Pengaruh Pemberian Omeprazole Terhadap Profil Farmakokinetika Piroxicam Dengan Metode Kromatografi Cair Kinerja Tinggi (KCKT)

Dasma Arihan Nauli Sipayung
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Abstract

Piroxicam is an anti-inflammatory drug belonging to the NSAID group and is also used as an analgesic and anti-rheumatic drug. Its use is often combined with stomach medicines, as the side effects of piroxicam can irritate the stomach. One of them is omeprazole. Since piroxicam and omeprazole act on the same enzyme, CYP450, they can affect the pharmacokinetic profile, especially at the metabolic stage and excretion of piroxicam. The purpose of this study was to determine the effect of omeprazole on the pharmacokinetic profile of piroxicam especially in the metabolic phase and excretion. The method used in this study was an experimental method using three male rabbits. These rabbits are divided into three groups. The first treatment group was giving pyroxicam solution 0.653 mg / kg body weight, the second treatment group gave piroxicam 0.653 mg / kg body weight that one hour before was given omeprazole 1.2 mg / kg body weight and the third group treated with piroxicam 0.7 mg / kg body weight at the same time with omeprazole 1,4 mg / kg body weight. Plasma levels of the drug piroxicam are measured using a high performance liquid chromatography (HPLC) tool. The verification method is executed. This is the determination of LOD and LOQ values, accuracy and accuracy testing. The result of data analysis using t-table. The results showed that there was an increase or difference in pharmacokinetic parameter values ​​during the absorption phase, but no significant effect was shown for each group. Pharmacokinetic parameter values ​​for metabolic stages and excretion were reduced and no significant difference was shown between the groups. Simultaneous administration of omeprazole and piroxicam and administration of piroxicam 1 hour before omeprazole may inhibit piroxicam-metabolizing enzymes and thus affect pharmacokinetic parameters and excretion during absorption, but are not significant.  
Omeprazole对Piroxicam药理学概况的影响,以及高性能的液体色谱方法
吡罗昔康是一种抗炎药,属于非甾体抗炎药组,也被用作镇痛和抗风湿药。它通常与胃药结合使用,因为吡罗昔康的副作用会刺激胃。其中之一是奥美拉唑。由于吡罗昔康和奥美拉唑作用于同一种酶CYP450,它们可以影响药代动力学特征,特别是在吡罗昔康的代谢阶段和排泄。本研究的目的是确定奥美拉唑对吡罗昔康的药代动力学特征的影响,特别是在代谢期和排泄。本研究采用3只雄性家兔的实验方法。这些兔子被分成三组。第一治疗组给予吡罗昔康溶液0.653 mg / kg体重,第二治疗组给予吡罗昔康0.653 mg / kg体重,1小时前给予奥美拉唑1.2 mg / kg体重,第三组给予吡罗昔康0.7 mg / kg体重,同时给予奥美拉唑1、4 mg / kg体重。使用高效液相色谱(HPLC)工具测量药物吡罗昔康的血浆水平。执行验证方法。这是LOD和LOQ值的测定,准确度和准确度的测试。数据分析结果采用t表。结果表明,吸收期药代动力学参数值有增加或差异,但各组间无显著影响。代谢阶段和排泄的药代动力学参数值降低,组间无显著差异。奥美拉唑与吡罗西康同时服用以及在奥美拉唑前1小时服用吡罗西康可能抑制吡罗西康代谢酶,从而影响吸收过程中的药代动力学参数和排泄,但不显著。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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