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来自根茎提取物的生物源银/氯化银纳米颗粒的生物活性:对艾氏腹水癌和人乳腺癌细胞系具有抗癌潜力的抗菌和抗氧化特性。

Bioactivity of biogenic silver/silver chloride nanoparticles from rhizome extract: Antibacterial and antioxidant properties with anticancer potential against Ehrlich ascites carcinoma and human breast cancer cell lines.

作者信息

Ruhul-Amin Md, Rahman Md Abdur, Khatun Nisa, Hasan Imtiaj, Kabir Syed Rashel, Asaduzzaman A K M

机构信息

Department of Biochemistry & Molecular Biology, Faculty of Science, University of Rajshahi, Rajshahi, 6205, Bangladesh.

Department of Biochemistry and Molecular Biology, Trust University, Barisal, 8200, Bangladesh.

出版信息

Heliyon. 2024 Oct 16;10(20):e39493. doi: 10.1016/j.heliyon.2024.e39493. eCollection 2024 Oct 30.

DOI:10.1016/j.heliyon.2024.e39493
PMID:39502215
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11535985/
Abstract

INTRODUCTION

This study explores the synthesis and characterization of silver/silver chloride nanoparticles (Ag/AgCl-NPs) using rhizome extract and evaluates their bioactivities, including antibacterial, antioxidant, and anticancer potentials.

METHODS

The synthesis of Ag/AgCl-NPs was initially confirmed by a color change and a sharp peak at 463 nm in UV-visible spectroscopy. Further characterization was conducted using scanning electron microscopy (SEM), X-ray powder diffraction (XRD), and fourier transform infrared spectroscopy (FTIR). Antibacterial properties were checked against four pathogenic bacteria ( and ), and antioxidant activities were assessed using DPPH (2,2-diphenyl-1-picrylhydrazyl) and ABTS (2,2-azino-bis-3-ethylbenzothiazoline-6-sulphonic acid) assay. In addition, the anticancer potential was evaluated using MTT (3-(4, 5-dimethylthiazolyl-2)-2, 5-diphenyltetrazolium bromide) colorimetric assay and using the mouse models. Finally, toxicity was determined by employing the brine shrimp nauplii lethality assay.

RESULTS

Ag/AgCl-NPs most effectively inhibited the growth of , showing maximum zone of inhibition and 7 μg/mL of minimum inhibitory concentration (MIC), and prevented the biofilm formation by at 40 μg/mL. They displayed antioxidant activities against DPPH and ABTS with IC values of 90.65 and 24.34 μg/mL, respectively. , they inhibited 61.96 % EAC and 49.63 % MCF-7 cells growth at 32 and 128 μg/mL, respectively. Subsequently, inhibition rates of EAC cells growth in mice were measured as 38.30 %, 57.38 %, and 31.81 % after employing 2.5, 5, and 10 mg/kg/day of Ag/AgCl-NPs, respectively. Moreover, Ag/AgCl-NPs treated mice were found to carry more apoptotic EAC cells with distorted morphology. Treated mice showed decreased tumor weight, increased mean survival time, and a lifespan increase of up to 30 %, with improved hematological parameters. Later, Ag/AgCl-NPs exhibited moderate toxicity with an LC value of 208.41 μg/mL in brine shrimp nauplii lethality assay.

CONCLUSION

The promising antibacterial, antioxidant, and anticancer activities along with mild toxicity suggest the potential biomedical uses of rhizome extract-mediated Ag/AgCl-NPs.

摘要

引言

本研究探索了利用根茎提取物合成及表征银/氯化银纳米颗粒(Ag/AgCl-NPs),并评估了它们的生物活性,包括抗菌、抗氧化和抗癌潜力。

方法

Ag/AgCl-NPs的合成最初通过颜色变化和紫外可见光谱中463nm处的尖锐峰得以确认。进一步的表征使用扫描电子显微镜(SEM)、X射线粉末衍射(XRD)和傅里叶变换红外光谱(FTIR)进行。针对四种致病细菌检测了抗菌性能,使用DPPH(2,2-二苯基-1-苦基肼)和ABTS(2,2-联氮-双-3-乙基苯并噻唑啉-6-磺酸)测定法评估了抗氧化活性。此外,使用MTT(3-(4,5-二甲基噻唑-2)-2,5-二苯基四氮唑溴盐)比色法并利用小鼠模型评估了抗癌潜力。最后,通过卤虫无节幼体致死率测定法确定了毒性。

结果

Ag/AgCl-NPs最有效地抑制了[细菌名称未给出]的生长,显示出最大抑菌圈和7μg/mL的最低抑菌浓度(MIC),并在40μg/mL时阻止了[细菌名称未给出]生物膜的形成。它们对DPPH和ABTS显示出抗氧化活性,IC值分别为90.65和24.34μg/mL。此外,它们在32和128μg/mL时分别抑制了61.96%的艾氏腹水癌细胞(EAC)和49.63%的MCF-7细胞生长。随后,在分别使用2.5、5和10mg/kg/天的Ag/AgCl-NPs后,测得小鼠体内EAC细胞生长的抑制率分别为38.30%、57.38%和31.81%。此外,发现经Ag/AgCl-NPs处理的小鼠携带更多形态扭曲的凋亡EAC细胞。经处理的小鼠肿瘤重量减轻,平均存活时间延长,寿命增加高达30%,血液学参数得到改善。后来,在卤虫无节幼体致死率测定中,Ag/AgCl-NPs表现出中等毒性,LC值为208.41μg/mL。

结论

有前景的抗菌、抗氧化和抗癌活性以及轻度毒性表明根茎提取物介导的Ag/AgCl-NPs具有潜在的生物医学用途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/460c/11535985/f0be8d334f74/gr10.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/460c/11535985/f0be8d334f74/gr10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/460c/11535985/ccce4fe86496/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/460c/11535985/ee36473a5da2/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/460c/11535985/94250c984ed3/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/460c/11535985/dad9edc5bd9e/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/460c/11535985/30931f17d4cc/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/460c/11535985/4f17e17e6be2/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/460c/11535985/ae303c5bfab4/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/460c/11535985/16802fde98ee/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/460c/11535985/3da3b4538197/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/460c/11535985/2c19cd197d05/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/460c/11535985/f0be8d334f74/gr10.jpg

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