One-Pot Synthesis of Biocompatible Silver Nanoparticle Composites from Cellulose and Keratin: Characterization and Antimicrobial Activity
Source abstract
Abstract
A novel, simple method was developed to synthesize biocompatible composites containing 50% cellulose (CEL) and 50% keratin (KER) and silver in the form of either ionic (Ag + ) or Ag 0 nanoparticles (Ag + NPs or Ag 0 NPs). In this method, butylmethylimmidazolium chloride ([BMIm + Cl – ]), a simple ionic liquid, was used as the sole solvent and silver chloride was added to the [BMIm + Cl – ] solution of [CEL+KER] during the dissolution process. The silver in the composites can be maintained as ionic silver (Ag + ) or completely converted to metallic silver (Ag 0 ) by reducing it with NaBH 4 . The results of spectroscopy [Fourier transform infrared and X-ray diffraction (XRD)] and imaging [scanning electron microscopy (SEM)] measurements confirm that CEL and KER remain chemically intact and homogeneously distributed in the composites. Powder XRD and SEM results show that the silver in the [CEL+KER+Ag + ] and [CEL+KER+Ag 0 ] composites is homogeneously distributed throughout the composites in either Ag + (in the form of AgClNPs) or Ag 0 NPs form with sizes of 27 ± 2 or 9 ± 1 nm, respectively. Both composites were found to exhibit excellent antibacterial activity against many bacteria including Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa, methicillin-resistant S. aureus (MRSA), and vancomycin-resistant Enterococus faecalis (VRE). The antibacterial activity of both composites increases with the Ag + or Ag 0 content in the composites. More importantly, for the same bacteria and the same silver content, the [CEL+KER+AgClNPs] composite is relatively more toxic than [CEL+KER+Ag 0 NPs] composite. Experimental results confirm that there was hardly any Ag 0 NPs release from the [CEL+KER+Ag 0 NPs] composite, and hence its antimicrobial activity and biocompatibility is due not to any released Ag 0 NPs but rather entirely to the Ag 0 NPs embedded in the composite. Both AgClNPs and Ag 0 NPs were found to be toxic to human fibroblasts at higher concentration (>0.72 mmol), and for the same silver content, the [CEL+KER+AgClNPs] composite is relatively more toxic than the [CEL+KER+Ag 0 NPs] composite. As expected, by lowering the Ag 0 NPs concentration to 0.48 mmol or less, the [CEL+KER+Ag 0 NPs] composite can be made biocompatible while still retaining its antimicrobial activity against bacteria such as E. coli, S. aureus, P. aeruginosa, MRSA, and VRE. These results, together with our previous finding that [CEL+KER] composites can be used for the controlled delivery of drugs such as ciprofloxacin, clearly indicate that the [CEL+KER+Ag 0 NPs] composite possesses all of the required properties for it to be successfully used as a high-performance dressing to treat chronic ulcerous infected wounds.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Dyeing and Modifying Textile Fibers · Nanoparticles: synthesis and applications · Pigment Synthesis and Properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, Marquette University, P.O. Box 1881, Milwaukee, Wisconsin 53201-1881, United States
Laboratory for Environmental Research, University of Nova Gorica, Vipavska 13, 5000 Nova Gorica, Slovenia
Funding
National Institute of General Medical Sciences
References (50)
Show source-provided references
1. 10.1021/acs.chemrev.5b0019310.1021/acs.chemrev.5b00193 ↗
2. 10.1021/jp306063p10.1021/jp306063p ↗
3. 10.1021/nn507071610.1021/nn5070716 ↗
4. 10.1021/nn303929a10.1021/nn303929a ↗
5. 10.1021/ja107934h10.1021/ja107934h ↗
6. 10.1021/nn305395p10.1021/nn305395p ↗
7. 10.1039/C4TC01006J10.1039/C4TC01006J ↗
8. 10.1039/C6CC04584G10.1039/C6CC04584G ↗
9. 10.1166/jbn.2013.165910.1166/jbn.2013.1659 ↗
10. 10.1166/jnn.2012.616910.1166/jnn.2012.6169 ↗
11. 10.1016/j.nano.2011.05.00710.1016/j.nano.2011.05.007 ↗
12. 10.1007/s00396-015-3581-010.1007/s00396-015-3581-0 ↗
13. 10.1016/j.watres.2010.06.05710.1016/j.watres.2010.06.057 ↗
14. 10.1016/j.carres.2009.09.00110.1016/j.carres.2009.09.001 ↗
15. 10.1007/s10853-011-5882-010.1007/s10853-011-5882-0 ↗
16. 10.1016/j.carbpol.2013.10.09310.1016/j.carbpol.2013.10.093 ↗
17. 10.1021/am101224v10.1021/am101224v ↗
18. 10.1016/j.apsusc.2015.04.04710.1016/j.apsusc.2015.04.047 ↗
19. 10.1016/j.biomaterials.2009.09.07610.1016/j.biomaterials.2009.09.076 ↗
20. 10.2174/138945011131405001010.2174/1389450111314050010 ↗
21. 10.1002/jbm.a.3291310.1002/jbm.a.32913 ↗
22. 10.1163/156856298X0064010.1163/156856298X00640 ↗
23. 10.1002/elsc.20110020610.1002/elsc.201100206 ↗
24. 10.1016/j.msec.2012.10.01110.1016/j.msec.2012.10.011 ↗
25. 10.1016/j.biomaterials.2011.07.05410.1016/j.biomaterials.2011.07.054 ↗
26. 10.1039/C5GC00715A10.1039/C5GC00715A ↗
27. 10.1016/j.eurpolymj.2008.06.00410.1016/j.eurpolymj.2008.06.004 ↗
28. Khosa M. A. · J. Food Proc. Beverages · 2013 · 1 · 8
29. 10.1149/06404.0499ecst10.1149/06404.0499ecst ↗
30. 10.1021/la503436710.1021/la5034367 ↗
31. 10.1021/acssuschemeng.6b0008410.1021/acssuschemeng.6b00084 ↗
32. 10.1016/j.carbpol.2016.06.02110.1016/j.carbpol.2016.06.021 ↗
33. 10.1002/jbm.a.3452010.1002/jbm.a.34520 ↗
34. 10.1002/jbm.b.3310310.1002/jbm.b.33103 ↗
35. Mututuvari, T. M.,Supramolecular Biopolymeric Composite Materials: Green Synthesis, Characterization and Applications. Dissertation, Marquette University, Wilwaukee, WI, 2014.
36. 10.1002/app.3752710.1002/app.37527 ↗
37. Peplow, P. V.; Roddick-Lanzilotta, A. D.Orthopaedic Materials Derived from Keratin. U.S. Patent 2005/0232963 A1, 2005.
38. 10.1248/cpb.54.15610.1248/cpb.54.156 ↗
39. JCPDS file No 31-1238.
40. 10.1021/jp311970k10.1021/jp311970k ↗
41. Veronica da Silva Ferreiraa V. D. S. · Enzym. Microbial. Tech. · 2016
42. Dhas T. S. · Acta A Mol. Biomol. Spectrosc. · 2014 · 120 · 41610.1016/j.saa.2013.10.044 ↗
43. 10.1016/j.jphotobiol.2016.08.01810.1016/j.jphotobiol.2016.08.018 ↗
44. 10.1039/c2ra00006g10.1039/c2ra00006g ↗
45. 10.1016/j.biortech.2010.05.05110.1016/j.biortech.2010.05.051 ↗
46. JCPDS 04-0783.
47. Scherrer P. · Nachr. Ges. Wiss. Göttingen · 1918 · 26 · 98
48. 10.1107/S002188987801284410.1107/S0021889878012844 ↗
49. 10.1007/s10765-010-0856-z10.1007/s10765-010-0856-z ↗
50. 10.1002/9780470027318.a907910.1002/9780470027318.a9079 ↗