Wu S T, Stampfli H F, Banks C M, Emm T A, Kapil R P, Padovani P K, Lee W M, Huang S M
DuPont Merck Pharmaceutical Company, Drug Metabolism and Pharmacokinetics Section, Newark, DE 19714.
J Chromatogr B Biomed Appl. 1994 Jul 1;657(1):254-60. doi: 10.1016/0378-4347(94)80097-9.
A specific and sensitive HPLC assay for the determination of DMP 728 in dog and rat plasma has been developed. The method involves solid-phase extraction of DMP 728 and the internal standard from plasma using a C2 column. The extracted compounds are derivatized with benzoin under alkaline conditions. Using a mixture of acetonitrile and 0.1 M potassium phosphate buffer (25:75, v/v, pH 7.4) as mobile phase, the derivatized products are separated on a Regis semipermeable surface C8 column and monitored fluorometrically using 325 nm and 425 nm as excitation and emission wavelengths, respectively. The assay is linear from 2.5 to 1000 ng/ml in dog plasma and from 5 to 1000 ng/ml in rat plasma. The limit of quantitation is 2.5 ng/ml using 0.5 ml of dog plasma and 5 ng/ml using 0.5 ml of rat plasma. The assay has been used in pharmacokinetic studies of DMP 728 in dogs and rats.
已开发出一种用于测定犬和大鼠血浆中DMP 728的特异性灵敏高效液相色谱法。该方法包括使用C2柱从血浆中固相萃取DMP 728和内标。萃取的化合物在碱性条件下用苯偶姻衍生化。使用乙腈和0.1 M磷酸钾缓冲液(25:75,v/v,pH 7.4)的混合物作为流动相,衍生化产物在Regis半透表面C8柱上分离,并分别使用325 nm和425 nm作为激发和发射波长进行荧光监测。该测定法在犬血浆中2.5至1000 ng/ml范围内呈线性,在大鼠血浆中5至1000 ng/ml范围内呈线性。使用0.5 ml犬血浆时定量限为2.5 ng/ml,使用0.5 ml大鼠血浆时定量限为5 ng/ml。该测定法已用于DMP 728在犬和大鼠中的药代动力学研究。