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在反相液相色谱法测定氟哌啶醇和还原氟哌啶醇过程中卡马西平和苯海拉明干扰的消除

Resolution of the interference from carbamazepine and diphenhydramine during reversed-phase liquid chromatographic determination of haloperidol and reduced haloperidol.

作者信息

Vatassery G T, Holden L A, Dysken M W

机构信息

Geriatric Research, Education and Clinical Center, Veterans Administration Medical Center, Minneapolis, MN 55417.

出版信息

J Anal Toxicol. 1993 Sep;17(5):304-6. doi: 10.1093/jat/17.5.304.

Abstract

Carbamazepine and diphenhydramine interfered with the assays of haloperidol and its metabolite, reduced haloperidol, by reversed-phase HPLC. Retention times of haloperidol, reduced haloperidol, and the interfering drugs were very sensitive to the percentage of potassium phosphate buffer in the mobile phase as well as to the final pH of the eluant. Retention times were not very dependent upon ionic strength of the eluting solvent mixture. Haloperidol and reduced haloperidol in the range of 0.5-10 ng/mL were analyzed in the presence of 0.2 micrograms/mL diphenhydramine and 5 micrograms/mL of carbamazepine. The concentrations of all drugs used were in their expected therapeutic ranges. The isocratic chromatographic conditions were as follows: 25-cm x 4.6-mm C-18 column; mobile phase, 75% phosphate buffer (final concentration, 0.06M) and 25% acetonitrile; final pH, 3.5; flow rate, 2.5 mL/min; and detection by UV absorption at 220 nm. Additional changes in the percent buffer in the mobile phase may be useful in achieving separation of other interfering compounds.

摘要

卡马西平和苯海拉明通过反相高效液相色谱法干扰了氟哌啶醇及其代谢产物还原氟哌啶醇的测定。氟哌啶醇、还原氟哌啶醇和干扰药物的保留时间对流动相中磷酸钾缓冲液的百分比以及洗脱液的最终pH值非常敏感。保留时间对洗脱溶剂混合物的离子强度依赖性不大。在存在0.2微克/毫升苯海拉明和5微克/毫升卡马西平的情况下,分析了0.5 - 10纳克/毫升范围内的氟哌啶醇和还原氟哌啶醇。所用所有药物的浓度均在其预期治疗范围内。等度色谱条件如下:25厘米×4.6毫米C - 18柱;流动相,75%磷酸盐缓冲液(最终浓度,0.06M)和25%乙腈;最终pH值,3.5;流速,2.5毫升/分钟;通过220纳米处的紫外吸收进行检测。流动相中缓冲液百分比的其他变化可能有助于实现其他干扰化合物的分离。

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