Construction of antibacterial nano-silver embedded bioactive hydrogel to repair infectious skin defects
Source abstract
Abstract
Abstract Background Hydrogels loaded with antimicrobial agents have been widely used for treating infected wound defects. However, hydrogels derived from a porcine dermal extracellular matrix (PADM), containing silver nanoparticles (AgNPs), have not yet been studied. Therefore, we investigated the therapeutic effect of an AgNP-impregnated PADM (AgNP–PADM) hydrogel on the treatment of infected wounds. Methods An AgNP–PADM hydrogel was synthesized by embedding AgNPs into a PADM hydrogel. We examined the porosity, moisture retention, degradation, antibacterial properties, cytotoxicity, antioxidant properties, and ability of the PADM and AgNP–PADM hydrogels to treat infected wounds in animals. Results The PADM and AgNP–PADM hydrogels were pH sensitive, which made them flow dynamically and solidify under acidic and neutral conditions, respectively. The hydrogels also exhibited porous network structures, satisfactory moisture retention, and slow degradation. Additionally, the AgNP–PADM hydrogel showed a slow and sustained release of AgNPs for at least 7 days without the particle size changing. Thus, the AgNPs exhibited adequate antibacterial ability, negligible toxicity, and antioxidant properties in vitro. Moreover, the AgNP–PADM hydrogel promoted angiogenesis and healed infected skin defects in vivo. Conclusions The AgNP–PADM hydrogel is a promising bioderived antibacterial material for clinical application to infected wound dressings.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Wound Healing and Treatments · Tissue Engineering and Regenerative Medicine · Corneal Surgery and Treatments
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Spine Surgery, The Central Hospital Affiliated to Shaoxing University, Shaoxing 312030, China.
Central laboratory, The Central Hospital Affiliated to Shaoxing University, Shaoxing 312030, China.
Funding
the Natural Science Foundation of Zhejiang Province · the Medical and Health Science and Technology Plan Project of Zhejiang Province
References (58)
Show source-provided references
1. Bruna T Maldonado-Bravo F Jara P Caro N. Silver nanoparticles and their antibacterial applications. Int J Mol Sci. 2021. https://doi.org/10.3390/ijms22137202.10.3390/ijms22137202 ↗
2. Xiao X Zhu Y Liao J Wang T Sun W Tong Z. High-efficient and synergetic antibacterial nanocomposite hydrogel with quaternized chitosan/ag nanoparticles prepared by one-pot UV photochemical synthesis. Biopolymers. 2020. https://doi.org/10.1002/bip.23354.10.1002/bip.23354 ↗
3. Yang K Han Q Chen B Zheng Y Zhang K Li Q et al. Antimicrobial hydrogels: promising materials for medical application. Int J Nanomedicine. 2018. https://doi.org/10.2147/ijn.S154748.10.2147/IJN.S154748 ↗
4. Chinnasamy G Chandrasekharan S Koh TW Bhatnagar S. Synthesis characterization antibacterial and wound healing efficacy of silver nanoparticles from Azadirachta indica. Front Microbiol. 2021. https://doi.org/10.3389/fmicb.2021.611560.10.3389/fmicb.2021.611560 ↗
5. Mathur P Jha S Ramteke S Jain NK. Pharmaceutical aspects of silver nanoparticles. Artif Cells Nanomed Biotechnol. 2018. https://doi.org/10.1080/21691401.2017.1414825.10.1080/21691401.2017.1414825 ↗
6. Sapkota K Narayanan KB Han SS. Environmentally sustainable synthesis of catalytically-active silver nanoparticles and their cytotoxic effect on human keratinocytes. J Clust Sci. 2017. https://doi.org/10.1007/s10876-017-1169-1.10.1007/s10876-017-1169-1 ↗
7. Pérez-Díaz M Alvarado-Gomez E Magaña-Aquino M Sánchez-Sánchez R Velasquillo C Gonzalez C et al. Anti-biofilm activity of chitosan gels formulated with silver nanoparticles and their cytotoxic effect on human fibroblasts. Mater Sci Eng C Mater Biol Appl. 2016. https://doi.org/10.1016/j.msec.2015.11.036.10.1016/j.msec.2015.11.036 ↗
8. Gao T Tian C Ma Z Chu Z Wang Z Zhang P. Stem cell seeded and silver nanoparticles loaded bilayer PLGA/PVA dressings for wound healing. Macromol Biosci. 2020. https://doi.org/10.1002/mabi.202000141.10.1002/mabi.202000141 ↗
9. Masood N Ahmed R Tariq M Ahmed Z Masoud MS Ali I et al. Silver nanoparticle impregnated chitosan-PEG hydrogel enhances wound healing in diabetes induced rabbits. Int J Pharm. 2019. https://doi.org/10.1016/j.ijpharm.2019.01.019.10.1016/j.ijpharm.2019.01.019 ↗
10. Diniz FR Maia R Rannier L Andrade LNMVC da Silva CF Corrêa CB et al. Silver nanoparticles-composing alginate/gelatine hydrogel improves wound healing in vivo. Nanomaterials (Basel). 2020. https://doi.org/10.3390/nano10020390.10.3390/nano10020390 ↗
11. Haidari H Kopecki Z Sutton AT Garg S Cowin AJ Vasilev K. pH-responsive “smart” hydrogel for controlled delivery of silver nanoparticles to infected wounds. Antibiotics (Basel). 2021. https://doi.org/10.3390/antibiotics10010049.10.3390/antibiotics10010049 ↗
12. Zhang M Wang D Ji N Lee S Wang G Zheng Y et al. Bioinspired design of sericin/chitosan/ag@MOF/GO hydrogels for efficiently combating resistant bacteria rapid hemostasis and wound healing. Polymers (Basel). 2021. https://doi.org/10.3390/polym13162812.10.3390/polym13162812 ↗
13. Li Y Li G Sha X Li L Zhang K Liu D et al. An intelligent vancomycin release system for preventing surgical site infections of bone tissues. Biomater Sci. 2020. https://doi.org/10.1039/d0bm00255k.10.1039/D0BM00255K ↗
14. Cai D Chen S Wu B Chen J Tao D Li Z et al. Construction of multifunctional porcine acellular dermal matrix hydrogel blended with vancomycin for hemorrhage control antibacterial action and tissue repair in infected trauma wounds. Mater Today Bio. 2021. https://doi.org/10.1016/j.mtbio.2021.100127.10.1016/j.mtbio.2021.100127 ↗
15. Haidari H Kopecki Z Bright R Cowin AJ Garg S Goswami N et al. Ultrasmall AgNP-impregnated biocompatible hydrogel with highly effective biofilm elimination properties. ACS Appl Mater Interfaces. 2020. https://doi.org/10.1021/acsami.0c09414.10.1021/acsami.0c09414 ↗
16. Qiu P Li M Chen K Fang B Chen P Tang Z et al. Periosteal matrix-derived hydrogel promotes bone repair through an early immune regulation coupled with enhanced angio- and osteogenesis. Biomaterials. 2020. https://doi.org/10.1016/j.biomaterials.2019.119552.10.1016/j.biomaterials.2019.119552 ↗
17. Farnebo S Woon CY Schmitt T Joubert LM Kim M Pham H et al. Design and characterization of an injectable tendon hydrogel: a novel scaffold for guided tissue regeneration in the musculoskeletal system. Tissue Eng Part A. 2014. https://doi.org/10.1089/ten.TEA.2013.0207.10.1089/ten.tea.2013.0207 ↗
18. Parmaksiz M Dogan A Odabas S Elçin AE Elçin YM. Clinical applications of decellularized extracellular matrices for tissue engineering and regenerative medicine. Biomed Mater. 2016. https://doi.org/10.1088/1748-6041/11/2/022003.10.1088/1748-6041/11/2/022003 ↗
19. Schoen B Avrahami R Baruch L Efraim Y Goldfracht I Elul O et al. Electrospun extracellular matrix: paving the way to tailor-made natural scaffolds for cardiac tissue regeneration. 2017. https://doi.org/10.1002/adfm.201700427.10.1002/adfm.201700427 ↗
20. Naahidi S Jafari M Logan M Wang Y Yuan Y Bae H et al. Biocompatibility of hydrogel-based scaffolds for tissue engineering applications. Biotechnol Adv. 2017. https://doi.org/10.1016/j.biotechadv.2017.05.006.10.1016/j.biotechadv.2017.05.006 ↗
21. Reátegui-Pinedo N Salirrosas D Sánchez-Tuesta L Quiñones C Jáuregui-Rosas SR Barraza G et al. Characterization of collagen from three genetic lines (gray red and F1) of Oreochromis niloticus (Tilapia) skin in young and old adults. Molecules. 2022. https://doi.org/10.3390/molecules27031123.10.3390/molecules27031123 ↗
22. Pan H Fan D Duan Z Zhu C Fu R Li X. Non-stick hemostasis hydrogels as dressings with bacterial barrier activity for cutaneous wound healing. Mater Sci Eng C Mater Biol Appl. 2019. https://doi.org/10.1016/j.msec.2019.110118.10.1016/j.msec.2019.110118 ↗
23. Derkach SR Kolotova DS Kuchina YA Shumskaya NV. Characterization of fish gelatin obtained from Atlantic cod skin using enzymatic treatment. Polymers (Basel). 2022. https://doi.org/10.3390/polym14040751.10.3390/polym14040751 ↗
24. Riaz M Mutreja V Sareen S Ahmad B Faheem M Zahid N et al. Exceptional antibacterial and cytotoxic potency of monodisperse greener AgNPs prepared under optimized pH and temperature. Sci Rep. 2021. https://doi.org/10.1038/s41598-021-82555-z.10.1038/s41598-021-82555-z ↗
25. Călina I Demeter M Scărișoreanu A Sătulu V Mitu B. One step e-beam radiation cross-linking of quaternary hydrogels dressings based on chitosan-poly (vinyl-pyrrolidone)-poly (ethylene glycol)-poly (acrylic acid). Int J Mol Sci. 2020. https://doi.org/10.3390/ijms21239236.10.20944/preprints202011.0194.v1 ↗
26. Chen X Zhang H Yang X Zhang W Jiang M Wen T et al. Preparation and application of quaternized chitosan- and AgNPs-base synergistic antibacterial hydrogel for burn wound healing. Molecules. 2021. https://doi.org/10.3390/molecules26134037.10.3390/molecules26134037 ↗
27. Chen Y Dan N Dan W Liu X Cong L. A novel antibacterial acellular porcine dermal matrix cross-linked with oxidized chitosan oligosaccharide and modified by in situ synthesis of silver nanoparticles for wound healing applications. Mater Sci Eng C Mater Biol Appl. 2019. https://doi.org/10.1016/j.msec.2018.10.036.10.1016/j.msec.2018.10.036 ↗
28. Zhang Y Chen Y Zhao B Gao J Xia L Xing F et al. Detection of type I and III collagen in porcine acellular matrix using HPLC-MS. Regen Biomater. 2020. https://doi.org/10.1093/rb/rbaa032.10.1093/rb/rbaa032 ↗
29. Taglietti A Diaz Fernandez YA Amato E Cucca L Dacarro G Grisoli P et al. Antibacterial activity of glutathione-coated silver nanoparticles against gram positive and gram negative bacteria. Langmuir. 2012. https://doi.org/10.1021/la3003838.10.1021/la3003838 ↗
30. Xiao L Hui F Tian T Yan R Xin J Zhao X et al. A novel conductive antibacterial nanocomposite hydrogel dressing for healing of severely infected wounds. Front Chem. 2021. https://doi.org/10.3389/fchem.2021.787886.10.3389/fchem.2021.787886 ↗
31. Wakabayashi N Sakai A Takada H Hoshi T Sano H Ichinose S et al. Noncontact phased-array ultrasound facilitates acute wound healing in mice. Plast Reconstr Surg. 2020. https://doi.org/10.1097/prs.0000000000006481.10.1097/PRS.0000000000006481 ↗
32. Koppe C Hoene A Walschus U Finke B Testrich H Pohl C et al. Local inflammatory response after intramuscularly implantation of anti-adhesive plasma-fluorocarbon-polymer coated Ti6AI4V discs in rats. Polymers (Basel). 2021. https://doi.org/10.3390/polym13162684.10.3390/polym13162684 ↗
33. Kobayashi H Kosaka T Mikami S Kimura T Hongo H Kosugi M et al. Vasohibin-1 expression as a biomarker of aggressive nature in ductal adenocarcinoma of the prostate: a retrospective cohort study at two centres in Japan. BMJ Open. 2021. https://doi.org/10.1136/bmjopen-2021-056439.10.1136/bmjopen-2021-056439 ↗
34. Chappell JC Wiley DM Bautch VL. Regulation of blood vessel sprouting. Semin Cell Dev Biol. 2011. https://doi.org/10.1016/j.semcdb.2011.10.006.10.1016/j.semcdb.2011.10.006 ↗
35. Tonnesen MG Feng X Clark RA. Angiogenesis in wound healing. J Investig Dermatol Symp Proc. 2000. https://doi.org/10.1046/j.1087-0024.2000.00014.x.10.1046/j.1087-0024.2000.00014.x ↗
36. Rao SQ Zhang RY Chen R Gao YJ Gao L Yang ZQ. Nanoarchitectonics for enhanced antibacterial activity with lactobacillus buchneri S-layer proteins-coated silver nanoparticles. J Hazard Mater. 2022. https://doi.org/10.1016/j.jhazmat.2021.128029.10.1016/j.jhazmat.2021.128029 ↗
37. Paramelle D Sadovoy A Gorelik S Free P Hobley J Fernig DG. A rapid method to estimate the concentration of citrate capped silver nanoparticles from UV-visible light spectra. Analyst. 2014. https://doi.org/10.1039/c4an00978a.10.1039/C4AN00978A ↗
38. Slepička P Slepičková Kasálková N Siegel J Kolská Z Švorčík V. Methods of gold and silver nanoparticles preparation. Materials (Basel). 2019. https://doi.org/10.3390/ma13010001.10.3390/ma13010001 ↗
39. Feng B Zhang S Wang D Li Y Zheng P Gao L et al. Study on antibacterial wood coatings with soybean protein isolate nano-silver hydrosol. Prog Org Coat. 2022. https://doi.org/10.1016/j.porgcoat.2022.106766.10.1016/j.porgcoat.2022.106766 ↗
40. El-Sherbiny GM Abou El-Nour SA Askar AA Mohammad NH Hammad AA. Solar radiation-induced synthesis of bacterial cellulose/silver nanoparticles (BC/AgNPs) composite using BC as reducing and capping agent. Bioprocess Biosyst Eng. 2022. https://doi.org/10.1007/s00449-021-02655-y.10.1007/s00449-021-02655-y ↗
41. Wroe JA Johnson CT García AJ. Bacteriophage delivering hydrogels reduce biofilm formation in vitro and infection in vivo. J Biomed Mater Res A. 2020. https://doi.org/10.1002/jbm.a.36790.10.1002/jbm.a.36790 ↗
42. Wolf MT Daly KA Brennan-Pierce EP Johnson SA Carruthers CA D'Amore A et al. A hydrogel derived from decellularized dermal extracellular matrix. Biomaterials. 2012. https://doi.org/10.1016/j.biomaterials.2012.06.051.10.1016/j.biomaterials.2012.06.051 ↗
43. Siah CR Childs C Chia CK Cheng KFK. An observational study of temperature and thermal images of surgical wounds for detecting delayed wound healing within four days after surgery. J Clin Nurs. 2019. https://doi.org/10.1111/jocn.14832.10.1111/jocn.14832 ↗
44. Ardan T Cejková J. Immunohistochemical expression of matrix metalloproteinases in the rabbit corneal epithelium upon UVA and UVB irradiation. Acta Histochem. 2012. https://doi.org/10.1016/j.acthis.2011.10.004.10.1016/j.acthis.2011.10.004 ↗
45. Wahl SM Wahl LM. Regulation of macrophage collagenase prostaglandin and fibroblast-activating-factor production by anti-inflammatory agents: different regulatory mechanisms for tissue injury and repair. Cell Immunol. 1985. https://doi.org/10.1016/0008-8749(85)90011-5.10.1016/0008-8749(85)90011-5 ↗
46. Buckley-Sturrock A Woodward SC Senior RM Griffin GL Klagsbrun M Davidson JM. Differential stimulation of collagenase and chemotactic activity in fibroblasts derived from rat wound repair tissue and human skin by growth factors. J Cell Physiol. 1989. https://doi.org/10.1002/jcp.1041380111.10.1002/jcp.1041380111 ↗
47. Müller SA van der Smissen A von Feilitzsch M Anderegg U Kalkhof S von Bergen M. Quantitative proteomics reveals altered expression of extracellular matrix related proteins of human primary dermal fibroblasts in response to sulfated hyaluronan and collagen applied as artificial extracellular matrix. J Mater Sci Mater Med. 2012. https://doi.org/10.1007/s10856-012-4760-x.10.1007/s10856-012-4760-x ↗
48. Thangavel N Jayakumar I Ravichandran M Vaidyanathan Ganesan V Nair BU. Photocrosslinking of collagen using Ru (II)-polypyridyl complex functionalized gold nanoparticles. Spectrochim Acta A Mol Biomol Spectrosc. 2019. https://doi.org/10.1016/j.saa.2019.02.098.10.1016/j.saa.2019.02.098 ↗
49. Gao Y Liu S Huang J Guo W Chen J Zhang L et al. The ECM-cell interaction of cartilage extracellular matrix on chondrocytes. Biomed Res Int. 2014. https://doi.org/10.1155/2014/648459.10.1155/2014/648459 ↗
50. Mott JD Werb Z. Regulation of matrix biology by matrix metalloproteinases. Curr Opin Cell Biol. 2004. https://doi.org/10.1016/j.ceb.2004.07.010.10.1016/j.ceb.2004.07.010 ↗
51. Sellaro TL Ranade A Faulk DM McCabe GP Dorko K Badylak SF et al. Maintenance of human hepatocyte function in vitro by liver-derived extracellular matrix gels. Tissue Eng Part A. 2010. https://doi.org/10.1089/ten.TEA.2008.0587.10.1089/ten.tea.2008.0587 ↗
52. Gong D Yu F Zhou M Dong W Yan D Zhang S et al. Ex vivo and in vivo properties of an injectable hydrogel derived from acellular ear cartilage extracellular matrix. Front Bioeng Biotechnol. 2021. https://doi.org/10.3389/fbioe.2021.740635.10.3389/fbioe.2021.740635 ↗
53. Fu W Xu P Feng B Lu Y Bai J Zhang J et al. A hydrogel derived from acellular blood vessel extracellular matrix to promote angiogenesis. J Biomater Appl. 2019. https://doi.org/10.1177/0885328219831055.10.1177/0885328219831055 ↗
54. Carrola J Bastos V Jarak I Oliveira-Silva R Malheiro E Daniel-da-Silva AL et al. Metabolomics of silver nanoparticles toxicity in HaCaT cells: structure-activity relationships and role of ionic silver and oxidative stress. Nanotoxicology. 2016. https://doi.org/10.1080/17435390.2016.1177744.10.1080/17435390.2016.1177744 ↗
55. Piao MJ Kang KA Lee IK Kim HS Kim S Choi JY et al. Silver nanoparticles induce oxidative cell damage in human liver cells through inhibition of reduced glutathione and induction of mitochondria-involved apoptosis. Toxicol Lett. 2011. https://doi.org/10.1016/j.toxlet.2010.12.010.10.1016/j.toxlet.2010.12.010 ↗
56. Avalos A Haza AI Mateo D Morales P. Interactions of manufactured silver nanoparticles of different sizes with normal human dermal fibroblasts. Int Wound J. 2016. https://doi.org/10.1111/iwj.12244.10.1111/iwj.12244 ↗
57. Preman NK E SS Prabhu A Shaikh SB C V Barki RR Bhandary YP Rekha PD Johnson RP. Bioresponsive supramolecular hydrogels for hemostasis infection control and accelerated dermal wound healing. J Mater Chem B. 2020. https://doi.org/10.1039/d0tb01468k.10.1039/D0TB01468K ↗
58. Dinda B Kyriakopoulos AM Dinda S Zoumpourlis V Thomaidis NS Velegraki A et al. Cornus mas L. (cornelian cherry) an important European and Asian traditional food and medicine: Ethnomedicine phytochemistry and pharmacology for its commercial utilization in drug industry. J Ethnopharmacol. 2016. https://doi.org/10.1016/j.jep.2016.09.042.10.1016/j.jep.2016.09.042 ↗