Uzu S, Imai K, Nakashima K, Akiyama S
Branch Hospital Pharmacy, University of Tokyo, Japan.
J Pharm Biomed Anal. 1992 Oct-Dec;10(10-12):979-84. doi: 10.1016/0731-7085(91)80107-k.
The high-performance liquid chromatographic determination of medroxyprogesterone acetate (MPA) with peroxyoxalate chemiluminescence (PO-CL) detection is described. The spiked serum containing MPA was extracted on Bond-Elut C18 columns and derivatized with 4-(N,N-dimethylaminosulphonyl)-7-hydrazino-2,1,3-benzoxadiazole (DBD-H). The hydrazone of MPA with DBD-H was confirmed to be a mono-DBD-derivative. The reaction mixture was separated by direct injection onto a C18 analytical column, and quantified by PO-CL detection. The linear range of the standard curve, in serum, was 15.6-96.6 ng ml-1 with a detection limit of 9 ng ml-1 using only 100 microliters of serum, while the detection limit of standard MPA derivatized with DBD-H was 8.7 fmol per injection. The relative standard deviation of the method was 7.4% at 19.3 ng and 1.7% at 77.3 ng ml-1.
描述了采用过氧草酸酯化学发光(PO-CL)检测的高效液相色谱法测定醋酸甲羟孕酮(MPA)。含MPA的加标血清在Bond-Elut C18柱上进行萃取,并用4-(N,N-二甲基氨基磺酰基)-7-肼基-2,1,3-苯并恶二唑(DBD-H)进行衍生化。MPA与DBD-H的腙被确认为单-DBD-衍生物。反应混合物通过直接进样到C18分析柱上进行分离,并用PO-CL检测进行定量。血清中标准曲线的线性范围为15.6 - 96.6 ng ml-1,仅使用100微升血清时检测限为9 ng ml-1,而用DBD-H衍生化的标准MPA每次进样的检测限为8.7 fmol。该方法的相对标准偏差在19.3 ng时为7.4%,在77.3 ng ml-1时为1.7%。