Tagesson C, Sjödahl R
Scand J Gastroenterol. 1984 May;19(3):315-20.
The urinary recovery of different-sized (282-1206 dalton) polyethylene glycols (PEGs) after intravenous administration was determined. Mixtures of different-sized PEGs were injected intravenously in anesthetized pigs, and the urinary recovery at different times was determined by means of reversed-phase high-performance liquid chromatography. PEGs in the 722-1206-dalton range were all recovered to the same extent, whereas the recovery of PEGs in the 282-678-dalton range was related to molecular size; that is, the smaller the molecule, the less the urinary recovery. Moreover, less was found of the 370-414-dalton PEGs than of the 678-722-dalton PEGs in the blood after intravenous injection. These findings have a bearing on the measurements of intestinal permeability to different-sized PEGs, in which absorption-molecular weight profiles are assessed by urinary recovery after oral load. Thus, if PEGs in the 282-678-dalton range are used for such measurements, the absorption-molecular weight profile should be corrected for non-intestinal, size-dependent filtration.
测定了静脉注射后不同大小(282 - 1206道尔顿)聚乙二醇(PEG)的尿回收率。将不同大小的PEG混合物静脉注射到麻醉的猪体内,通过反相高效液相色谱法测定不同时间的尿回收率。722 - 1206道尔顿范围内的PEG回收率相同,而282 - 678道尔顿范围内的PEG回收率与分子大小有关;即分子越小,尿回收率越低。此外,静脉注射后血液中370 - 414道尔顿的PEG比678 - 722道尔顿的PEG含量少。这些发现与不同大小PEG的肠道通透性测量有关,其中口服负荷后通过尿回收率评估吸收 - 分子量分布。因此,如果使用282 - 678道尔顿范围内的PEG进行此类测量,吸收 - 分子量分布应针对非肠道的、大小依赖性过滤进行校正。