Yoshikawa H, Takada K, Muranishi S
Department of Drug Dosage Form Design, Faculty of Pharmaceutical Sciences, Toyama Medical & Pharmaceutical University, Japan.
Chem Pharm Bull (Tokyo). 1992 May;40(5):1277-9. doi: 10.1248/cpb.40.1277.
Transfer selectivity to the blood and the lymph of exogenous dextrans of various average molecular weight (approximate 4, 10, 18, 39 and 70 kilodaltons (kDa)) after dosing to the subserosal layer of the rat stomach wall was investigated by measuring the fluorescein isothiocyanate labelled dextran concentrations in the lymph of the thoracic duct and the peripheral plasma. The lymph/plasma level ratio of the dextrans rose greatly with the increase in molecular weight (over 10kDa) owing largely to the lower plasma concentration, although the lymph levels of small dextran (4kDa) were not significantly higher than the plasma levels. These results indicate that there is an inverse relation between plasma levels of dextrans and their molecular weight, and also suggest that the molecular weight threshold of transfer selectivity of dextran to the blood and the lymph administered in the rat stomach wall is between 4-10 kDa.
通过测量大鼠胃壁浆膜下层给药后不同平均分子量(约4、10、18、39和70千道尔顿(kDa))的外源性右旋糖酐在血液和淋巴中的转移选择性,研究人员测定了胸导管淋巴液和外周血浆中异硫氰酸荧光素标记的右旋糖酐浓度。尽管小分子量右旋糖酐(4kDa)的淋巴水平并不显著高于血浆水平,但由于血浆浓度较低,右旋糖酐的淋巴/血浆水平比值随着分子量增加(超过10kDa)而大幅上升。这些结果表明,右旋糖酐的血浆水平与其分子量呈负相关,也表明在大鼠胃壁给药时,右旋糖酐向血液和淋巴转移选择性的分子量阈值在4 - 10 kDa之间。