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新型杂化甾体杂环作为基于聚乙二醇的纳米颗粒的合成、表征及细胞毒性作用评估

Synthesis, Characterization, and Evaluation of Cytotoxic Effects of Novel Hybrid Steroidal Heterocycles as PEG Based Nanoparticles.

作者信息

Abd Elhalim Mervat M, Ismail Nasser S M, M Yahya Shaymaa M, Omar Yasmin Y, Abd Rabou Ahmed A, Lasheen Deena S, Zawrah Mahmoud F, Elmegeed Gamal A

机构信息

Hormones Department, Medical Research Division, National Research Centre, Dokki, Cairo, Egypt. Email:

出版信息

Asian Pac J Cancer Prev. 2017 Jul 27;18(7):1937-1946. doi: 10.22034/APJCP.2017.18.7.1937.

Abstract

Anticancer agents featuring hybrid molecules can improve effectiveness and diminish drug resistance. The current study aimed to introduce newly synthesized heterocyclic steroids of promising anticancer effects loaded in polyethylene glycol (PEG)•based nanoparticles form. Several heterocyclic steroids (1-9) were synthesized via multicomponent reactions (MCRs) and confirmed via the analytical and spectral data. Compounds 1, 2, 3, 4, 5, 6, 7 and 9, were investigated individually in their free and PEG based nano-size hybrid forms as anticancer agents against three human cell lines: hepatocellular carcinoma cells (HepG2); breast cancer cells (MCF-7); and colon cancer cells (HCT116). The neutral red supravital dye uptake assay was employed. Compound 6 in its PEG based nano-size form exhibited the best cytotoxic effects against HepG2 and HCT116 cell lines, with IC50 values of 2.44 μmol/l and 2.59 μmol/l, respectively. In addition, it demonstrated a low IC50 value against MCF-7 (3.46μmol/l) cells. This study introduced promising anticancer agents acting through conversion into PEG-based nanoparticles.

摘要

具有杂化分子的抗癌药物可以提高疗效并降低耐药性。当前的研究旨在引入新合成的具有良好抗癌效果的杂环甾体,其以聚乙二醇(PEG)基纳米颗粒的形式存在。通过多组分反应(MCRs)合成了几种杂环甾体(1-9),并通过分析和光谱数据进行了确认。化合物1、2、3、4、5、6、7和9,分别以其游离形式和基于PEG的纳米尺寸杂化形式作为抗癌剂,针对三种人类细胞系进行了研究:肝癌细胞(HepG2);乳腺癌细胞(MCF-7);和结肠癌细胞(HCT116)。采用中性红活体染料摄取试验。化合物6的基于PEG的纳米尺寸形式对HepG2和HCT116细胞系表现出最佳的细胞毒性作用,IC50值分别为2.44μmol/l和2.59μmol/l。此外,它对MCF-7(3.46μmol/l)细胞也表现出较低的IC50值。本研究引入了通过转化为基于PEG的纳米颗粒而起作用的有前景的抗癌药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f35/5648402/2cfcaef6b6e9/APJCP-18-1937-g001.jpg

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