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pH 响应性透明质酸脂质体用于多西他赛递送。

pH-Responsive hyaluronated liposomes for docetaxel delivery.

机构信息

Department of Biotechnology, The Catholic University of Korea, 43 Jibong-ro, Bucheon-si, Gyeonggi-do 14662, Republic of Korea.

Division of Endocrinology, Metabolism and Lipid Research, Washington University School of Medicine, Saint Louis, MO 63110, USA.

出版信息

Int J Pharm. 2018 Aug 25;547(1-2):377-384. doi: 10.1016/j.ijpharm.2018.06.028. Epub 2018 Jun 11.

Abstract

In this study, we report pH-responsive liposomes consisting of hydrogenated soy phosphatidylcholine (HSPC) as a lipid, hyaluronic acid (HA) grafted with functional 3-diethylaminopropyl (DEAP) groups (hereafter denoted as HA-g-DEAP) as a pH-responsive polymer, and docetaxel (DTX) as an antitumor drug. DTX-loaded HSPC liposomes were prepared via a conventional liposome manufacturing procedure and then were decorated with HA-g-DEAP (HA-g-DEAP, HA-g-DEAP, and HA-g-DEAP, according to the molar conjugate ratio of DEAP to HA) in an aqueous solution (pH 7.4), by sonication. The liposomes with HA-g-DEAP allowed the efficient release of the encapsulated DTX content when the pH of the solution decreased to 6.5 (i.e., endosomal pH), owing to the acidic pH-induced protonation of the DEAP anchored to the vesicular lipid bilayers. These hyaluronated liposomes were effective at entering the human colon carcinoma HCT-116 cells with a CD44 receptor overexpression. In an in vitro tumor cell cytotoxicity test, the DTX-loaded liposomes caused a significant increase in HCT-116 tumor cell death, revealing their pharmaceutical potential in tumor therapy.

摘要

在这项研究中,我们报告了一种 pH 响应性脂质体,由氢化大豆磷脂酰胆碱(HSPC)作为脂质、接枝有功能的 3-二乙氨基丙基(DEAP)基团的透明质酸(HA)(以下表示为 HA-g-DEAP)作为 pH 响应性聚合物,以及多西紫杉醇(DTX)作为抗肿瘤药物。通过常规脂质体制备程序制备负载 DTX 的 HSPC 脂质体,然后在水溶液(pH 7.4)中通过超声处理,用 HA-g-DEAP(根据 DEAP 与 HA 的摩尔偶联比,HA-g-DEAP、HA-g-DEAP 和 HA-g-DEAP)进行修饰。当溶液的 pH 值降低至 6.5(即内体 pH)时,带 HA-g-DEAP 的脂质体允许包封的 DTX 内容物有效释放,这是由于酸性 pH 诱导固定在囊泡脂质双层上的 DEAP 质子化。这些透明质酸化的脂质体能够有效地进入过表达 CD44 受体的人结肠癌细胞 HCT-116。在体外肿瘤细胞细胞毒性试验中,负载 DTX 的脂质体导致 HCT-116 肿瘤细胞死亡显著增加,揭示了它们在肿瘤治疗中的药物潜力。

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