Suppr超能文献

提取负载新型无胆固醇脂质体用于治疗肝细胞癌。

extract loaded novel cholesterol-free liposome for the treatment of hepatocellular carcinoma.

作者信息

Yang Siqi, Lan Jinshuai, Li Zhe, Li Ming, Wu Ya, Sun Liyan, Zhang Tong, Ding Yue

机构信息

School of Pharmacy, Shanghai University of Traditional Chinese Medicine, Shanghai, China.

State Key Laboratory of Integration and Innovation of Classic Formula and Modern Chinese Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, China.

出版信息

Front Pharmacol. 2024 Nov 25;15:1486742. doi: 10.3389/fphar.2024.1486742. eCollection 2024.

Abstract

BACKGROUND

This study aims to improve the solubility and the toxicity of Bufonis venenum, and finally enhance the therapeutic outcomes of hepatocellular carcinoma (HCC).

METHODS

The cholesterol-free liposomes simultaneously encapsulate bufadienolides and indolealkylamines (Non-Cholesterol-Bufonis Venenum Extract-Liposome, Non-Chol-BVE-LP) was prepared by the thin-film evaporation technique. , the cytotoxicity, cell apoptosis study, cellular uptake and hemolysis studies were evaluated in HepG2 cells. , the biodistribution and anti-tumor activity studies were conducted in BALB/C mice with HepG2 cells.

RESULTS

The liposomes showed good size distribution, encapsulation efficiency drug loading capacity and slower drug release. Non-Chol-BVE-LP had higher cytotoxicity on HepG2 cells and induced more apoptosis on HepG2 Cells compared with BVE. In addition, the liposomes could accumulate in tumor by passive targeting, thus facilitating the anti-tumor effects. , Non-Chol-BVE-LP showed equivalent anti-tumor efficacy to the first-line anti-HCC drug sorafenib.

CONCLUSION

The study provided new ideas for the development and clinical application of Bufonis venenum related formulation and offered new drug for the treatment of HCC.

摘要

背景

本研究旨在提高蟾酥的溶解度和降低其毒性,最终提高肝细胞癌(HCC)的治疗效果。

方法

采用薄膜蒸发技术制备同时包封蟾毒配基和吲哚烷基胺的无胆固醇脂质体(非胆固醇蟾酥提取物脂质体,Non-Chol-BVE-LP)。在HepG2细胞中评估其细胞毒性、细胞凋亡研究、细胞摄取和溶血研究。在接种HepG2细胞的BALB/C小鼠中进行生物分布和抗肿瘤活性研究。

结果

脂质体显示出良好的粒径分布、包封率、载药量和较慢的药物释放。与蟾酥提取物(BVE)相比,Non-Chol-BVE-LP对HepG2细胞具有更高的细胞毒性,并诱导HepG2细胞更多凋亡。此外,脂质体可通过被动靶向在肿瘤中蓄积,从而促进抗肿瘤作用。而且,Non-Chol-BVE-LP显示出与一线抗HCC药物索拉非尼相当的抗肿瘤疗效。

结论

本研究为蟾酥相关制剂的开发和临床应用提供了新思路,并为HCC的治疗提供了新药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a481/11625546/f5dcfa4c2db9/fphar-15-1486742-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验