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一种新型脂质纳米乳液系统,可提高格拉司琼的渗透。

A novel lipid nanoemulsion system for improved permeation of granisetron.

机构信息

College of Pharmacy, Pusan National University, Busan 609-735, Republic of Korea.

出版信息

Colloids Surf B Biointerfaces. 2013 Jan 1;101:475-80. doi: 10.1016/j.colsurfb.2012.07.019. Epub 2012 Jul 21.

Abstract

A new lipid nanoemulsion (LNE) system containing granisetron (GRN) was developed and its in vitro permeation-enhancing effect was evaluated using Caco-2 cell monolayers. Particle size, polydispersity index (PI) and stability of the prepared GRN-loaded LNE systems were also characterized. The mean diameters of prepared LNEs were around 50 nm with PI<0.2. Developed LNEs were stable at 4°C in the dark place over a period of 12 weeks. In vitro drug dissolution and cytotoxicity studies of GRN-loaded LNEs were performed. GRN-loaded LNEs exhibited significantly higher drug dissolution than GRN suspension at pH 6.8 for 2h (P<0.05). In vitro permeation study in Caco-2 cell monolayers showed that the LNEs significantly enhanced the drug permeation compared to GRN powder. The in vivo toxicity study in the rat jejunum revealed that the prepared GRN-loaded LNE was as safe as the commercial formulation (Kytril). These results suggest that LNE could be used as a potential oral liquid formulation of GRN for anti-emetic treatment on the post-operative and chemotherapeutic patients.

摘要

一种新的载格拉司琼(GRN)的脂质纳米乳(LNE)系统被开发出来,并使用 Caco-2 细胞单层评估了其体外渗透增强效果。还对所制备的 GRN 载 LNE 系统的粒径、多分散指数(PI)和稳定性进行了表征。制备的 LNEs 的平均粒径约为 50nm,PI<0.2。在 4°C 暗处,LNEs 在 12 周内稳定。对 GRN 载 LNEs 的体外药物溶出度和细胞毒性进行了研究。在 pH6.8 下 2 小时,GRN 载 LNEs 的药物溶出度明显高于 GRN 混悬液(P<0.05)。在 Caco-2 细胞单层中的体外渗透研究表明,与 GRN 粉末相比,LNEs 显著增强了药物渗透。在大鼠空肠的体内毒性研究中,发现所制备的 GRN 载 LNE 与商业制剂(Kytril)一样安全。这些结果表明,LNE 可用作 GRN 的潜在口服液体制剂,用于术后和化疗患者的止吐治疗。

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