Silver Decorated Mesoporous Carbons for the Treatment of Acute and Chronic Wounds, in a Tissue Regeneration Context

References

• Järbrink K, Ni G, Sönnergren H, et al. The humanistic and economic burden of chronic wounds: a protocol for a systematic review. Syst Rev. 2017;6(1):15. doi:10.1186/s13643-016-0400-828118847
   PubMed Web of Science ®Google Scholar
• Frykberg RG, Banks J. Challenges in the treatment of chronic wounds. Adv Wound Care. 2015;4(9):560–582. doi:10.1089/wound.2015.0635
   PubMed Web of Science ®Google Scholar
• Velnar T, Bailey T, Smrkolj V. The wound healing process: an overview of the cellular and molecular mechanisms. J Int Med Res. 2009;37:1528–1542. doi:10.1177/14732300090370053119930861
   PubMed Web of Science ®Google Scholar
• Mofazzal Jahromi MA, Sahandi Zangabad P, Moosavi Basri SM, et al. Nanomedicine and advanced technologies for burns: preventing infection and facilitating wound healing. Adv Drug Deliv Rev. 2018;1(123):33–64. doi:10.1016/j.addr.2017.08.001
   Google Scholar
• Mosser DM, Edwards JP. Exploring the full spectrum of macrophage activation. Nat Rev Immunol. 2008;8(12):958–969. doi:10.1038/nri244819029990
   PubMed Web of Science ®Google Scholar
• Morán GAG, Parra-Medina R, Cardona AG, Ronderos PQ, Rodríguez ÉG. Cytokines, Chemokines and Growth Factors. 1st ed, (Anaya JM, Shoenfeld Y, Rojas-Villarraga A. et al., editors) Bogota: El Rosario University Press; 2013; 133–164
   Google Scholar
• Jones SG, Edwards R, Thomas DW. Inflammation and wound healing: the role of bacteria in the immuno-regulation of wound healing. Int J Low Extrem Wounds. 2004;3(4):201–208. doi:10.1177/153473460427181015866816
   PubMedGoogle Scholar
• Lau PS, Bidin N, Islam S, et al. Influence of gold nanoparticles on wound healing treatment in rat model: photobiomodulation therapy. Lasers Surg Med. 2017;49(4):380–386. doi:10.1002/lsm.2261427859389
   PubMed Web of Science ®Google Scholar
• Arafa MG, El-Kased RF, Elmazar MM. Thermoresponsive gels containing gold nanoparticles as smart antibacterial and wound healing agents. Sci Rep. 2018;8:13674. doi:10.1038/s41598-018-31895-430209256
   PubMed Web of Science ®Google Scholar
• Oyarzun-Ampuero F, Vidal A, Concha M, Morales J, Orellana S, Moreno-Villoslada I. Nanoparticles for the treatment of wounds. Curr Pharm Des. 2015;21(29):4329–4341. doi:10.2174/138161282166615090110460126323420
   PubMedGoogle Scholar
• Politano AD, Campbell KT, Rosenberger LH, Sawyer RG. Use of silver in the prevention and treatment of infections: silver review. Surg Infect (Larchmt). 2013;14(1):8–20. doi:10.1089/sur.2011.09723448590
   PubMed Web of Science ®Google Scholar
• Martínez-Castañón GA, Niño-Martínez N, Martínez-Gutierrez F, Martínez-Mendoza JR, Ruiz F. Synthesis and antibacterial activity of silver nanoparticles with different sizes. J Nanopart Res. 2008;10(8):1343–1348. doi:10.1007/s11051-008-9428-6
   Web of Science ®Google Scholar
• Pal S, Tak YK, Song JM. Does the antibacterial activity of silver nanoparticles depend on the shape of the nanoparticle? A study of the gram-negative bacterium Escherichia coli. J Biol Chem. 2007;73(6):1712–1720. doi:10.1128/AEM.02218-06
   Google Scholar
• Sau TK, Rogach AL. Complex-Shaped Metal Nanoparticles: Bottom-Up Syntheses and Applications. Wiley-VCH Verlag GmbH & Co. KGaA; 2012. doi:10.1002/9783527652570
   Google Scholar
• Marambio-Jones C, Hoek EMV. A review of the antibacterial effects of silver nanomaterials and potential implications for human health and the environment. J Nanopart Res. 2010;12(5):1531–1551. doi:10.1007/s11051-010-9900-y
   Web of Science ®Google Scholar
• Chen Y, Shi J. Mesoporous carbon biomaterials. Sci China Mater. 2015;58(3):241–257. doi:10.1007/s40843-015-0037-2
   Web of Science ®Google Scholar
• Zhao Q, Lin Y, Han N, et al. Mesoporous carbon nanomaterials in drug delivery and biomedical application. Drug Deliv. 2017;24(sup1):94–107. doi:10.1080/10717544.2017.139930029124979
   PubMedGoogle Scholar
• Ryoo R, Joo SH, Jun S. Synthesis of highly ordered carbon molecular sieves via template-mediated structural transformation. J Phys Chem B. 1999;103(37):7743–7746. doi:10.1021/jp991673a
   Web of Science ®Google Scholar
• Jun S, Joo SH, Ryoo R, et al. Synthesis of new, nanoporous carbon with hexagonally ordered mesostructure. J Am Chem Soc. 2000;122(43):10712–10713. doi:10.1021/ja002261e
   Web of Science ®Google Scholar
• Zhao D, Feng J, Huo Q, et al. Triblock copolymer syntheses of mesoporous silica with periodic 50 to 300 angstrom pores. Science. 1998;279(5350):548–552. doi:10.1126/science.279.5350.5489438845
   PubMed Web of Science ®Google Scholar
• Shin HJ, Ryoo R, Kruk M, Jaroniec M. Modification of SBA-15 pore connectivity by high-temperature calcination investigated by carbon inverse replication. Chem Commun. 2001;340–349. doi:10.1039/b009762o
   Web of Science ®Google Scholar
• Lu AH, Li WC, Schmidt W, Schüth F. Template synthesis of large pore ordered mesoporous carbon. Microporous Mesoporous Mater. 2005;80(1–3):117–128. doi:10.1016/j.micromeso.2004.12.007
   Web of Science ®Google Scholar
• Hammer Ø, Harper D, Ryan P. Past: paleontological statistics software package for education and data analysis. Paleontol Electron. 2001;4(1):9.
   Google Scholar
• Karavasili C, Amanatiadou EP, Sygellou L, et al. Development of new drug delivery system based on ordered mesoporous carbons: characterisation and cytocompatibility studies. J Mater Chem B. 2013;1(25):3167–3174. doi:10.1039/c3tb20304b
   PubMed Web of Science ®Google Scholar
• Khan MAM, Kumar S, Ahamed M, Alrokayan SA, AlSalhi MS. Structural and thermal studies of silver nanoparticles and electrical transport study of their thin films. Nanoscale Res Lett. 2011;6(1):434. doi:10.1186/1556-276X-6-43421711498
   PubMedGoogle Scholar
• Agasti N, Kaushik NK. One pot synthesis of crystalline silver nanoparticles. Am J Nanomater. 2014;2(1):4–7. doi:10.12691/ajn-2-1-2
   Google Scholar
• Lee JH, El-Fiqi A, Mandakhbayar N, Lee HH, Kim HW. Drug/ion co-delivery multi-functional nanocarrier to regenerate infected tissue defect. Biomaterials. 2017;142:62–76. doi:10.1016/j.biomaterials.2017.07.01428727999
   PubMedGoogle Scholar
• Hackenberg S, Scherzed A, Kessler M, et al. Silver nanoparticles: evaluation of DNA damage, toxicity and functional impairment in human mesenchymal stem cells. Toxicol Lett. 2011;201(1):27–33. doi:10.1016/j.toxlet.2010.12.00121145381
   PubMed Web of Science ®Google Scholar
• Manshian BB, Jimenez J, Himmelreich U, Soenen SJ. Presence of an immune system increases anti-tumor effect of Ag nanoparticle treated mice. Adv Healthc Mater. 2017;6(1):1601099. doi:10.1002/adhm.201601099
   Web of Science ®Google Scholar
• Mishra AR, Zheng J, Tang X, Goering PL. Silver nanoparticle-induced autophagic-Lysosomal disruption and NLRP3-inflammasome activation in HepG2 cells is size-dependent. Toxicol Sci. 2016;150(2):473–487. doi:10.1093/toxsci/kfw01126801583
   PubMed Web of Science ®Google Scholar
• Park EJ, Bae E, Yi J, et al. Repeated-dose toxicity and inflammatory responses in mice by oral administration of silver nanoparticles. Environ Toxicol Pharmacol. 2010;30(2):162–168. doi:10.1016/j.etap.2010.05.00421787647
   PubMed Web of Science ®Google Scholar
• Tian J, Wong KKY, Ho CM, et al. Topical delivery of silver nanoparticles promotes wound healing. ChemMedChem. 2007;2(1):129–136. doi:10.1002/cmdc.20060017117075952
   PubMed Web of Science ®Google Scholar
• Wong KKY, Cheung SOF, Huang L, et al. Further evidence of the anti-inflammatory effects of silver nanoparticles. ChemMedChem. 2009;4(7):1129–1135. doi:10.1002/cmdc.20090004919405063
   PubMed Web of Science ®Google Scholar
• Kwan KHL, Liu X, To MKT, Yeung KWK, Ho CM, Wong KKY. Modulation of collagen alignment by silver nanoparticles results in better mechanical properties in wound healing. Nanomed Nanotechnol Biol Med. 2011;7(4):497–504. doi:10.1016/j.nano.2011.01.003
   PubMed Web of Science ®Google Scholar
• Liu X, Lee PY, Ho CM, et al. Silver nanoparticles mediate differential responses in keratinocytes and fibroblasts during skin wound healing. ChemMedChem. 2010;5(3):468–475. doi:10.1002/cmdc.20090050220112331
   PubMed Web of Science ®Google Scholar
• Seo SB, Dananjaya SHS, Nikapitiya C, et al. Silver nanoparticles enhance wound healing in zebrafish (Danio rerio). Fish Shellfish Immunol. 2017;68:536–545. doi:10.1016/j.fsi.2017.07.05728757200
   PubMedGoogle Scholar
• Pakyari M, Farrokhi A, Maharlooei MK, Ghahary A. Critical role of transforming growth factor beta in different phases of wound healing. Adv Wound Care. 2013;2(5):215–224. doi:10.1089/wound.2012.0406
   PubMedGoogle Scholar
• Kulkarni AB, Huh CG, Becker D, et al. Transforming growth factor beta 1 null mutation in mice causes excessive inflammatory response and early death. Proc Natl Acad Sci U S A. 1993;90(2):770–774. doi:10.1073/pnas.90.2.7708421714
   PubMed Web of Science ®Google Scholar
• Ferrari G, Cook BD, Terushkin V, Pintucci G, Mignatti P. Transforming growth factor-beta 1 (TGF-β1) induces angiogenesis through vascular endothelial growth factor (VEGF)-mediated apoptosis. J Cell Physiol. 2009;219(2):449–458. doi:10.1002/jcp.2170619180561
   PubMed Web of Science ®Google Scholar
• Clark RAF, McCoy GA, Folkvord JM, McPherson JM. TGF-β1 stimulates cultured human fibroblasts to proliferate and produce tissue-like fibroplasia: a fibronectin matrix-dependent event. J Cell Physiol. 1997;170:5. doi:10.1002/(SICI)1097-4652(199701)170:1<69::AID-JCP8>3.0.CO;2-J
   Web of Science ®Google Scholar
• Xiao L, Du Y, Shen Y, He Y, Zhao H, Li Z. TGF-beta 1 induced fibroblast proliferation is mediated by the FGF-2/ERK pathway. Front Biosci. 2012;17:2667–2674. doi:10.2741/4077
   Web of Science ®Google Scholar
• Verrecchia F, Mauviel A. Transforming growth factor-β signaling through the Smad pathway: role in extracellular matrix gene expression and regulation. J Invest Dermatol. 2002;118(2):211–215. doi:10.1046/j.1523-1747.2002.01641.x11841535
   PubMed Web of Science ®Google Scholar
• White LA, Mitchell TI, Brinckerhoff CE. Transforming growth factor β inhibitory element in the rabbit matrix metalloproteinase-1 (collagenase-1) gene functions as a repressor of constitutive transcription. Biochim Biophys Acta - Gene Struct Expr. 2000;1490(3):259–268. doi:10.1016/S0167-4781(00)00002-6
   PubMedGoogle Scholar
• Leivonen SK, Lazaridis K, Decock J, Chantry A, Edwards DR, Kähäri VM. TGF-β-elicited induction of tissue inhibitor of metalloproteinases (TIMP)-3 expression in fibroblasts involves complex interplay between Smad3, p38α, and ERK1/2. Biochim Biophys Acta. 2013;1490(3):259–268. doi:10.1371/journal.pone.0057474
   Google Scholar
• Qureshi HY, Sylvester J, El Mabrouk M, Zafarullah M. TGF-β-induced expression of tissue inhibitor of metalloproteinases-3 gene in chondrocytes is mediated by extracellular signal-regulated kinase pathway and Sp1 transcription factor. J Cell Physiol. 2005;203(2):345–352. doi:10.1002/jcp.2022815468069
   PubMedGoogle Scholar
• Luo DD, Fielding C, Phillips A, Fraser D. Interleukin-1 beta regulates proximal tubular cell transforming growth factor beta-1 signalling. Nephrol Dial Transplant. 2009;24(9):2655–2665. doi:10.1093/ndt/gfp20819420104
   PubMedGoogle Scholar
• Das L, Levine AD. TGF-β inhibits IL-2 production and promotes cell cycle arrest in TCR-activated effector/memory T cells in the presence of sustained TCR signal transduction. J Immunol. 2014;180(3):1490–1498. doi:10.4049/jimmunol.180.3.1490
   Google Scholar
• Han HS, Jun HS, Utsugi T, Yoon JW. Molecular role of TGF-β, secreted from a new type of CD4+ suppressor T cell, NY4.2, in the prevention of autoimmune IDDM in NOD mice. J Autoimmun. 1997;10(3):299–307. doi:10.1006/jaut.1997.01379218758
   PubMedGoogle Scholar
• An Y, Liu WJ, Xue P, et al. Autophagy promotes MSC-mediated vascularization in cutaneous wound healing via regulation of VEGF secretion article. Cell Death Dis. 2018;9:58. doi:10.1038/s41419-017-0082-829352190
   PubMed Web of Science ®Google Scholar
• Xiao M, Li L, Li C, et al. Role of autophagy and apoptosis in wound tissue of deep second-degree burn in rats. Acad Emerg Med. 2014;21(4):383–391. doi:10.1111/acem.1235224730400
   PubMedGoogle Scholar
• Li L, Xiao M. Role of autophagy in burn wound progression and wound healing In: Gorbunov NV, Schneider M, editors. Autophagy in Current Trends in Cellular Physiology and Pathology. IntechOpen;2016. doi:10.5772/63711
   Google Scholar
• Xiao M, Li L, Hu Q, et al. Rapamycin reduces burn wound progression by enhancing Autophagy in deep second-degree burn in rats. Wound Repair Regen. 2013;21(6):852–859. doi:10.1111/wrr.1209023980869
   PubMed Web of Science ®Google Scholar
• Shi J, Shi S, Wu B, et al. Autophagy protein LC3 regulates the fibrosis of hypertrophic scar by controlling Bcl-xL in dermal fibroblasts. Oncotarget. 2017;8(55):93757–93770. doi:10.18632/oncotarget.2077129212187
   PubMedGoogle Scholar
• Lin J, Liu Y, Wu H, et al. Key role of TFEB nucleus translocation for silver nanoparticle-induced cytoprotective autophagy. Small. 2018;14:13. doi:10.1002/smll.201703711
   Web of Science ®Google Scholar
• Xu Y, Wang L, Bai R, Zhang T, Chen C. Silver nanoparticles impede phorbol myristate acetate-induced monocyte-macrophage differentiation and autophagy. Nanoscale. 2015;7(38):16100–16109. doi:10.1039/c5nr04200c26372376
   PubMedGoogle Scholar
• Gibbs S. In vitro irritation models and immune reactions. Skin Pharmacol Physiol. 2009;22(2):103–113. doi:10.1159/00017886919188758
   PubMedGoogle Scholar
• Duan X, Peng D, Zhang Y, et al. Sub-cytotoxic concentrations of ionic silver promote the proliferation of human keratinocytes by inducing the production of reactive oxygen species. Front Med. 2018;12(3):289–300. doi:10.1007/s11684-017-0550-729101755
   PubMedGoogle Scholar
• Patel GK, Wilson CH, Harding KG, Finlay AY, Bowden PE. Numerous keratinocyte subtypes involved in wound re-epithelialization. J Invest Dermatol. 2006;126(2):497–502. doi:10.1038/sj.jid.570010116374449
   PubMedGoogle Scholar
• Kirfel J, Magin TM, Reichelt J. Keratins: a structural scaffold with emerging functions. Cell Mol Life Sci. 2003;60(1):56–71. doi:10.1007/s00018030000412613658
   PubMedGoogle Scholar
• Takahashi K, Yan B, Yamanishi K, Imamura S, Coulombe PA. The two functional keratin 6 genes of mouse are differentially regulated and evolved independently from their human orthologs. Genomics. 1998;53(2):170–183. doi:10.1006/geno.1998.54769790766
   PubMedGoogle Scholar
• Giangreco A, Jensen KB, Takai Y, Miyoshi J, Watt FM. Necl2 regulates epidermal adhesion and wound repair. Development. 2009;136(20):3505–3514. doi:10.1242/dev.03823219783739
   PubMedGoogle Scholar
• Paladini RD, Takahashi K, Bravo NS, Coulombe PA. Onset of re-epithelialization after skin injury correlates with a reorganization of keratin filaments in wound edge keratinocytes: defining a potential role for keratin 16. J Cell Biol. 1996;132(3):381–397. doi:10.1083/jcb.132.3.3818636216
   PubMedGoogle Scholar
• Freedberg IM, Tomic-Canic M, Komine M, Blumenberg M. Keratins and the keratinocyte activation cycle. J Invest Dermatol. 2001;116(5):633–640. doi:10.1046/j.1523-1747.2001.01327.x11348449
   PubMedGoogle Scholar
• Ramirez H, Patel SB, Pastar I. The role of TGFβ signaling in wound epithelialization. Adv Wound Care. 2013;3(7):482–491. doi:10.1089/wound.2013.0466
   Google Scholar
• Eckert RL, Yaffe MB, Crish JF, Murthy S, Rorke EA, Welter JF. Involucrin-structure and role in envelope assembly. J Invest Dermatol. 1993;100(5):613–617. doi:10.1111/1523-1747.ep124722888098344
   PubMedGoogle Scholar
• Nemes Z, Marekov LN, Steinert PM. Involucrin Cross-linking by Transglutaminase 1. J Biol Chem. 1999;274(16):11013–11021. doi:10.1074/jbc.274.16.1101310196183
   PubMedGoogle Scholar
• Deucher A, Efimova T, Eckert RL. Calcium-dependent involucrin expression is inversely regulated by protein kinase C (PKC)α and PKCδ. J Biol Chem. 2002;277(19):17032–17040. doi:10.1074/jbc.M10907620011864971
   PubMedGoogle Scholar
• Deyrieux AF, Wilson VG. In vitro culture conditions to study keratinocyte differentiation using the HaCaT cell line. Cytotechnology. 2007;113(5):851–855. doi:10.1007/s10616-007-9076-1
   Google Scholar
• Löffek S, Schilling O, Franzke C-W. Biological role of matrix metalloproteinases: a critical balance. Eur Respir J. 2011;38(1):191–208. doi:10.1183/09031936.0014651021177845
   PubMed Web of Science ®Google Scholar
• Gill SE, Parks WC. Metalloproteinases and their inhibitors: regulators of wound healing. Int J Biochem Cell Biol. 2008;40(6–7):1334–1347. doi:10.1016/j.biocel.2007.10.02418083622
   PubMed Web of Science ®Google Scholar
• McCawley LJ, O’Brien P, Hudson LG. Epidermal growth factor (EGF)- and scatter factor/hepatocyte growth factor (SF/HGF)- mediated keratinocyte migration is coincident with induction of matrix metalloproteinase (MMP)-9. J Cell Physiol. 1998;176(2):255–265. doi:10.1002/(SICI)1097-4652(199808)176:2<255::AID-JCP4>3.0.CO;2-N9648913
   PubMedGoogle Scholar
• Bove PF, Wesley UV, Greul AK, Hristova M, Dostmann WR, Van Der Vliet A. Nitric oxide promotes airway epithelial wound repair through enhanced activation of MMP-9. Am J Respir Cell Mol Biol. 2007;36(2):138–146. doi:10.1165/rcmb.2006-0253SM16980554
   PubMedGoogle Scholar
• Handsley MM, Edwards DR. Metalloproteinases and their inhibitors in tumor angiogenesis. Int J Cancer. 2005;115(6):849–860. doi:10.1002/ijc.2094515729716
   PubMed Web of Science ®Google Scholar
• Mohammed FF, Smookler DS, Taylor SEM, et al. Abnormal TNF activity in Timp3-/-mice leads to chronic hepatic inflammation and failure of liver regeneration. Nat Genet. 2004;36(9):969–977. doi:10.1038/ng141315322543
   PubMed Web of Science ®Google Scholar
• Qi JH, Ebrahem Q, Moore N, et al. A novel function for tissue inhibitor of metalloproteinases-3 (TIMP3): inhibition of angiogenesis by blockage of VEGF binding to VEGF receptor-2. Nat Med. 2003;9(4):407–415. doi:10.1038/nm84612652295
   PubMed Web of Science ®Google Scholar
• Saunders WB, Bohnsack BL, Faske JB, et al. Coregulation of vascular tube stabilization by endothelial cell TIMP-2 and pericyte TIMP-3. J Cell Biol. 2006;175(1):179–191. doi:10.1083/jcb.20060317617030988
   PubMedGoogle Scholar
• Johnson KE, Wilgus TA. Vascular endothelial growth factor and angiogenesis in the regulation of cutaneous wound repair. Adv Wound Care. 2014;3(10):647–661. doi:10.1089/wound.2013.0517
   PubMedGoogle Scholar
• Hotowy A, Sawosz E, Pineda L, Sawosz F, Grodzik M, Chwalibog A. Silver nanoparticles administered to chicken affect VEGFA and FGF2 gene expression in breast muscle and heart. Nanoscale Res Lett. 2012;7(1):418. doi:10.1186/1556-276X-7-41822827927
   PubMedGoogle Scholar
• Maulik N, Das DK. Redox signaling in vascular angiogenesis. Free Radic Biol Med. 2002;33(8):1047–1060. doi:10.1016/S0891-5849(02)01005-512374616
   PubMedGoogle Scholar
• Kim YW, Byzova TV. Oxidative stress in angiogenesis and vascular disease. Blood. 2014. doi:10.1182/blood-2013-09-512749
   Google Scholar
• Augustine R, Dalvi YB, Yadu Nath VK, et al. Yttrium oxide nanoparticle loaded scaffolds with enhanced cell adhesion and vascularization for tissue engineering applications. Mater Sci Eng C. 2019;103:109801. doi:10.1016/j.msec.2019.109801
   PubMed Web of Science ®Google Scholar
• Augustine R, Dalvi YB, Dan P, et al. Nanoceria can act as the cues for angiogenesis in tissue-engineering scaffolds: toward next-generation in situ tissue engineering. ACS Biomater Sci Eng. 2018;4:4338–4353. doi:10.1021/acsbiomaterials.8b01102
   PubMed Web of Science ®Google Scholar
• Mroczek-Sosnowska N, Sawosz E, Vadalasetty KP, et al. Nanoparticles of copper stimulate angiogenesis at systemic and molecular level. Int J Mol Sci. 2015;16:4838–4849. doi:10.3390/ijms1603483825741768
   PubMed Web of Science ®Google Scholar
• Augustine R, Dominic EA, Reju I, Kaimal B, Kalarikkal N, Thomas S. Investigation of angiogenesis and its mechanism using zinc oxide nanoparticle-loaded electrospun tissue engineering scaffolds. RSC Adv. 2014;4:51528–51536. doi:10.1039/c4ra07361d
   Web of Science ®Google Scholar
• Augustine R, Nethi SK, Kalarikkal N, Thomas S, Patra CR. Electrospun polycaprolactone (PCL) scaffolds embedded with europium hydroxide nanorods (EHNs) with enhanced vascularization and cell proliferation for tissue engineering applications. J Mater Chem B. 2017;5:4660–4672. doi:10.1039/c7tb00518k
   PubMed Web of Science ®Google Scholar
• Behravan M, Hossein Panahi A, Naghizadeh A, Ziaee M, Mahdavi R, Mirzapour A. Facile green synthesis of silver nanoparticles using Berberis vulgaris leaf and root aqueous extract and its antibacterial activity. Int J Biol Macromol. 2019;124:148–154. doi:10.1016/j.ijbiomac.2018.11.10130447360
   PubMed Web of Science ®Google Scholar
• Gunasekaran T, Nigusse T, Dhanaraju MD. Silver nanoparticles as real topical bullets for wound healing. J Am Coll Clin Wound Spec. 2011;3(4):82–96. doi:10.1016/j.jcws.2012.05.00124527370
   PubMedGoogle Scholar
• Percival SL, Bowler PG, Russell D. Bacterial resistance to silver in wound care. J Hosp Infect. 2005;60(1):1–7. doi:10.1016/j.jhin.2004.11.01415823649
   PubMed Web of Science ®Google Scholar
• Rupp ME, Archer GL. Coagulase-negative staphylococci: pathogens associated with medical progress. Clin Infect Dis. 1994;19:231–245. doi:10.1093/clinids/19.2.2317986894
   PubMed Web of Science ®Google Scholar
• Pazos-Ortiz E, Roque-Ruiz JH, Hinojos-Márquez EA, et al. Dose-dependent antimicrobial activity of silver nanoparticles on polycaprolactone fibers against gram-positive and gram-negative bacteria. J Nanomater. 2017;2017:1–9. doi:10.1155/2017/4752314
   Web of Science ®Google Scholar