Pengaruh Pemberian Omeprazole Terhadap Profil Farmakokinetika Piroxicam Dengan Metode Kromatografi Cair Kinerja Tinggi (KCKT)
Pengaruh Pemberian Omeprazole Terhadap Profil Farmakokinetika Piroxicam Dengan Metode Kromatografi Cair Kinerja Tinggi (KCKT)
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.
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References
Khrishna, M.B., Pallavi, S.S., Madhu.P., Kumar, S.S., Ramu, V., dan Satyanarayana, D. (2011). Drug Interaction; Principles, Methodology and Applications (General Aspects). Pharmanest.
Rahmawati. F, Handayani. R, dan Gosal. V. (2006). Kajian Retrospektif Interaksi Obat di Rumah Sakit Pendidikan Dr. Sardjito Yogyakarta. Majalah Farmasi Indonesia.
Aslam, M., Kaw Tan, C., dan Prayitno, A. (2003). Farmasi Klinis (Clinical Pharmacy) Menuju Pengobatan Rasional dan Penghargaan Pilihan Pasien. Jakarta:
Forceia, MA.,et al. (2004). Geriatric Secrets, Third Edition. United States: Independence Square West.
Hakim, L. (2012). Farmakokinetik Klinik. Yogyakarta: Bursa Ilmu.
Siswandono dan Soekardjo, B. 2000. Kimia Medisinal Edisi 2. Surabaya: Airlangga University Press.
Anief, M. (1995). Ilmu Meracik Obat. Cetakan V. Yogyakarta: Gajah Mada University Press.
Iersa, R. (2012). Pengaruh Vitamin C pada Profil Farmakokinetika Natrium Diklofenak Terhadap Hewan Uji Kelinci. Fakultas Farmasi Universitas Sumatera Utara. E-USU Repository. Tanggal akses 6 April 2013.
Emami, J., Ghassami, N., dan Talari, R. (2007). A Rapid and Sensitive Modified HPLC Method for Determination of Diclofenac in Human Plasma and its Application in Pharmacokinetic Studies. Daru.
Harmita, (2004). Petunjuk Pelaksanaan Validasi Metode Dan Cara Perhitungannya. Majalah Ilmu Kefarmasian.
Mirakel Agatha Devi. (2007). Pengaruh Pemberian Air Berkarbonasi Terhadap Profil Farmakokinetika Parasetamol Pada Tikus Putih Jantan. Fakultas Farmasi Universitas Sanata Dharma. Yogyakarta