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基于 种子提取物介导的银纳米粒子对人结肠(HCT-116)、胰腺(PANC-1)和乳腺(MDA-MB 231)癌细胞系的特性和抗癌作用的比较研究。

Characterization and Anti-Cancerous Effect of Seed Extract Mediated Silver Nanoparticles on Human Colon (HCT-116), Pancreatic (PANC-1) and Breast (MDA-MB 231) Cancer Cell Lines: A Comparative Study.

机构信息

Drug Discovery and Development Division, Patanjali Research Foundation Trust, Haridwar, Uttarakhand 249405, India.

University of Patanjali, Haridwar, Uttarakhand 249405, India.

出版信息

Int J Nanomedicine. 2020 Jan 24;15:573-585. doi: 10.2147/IJN.S230244. eCollection 2020.

Abstract

INTRODUCTION

A comparative study of . seed extract and developed silver nanoparticles (PJSNPs) for improving bioavailability that enhance their anti-cancer activity against HCT-116 (colon carcinoma), PANC-1 (pancreatic carcinoma), MDA-MB 231 (breast carcinoma) cell lines was performed.

MATERIALS AND METHODS

The green synthesis of PJSNPs ( silver nanoparticles) was performed using PJ () extract, and characterization of synthesized nanoparticles was accomplished through UV-Vis spectrum, X-ray diffraction (XRD), transmission electron microscopy, energy-dispersive X-ray spectroscopy (TEM-EDAX), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), atomic force microscopy (AFM), and Raman spectroscopy.

RESULTS

The results revealed that PJSNPs are homogeneous, spherical in shape, ~8±2 nm in size, and negatively charged with a zeta potential of about -26.71 mV. The cytotoxicity pattern observed was AgNO > PJSNPs > PJ extract. The morphological changes of the cells were observed by flow cytometry and also by the DNA ladder pattern on gel electrophoresis, which indicated that the process of cell death occurred via the apoptosis mechanism and PJSNPs were exerting late-stage apoptosis in all the tested cell lines. The small size and negative value of zeta potential could be the factors responsible for greater bioavailability and thus increased uptake by the tumor cells.

CONCLUSION

The MTT assay and morphological changes observed by various methods indicate that the novel PJSNPs are a better anticancer agent than PJ extract. All the above properties make biologically synthesized PJSNPs an important target in the field of anti-cancer drug discovery.

摘要

简介

为了提高生物利用度,增强其对 HCT-116(结肠癌)、PANC-1(胰腺癌)、MDA-MB 231(乳腺癌)细胞系的抗癌活性,对. 种子提取物和开发的银纳米粒子(PJSNPs)进行了比较研究。

材料和方法

使用 PJ()提取物进行 PJSNPs(银纳米粒子)的绿色合成,并通过紫外-可见光谱、X 射线衍射(XRD)、透射电子显微镜、能谱(TEM-EDAX)、扫描电子显微镜(SEM)、傅里叶变换红外光谱(FTIR)、原子力显微镜(AFM)和拉曼光谱对合成的纳米粒子进行表征。

结果

结果表明,PJSNPs 是均匀的、球形的,大小约为 8±2nm,带负电荷,zeta 电位约为-26.71mV。观察到的细胞毒性模式是 AgNO > PJSNPs > PJ 提取物。通过流式细胞术和凝胶电泳上的 DNA 梯图案观察到细胞形态变化,这表明细胞死亡过程是通过凋亡机制发生的,并且 PJSNPs 在所有测试的细胞系中都发挥晚期凋亡作用。小尺寸和负的 zeta 电位值可能是生物利用度更高的原因,从而增加了肿瘤细胞的摄取。

结论

MTT 测定和各种方法观察到的形态变化表明,新型 PJSNPs 是比 PJ 提取物更好的抗癌剂。所有上述特性使生物合成的 PJSNPs 成为抗癌药物发现领域的一个重要目标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c3f/6986406/bce320b9e9e2/IJN-15-573-g0001.jpg

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