Yeh P Y, Smith P L, Ellens H
Department of Pharmaceutics and Pharmaceutical Chemistry, University of Utah, Salt Lake.
Pharm Res. 1994 Aug;11(8):1148-54. doi: 10.1023/a:1018988832492.
Medium chain glycerides (MCGs) have been reported to enhance intestinal absorption of hydrophilic drugs. However, the mechanisms involved in absorption enhancement are not well understood. The effects of MCGs (CapMul MCM) on physiological properties of rabbit ileum and distal colon, including active ion transport, transepithelial resistance (Rt) and passive permeability, have been investigated in vitro. CapMul MCM inhibited active ion transport (measured as a decrease in short-circuit current, Isc) in both intestinal segments in a concentration-dependent manner. The inhibition of Isc was rapidly reversible (within 100 min) upon removal of CapMul MCM. The data indicate that CapMul MCM preferentially affected ion transport by villus cells in the ileum and surface cells in the distal colon. Ion transport in crypt cells in both segments was not significantly altered. Rt of the ileum was not significantly affected by 5% CapMul MCM, while mannitol transport was 6 fold enhanced. Treatment of distal colon with 1% CapMul MCM reduced Rt by 95%, while mannitol transport was 100 fold enhanced. In a parallel experiment, mucosal(m)-to-serosal(s) transport of cephalexin, a beta-lactam antibiotic, in the ileum was about 40% reduced in the presence of 5% CapMul MCM, whereas transport in the s-to-m direction was 2.5 fold enhanced. Treatment of the distal colon with 1% CapMul MCM resulted in 25 fold enhancement of cephalexin transport in either direction. These results suggest that absorption enhancement by MCGs results from an increased permeability of the intestine confined to the villus or surface epithelium.
据报道,中链甘油酯(MCGs)可增强亲水性药物的肠道吸收。然而,其吸收增强所涉及的机制尚未完全明确。本研究在体外考察了MCGs(CapMul MCM)对兔回肠和远端结肠生理特性的影响,包括主动离子转运、跨上皮电阻(Rt)和被动通透性。CapMul MCM以浓度依赖性方式抑制了两个肠段的主动离子转运(以短路电流Isc降低来衡量)。去除CapMul MCM后,Isc的抑制作用迅速逆转(100分钟内)。数据表明,CapMul MCM优先影响回肠绒毛细胞和远端结肠表面细胞的离子转运。两个肠段隐窝细胞的离子转运未发生显著改变。5%CapMul MCM对回肠的Rt无显著影响,但甘露醇转运增强了6倍。用1%CapMul MCM处理远端结肠可使Rt降低95%,而甘露醇转运增强了100倍。在一项平行实验中,在5%CapMul MCM存在的情况下,β-内酰胺抗生素头孢氨苄在回肠中的黏膜(m)到浆膜(s)转运降低了约40%,而在s到m方向的转运增强了2.5倍。用1%CapMul MCM处理远端结肠导致头孢氨苄在任一方向的转运增强了25倍。这些结果表明,MCGs引起的吸收增强是由于绒毛或表面上皮处肠道通透性增加所致。