Optimization of silver nanoparticle synthesis by chemical reduction and evaluation of its antimicrobial and toxic activity

Chemical reduction has become an accessible and useful alternative to obtain silver nanoparticles (AgNPs). However, its toxicity capacity depends on multiple variables that generate differences in the ability to inhibit the growth of microorganisms. Thus, optimazing parameters for the synthesis of A...

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Veröffentlicht in:Biomaterials research 2020, 24(1), , pp.53-67
Hauptverfasser: Quintero-Quiroz, Catalina, Acevedo, Natalia, Zapata-Giraldo, Jenniffer, Botero, Luz E, Quintero, Julián, Zárate-Triviño, Diana, Saldarriaga, Jorge, Pérez, Vera Z
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Sprache:eng
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Zusammenfassung:Chemical reduction has become an accessible and useful alternative to obtain silver nanoparticles (AgNPs). However, its toxicity capacity depends on multiple variables that generate differences in the ability to inhibit the growth of microorganisms. Thus, optimazing parameters for the synthesis of AgNPs can increase its antimicrobial capacity by improving its physical-chemical properties. In this study a Face Centered Central Composite Design (FCCCD) was carried out with four parameters: concentration, sodium citrate (TSC) concentration, concentration and the pH of the reaction with the objective of inhibit the growth of microorganisms. The response variables were the average size of AgNPs, the peak with the greatest intensity in the size distribution, the polydispersity of the nanoparticle size and the yield of the process. AgNPs obtained from the optimization were characterized physically and chemically. The antimicrobial activity of optimized AgNPs was evaluated against , , AmpC resistant, and and compared with AgNPs before optimization. In addition, the cytotoxicity of the optimized AgNPs was evaluated by the colorimetric assay MTT (3- (4,5- Dimethylthiazol- 2- yl)- 2, 5 - Diphenyltetrazolium Bromide). It was found that the four factors studied were significant for the response variables, and a significant model (p
ISSN:1226-4601
2055-7124
2055-7124
DOI:10.1186/s40824-019-0173-y