Comparative cytotoxicity of a glycolipopeptide biosurfactant from Lactobacillus plantarum and its derived silver nanoparticles against breast cancer cells

Q2 Medicine
Zaid Mohammed Joodi Al-Janabi , Waseem Yousif M. Al-dulaimy , Maryam Hekmat Abdulateef , Aeshah Abbood Ahmed , Mohammed Kadhom
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Abstract

The present study describes the green synthesis of silver nanoparticles (AgNPs) using a glycolipopeptide (GLP) biosurfactant produced by Lactobacillus plantarum, and evaluates their physicochemical characteristics and anticancer potential. The formation of AgNPs was visually confirmed by a color change and further characterized by UV–Vis, XRD, AFM, and TEM, revealing spherical particles ranging from 20 to 300 nm. Zeta potential analysis (−32.1 mV) confirmed strong colloidal stability. FTIR and GC-MS analyses identified key functional groups and bioactive compounds in the GLP, including fatty acids and lipopeptides responsible for both surface activity and biological effects. Surface tension (32.4 mN/m) and emulsification index (61.5 %) further validated the biosurfactant's amphiphilic nature. In vitro cytotoxicity assays against MCF-7 breast cancer cells demonstrated dose-dependent effects, with the GLP and AgNPs showing 60.59 % and 54.77 % inhibition, respectively, at 400 μg/mL. Their combination enhanced cytotoxicity to 69.14 % while maintaining minimal toxicity toward WRL-68 normal liver cells, indicating selective activity. Compared to doxorubicin (IC50 ≈ 0.98 μg/mL, SI ≈ 1.01), the green formulations displayed a higher selectivity index (SI ≈ 2.71). The enhanced cytotoxicity is likely attributed to reactive oxygen species (ROS) generation, apoptosis induction, and membrane disruption. Although our findings highlight the dual functionality of the GLP biosurfactant as both a nanoparticle stabilizer and a bioactive agent, further in vivo studies and mechanistic investigations are warranted to validate its potential in cancer therapy.
植物乳杆菌糖多糖肽生物表面活性剂及其衍生银纳米颗粒对乳腺癌细胞的细胞毒性比较
本研究利用植物乳杆菌生产的糖多糖肽(GLP)生物表面活性剂绿色合成纳米银(AgNPs),并对其理化特性和抗癌潜力进行了评价。通过颜色变化直观地证实了AgNPs的形成,并进一步通过UV-Vis, XRD, AFM和TEM进行了表征,揭示了20 ~ 300 nm的球形颗粒。Zeta电位分析(−32.1 mV)证实了较强的胶体稳定性。FTIR和GC-MS分析确定了GLP中的关键官能团和生物活性化合物,包括负责表面活性和生物效应的脂肪酸和脂肽。表面张力(32.4 mN/m)和乳化指数(61.5%)进一步验证了生物表面活性剂的两亲性。对MCF-7乳腺癌细胞的体外细胞毒性试验显示出剂量依赖性,400 μg/mL时,GLP和AgNPs分别表现出60.59%和54.77%的抑制作用。两种药物联合使用可将细胞毒性提高至69.14%,同时对WRL-68正常肝细胞保持最小毒性,表明其具有选择性活性。与阿霉素(IC50≈0.98 μg/mL, SI≈1.01)相比,绿色配方具有更高的选择性指数(SI≈2.71)。增强的细胞毒性可能归因于活性氧(ROS)的产生、细胞凋亡的诱导和膜的破坏。尽管我们的研究结果强调了GLP生物表面活性剂作为纳米颗粒稳定剂和生物活性剂的双重功能,但需要进一步的体内研究和机制研究来验证其在癌症治疗中的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Medicine in Microecology
Medicine in Microecology Medicine-Gastroenterology
CiteScore
5.60
自引率
0.00%
发文量
16
审稿时长
76 days
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