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A novel lipid nanoemulsion system for improved permeation of granisetron

机译:一种新型脂质纳米乳剂体系,可提高格拉司琼的渗透性

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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 2 h (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.
机译:开发了一种新的含Granisetron(GRN)的脂质纳米乳剂(LNE)系统,并使用Caco-2细胞单层膜评估了其体外渗透增强作用。还对制备的GRN负载LNE系统的粒径,多分散指数(PI)和稳定性进行了表征。制备的LNE的平均直径约为50 nm,PI <0.2。发达的LNE在12周的黑暗环境中在4°C稳定。进行了载有GRN的LNE的体外药物溶解和细胞毒性研究。装载GRN的LNEs在pH 6.8的情况下显示2小时显着高于GRN悬浮液的药物溶解度(P <0.05)。在Caco-2细胞单层中进行的体外渗透研究表明,与GRN粉末相比,LNEs显着增强了药物渗透。在大鼠空肠中的体内毒性研究表明,制备的GRN负载的LNE与市售制剂(Kytril)一样安全。这些结果表明,LNE可用作GRN的潜在口服液制剂,可用于术后和化疗患者的止吐治疗。

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