Krishna D R, Ramana D V, Mamidi N V
University College of Pharmaceutical Sciences, Kakatiya University, Warangal, India.
Drug Metabol Drug Interact. 1995;12(1):53-63. doi: 10.1515/dmdi.1995.12.1.53.
In vitro protein binding of D(+) usnic acid in rabbit plasma and purified bovine serum albumin was investigated by equilibrium dialysis. The drug was highly protein bound, approximately 99.2%, and the extent of protein binding remained constant at usnic acid concentrations in the range of 1-5 micrograms/ml. The extent of binding, however, tended to decrease at low albumin concentrations and higher drug concentrations; Scatchard plot analysis indicated the existence of two classes of binding sites with association constants of 34.3 x 10(-6) and 1.43 x 10(-6) M respectively. Tissue distribution studies of usnic acid were undertaken in rats following i.p. administration. Usnic acid was well distributed into well perfused organs. The tissue/plasma ratio in lungs was high, which could be advantageous in a therapeutic agent for pulmonary tuberculosis.
通过平衡透析研究了兔血浆和纯化牛血清白蛋白中D(+)松萝酸的体外蛋白结合情况。该药物与蛋白高度结合,约为99.2%,在松萝酸浓度为1 - 5微克/毫升范围内,蛋白结合程度保持恒定。然而,在低白蛋白浓度和高药物浓度下,结合程度趋于降低;Scatchard图分析表明存在两类结合位点,其缔合常数分别为34.3×10⁻⁶和1.43×10⁻⁶ M。在大鼠腹腔注射松萝酸后进行了组织分布研究。松萝酸在灌注良好的器官中分布良好。肺中的组织/血浆比值较高,这对于治疗肺结核的药物可能是有利的。