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“特洛伊木马”策略:用于制备胆汁酸修饰盐酸伊立替康纳米脂质体的肝靶向抗癌药物传递系统研究。

A "Trojan Horse" Strategy: The Preparation of Bile Acid-Modifying Irinotecan Hydrochloride Nanoliposomes for Liver-Targeted Anticancer Drug Delivery System Study.

机构信息

State Key Laboratory of Southwestern Chinese Medicine Resources, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China.

College of Pharmacy, School of Modern Chinese Medicine Industry, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China.

出版信息

Molecules. 2023 Feb 7;28(4):1577. doi: 10.3390/molecules28041577.

Abstract

The bile acid transport system is a natural physiological cycling process between the liver and the small intestine, occurring approximately 6-15 times during the day. There are various bile acid transporter proteins on hepatocytes that specifically recognize bile acids for transport. Therefore, in this paper, a novel liposome, cholic acid-modified irinotecan hydrochloride liposomes (named CA-CPT-11-Lip), was prepared based on the "Trojan horse" strategy. The liposomes preparation process was optimized, and some important quality indicators were investigated. The distribution of irinotecan hydrochloride in mice was then analyzed by high-performance liquid chromatography (HPLC), and the toxicity of liposomes to hepatocellular carcinoma cells (HepG-2) was evaluated in vitro. As a result, CA-CPT-11-Lip was successfully prepared. It was spherical with a particle size of 154.16 ± 4.92 nm, and the drug loading and encapsulation efficiency were 3.72 ± 0.04% and 82.04 ± 1.38%, respectively. Compared with the conventional liposomes (without cholic acid modification, named CPT-11-Lip), CA-CPT-11-Lip had a smaller particle size and higher encapsulation efficiency, and the drug accumulation in the liver was more efficient, enhancing the anti-hepatocellular carcinoma activity of irinotecan hydrochloride. The novel nanoliposome modified by cholic acid may help to expand the application of irinotecan hydrochloride in the treatment of hepatocellular carcinoma and construct the drug delivery system mode of drug liver targeting.

摘要

胆汁酸转运系统是肝脏和小肠之间自然的生理循环过程,每天大约发生 6-15 次。肝细胞上有各种胆汁酸转运蛋白,专门识别胆汁酸进行转运。因此,本文基于“特洛伊木马”策略,制备了一种新型的脂质体,即胆酸修饰的盐酸伊立替康脂质体(命名为 CA-CPT-11-Lip)。对脂质体的制备工艺进行了优化,并考察了一些重要的质量指标。然后通过高效液相色谱法(HPLC)分析盐酸伊立替康在小鼠体内的分布,并在体外评价脂质体对肝癌细胞(HepG-2)的毒性。结果成功制备了 CA-CPT-11-Lip。它呈球形,粒径为 154.16±4.92nm,载药量和包封率分别为 3.72±0.04%和 82.04±1.38%。与未修饰胆酸的常规脂质体(命名为 CPT-11-Lip)相比,CA-CPT-11-Lip 的粒径更小,包封率更高,药物在肝脏中的积累更有效,增强了盐酸伊立替康的抗肝癌活性。胆酸修饰的新型纳米脂质体可能有助于扩大盐酸伊立替康在肝癌治疗中的应用,并构建药物肝靶向的药物传递系统模式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81f2/9963329/bf41a07d89ec/molecules-28-01577-g001.jpg

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