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Disposition Characteristics of Protein Drugs in the Perfused Rat Kidney
Authors:Mihara  Kiyoshi  Hojo  Takami  Fujikawa  Makoto  Takakura  Yoshinobu  Sezaki  Hitoshi  Hashida  Mitsuru
Institution:(1) Department of Basic Pharmaceutics, Faculty of Pharmaceutical Sciences, Kyoto University, Sakyo-ku, Kyoto, 606-01, Japan;(2) Department of Basic Pharmaceutics, Faculty of Pharmaceutical Sciences, Setsunan University, Osaka, 573-01, Japan;(3) Faculty of Pharmaceutical Sciences, Kyoto University, Sakyo-ku, Kyoto, 606-01, Japan
Abstract:The renal disposition characteristics of 111In-labeled neocarzinostatin (NCS), soybean trypsin inhibitor (STI), and superoxide dismutase (SOD) were studied in the perfused rat kidney. In a single-pass indicator dilution experiment, venous and urinary recovery profiles and tissue accumulation of proteins were determined under filtering or nonfiltering conditions. In the nonfiltering kidney perfusion experiment, no significant tissue accumulation was observed, suggesting minimal uptake from the glomerular and peritubular capillary sides. Therefore, tissue recovery corresponded to that with tubular reabsorption after glomerular filtration. The total amount of NCS or STI being filtrated through glomeruli, the sum of tissue and urinary recoveries, was similar to that of inulin, but that of SOD was about half. Similarly, the steady-state distribution volumes (V d) of NCS and STI obtained by moment analysis of their venous outflow curves were similar to that of inulin, while the V d value of SOD was significantly lower. These results suggest the restricted passage of SOD through the glomerular and postglomerular capillary wall. The tubular reabsorption ratio of proteins against the total filtrated amount decreased with an increase in the administered dose, suggesting nonlinearity of reabsorption. SOD had the largest reabsorption ratio. Thus, this experimental system is useful for quantitative analysis of renal disposition of proteins.
Keywords:protein drugs  rat kidney perfusion  moment analysis  glomerular and postglomerular permselectivity  tubular reabsorption
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