Julkunen R J, Himberg J J
Arzneimittelforschung. 1976 Apr;26(4):560-3.
The validity of a new technique for studying drug protein binding is tested. By this gel diffusion or batch method using dry polyacrylamide, sulfadiazine and sulfafurazole are bound by human plasma proteins to the same extent as reported by other authors with different techniques. The binding of warfarin to fresh human plasma was quantitatively less than expected. This might be due to the possibility that other plasma constituents of non-fasted test persons displace warfarin from protein binding sites, since it is bound more in buffer solutions containing physiological concentrations of human albumin. Phenylbutazone displaced warfarin from its binding sites in diluted human serum albumin concentrations. Quinidine was found to be adsorbed by the otherwise inert polyacrylamide gel and the method is therefore not applicable to quinidine binding studies.
一种用于研究药物与蛋白质结合的新技术的有效性得到了检验。通过这种使用干燥聚丙烯酰胺的凝胶扩散或批量方法,磺胺嘧啶和磺胺异恶唑与人类血浆蛋白的结合程度与其他作者使用不同技术所报道的相同。华法林与新鲜人类血浆的结合在定量上低于预期。这可能是由于非空腹测试者的其他血浆成分有可能将华法林从蛋白质结合位点上置换下来,因为它在含有生理浓度人白蛋白的缓冲溶液中结合得更多。在稀释的人血清白蛋白浓度下,保泰松将华法林从其结合位点上置换下来。发现奎尼丁被原本惰性的聚丙烯酰胺凝胶吸附,因此该方法不适用于奎尼丁结合研究。