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基于姜黄素自微乳浮动片的 caco-2 单层的开发、表征和渗透性评估。

Development, characterization and permeability assessment based on caco-2 monolayers of self-microemulsifying floating tablets of tetrahydrocurcumin.

机构信息

Department of Pharmaceutical Technology, Faculty of Pharmaceutical Sciences, Prince of Songkla University, Hat Yai, Songkhla, 90112, Thailand.

出版信息

AAPS PharmSciTech. 2013 Mar;14(1):321-31. doi: 10.1208/s12249-012-9912-2. Epub 2013 Jan 15.

DOI:10.1208/s12249-012-9912-2
PMID:23319299
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3581676/
Abstract

Novel self-microemulsifying floating tablets were developed to enhance the dissolution and oral absorption of the poorly water-soluble tetrahydrocurcumin (THC). Their physicochemical properties and THC permeability across Caco-2 cell monolayers were assessed. The self-microemulsifying liquid containing THC was adsorbed onto colloidal silicon dioxide, mixed with HPMC, gas-generating agents (sodium bicarbonate and tartaric acid), lactose and silicified-microcrystalline cellulose and transformed into tablets by direct compression. The use of different types/concentrations of HPMC and sodium bicarbonate in tablet formulations had different effects on the floating characteristics and in vitro THC release. The optimum tablet formulation (F2) provided a short floating lag time (∼23 s) together with a prolonged buoyancy (>12 h). About 72% of THC was released in 12 h with an emulsion droplet size in aqueous media of 33.9±1.0 nm while that of a self-microemulsifying liquid was 29.9±0.3 nm. The tablet formulation was stable under intermediate and accelerated storage conditions for up to 6 months. The THC released from the self-microemulsifying liquid and tablet formulations provided an approximately three- to fivefold greater permeability across the Caco-2 cell monolayers than the unformulated THC and indicated an enhanced absorption of THC by the formulations. The self-microemulsifying floating tablet could provide a dosage form with the potential to improve the oral bioavailability of THC and other hydrophobic compounds.

摘要

研制了新型自微乳浮动片剂,以提高水中溶解度差的四氢姜黄素(THC)的溶解和口服吸收。评估了它们的物理化学性质和 THC 通过 Caco-2 细胞单层的渗透性。将含有 THC 的自微乳液体吸附到胶体二氧化硅上,与 HPMC、产气剂(碳酸氢钠和酒石酸)、乳糖和硅化微晶纤维素混合,并通过直接压片制成片剂。片剂配方中使用不同类型/浓度的 HPMC 和碳酸氢钠对漂浮特性和体外 THC 释放有不同的影响。最佳片剂配方(F2)提供了短的漂浮滞后时间(约 23 秒)和延长的浮力(>12 小时)。约 72%的 THC 在 12 小时内释放,水介质中的乳滴粒径为 33.9±1.0nm,而自微乳液的粒径为 29.9±0.3nm。在中间和加速储存条件下,片剂配方稳定长达 6 个月。自微乳液和片剂配方释放的 THC 穿过 Caco-2 细胞单层的渗透性比未成型的 THC 大约高出三到五倍,表明这些配方增强了 THC 的吸收。自微乳浮动片剂可以提供一种具有提高 THC 和其他疏水性化合物口服生物利用度潜力的剂型。

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