Sundqvist T, Magnusson K E, Sjödahl R, Stjernström I, Tagesson C
Gut. 1980 Mar;21(3):208-14. doi: 10.1136/gut.21.3.208.
The intestinal permeability to low molecular weight polyethyleneglycol (PEG) has been evaluated by means of a simple mathematical model and computer-aided curve-fitting procedures. Macrogolum 400, a mixture of 11 PEGs with molecular weights ranging from 194 to 634 daltons, was taken together with a liquid meal and a six-hour portion of urine collected. The different PEGs were then extracted from the urine, separated from each other by gas-liquid chromatography, and the relative peak area of each individual PEG determined. The distribution of different PEGs in the urine was then compared with the original PEG-distribution in three different ways: (1) by comparing the median values of the molecular weights, (2) by comparing the mean and standard deviation after curve fitting to the normal distribution, and (3) by curve fitting to mathematical filter functions demonstrating molecular exclusion due to size. It thus appeared that molecules were excluded both in the high and in the low molecular weight range, possibly by a combined effect of the intestinal permeability barrier and an escape to other compartments than the urine. However, relatively more of the larger PEGs passed from the intestine to the urine in a patient with Crohn's disease than in an apparently healthy individual.
已通过一个简单的数学模型和计算机辅助曲线拟合程序评估了肠道对低分子量聚乙二醇(PEG)的通透性。将分子量范围为194至634道尔顿的11种PEG的混合物聚乙二醇400与流食一起服用,并收集6小时的尿液样本。然后从尿液中提取不同的PEG,通过气液色谱法将它们彼此分离,并测定每种PEG的相对峰面积。随后,以三种不同方式将尿液中不同PEG的分布与原始PEG分布进行比较:(1)通过比较分子量的中位数;(2)通过将曲线拟合到正态分布后比较均值和标准差;(3)通过将曲线拟合到显示因大小导致分子排斥的数学过滤函数。结果显示,在高分子量和低分子量范围内分子均被排斥,这可能是肠道通透性屏障以及分子逃逸到尿液以外其他隔室的综合作用所致。然而,与明显健康的个体相比,克罗恩病患者中相对更多的较大PEG从肠道进入尿液。