Wils P, Legrain S, Frenois E, Scherman D
UMR 133 CNRS/RPR, Centre de Recherche de Vitry-Alfortville, Vitry-sur-Seine, France.
Biochim Biophys Acta. 1993 Jun 6;1177(2):134-8. doi: 10.1016/0167-4889(93)90032-k.
A polarized differentiated subclone of HT29, a human colon carcinoma cell line, was used to measure the passage of drugs across the intestinal epithelium. These cells, HT29-18-C1, when grown on permeable filters, formed tight monolayers of high electrical resistance (> 400 omega cm2). Electron micrographs revealed the presence of numerous apical microvilli and well developed junctional complexes. The transepithelial passage of various drugs was studied: the transepithelial permeability coefficients ranged from 0.8 x 10(-6) cm/s for fluorescein, to 4.8 x 10(-5) cm/s for the most lipophilic molecule, testosterone. For the five compounds tested, there was a coarse correlation between the apparent transepithelial permeability coefficient and the octanol/buffer distribution coefficient. The HT29-18-C1 subclone thus represents a new in-vitro model for studying the intestinal absorption of drugs.
人结肠癌细胞系HT29的一个极化分化亚克隆用于测定药物跨肠上皮的转运。这些细胞(HT29-18-C1)在可渗透滤膜上生长时,形成了高电阻(>400Ω·cm²)的紧密单层。电子显微镜照片显示存在大量顶端微绒毛和发育良好的连接复合体。研究了多种药物的跨上皮转运:跨上皮渗透系数范围从荧光素的0.8×10⁻⁶cm/s到亲脂性最强的分子睾酮的4.8×10⁻⁵cm/s。对于所测试的五种化合物,表观跨上皮渗透系数与正辛醇/缓冲液分配系数之间存在粗略的相关性。因此,HT29-18-C1亚克隆代表了一种研究药物肠道吸收的新体外模型。