Jaworowicz D J, Filipowski M T, Boje K M
Department of Pharmaceutics, School of Pharmacy, University at Buffalo, NY 14260, USA.
J Chromatogr B Biomed Sci Appl. 1999 Feb 19;723(1-2):293-9. doi: 10.1016/s0378-4347(98)00559-3.
An improved, validated HPLC assay was developed for the non-steroidal anti-inflammatory agent, nimesulide. In contrast to previous methods, the present assay requires smaller plasma volumes (0.2 ml) and utilizes a commercially available, structurally similar analogue of nimesulide, NS-398. The method involves a liquid-liquid extraction procedure that can be completed within 4 h, followed by reversed-phase HPLC analysis. Briefly, the extraction protocol required toluene extraction of acidified plasma samples, followed by back-extraction of the retained toluene phase with aqueous base. The retained aqueous alkaline phase was concentrated by toluene re-extraction. The retained toluene phase was evaporated to dryness and reconstituted with 100 microl of mobile phase. Extracted samples were injected (50 microl) onto a Shandon Hypersil BDS C18 column (5 microm particle size; 250x4.6 mm) equilibrated with 1.0 ml/min of 68:32 (v/v) methanol-citrate (0.08 M)-phosphate (0.04 M) buffer (pH 3.0) at room temperature, with detection at 240 nm. The chromatographic run time was 12 min with retention times of 5.9 min and 9.1 min for nimesulide and NS-398, respectively. The analytical method was successfully utilized for a pilot pharmacokinetic study.
已开发出一种改进的、经过验证的高效液相色谱法(HPLC)用于测定非甾体抗炎药尼美舒利。与先前的方法不同,本测定法所需血浆量较少(0.2毫升),并使用了一种市售的、结构与尼美舒利相似的类似物NS - 398。该方法包括一个液 - 液萃取过程,此过程可在4小时内完成,随后进行反相高效液相色谱分析。简要地说,萃取方案要求用甲苯萃取酸化的血浆样品,然后用碱性水溶液对保留的甲苯相进行反萃取。保留的碱性水相通过甲苯再萃取进行浓缩。保留的甲苯相蒸发至干,并以100微升流动相复溶。将萃取后的样品(50微升)注入到一根Shandon Hypersil BDS C18柱(粒径5微米;250×4.6毫米)上,该柱在室温下用流速为1.0毫升/分钟的68:32(v/v)甲醇 - 柠檬酸盐(0.08 M) - 磷酸盐(0.04 M)缓冲液(pH 3.0)平衡,检测波长为240纳米。色谱运行时间为12分钟,尼美舒利和NS - 398的保留时间分别为5.9分钟和9.1分钟。该分析方法已成功用于一项初步的药代动力学研究。