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禁食状态模拟肠液“FaSSIF-C”,一种用于体外药物递送研发的含胆固醇的肠道模型介质。

Fasted-state simulated intestinal fluid "FaSSIF-C", a cholesterol containing intestinal model medium for in vitro drug delivery development.

作者信息

Khoshakhlagh Pooneh, Johnson Raphael, Langguth Peter, Nawroth Thomas, Schmueser Lars, Hellmann Nadja, Decker Heinz, Szekely Noemi Kinga

机构信息

Johannes Gutenberg University, Pharmacy and Biochemistry Institute, Division Pharmaceutical Technology, Mainz, D-55099, Germany.

Max Planck Institute for Polymer Research, Mainz, D-55128, Germany.

出版信息

J Pharm Sci. 2015 Jul;104(7):2213-24. doi: 10.1002/jps.24470. Epub 2015 May 11.

DOI:10.1002/jps.24470
PMID:25964103
Abstract

A set of biorelevant media "fasted-state simulated intestinal fluid with cholesterol (FaSSIF-C)" for the in vitro study of intestinal drug dissolution in the duodenum was developed. These contain cholesterol at the same levels as in human bile: the cholesterol content of FaSSIF-7C is equivalent to healthy female, FaSSIF-10C to healthy male persons, and FaSSIF-13C to several disease cases that lead to gallstones. The fluids were studied in three aspects: biocompatibility, intestinal nanostructure, and solubilizing power of hydrophobic drugs of the BCS class II. The biocompatibility study showed no toxic effects in a Caco-2 cell system. The drug-solubilizing capacity toward Fenofibrate, Danazol, Griseofulvin, and Carbamazepine was assessed as example. It varied with the cholesterol content widely from a fourfold improvement to a twofold reduction. The nanostructure study by dynamic light scattering and small-angle neutron scattering indicated vesicles as the main component of FaSSIF-C in equilibrium (>1 h), but at high cholesterol content, larger particles were observed as a minor contribution. The neutron experiments indicated the presence of complex micelle-vesicle mixtures, even after 1 h development of fed-state bile model to FaSSIF. The results indicate that cholesterol affects some drugs in solubilization and particle size in intestinal model fluids.

摘要

开发了一组用于十二指肠肠道药物溶解体外研究的生物相关介质“含胆固醇的禁食状态模拟肠液(FaSSIF-C)”。这些介质中胆固醇的含量与人胆汁中的含量相同:FaSSIF-7C的胆固醇含量相当于健康女性,FaSSIF-10C相当于健康男性,FaSSIF-13C相当于几种导致胆结石的疾病病例。对这些液体从三个方面进行了研究:生物相容性、肠道纳米结构以及BCS II类疏水药物的增溶能力。生物相容性研究表明在Caco-2细胞系统中没有毒性作用。以非诺贝特、达那唑、灰黄霉素和卡马西平为例评估了药物增溶能力。其随胆固醇含量变化很大,从提高四倍到降低两倍不等。通过动态光散射和小角中子散射进行的纳米结构研究表明,在平衡状态(>1小时)下,囊泡是FaSSIF-C的主要成分,但在高胆固醇含量时,观察到较大颗粒作为次要成分存在。中子实验表明,即使在将进食状态胆汁模型发展为FaSSIF 1小时后,仍存在复杂的胶束 - 囊泡混合物。结果表明,胆固醇在肠道模型液体中会影响某些药物的溶解和粒径。

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