development? Nanomedicine (Lond) 16:731–738. https://doi.org/10.2217/nnm-2021-003510.2217/nnm-2021-0035 ↗
3. Chen L, Liang J (2020) An overview of functional nanoparticles as novel emerging antiviral therapeutic agents. Mater Sci Eng C 112:110924. https://doi.org/10.1016/j.msec.2020.11092410.1016/j.msec.2020.110924 ↗
4. Mallapaty S (2021) Laos bats host closest known relatives of virus behind COVID. Nature 597:603. https://doi.org/10.1038/d41586-021-02596-210.1038/d41586-021-02596-2 ↗
5. Sportelli MC, Izzi M, Kukushkina EA, Hossain SI, Picca RA, Ditaranto N, Cioffi N (2020) Can nanotechnology and materials science help the fight against SARS-CoV-2? Nanomaterials 10:731–738. https://doi.org/10.3390/nano1004080210.3390/nano10040802 ↗
6. Silva LF, Dotto GL, Pinto D, Oliveira ML (2021) Nanoparticles and interfaces with toxic elements in fluvial suspended sediment. Mar Pollut Bull 168:112405. https://doi.org/10.1016/j.marpolbul.2021.11240510.1016/j.marpolbul.2021.112405 ↗
7. Oliveira ML, Dotto GL, Pinto D, Neckel A, Silva LF (2021) Nanoparticles as vectors of other contaminants in estuarine suspended sediments: natural and real conditions. Mar Pollut Bull 168:112429. https://doi.org/10.1016/j.marpolbul.2021.11242910.1016/j.marpolbul.2021.112429 ↗
8. López AF, Fabiani M, Lassalle V, Spetter C, Severini MF (2022) Critical review of the characteristics, interactions, and toxicity of micro/nanomaterials pollutants in aquatic environments. Mar Pollut Bull 174:731–738. https://doi.org/10.1016/j.marpolbul.2021.11327610.1016/j.marpolbul.2021.113276 ↗
9. Krantz MS, Phillips EJ (2022) COVID-19 mRNA vaccine safety during the first 6 months of roll-out in the USA. Lancet Infect Dis 35:731–738. https://doi.org/10.1016/S1473-3099(22)00123-210.1016/S1473-3099(22)00123-2 ↗
10. De-la-Torre GE, Pizarro-Ortega CI, Dioses-Salinas DC, Ammendolia J, Okoffo ED (2021) Investigating the current status of COVID-19 related plastics and their potential impact on human health. Curr Opin Toxicol 35:731–738. https://doi.org/10.1016/j.cotox.2021.08.00210.1016/j.cotox.2021.08.002 ↗
11. Campos EV, Pereira AE, De Oliveira JL, Carvalho LB, Guilger-Casagrande M, De Lima R, Fraceto LF (2020) How can nanotechnology help to combat COVID-19? Opportunities and urgent need. J Nanobiotechnology 18:1–23. https://doi.org/10.1186/s12951-020-00685-410.1186/s12951-020-00685-4 ↗
12. Seidi F, Deng C, Zhong Y, Liu Y, Huang Y, Li C, Xiao H (2021) Functionalized masks: powerful materials against COVID-19 and future pandemics. Small 17:2102453. https://doi.org/10.1002/smll.20210245310.1002/smll.202102453 ↗
13. Bradley D (2020) Copper against COVID. Mater Today (Kidlington, England) 40:2. https://doi.org/10.1016/j.mattod.2020.09.01610.1016/j.mattod.2020.09.016 ↗
14. Skalny AV, Rink L, Ajsuvakova OP, Aschner M, Gritsenko VA, Alekseenko SI, Svistunov AA, Petrakis D, Spandidos DA, Aaseth J (2020) Zinc and respiratory tract infections: perspectives for COVID-19. Int J Mol Med 46:17–26. https://doi.org/10.3892/ijmm.2020.457510.3892/ijmm.2020.4575 ↗
15. Sousa BC, Cote DL (2020) Antimicrobial copper cold spray coatings and SARS-CoV-2 surface inactivation. MRS Adv 5:2873–2880. https://doi.org/10.1557/adv.2020.36610.1557/adv.2020.366 ↗
16. Joost U, Juganson K, Visnapuu M, Mortimer M, Kahru A, Nõmmiste E, Kisand V, Ivask A (2015) Photocatalytic antibacterial activity of nano-TiO2 (anatase)-based thin films: effects on Escherichia coli cells and fatty acids. J Photochem Photobiol B Biol 142:178–185. https://doi.org/10.1016/j.jphotobiol.2014.12.01010.1016/j.jphotobiol.2014.12.010 ↗
17. Xiao MF, Zeng C, Li SH, Yuan FL (2021) Applications of nanomaterials in COVID-19 pandemic. Rare Met 41:1–13. https://doi.org/10.1007/s12598-021-01789-y10.1007/s12598-021-01789-y ↗
18. Bhattacharjee S, Joshi R, Chughtai AA, Macintyre CR (2019) Graphene modified multifunctional personal protective clothing. Adv Mater Interfaces 6:1900622. https://doi.org/10.1002/admi.20190062210.1002/admi.201900622 ↗
19. Palmieri V, De Maio F, De Spirito M, Papi M (2021) Face masks and nanotechnology: keep the blue side up. Nano Today 37:101077. https://doi.org/10.1016/j.nantod.2021.10107710.1016/j.nantod.2021.101077 ↗
20. El-Atab N, Qaiser N, Badghaish H, Shaikh SF, Hussain MM (2020) Flexible nanoporous template for the design and development of reusable anti-COVID-19 hydrophobic face masks. ACS Nano 14:7659–7665. https://doi.org/10.1021/acsnano.0c0397610.1021/acsnano.0c03976 ↗
21. Choi S, Jeon H, Jang M, Kim H, Shin G, Koo JM, Lee M, Sung HK, Eom Y, Yang HS (2021) Biodegradable, efficient, and breathable multi-use face mask filter. Adv Sci 8:2003155. https://doi.org/10.1002/advs.20200315510.1002/advs.202003155 ↗
22. Almanza-Reyes H, Moreno S, Plascencia-López I, Alvarado-Vera M, Patrón-Romero L, Borrego B, Reyes-Escamilla A, Valencia-Manzo D, Brun A, Pestryakov A (2021) Evaluation of silver nanoparticles for the prevention of SARS-CoV-2 infection in health workers: in vitro and in vivo. Plos One 16:e0256401. https://doi.org/10.1371/journal.pone.025640110.1371/journal.pone.0256401 ↗
23. ClinicalTrials.gov (2021) Evaluation of silver nanoparticles for the prevention of COVID-19 (COVID-19). (NCT04894409). https://clinicaltrials.gov/ct2/show/NCT04894409
24. Talebian S, Wallace GG, Schroeder A, Stellacci F, Conde J (2020) Nanotechnology-based disinfectants and sensors for SARS-CoV-2. Nat Nanotechnol 15:618–621. https://doi.org/10.1038/s41565-020-0751-010.1038/s41565-020-0751-0 ↗
25. Yasugi M, Komura Y, Ishigami Y (2022) Mechanisms underlying inactivation of SARS-CoV-2 by nano-sized electrostatic atomized water particles. J Nanopart Res 24:99. https://doi.org/10.1007/s11051-022-05485-510.1007/s11051-022-05485-5 ↗
26. Hora PI, Pati SG, McNamara PJ, Arnold WA (2020) Increased use of quaternary ammonium compounds during the SARS-CoV-2 pandemic and beyond: consideration of environmental implications. Environ Sci Technol Lett 7:622–631. https://doi.org/10.1021/acs.estlett.0c0043710.1021/acs.estlett.0c00437 ↗
27. Riva L, Yuan S, Yin X, Martin-Sancho L, Matsunaga N, Pache L, Burgstaller-Muehlbacher S, De Jesus PD, Teriete P, Hull MV (2020) Discovery of SARS-CoV-2 antiviral drugs through large-scale compound repurposing. Nature 586:113–119. https://doi.org/10.1038/s41586-020-2577-110.1038/s41586-020-2577-1 ↗
28. De Clercq E (2006) Antiviral agents active against influenza A viruses. Nat Rev Drug Discov 5:1015–1025. https://doi.org/10.1038/nrd217510.1038/nrd2175 ↗
29. Abo-Zeid Y, Ismail NS, McLean GR, Hamdy NM (2020) A molecular docking study repurposes FDA approved iron oxide nanoparticles to treat and control COVID-19 infection. Eur J Pharm Sci 153:105465. https://doi.org/10.1016/j.ejps.2020.10546510.1016/j.ejps.2020.105465 ↗
30. Behbahanipour M, Benoit R, Navarro S, Ventura S (2023) Oligobinders: bioengineered soluble amyloid-like nanoparticles to bind and neutralize SARS-CoV-2. ACS Appl Mater Interfaces 15:11444–11457. https://doi.org/10.1021/acsami.2c1830510.1021/acsami.2c18305 ↗
31. Page TM, Nie C, Neander L, Povolotsky TL, Sahoo AK, Nickl P, Adler JM, Bawadkji O, Radnik J, Achazi K (2023) Functionalized fullerene for inhibition of SARS-CoV-2 variants. Small 19:2206154. https://doi.org/10.1002/smll.20220615410.1002/smll.202206154 ↗
32. Li Z, Wang Z, Dinh P-UC, Zhu D, Popowski KD, Lutz H, Hu S, Lewis MG, Cook A, Andersen H (2021) Cell-mimicking nanodecoys neutralize SARS-CoV-2 and mitigate lung injury in a non-human primate model of COVID-19. Nat Nanotechnol 16:942–951. https://doi.org/10.1038/s41565-021-00923-210.1038/s41565-021-00923-2 ↗
33. Milovanovic M, Arsenijevic A, Milovanovic J, Kanjevac T, Arsenijevic N (2017) Nanoparticles in antiviral therapy. In: Antimicrobial nanoarchitectonics. Elsevier, pp 383–410. https://doi.org/10.1016/B978-0-323-52733-0.00014-810.1016/B978-0-323-52733-0.00014-8 ↗
34. Sanna V, Satta S, Hsiai T, Sechi M (2022) Development of targeted nanoparticles loaded with antiviral drugs for SARS-CoV-2 inhibition. Eur J Med Chem 231:114121. https://doi.org/10.1016/j.ejmech.2022.11412110.1016/j.ejmech.2022.114121 ↗
35. Khater SE, El-Khouly A, Abdel-Bar HM, Al-Mahallawi AM, Ghorab DM (2021) Fluoxetine hydrochloride loaded lipid polymer hybrid nanoparticles showed possible efficiency against SARS-CoV-2 infection. Int J Pharm 607:121023. https://doi.org/10.1016/j.ijpharm.2021.12102310.1016/j.ijpharm.2021.121023 ↗
36. Naseem T, Durrani T (2021) The role of some important metal oxide nanoparticles for wastewater and antibacterial applications: a review. Environ Chem Ecotoxicol 3:59–75. https://doi.org/10.1016/j.enceco.2020.12.00110.1016/j.enceco.2020.12.001 ↗
37. Uheida A, Mejía HG, Abdel-Rehim M, Hamd W, Dutta J (2021) Visible light photocatalytic degradation of polypropylene microplastics in a continuous water flow system. J Hazard Mater 406:124299. https://doi.org/10.1016/j.jhazmat.2020.12429910.1016/j.jhazmat.2020.124299 ↗
38. Hydzik P (2012) Nanoparticles toxicity--selective examples. Przegl Lek 69:486–489. PMID: 23243914 https://europepmc.org/article/med/23243914
39. Shirvanimoghaddam K, Czech B, Yadav R, Gokce C, Fusco L, Delogu LG, Yilmazer A, Brodie G, Al-Othman AK, Al-Tamimi AK (2022) Facemask global challenges: the case of effective synthesis, utilization, and environmental sustainability. Sustainability 14:737. https://doi.org/10.3390/su1402073710.3390/su14020737 ↗
40. Vishwakarma K, Upadhyay N, Singh J, Liu S, Singh VP, Prasad SM, Chauhan DK, Tripathi DK, Sharma S (2017) Differential phytotoxic impact of plant-mediated silver nanoparticles (AgNPs) and silver nitrate (AgNO3) on Brassica sp. Front Plant Sci 8:1501. https://doi.org/10.1016/j.aquatox.2016.04.01910.1016/j.aquatox.2016.04.019 ↗
41. Dietz K-J, Herth S (2011) Plant nanotoxicology. Trends Plant Sci 16:582–589. https://doi.org/10.1016/j.tplants.2011.08.00310.1016/j.tplants.2011.08.003 ↗
42. Begum P, Fugetsu B (2012) Phytotoxicity of multi-walled carbon nanotubes on red spinach (Amaranthus tricolor L) and the role of ascorbic acid as an antioxidant. J Hazard Mater 243:212–222. https://doi.org/10.1016/j.jhazmat.2012.10.02510.1016/j.jhazmat.2012.10.025 ↗
43. Slomberg DL, Schoenfisch MH (2012) Silica nanoparticle phytotoxicity to Arabidopsis thaliana. Environ Sci Technol 46:10247–10254. https://doi.org/10.1021/es300949f10.1021/es300949f ↗
44. Khan M, Khan MSA, Borah KK, Goswami Y, Hakeem KR, Chakrabartty I (2021) The potential exposure and hazards of metal-based nanoparticles on plants and environment, with special emphasis on ZnO NPs, TiO2 NPs, and AgNPs: a review. Environ Adv 6:100128. https://doi.org/10.1016/j.envadv.2021.10012810.1016/j.envadv.2021.100128 ↗
45. Dağhan H (2018) Effects of TiO2 nanoparticles on maize (Zea mays L.) growth, chlorophyll content, and nutrient uptake. Appl Ecol Environ Res 16:6873–6883. https://doi.org/10.15666/aeer/1605_6873688310.15666/aeer/1605_68736883 ↗
46. Lin D, Xing B (2008) Root uptake and phytotoxicity of ZnO nanoparticles. Environ Sci Technol 42:5580–5585. https://doi.org/10.1021/es800422x10.1021/es800422x ↗
47. Monica RC, Cremonini R (2009) Nanoparticles and higher plants. Caryologia 62:161–165. https://doi.org/10.1080/00087114.2004.1058968110.1080/00087114.2004.10589681 ↗
48. Raskar S, Laware S (2014) Effect of zinc oxide nanoparticles on cytology and seed germination in onion. Int J Curr Microbiol App Sci 3:467–473. https://www.ijcmas.com/vol-3-2/S.V.Raskar%20and%20S.L.Laware.pdf
49. Li CC, Wang YJ, Dang F, Zhou DM (2016) Mechanistic understanding of reduced AgNP phytotoxicity induced by extracellular polymeric substances. J Hazard Mater 308:21–28. https://doi.org/10.1016/j.jhazmat.2016.01.03610.1016/j.jhazmat.2016.01.036 ↗
50. Wang C, Jiang K, Wu B, Zhou J, Lv Y (2018) Silver nanoparticles with different particle sizes enhance the allelopathic effects of Canada goldenrod on the seed germination and seedling development of lettuce. Ecotoxicology 27:1116–1125. https://doi.org/10.1007/s10646-018-1966-910.1007/s10646-018-1966-9 ↗
51. Federici G, Shaw BJ, Handy RD (2007) Toxicity of titanium dioxide nanoparticles to rainbow trout (Oncorhynchus mykiss): gill injury, oxidative stress, and other physiological effects. Aquat Toxicol 84:415–430. https://doi.org/10.1016/j.aquatox.2007.07.00910.1016/j.aquatox.2007.07.009 ↗
52. Huang CW, Li SW, Liao VH-C (2017) Chronic ZnO-NPs exposure at environmentally relevant concentrations results in metabolic and locomotive toxicities in Caenorhabditis elegans. Environ Pollut 220:1456–1464. https://doi.org/10.1016/j.envpol.2016.10.08610.1016/j.envpol.2016.10.086 ↗
53. Bundschuh M, Filser J, Lüderwald S, McKee MS, Metreveli G, Schaumann GE, Schulz R, Wagner S (2018) Nanoparticles in the environment: where do we come from, where do we go to? Environ Sci Europe 30:1–17. https://doi.org/10.1186/s12302-018-0132-610.1186/s12302-018-0132-6 ↗
54. Labille J, Slomberg D, Catalano R, Robert S, Apers-Tremelo M-L, Boudenne J-L, Manasfi T, Radakovitch O (2020) Assessing UV filter inputs into beach waters during recreational activity: a field study of three French Mediterranean beaches from consumer survey to water analysis. Sci Total Environ 706:136010. https://doi.org/10.1016/j.scitotenv.2019.13601010.1016/j.scitotenv.2019.136010 ↗
55. Wang J, Zhu X, Zhang X, Zhao Z, Liu H, George R, Wilson-Rawls J, Chang Y, Chen Y (2011) Disruption of zebrafish (Danio rerio) reproduction upon chronic exposure to TiO2 nanoparticles. Chemosphere 83:461–467. https://doi.org/10.1016/j.chemosphere.2010.12.06910.1016/j.chemosphere.2010.12.069 ↗
56. Bodamyali T, Stevens CR, Blake DR, Winyard PG (2000) Reactive oxygen/nitrogen species and acute inflammation: a physiological process. In: Free Radicals and Inflammation. Springer, pp 11–16. https://doi.org/10.1007/978-3-0348-8482-2_210.1007/978-3-0348-8482-2_2 ↗
57. Jakubczyk K, Dec K, Kałduńska J, Kawczuga D, Kochman J, Janda K (2020) Reactive oxygen species-sources, functions, oxidative damage. Pol Merkur Lekarski 48:124–127
58. Valko M, Leibfritz D, Moncol J, Cronin MTD, Mazur M, Telser J (2007) Free radicals and antioxidants in normal physiological functions and human disease. Int J Biochem Cell Biol 39:44–84. https://doi.org/10.1016/j.biocel.2006.07.00110.1016/j.biocel.2006.07.001 ↗
59. Natarajan P, Tomich JM (2020) Understanding the influence of experimental factors on bio-interactions of nanoparticles: towards improving correlation between in vitro and in vivo studies. Arch Biochem Biophys 694:108592. https://doi.org/10.1016/j.abb.2020.10859210.1016/j.abb.2020.108592 ↗
60. Sohal IS, Cho YK, O’Fallon KS, Gaines P, Demokritou P, Bello D (2018) Dissolution behavior and biodurability of ingested engineered nanomaterials in the gastrointestinal environment. ACS Nano 12:8115–8128. https://doi.org/10.1021/acsnano.8b0297810.1021/acsnano.8b02978 ↗
61. De Matteis V (2017) Exposure to inorganic nanoparticles: routes of entry, immune response, biodistribution and in vitro/in vivo toxicity evaluation. Toxics 5:29. https://doi.org/10.3390/toxics504002910.3390/toxics5040029 ↗
62. Yang L, Ji W, Mao M, Huang J-n (2020) An updated review on the properties, fabrication and application of hybrid-nanofluids along with their environmental effects. J Clean Prod 257:120408. https://doi.org/10.1016/j.jclepro.2020.12040810.1016/j.jclepro.2020.120408 ↗
63. Hsin Y-H, Chen C-F, Huang S, Shih T-S, Lai P-S, Chueh PJ (2008) The apoptotic effect of nanosilver is mediated by a ROS-and JNK-dependent mechanism involving the mitochondrial pathway in NIH3T3 cells. Toxicol Lett 179:130–139. https://doi.org/10.1016/j.toxlet.2008.04.01510.1016/j.toxlet.2008.04.015 ↗
64. ATSDR (2014) Agency for Toxic Substances and Disease Registry (ATSDR), Toxicological profile for silver. https://wwwn.cdc.gov/TSP/ToxProfiles/ToxProfiles.aspx?id=539&tid=97. Accessed 26 March 2014
65. Rezvani E, Rafferty A, McGuinness C, Kennedy J (2019) Adverse effects of nanosilver on human health and the environment. Acta Biomater 94:145–159. https://doi.org/10.1016/j.actbio.2019.05.04210.1016/j.actbio.2019.05.042 ↗
66. Kiss B, Bíró T, Czifra G, Tóth BI, Kertész Z, Szikszai Z, Kiss ÁZ, Juhász I, Zouboulis CC, Hunyadi J (2008) Investigation of micronized titanium dioxide penetration in human skin xenografts and its effect on cellular functions of human skin-derived cells. Exp Dermatol 17:659–667. https://doi.org/10.1111/j.1600-0625.2007.00683.x10.1111/j.1600-0625.2007.00683.x ↗
67. Lademann J, Weigmann H-J, Rickmeyer C, Barthelmes H, Schaefer H, Mueller G, Sterry W (1999) Penetration of titanium dioxide microparticles in a sunscreen formulation into the horny layer and the follicular orifice. Skin Pharmacol Physiol 12:247–256. https://doi.org/10.1159/00006624910.1159/000066249 ↗
68. Bennat C, Müller-Goymann C (2000) Skin penetration and stabilization of formulations containing microfine titanium dioxide as physical UV filter. Int J Cosmet Sci 22:271–283. https://doi.org/10.1046/j.1467-2494.2000.00009.x10.1046/j.1467-2494.2000.00009.x ↗
69. Mavon A, Miquel C, Lejeune O, Payre B, Moretto P (2007) In vitro percutaneous absorption and in vivo stratum corneum distribution of an organic and a mineral sunscreen. Skin Pharmacol Physiol 20:10–20. https://doi.org/10.1159/00009616710.1159/000096167 ↗
70. Christensen FM, Johnston HJ, Stone V, Aitken RJ, Hankin S, Peters S, Aschberger K (2011) Nano-TiO2–feasibility and challenges for human health risk assessment based on open literature. Nanotoxicology 5:110–124. https://doi.org/10.3109/17435390.2010.50489910.3109/17435390.2010.504899 ↗
71. Oberdörster G, Sharp Z, Atudorei V, Elder A, Gelein R, Kreyling W, Cox C (2004) Translocation of inhaled ultrafine particles to the brain. Inhal Toxicol 16:437–445. https://doi.org/10.1080/0895837049043959710.1080/08958370490439597 ↗
72. Gutwein LG, Webster TJ (2004) Increased viable osteoblast density in the presence of nanophase compared to conventional alumina and titania particles. Biomaterials 25:4175–4183. https://doi.org/10.1016/j.biomaterials.2003.10.09010.1016/j.biomaterials.2003.10.090 ↗
73. Pollard ZA, Karod M, Goldfarb JL (2021) Metal leaching from antimicrobial cloth face masks intended to slow the spread of COVID-19. Sci Rep 11:19216. https://doi.org/10.1038/s41598-021-98577-610.1038/s41598-021-98577-6 ↗
74. Mercer RR, Scabilloni JF, Wang L, Battelli LA, Antonini JM, Roberts JR, Qian Y, Sisler JD, Castranova V, Porter DW (2018) The fate of inhaled nanoparticles: detection and measurement by enhanced dark-field microscopy. Toxicol Pathol 46:28–46. https://doi.org/10.1177/019262331773232110.1177/0192623317732321 ↗
75. Coreas R, Cao X, DeLoid GM, Demokritou P, Zhong W (2020) Lipid and protein corona of food-grade TiO2 nanoparticles in simulated gastrointestinal digestion. NanoImpact 20:100272. https://doi.org/10.1016/j.impact.2020.10027210.1016/j.impact.2020.100272 ↗
76. Baimanov D, Wang J, Zhang J, Liu K, Cong Y, Shi X, Zhang X, Li Y, Li X, Qiao R (2022) In situ analysis of nanoparticle soft corona and dynamic evolution. Nat Commun 13:5389. https://doi.org/10.1038/s41467-022-33044-y10.1038/s41467-022-33044-y ↗
77. Zhou H, McClements DJ (2022) Recent advances in the gastrointestinal fate of organic and inorganic nanoparticles in foods. Nanomaterials 12:1099. https://doi.org/10.3390/nano1207109910.3390/nano12071099 ↗
78. Li L, Huang J, Almutairi AW, Lan X, Zheng L, Lin Y, Chen L, Fu N, Lin Z, Abomohra AE-F (2021) Integrated approach for enhanced bio-oil recovery from disposed face masks through co-hydrothermal liquefaction with Spirulina platensis grown in wastewater. Biomass Conv Bioref 13:11109–11120. https://doi.org/10.1007/s13399-021-01891-210.1007/s13399-021-01891-2 ↗
79. Li S, Ding J, Zheng X, Sui Y (2021) Beach tourists behavior and beach management strategy under the ongoing prevention and control of the COVID-19 pandemic: a case study of Qingdao. China Ocean Coast Manage 215:105974. https://doi.org/10.1016/j.ocecoaman.2021.10597410.1016/j.ocecoaman.2021.105974 ↗
80. Hatami T, Rakib MRJ, Madadi R, De-la-Torre GE, Idris AM (2022) Personal protective equipment (PPE) pollution in the Caspian Sea, the largest enclosed inland water body in the world. Sci Total Environ 824:153771. https://doi.org/10.1016/j.scitotenv.2022.15377110.1016/j.scitotenv.2022.153771 ↗
81. Lee G, Lee ME, Kim SS, Joh H-I, Lee S (2022) Efficient upcycling of polypropylene-based waste disposable masks into hard carbons for anodes in sodium ion batteries. J Ind Eng Chem 105:268–277. https://doi.org/10.1016/j.jiec.2021.09.02610.1016/j.jiec.2021.09.026 ↗
82. Zhao X, Klemeš JJ, You F (2022) Energy and environmental sustainability of waste personal protective equipment (PPE) treatment under COVID-19. Renew Sustain Energy Rev 153:111786. https://doi.org/10.1016/j.rser.2021.11178610.1016/j.rser.2021.111786 ↗
83. Aragaw TA, Mekonnen BA (2021) Current plastics pollution threats due to COVID-19 and its possible mitigation techniques: a waste-to-energy conversion via pyrolysis. Environ Syst Res 10. https://doi.org/10.1186/s40068-020-00217-x10.1186/s40068-020-00217-x ↗
84. Sani A, Cao C, Cui D (2021) Toxicity of gold nanoparticles (AuNPs): a review. Biochem Biophys Rep 26:100991. https://doi.org/10.1016/j.bbrep.2021.10099110.1016/j.bbrep.2021.100991 ↗
85. Kim K-T, Truong L, Wehmas L, Tanguay RL (2013) Silver nanoparticle toxicity in the embryonic zebrafish is governed by particle dispersion and ionic environment. Nanotechnology 24:115101. https://doi.org/10.1093/toxsci/kft08110.1093/toxsci/kft081 ↗
86. Park MV, Neigh AM, Vermeulen JP, de la Fonteyne LJ, Verharen HW, Briedé JJ, van Loveren H, de Jong WH (2011) The effect of particle size on the cytotoxicity, inflammation, developmental toxicity, and genotoxicity of silver nanoparticles. Biomaterials 32:9810–9817. https://doi.org/10.1016/j.biomaterials.2011.08.08510.1016/j.biomaterials.2011.08.085 ↗
87. Renwick L, Brown D, Clouter A, Donaldson K (2004) Increased inflammation and altered macrophage chemotactic responses caused by two ultrafine particle types. Occup Environ Med 61:442–447. https://doi.org/10.1136/oem.2003.00822710.1136/oem.2003.008227 ↗
88. Sager TM, Kommineni C, Castranova V (2008) Pulmonary response to intratracheal instillation of ultrafine versus fine titanium dioxide: role of particle surface area. Part Fibre Toxicol 5:17. https://doi.org/10.1186/1743-8977-5-1710.1186/1743-8977-5-17 ↗
89. Hunt PR, Keltner Z, Gao X, Oldenburg SJ, Bushana P, Olejnik N, Sprando RL (2014) Bioactivity of nanosilver in Caenorhabditis elegans: effects of size, coat, and shape. Toxicol Rep 1:923–944. https://doi.org/10.1016/j.toxrep.2014.10.02010.1016/j.toxrep.2014.10.020 ↗
90. Nativo P, Prior IA, Brust M (2008) Uptake and intracellular fate of surface-modified gold nanoparticles. ACS Nano 2:1639–1644. https://doi.org/10.1021/nn800330a10.1021/nn800330a ↗
91. Cruje C, Chithrani B (2015) Integration of peptides for enhanced uptake of pegylated gold nanoparticles. J Nanosci Nanotechnol 15:2125–2131. https://doi.org/10.1166/jnn.2015.1032110.1166/jnn.2015.10321 ↗
92. Zhang X-D, Wu D, Shen X, Liu P-X, Fan F-Y, Fan S-J (2012) In vivo renal clearance, biodistribution, toxicity of gold nanoclusters. Biomaterials 33:4628–4638. https://doi.org/10.1016/j.biomaterials.2012.03.02010.1016/j.biomaterials.2012.03.020 ↗
93. Pollard AJ, Bijker EM (2021) A guide to vaccinology: from basic principles to new developments. Nat Rev Immunol 21:83–100. https://doi.org/10.1038/s41577-020-00497-510.1038/s41577-020-00497-5 ↗
94. Riedel S (2005) Edward Jenner and the history of smallpox and vaccination. Baylor University Med Center Proc 2005. Taylor & Francis. https://doi.org/10.1080/08998280.2005.1192802810.1080/08998280.2005.11928028 ↗
95. Nascimento I, Leite L (2012) Recombinant vaccines and the development of new vaccine strategies. Braz J Med Biol Res 45:1102–1111. https://pubmed.ncbi.nlm.nih.gov/22948379/, https://doi.org/10.1590/s0100-879x201200750014210.1590/s0100-879x2012007500142 ↗
96. Lozano D, Larraga V, Vallet-Regí M, Manzano M (2023) An overview of the use of nanoparticles in vaccine development. Nanomaterials 13:1828. https://doi.org/10.3390/nano1312182810.3390/nano13121828 ↗
97. Delany I, Rappuoli R, De Gregorio E (2014) Vaccines for the 21st century. EMBO Mol Med 6:708–720. https://doi.org/10.1002/emmm.20140387610.1002/emmm.201403876 ↗
98. Kirtane AR, Verma M, Karandikar P, Furin J, Langer R, Traverso G (2021) Nanotechnology approaches for global infectious diseases. Nat Nanotechnol 16:369–384. https://doi.org/10.1038/s41565-021-00866-810.1038/s41565-021-00866-8 ↗
99. Gregory AE, Titball R, Williamson D (2013) Vaccine delivery using nanoparticles. Front Cell Infect Microbiol 3:13. https://doi.org/10.3389/fcimb.2013.0001310.3389/fcimb.2013.00013 ↗
100. Lee J, Kim D, Byun J, Wu Y, Park J, Oh Y-K (2022) In vivo fate and intracellular trafficking of vaccine delivery systems. Adv Drug Deliv Rev 186:114325. https://doi.org/10.1016/j.addr.2022.11432510.1016/j.addr.2022.114325 ↗