Feldman S, Reinhard M
J Pharm Sci. 1976 Oct;65(10):1460-2. doi: 10.1002/jps.2600651011.
The effect of sodium alkyl sulfates (C6-C14) on the loss of protein from the everted rat small intestine was measured. At a surfactant concentration of 10 mM, a peak effect on protein release was noted with sodium decyl sulfate (C10). Measurement of proten release as a function of sidium lauryl sulfate (C12) concentration resulted in the observation that the effect appears to be due to the micellar phaseof the surfactant solution. At concentrations of C12 above the CMC, the loss of protein from the intestinal preparation increased as the concentration of surfactant was increased. There may be a maximum amount of protein that can be released from the everted rat small intestinal sacs by surface-active agents. At equivalent micellar concentrations of C8-C14 (12.5 times the CMC), there was no difference in the amount of protein released in the presence of the individual alkyl sulfate solutions. Other studies on salicylate transfer across the everted rat small intestine indicate that permeability changes occur with anionic and cationic surfactants but not with nonionics.
测定了烷基硫酸钠(C6 - C14)对外翻大鼠小肠蛋白质损失的影响。在表面活性剂浓度为10 mM时,观察到癸基硫酸钠(C10)对蛋白质释放有峰值效应。测量蛋白质释放量与月桂基硫酸钠(C12)浓度的关系,结果表明该效应似乎归因于表面活性剂溶液的胶束相。在C12浓度高于临界胶束浓度(CMC)时,肠道制剂中蛋白质的损失随着表面活性剂浓度的增加而增加。表面活性剂可能存在一个能从外翻大鼠小肠囊中释放的最大蛋白质量。在C8 - C14的等效胶束浓度(CMC的12.5倍)下,在各个烷基硫酸盐溶液存在时释放的蛋白质量没有差异。其他关于水杨酸盐通过外翻大鼠小肠转运的研究表明,阴离子和阳离子表面活性剂会引起通透性变化,而非离子表面活性剂则不会。