Fremstad D
Acta Pharmacol Toxicol (Copenh). 1977 Aug;41(2):148-60. doi: 10.1111/j.1600-0773.1977.tb02135.x.
The blood cell/plasma concentration ratio of quinidine, as influenced by the plasma protein binding, was studied in normal and anuric rats by applying incubation and equilibrium dialysis techniques on blood and plasma, respectively, from normal and anuric rats. The plasma protein binding of quinidine in anuria was increased at concentrations of unbound drug of less than 1.75 X 10(-4) M and decreased above this concentration. At an assumed "therapeutic" quinidine concentration (1 X 10(-5) M), the mean concentration ratio (total quinidine in blood cells)/(total quinidine in plasma) was 1.84 in normals and 0.46 in anuria, and the mean ratio (total quinidine in blood cells)/(unbound in plasma) was 4.45 and 1.81, respectively. As the latter ratios were concentration dependent and greater than could be accounted for by pH-dependent distribution, quinidine is presumably bound in/on the blood cells. Reduced distribution ratio in anuria, even when related to unbound quinidine in plasma, also indicates changed binding in blood cells, a finding confirmed by applying the data to modified Scatchard plot. this may have implication for the use of blood cell/plasma concentration ratio as screening procedure for the altered plasma binding of quinidine in patients.
通过分别对正常大鼠和无尿大鼠的血液和血浆应用孵育和平衡透析技术,研究了受血浆蛋白结合影响的奎尼丁血细胞/血浆浓度比。在无尿状态下,当未结合药物浓度低于1.75×10⁻⁴ M时,奎尼丁的血浆蛋白结合增加,而高于该浓度时则降低。在假定的“治疗”奎尼丁浓度(1×10⁻⁵ M)下,正常大鼠的平均浓度比(血细胞中总奎尼丁)/(血浆中总奎尼丁)为1.84,无尿大鼠为0.46,平均比值(血细胞中总奎尼丁)/(血浆中未结合奎尼丁)分别为4.45和1.81。由于后一个比值与浓度有关且大于由pH依赖性分布所解释的值,推测奎尼丁在血细胞内/上结合。无尿状态下分布比降低,即使与血浆中未结合的奎尼丁相关,也表明血细胞中的结合发生了变化,将数据应用于修正的Scatchard图证实了这一发现。这可能对使用血细胞/血浆浓度比作为筛选患者中奎尼丁血浆结合改变的程序有影响。