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亚马逊水果的生物技术应用:基于(图库马)提取物,由细菌纤维素和银纳米颗粒制备活性纳米复合材料。

Biotechnological Utilization of Amazonian Fruit: Development of Active Nanocomposites from Bacterial Cellulose and Silver Nanoparticles Based on (Tucumã) Extract.

作者信息

Dos Santos Sidney S, Cerqueira Miguel Ângelo, Azevedo Ana Gabriela, Pastrana Lorenzo M, Aouada Fauze Ahmad, Tanaka Fabrício C, Perotti Gustavo Frigi, de Moura Marcia Regina

机构信息

Hybrid Composites and Nanocomposites Group (GCNH), Department of Physics and Chemistry, Ilha Solteira School of Engineering, São Paulo State University (UNESP), Ilha Solteira CEP 15385-000, SP, Brazil.

Instituto de Ciências Exatas e Tecnologia, Universidade Federal do Amazonas (UFAM), Itacoatiara CEP 69104-404, AM, Brazil.

出版信息

Pharmaceuticals (Basel). 2025 May 26;18(6):799. doi: 10.3390/ph18060799.

DOI:10.3390/ph18060799
PMID:40573196
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12195901/
Abstract

The rise of bacterial resistance and the search for alternative, biocompatible antimicrobial materials have driven interest in natural-based nanocomposites. In this context, silver nanoparticles (AgNPs) have shown broad-spectrum antibacterial activity, and bacterial cellulose (BC) is widely recognized for its high purity, hydrophilicity, and biocompatibility. This study aimed to develop a bio-based BC-AgNP nanocomposite via green synthesis using (tucumã) extract and assess its antimicrobial performance for wound dressing applications. BC was biosynthesized via green tea fermentation (20 g/L tea and 100 g/L sugar) and purified prior to use. AgNPs were obtained by reacting aqueous tucumã extract with silver nitrate (0.1 mmol/L) at pH (9) and temperature (40 °C). BC membranes were immersed in the AgNPs dispersion for 7 days to form the nanocomposite. Characterization was performed using UV-Vis, DLS, TEM, SEM-EDS, FTIR, XRD, ICP-OES, and swelling analysis. Antibacterial activity was evaluated using the disk diffusion method against and (ATCC 6538 and 4388). The UV-Vis spectra revealed a gradual decrease in the surface plasmon resonance (SPR) band over 7 days of incubation with BC, indicating progressive incorporation of AgNPs into the membrane. ICP analysis confirmed silver incorporation in the BC membrane at 0.00215 mg/mL, corresponding to 15.5% of the initial silver content. Antimicrobial assays showed inhibition zones of 6.5 ± 0.5 mm for and 4.3 ± 0.3 mm for . These findings validate the successful formation and antimicrobial performance of the BC-AgNP nanocomposite, supporting its potential use in wound care applications.

摘要

细菌耐药性的增加以及对替代的、生物相容性抗菌材料的探索,激发了人们对天然基纳米复合材料的兴趣。在这种背景下,银纳米颗粒(AgNPs)已显示出广谱抗菌活性,而细菌纤维素(BC)因其高纯度、亲水性和生物相容性而被广泛认可。本研究旨在通过使用图康(tucumã)提取物进行绿色合成来开发一种生物基BC-AgNP纳米复合材料,并评估其在伤口敷料应用中的抗菌性能。BC通过绿茶发酵(20 g/L茶叶和100 g/L糖)进行生物合成,并在使用前进行纯化。通过使图康水提取物与硝酸银(0.1 mmol/L)在pH值为9和温度为40°C的条件下反应获得AgNPs。将BC膜浸入AgNPs分散液中7天以形成纳米复合材料。使用紫外可见光谱(UV-Vis)、动态光散射(DLS)、透射电子显微镜(TEM)、扫描电子显微镜-能谱分析(SEM-EDS)、傅里叶变换红外光谱(FTIR)、X射线衍射(XRD)、电感耦合等离子体质谱(ICP-OES)和溶胀分析进行表征。使用纸片扩散法针对金黄色葡萄球菌(Staphylococcus aureus)和大肠杆菌(Escherichia coli)(ATCC 6538和4388)评估抗菌活性。紫外可见光谱显示,在与BC孵育的7天内,表面等离子体共振(SPR)带逐渐下降,表明AgNPs逐渐掺入膜中。ICP分析证实BC膜中银的掺入量为0.00215 mg/mL,相当于初始银含量的15.5%。抗菌试验显示,对金黄色葡萄球菌的抑菌圈为6.5±0.5 mm,对大肠杆菌的抑菌圈为4.3±0.3 mm。这些发现证实了BC-AgNP纳米复合材料的成功形成及其抗菌性能,支持了其在伤口护理应用中的潜在用途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc76/12195901/84caf4f1709c/pharmaceuticals-18-00799-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc76/12195901/9a62c527a482/pharmaceuticals-18-00799-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc76/12195901/34146fadb1fc/pharmaceuticals-18-00799-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc76/12195901/150f56098c37/pharmaceuticals-18-00799-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc76/12195901/2a833c502d8c/pharmaceuticals-18-00799-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc76/12195901/a794eff48dc9/pharmaceuticals-18-00799-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc76/12195901/db5b453fd671/pharmaceuticals-18-00799-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc76/12195901/3c426a7f4cc1/pharmaceuticals-18-00799-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc76/12195901/84caf4f1709c/pharmaceuticals-18-00799-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc76/12195901/9a62c527a482/pharmaceuticals-18-00799-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc76/12195901/34146fadb1fc/pharmaceuticals-18-00799-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc76/12195901/150f56098c37/pharmaceuticals-18-00799-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc76/12195901/2a833c502d8c/pharmaceuticals-18-00799-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc76/12195901/a794eff48dc9/pharmaceuticals-18-00799-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc76/12195901/db5b453fd671/pharmaceuticals-18-00799-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc76/12195901/3c426a7f4cc1/pharmaceuticals-18-00799-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc76/12195901/84caf4f1709c/pharmaceuticals-18-00799-g008.jpg

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