Wiedmann T S, Deye C, Kallick D
Department of Pharmaceutics, University of Minnesota, Minneapolis 55455, USA.
Pharm Res. 2001 Jan;18(1):45-53. doi: 10.1023/a:1011022626030.
The purpose of this study was to determine the distribution and diffusion of sodium taurocholate-phospholipid micelles with mucin in order to provide the foundation for understanding the transport of ingested fat and poorly water-soluble drugs through the intestinal mucous layer.
Sodium taurocholate (NaTC) was dispersed with egg phosphatidylcholines (PC) to yield mixed micelles of a specific size and concentration. A preliminary study was conducted to determine the time required for equilibration of PC/TC micellar solutions with mucin. PC/TC micellar solutions were dialyzed against fixed and variable concentrations of bovine submaxillary mucin after which the concentration of PC and NaTC was measured by an assay for total phosphorus and by HPLC, respectively. In addition, a quantitative assay of TC and PC by NMR was developed and used to estimate the mobile fraction of lipids in the samples. Finally, pulsed-field gradient spin echo NMR self-diffusion measurements were made of the water, TC, and PC in the samples obtained from dialysis.
TC/PC micellar solutions achieved equilibrium with mucin in 7 days. Mucin did not affect the equilibrium concentration of PC or TC, except at high concentrations of mucin (5%), and then the effect was small. NMR quantitation was valid for PC and TC systems containing small micelles, but deviated significantly with systems containing large micelles. Mucin decreased the diffusivity of water and the phospholipids, but the effect was relatively small. Mucin dramatically affected the mobility of TC, which prevented a straightforward interpretation of the calculated diffusion coefficients.
Mucin has a minor effect on the equilibrium distribution of phospholipids and bile salts. However, lipids are readily accommodated by mucus, which can significantly increase the permeability of the mucous layer, particularly for poorly water-soluble drugs.
本研究旨在确定牛磺胆酸钠 - 磷脂胶束与粘蛋白的分布和扩散情况,为理解摄入的脂肪和难溶性药物通过肠道粘液层的转运提供基础。
将牛磺胆酸钠(NaTC)与蛋黄卵磷脂(PC)分散,以产生特定大小和浓度的混合胶束。进行了一项初步研究,以确定PC/TC胶束溶液与粘蛋白达到平衡所需的时间。将PC/TC胶束溶液与固定和可变浓度的牛下颌粘蛋白进行透析,之后分别通过总磷测定法和高效液相色谱法测量PC和NaTC的浓度。此外,开发了一种通过核磁共振对TC和PC进行定量分析的方法,并用于估计样品中脂质的可移动部分。最后,对透析获得的样品中的水、TC和PC进行了脉冲场梯度自旋回波核磁共振自扩散测量。
TC/PC胶束溶液在7天内与粘蛋白达到平衡。粘蛋白对PC或TC的平衡浓度没有影响,除非在高浓度粘蛋白(5%)时,且此时影响较小。核磁共振定量分析对于含有小胶束的PC和TC系统是有效的,但对于含有大胶束的系统则有显著偏差。粘蛋白降低了水和磷脂的扩散率,但影响相对较小。粘蛋白显著影响了TC的流动性,这使得对计算出的扩散系数的直接解释变得困难。
粘蛋白对磷脂和胆盐的平衡分布影响较小。然而,脂质很容易被粘液容纳,这可以显著增加粘液层的通透性,特别是对于难溶性药物。