Khoshakhlagh Pooneh, Johnson Raphael, Langguth Peter, Nawroth Thomas, Schmueser Lars, Hellmann Nadja, Decker Heinz, Szekely Noemi Kinga
Johannes Gutenberg University, Pharmacy and Biochemistry Institute, Division Pharmaceutical Technology, Mainz, D-55099, Germany.
Max Planck Institute for Polymer Research, Mainz, D-55128, Germany.
J Pharm Sci. 2015 Jul;104(7):2213-24. doi: 10.1002/jps.24470. Epub 2015 May 11.
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.
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。