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利用罗勒水提取物绿色合成银纳米颗粒并评估其对临床和食品病原体的抗菌活性

Green Synthesis of Silver Nanoparticles Using L. Aqueous Extract with the Evaluation of Its Antibacterial Activity against Clinical and Food Pathogens.

作者信息

Alahmad Abdalrahim, Al-Zereini Wael A, Hijazin Tahani J, Al-Madanat Osama Y, Alghoraibi Ibrahim, Al-Qaralleh Omar, Al-Qaraleh Samer, Feldhoff Armin, Walter Johanna-Gabriela, Scheper Thomas

机构信息

Institut für Technische Chemie, Leibniz Universität Hannove, Callinstraße 5, 30167 Hannover, Germany.

Department of Biological Sciences, Faculty of Scince, Mutah University, P.O. Box 7, Mutah 61710, Jordan.

出版信息

Pharmaceutics. 2022 May 21;14(5):1104. doi: 10.3390/pharmaceutics14051104.

DOI:10.3390/pharmaceutics14051104
PMID:35631691
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9144328/
Abstract

The rapid development of nanotechnology and its applications in medicine has provided the perfect solution against a wide range of different microbes, especially antibiotic-resistant ones. In this study, a one-step approach was used in preparing silver nanoparticles (AgNPs) by mixing silver nitrate with hot (St. John's wort) aqueous extract under high stirring to prevent agglomeration. The formation of silver nanoparticles was monitored by continuous measurement of the surface plasma resonance spectra (UV-VIS). The effect of St. John's wort aqueous extract on the formation of silver nanoparticles was evaluated and fully characterized by using different physicochemical techniques. The obtained silver nanoparticles were spherical, monodisperse, face-centered cubic (fcc) crystal structures, and the size ranges between 20 to 40 nm. They were covered with a capping layer of organic compounds considered as a nano dimension protective layer that prevents agglomeration and sedimentation. AgNPs revealed antibacterial activity against both tested Gram-positive and Gram-negative bacterial strains causing the formation of 13-32 mm inhibition zones with MIC 6.25-12.5 µg/mL; strains were resistant to tested AgNPs. The specific growth rate of was significantly reduced due to tested AgNPs at concentrations ≥½ MIC. AgNPs did not affect wound migration in fibroblast cell lines compared to control. Our results highlighted the potential use of AgNPs capped with plant extracts in the pharmaceutical and food industries to control bacterial pathogens' growth; however, further studies are required to confirm their wound healing capability and their health impact must be critically evaluated.

摘要

纳米技术的迅速发展及其在医学中的应用为应对多种不同微生物,尤其是对抗生素耐药的微生物提供了完美的解决方案。在本研究中,采用了一种一步法,通过在高速搅拌下将硝酸银与热的(圣约翰草)水提取物混合来制备银纳米颗粒(AgNPs),以防止团聚。通过连续测量表面等离子体共振光谱(紫外 - 可见光谱)监测银纳米颗粒的形成。利用不同的物理化学技术评估并全面表征了圣约翰草水提取物对银纳米颗粒形成的影响。所获得的银纳米颗粒呈球形、单分散,具有面心立方(fcc)晶体结构,尺寸范围在20至40纳米之间。它们覆盖有一层有机化合物封端层,被视为纳米尺寸的保护层,可防止团聚和沉淀。AgNPs对测试的革兰氏阳性和革兰氏阴性细菌菌株均显示出抗菌活性,形成了13 - 32毫米的抑菌圈,最低抑菌浓度(MIC)为6.25 - 12.5微克/毫升; 菌株对测试的AgNPs具有抗性。在浓度≥½ MIC时,测试的AgNPs显著降低了 的比生长速率。与对照相比,AgNPs对成纤维细胞系中的伤口迁移没有影响。我们的结果突出了用植物提取物封端的AgNPs在制药和食品工业中控制细菌病原体生长的潜在用途;然而,需要进一步研究来证实它们的伤口愈合能力,并且必须严格评估它们对健康的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e6/9144328/6273b8d81b41/pharmaceutics-14-01104-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e6/9144328/f574610412de/pharmaceutics-14-01104-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e6/9144328/a8ef9cff06ba/pharmaceutics-14-01104-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e6/9144328/21419e4e08c8/pharmaceutics-14-01104-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e6/9144328/1ce75daa2bf2/pharmaceutics-14-01104-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e6/9144328/1f3589e7aed2/pharmaceutics-14-01104-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e6/9144328/97a4d2c8e599/pharmaceutics-14-01104-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e6/9144328/57116733c1f4/pharmaceutics-14-01104-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e6/9144328/a40c78e4a70b/pharmaceutics-14-01104-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e6/9144328/6273b8d81b41/pharmaceutics-14-01104-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e6/9144328/f574610412de/pharmaceutics-14-01104-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e6/9144328/a8ef9cff06ba/pharmaceutics-14-01104-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e6/9144328/21419e4e08c8/pharmaceutics-14-01104-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e6/9144328/1ce75daa2bf2/pharmaceutics-14-01104-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e6/9144328/1f3589e7aed2/pharmaceutics-14-01104-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e6/9144328/97a4d2c8e599/pharmaceutics-14-01104-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e6/9144328/57116733c1f4/pharmaceutics-14-01104-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e6/9144328/a40c78e4a70b/pharmaceutics-14-01104-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e6/9144328/6273b8d81b41/pharmaceutics-14-01104-g009.jpg

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