These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
81 related articles for article (PubMed ID: 17341027)
1. RP-HPLC analysis of flucloxacillin in human plasma: validation and application to a bioequivalence study. Zhou Q; Ruan Z; Yuan H; Jiang B; Xu D Pharmazie; 2007 Feb; 62(2):101-4. PubMed ID: 17341027 [TBL] [Abstract][Full Text] [Related]
2. A simple sample preparation with HPLC-UV method for estimation of tiropramide from plasma: application to bioequivalence study. Imran K; Punnamchand L; Natvarlal SM J Pharm Biomed Anal; 2007 Feb; 43(3):1135-40. PubMed ID: 17127027 [TBL] [Abstract][Full Text] [Related]
3. HPLC determination of amoxicillin comparative bioavailability in healthy volunteers after a single dose administration. Pires de Abreu LR; Ortiz RM; de Castro SC; Pedrazzoli J J Pharm Pharm Sci; 2003; 6(2):223-30. PubMed ID: 12935434 [TBL] [Abstract][Full Text] [Related]
4. Determination of secnidazole in human plasma by high-performance liquid chromatography with UV detection and its application to the bioequivalence studies. Li X; Sun J; Wang G; Zheng Y; Yan B; Xie H; Gu Y; Ren H Biomed Chromatogr; 2007 Mar; 21(3):304-9. PubMed ID: 17221933 [TBL] [Abstract][Full Text] [Related]
5. [Pharmacokinetics and bioequivalence of trimebutine dispersive tablet in healthy subjects]. Jiang H; Ding L; Yang J; Huang X; Liu GY; Zhang ZX Yao Xue Xue Bao; 2004 Mar; 39(3):208-11. PubMed ID: 15171657 [TBL] [Abstract][Full Text] [Related]
6. Validation of a reversed-phase high-performance liquid chromatography method with fluorescence detection for the bioequivalence study of norfloxacin in plasma samples. Maia MB; Martins IL; do Nascimento DF; Cunha AN; de Lima FE; Bezerra FA; Moraes MO; Moraes ME Ther Drug Monit; 2008 Jun; 30(3):341-6. PubMed ID: 18520606 [TBL] [Abstract][Full Text] [Related]
7. Quantification of gliclazide by semi-micro high-performance liquid chromatography: application to a bioequivalence study of two formulations in healthy subjects. Park JY; Kim KA; Kim SL; Park PW J Pharm Biomed Anal; 2004 Jun; 35(4):943-9. PubMed ID: 15193740 [TBL] [Abstract][Full Text] [Related]
8. Bioequivalence evaluation of two D-limonene capsule formulations in healthy Chinese volunteers. Liu T; Guo Y; Gao Z; Chen Z; Jiang X Pharmazie; 2008 Oct; 63(10):718-20. PubMed ID: 18972832 [TBL] [Abstract][Full Text] [Related]
9. Determination of azithromycin in human plasma by LC-MS-MS and its pharmacokinetics. Xue-Min Z; Jie L; Juan G; Quan-Sheng Y; Wen-Yan W Pharmazie; 2007 Apr; 62(4):255-7. PubMed ID: 17484278 [TBL] [Abstract][Full Text] [Related]
10. Determination of mianserin in human plasma by high performance liquid chromatography-electrospray ionization mass spectrometry (HPLC-ESI/MS): application to a bioequivalence study in Chinese volunteers. Xu P; Li HD; Chen BM; Ma N; Yan M; Zhu YG J Pharm Biomed Anal; 2008 Aug; 47(4-5):994-9. PubMed ID: 18514457 [TBL] [Abstract][Full Text] [Related]
11. A sensitive validated LC-MS/MS method for quantification of itraconazole in human plasma for pharmacokinetic and bioequivalence study in 24 Korean volunteers. Rhim SY; Park JH; Park YS; Kim DS; Lee MH; Shaw LM; Kang JS Pharmazie; 2009 Feb; 64(2):71-5. PubMed ID: 19320276 [TBL] [Abstract][Full Text] [Related]
12. Bioavailability and bioequivalence of two oral formulations of alendronate sodium 70 mg: an open-label, randomized, two-period crossover comparison in healthy Korean adult male volunteers. Rhim SY; Park JH; Park YS; Lee MH; Kim DS; Shaw LM; Yang SC; Kang JS Clin Ther; 2009 May; 31(5):1037-45. PubMed ID: 19539104 [TBL] [Abstract][Full Text] [Related]
13. A selective HPLC method for the determination of indapamide in human whole blood: application to a bioequivalence study in Chinese volunteers. Hang TJ; Zhao W; Liu J; Song M; Xie Y; Zhang Z; Shen J; Zhang Y J Pharm Biomed Anal; 2006 Jan; 40(1):202-5. PubMed ID: 16111851 [TBL] [Abstract][Full Text] [Related]
14. Determination of tegaserod by LC-ESI-MS/MS and its application to a pharmacokinetic study in healthy Chinese volunteers. Zou JJ; Bian XJ; Ding L; Zhu YB; Fan HW; Xiao DW J Chromatogr B Analyt Technol Biomed Life Sci; 2008 Jan; 861(1):151-7. PubMed ID: 18069077 [TBL] [Abstract][Full Text] [Related]
15. Determination of nifedipine in human plasma and its use in bioequivalence study. Guo Y; Dai J; Qian G; Guo N; Ma Z; Guo X Int J Pharm; 2007 Aug; 341(1-2):91-6. PubMed ID: 17507190 [TBL] [Abstract][Full Text] [Related]
16. Evaluation of the bioequivalence of single 100-mg doses of two oral formulations of cyclosporin A microemulsion: a randomized, open-label, two-period crossover study in healthy adult male Mexican volunteers. Piñeyro-López A; Piñeyro-Garza E; Torres-Alanís O; Reyes-Araiza R; Gómez-Silva M; Waksman N; E Salazar-Leal M; Luján-Rangel R Clin Ther; 2007 Sep; 29(9):2049-54. PubMed ID: 18035203 [TBL] [Abstract][Full Text] [Related]
17. Evaluation of the bioequivalence of zidovudine 100 mg capsules in healthy Thai male volunteers. Chompootaweep S; Poonsrisawat J; Xumseang P J Med Assoc Thai; 2006 Sep; 89 Suppl 3():S79-85. PubMed ID: 17722305 [TBL] [Abstract][Full Text] [Related]
18. A rapid and simple high-performance liquid chromatography method for the determination of human plasma levofloxacin concentration and its application to bioequivalence studies. Zhou ZL; Yang M; Yu XY; Peng HY; Shan ZX; Chen SZ; Lin QX; Liu XY; Chen TF; Zhou SF; Lin SG Biomed Chromatogr; 2007 Oct; 21(10):1045-51. PubMed ID: 17549677 [TBL] [Abstract][Full Text] [Related]
19. Assessment of the bioequivalence of two formulations of clarithromycin extended-release 500-mg tablets under fasting and fed conditions: a single-dose, randomized, open-label, two-period, two-way crossover study in healthy Jordanian male volunteers. Alkhalidi BA; Tamimi JJ; Salem II; Ibrahim H; Sallam AA Clin Ther; 2008 Oct; 30(10):1831-43. PubMed ID: 19014838 [TBL] [Abstract][Full Text] [Related]
20. A new method for plasma citrate determination by reversed-phase high-performance liquid chromatography after ultrafiltration extraction: an example for bioequivalence evaluation of a medicinal endogenous substance. Gu Y; Wang GJ; Sun JG; Zhang XY; Sai Y Methods Find Exp Clin Pharmacol; 2008 Sep; 30(7):513-20. PubMed ID: 18985179 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]