Péhourcq F, Matoga M, Jarry C, Bannwarth B
EA 525, Université Victor Segalen Bordeaux 2, Bordeaux, France.
Biomed Chromatogr. 2004 Jun;18(5):330-4. doi: 10.1002/bmc.328.
A rapid and stereospecific HPLC micromethod to quantify flurbiprofen enantiomers was developed. Both flurbiprofen enantiomers and indomethacin, used as internal standard, were extracted with methylene chloride from 100 microL of acidified plasma. The resolution of the R- and S-forms was performed on a bonded vancomycin chiral stationary phase (Chirobiotic V) with 20% of tetrahydrofuran in ammonium nitrate (100 mM, pH 5) as mobile phase. Calibration curves were linear in the range 0.5-10 microg/mL for both enantiomers. A good accuracy (< or = 5%) was obtained for all quality controls, with intra-day and inter-day variation coefficients equal or less than 7.7%. Recovery of both enantiomers was found in the range 77.4-86.3%. The lower limit of quantitation was 0.25 microg/mL for both enantiomers, without interference of endogenous components. This validated micromethod has been successfully applied for quantifying R- flurbiprofen and S- flurbiprofen in rat plasma.
建立了一种快速、立体专一的HPLC微量方法来定量氟比洛芬对映体。氟比洛芬对映体和用作内标的吲哚美辛,用二氯甲烷从100 μL酸化血浆中提取。R型和S型的分离在键合万古霉素手性固定相(Chirobiotic V)上进行,流动相为含20%四氢呋喃的硝酸铵(100 mM,pH 5)。两种对映体的校准曲线在0.5-10 μg/mL范围内呈线性。所有质量控制的准确度良好(≤5%),日内和日间变异系数均等于或小于7.7%。两种对映体的回收率在77.4-86.3%范围内。两种对映体的定量下限均为0.25 μg/mL,无内源性成分干扰。这种经过验证的微量方法已成功应用于大鼠血浆中R-氟比洛芬和S-氟比洛芬的定量。