Winne D, Verheyen W
Abteilung für Molekularpharmakologie, Universität Tübingen, FRG.
J Pharm Pharmacol. 1990 Jul;42(7):517-9. doi: 10.1111/j.2042-7158.1990.tb06611.x.
The diffusion coefficients of [3H] water, urea, benzoic acid, antipyrine, aminopyrine, alpha-methyl-glucoside, L-phenylalanine and of hydrogen ions were measured at 38 degrees C in native mucus gel from rat small intestine. The diffusion in the gel was reduced to 37-53% (for hydrogen ions to 7%) compared with buffer solution. In addition, the buffering capacity of the gel retarded the permeation of hydrogen ions before a steady state flux was attained. A model calculation revealed that in the preparation a gel layer of 80 microns thickness represents 23% of the total permeation resistance for substances with high epithelial permeability. The aqueous part of the pre-epithelial diffusion resistance amounts to 77% of the total resistance.
在38摄氏度下,测定了[3H]水、尿素、苯甲酸、安替比林、氨基比林、α-甲基葡萄糖苷、L-苯丙氨酸以及氢离子在大鼠小肠天然黏液凝胶中的扩散系数。与缓冲溶液相比,凝胶中的扩散降低至37% - 53%(氢离子降至7%)。此外,在达到稳态通量之前,凝胶的缓冲能力阻碍了氢离子的渗透。模型计算表明,在该制剂中,80微米厚的凝胶层占上皮高通透性物质总渗透阻力的23%。上皮前扩散阻力的水相部分占总阻力的77%。