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Effect of omeprazole, rabeprazole, and rebamipide on the accuracy of urea breath test in patients with Helicobacter pylori infection

pharmacokinetics. Acid suppression and efficacy of proton pump inhibitors. Aliment Pharmacol Ther. 2000; 14:963-78. 6. John H. The proton pump inhibitors: similarities and differences. Clinical Therapeutics. 2000; 22:266-79. 7. Chey WD, Spybrook M, Carpenter S, Nostrant TT, Elta GH, Scheiman JM. Prolonged effect of omeprazole on the 14C-urea breath test. Am J Gastroenterol. 1996; 91:89-92. 8. Connor SJ, Seow F, Ngu MC, Katelaris PH. The effect of dosing with omeprazole on the accuracy of 13C-urea breath test in Helicobacter pylori

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Validation and application of hair analysis for the detection of methamphetamine in young Thai adults

, Balikova MA. State of the art in hair analysis for detection of drug and alcohol abuse. Clin Chim Acta. 2006; 370:17-49. 28. Zhang X, Es-haghi A, Cai J, Pawliszyn J. Simplified kinetic calibration of solid-phase microextraction for in vivo pharmacokinetics. J Chromatogr A. 2009; 1216: 7664-9. 29. Bruheim P, Kvitvang HFN, Villas-Boas SG. Stable isotope coded derivatizing reagents as internal standards in metabolite profiling. J Chromatogr A. 3013; 1296:196-203. 30. Han E, Park Y, Yang W, Lee J, Lee S, Kim E, Lim M, Chung H

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Guidelines for the management of haemophilia in Egypt

-8. 25. Fischer K, van der Bom JG, Molho P, et al. Prophylactic versus on-demand treatment strategies for severe haemophilia: a comparison of costs and long-term outcome. Haemophilia 2002; 8: 745-52. 26. Elekiaby A, El Saied H, Elekiaby M. Five years of tailored low dose prophylaxis in a small cohort of kids with severe hemophilia A using SD-F cryoprecipitate. Poster no. PO169 presented at the World Federation of Hemophilia Congress; 24-28 July 2016; Orlando, FL. 27. El-Kiaby M, Goubran HA, Radosevich M, et al. Pharmacokinetic study of

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Statin use and histopathological change in patients with non-alcoholic fatty liver disease: a systematic review and meta-analysis

-up time of the included study might present only the early stage of fibrotic change. From the meta-analysis, the average rate of fibrosis progression of one stage is more than 7.7 years in patients with NASH and 14.3 years in patients with NAFLD [ 55 ]. The heterogeneous findings from the present study may be the result of several factors. First, the pharmacokinetics of each statin varies in metabolism and excretion. Most statin metabolism takes place in liver, while the excretion depends on hydrophobicity. The liver mostly excretes hydrophobic compounds, such as

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Second line antiretroviral therapy for treatment of HIV in Asia

al. The LOPSAQ study: 48 week analysis of a boosted double protease inhibitor regimen containing lopinavir/ritonavir plus saquinavir without additional antiretroviral therapy. J AntimicrobChemother. 2006; 58: 1024-30. 27. Ribera E, Azuaje C, Lopez RM, Diaz M, Feijoo M, Pou L, et al. Atazanavir and lopinavir/ritonavir: pharmacokinetics, safety and efficacy of a promising double-boosted protease inhibitor regimen. AIDS. 2006. 20: 1131-9. 28. Chetchotisakd P, Anunnatsiri S, Mootsikapun P, Kiertiburanakul S, Anekthananon T

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Comparison Between Lignocaine Hydrochloride and Ropivacaine Hydrochloride as Lumbosacral Epidural Anaesthetic Agents in Goats Undergoing Laparoscopy Assisted Embryo Transfer

. Fubini, S.L and Ducharme, N.G (eds.), first edition, Saunders, Missouri. 9. Ala-Kokko, T.I., Partanen, A., Kainen, J., Kiviluoma, K., Alahuhta, S. (2000). Pharmacokinetics of 0.2 % ropivacaine and 0.2 % bupivacaine following caudal blocks in children. Acta Anaesthesiol. Scand. 44, 1099-1102. PMid:11028730 10. Singh, K., Kinjavdekar., Amarpal., Aithal, H.P., Gopinathan, A., Singh, G.R., Singh, T., Pawde, A.M. Pratap, K. (2005). Clinicophysiological and hematobiochemical effects of

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Inhibition of cell cycle progression and apoptotic activity of resveratrol in human intrahepatic cholangiocarcinoma cell lines

; 90:1325-38. 41. Brown VA, Patel KR, Viskaduraki M, Crowell JA, Perloff M, Booth TD, et al. Repeat dose study of the cancer chemopreventive agent resveratrol in healthy volunteers: safety, pharmacokinetics, and effect on the insulin-like growth factor axis. Cancer Res. 2010; 70:9003-11. 42. Baur JA, Sinclair DA. Therapeutic potential of resveratrol: the in vivo evidence. Nat Rev Drug Discov. 2006; 5:493-506.

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Genotype distributions of CYP2C9 and VKORC1 in southern Thais and their association with warfarin maintenance dose in patients with cardiac surgery

are associated with altered warfarin pharmacokinetics. Two minor variants, CYP2C9 * 2 (rs1799853, C>T) and CYP2C9 * 3 (rs1057910, A>C), have been proven to reduce warfarin metabolism and thus reduce the dose requirement in patients taking regular warfarin. The frequencies of CYP2C9 polymorphisms differ with ethnicity. In Thailand, the frequency of CYP2C9 * 1 /* 3 (heterozygous AC of rs1057910) has been reported at 2.8%–8.6% [ 7 , 8 , 10 ], CYP2C9 * 3 /* 3 (homozygous CC of rs1057910) as a very rare genotype, and CYP2C9 * 2 has never been reported

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Thai national guidelines for antiretroviral therapy in HIV-1 infected adults and adolescents 2010

efficacy of nevirapine-based antiretroviral therapy in HIV-infected patients with tuberculosis. Clin Infect Dis. 2007; 44:141-4. 42. Avihingsanon A, Manosuthi W, Kantipong P, Chuchotaworn C, Moolphate S, Yamada N, et al. Pharmacokinetics and 48 weeks efficacy of nevirapine: 400 mg versus 600 mg per day in HIV-Tuberculosis coinfection receiving rifampicin. Antivir Ther. 2008; 13: 529-36. 43. Hammer SM, Saag MS, Schechter M, Montaner JSG, Schooley RT, Jacobsen DM, et al. Antiretroviral treatment of adult HIV infection: 2008 recommendations

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Human immunodeficiency virus and acquired immune deficiency syndrome in Asia: an update

regimens [ 52 ]. Efavirenz causes central neurological side-effects and rash in 5%–10% of treated patients which limits the tolerability of the drug, and this may prove a challenge for Asia, while implementing recommendations to commence ART at a 500 cell/mm 3 CD4 count or higher threshold. Optimizing antiretroviral therapy in Asia In general, ARV drug development for licensing has been based on pharmacokinetic results among Western volunteers. Furthermore, the final dose selected for phase III trials and approval is decided by the principle of selecting the

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