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RP-HPLC-DAD method for determination of olmesartan medoxomil in bulk and tablets exposed to forced conditions

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FDA, Draft Guidance for Industry: Stability Testing of Drug Substances and Drug Products, FDA, Rockville 1998.Search in Google Scholar

International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use, ICH Harmonised Tripartite Guideline: Stability Testing of New Drug Substances and Products Q1A (R2), Step 5, ICH Geneva, Aug. 2003.Search in Google Scholar

H.R. Brunner, The new oral angiotensin II antagonist olmesartan medoxomil: a concise overview, J. Hum. Hypertens. 16 (2002) S13-S16; DOI: 10.1038/sj/jhh/1001391.Search in Google Scholar

H. Koike, T. Konse, T. Sada, T. Ikeda, S. Hyogo, D. Hinman, H. Saito, and H. Yanagisawa, Olmesartan medoxomil, a novel potent angiotensin II blocker, Ann. Rep. Snakyo Res. Lab. 55 (2003) 1-91.Search in Google Scholar

D.E. Mire, T.N. Silfani and M.K. Pugsley, A review of the structural and functional features of olmesartan medoxomil, an angiotensin receptor blocker, J. Cardiovasc. Pharmacol. 46 (2005) 585-593; DOI: 10.1097/01.fjc.0000180902.78230.fd.10.1097/01.fjc.0000180902.78230.fd16220064Search in Google Scholar

H. Koike, T. Sada and M. Mizuno, In vitro and in vivo pharmacology of olmesartan medoxomil, an angiotensin II type AT1 receptor antagonist, J. Hypertens. 19 (Suppl) (2001) S3-S14.10.1097/00004872-200106001-0000211451212Search in Google Scholar

G.T. Warner and B. Jarvis, Olmesartan medoxomil, Drugs 62 (2002) 1345-1353.10.2165/00003495-200262090-0000512076183Search in Google Scholar

O. Sagirli, A. Önal, S.E. Toker and D. Sensoy, Simultaneous HPLC analysis of olmesartan and hydrochlorothiazide in combined tablets and in vitro dissolution studies, Chromatographia 66 (2007) 213-218; DOI: 10.1365/s10337-007-0304-9.10.1365/s10337-007-0304-9Search in Google Scholar

K. Yoshihara, Y. Gao, H. Shiga, D.R. Wada and M. Hisaoka, Population pharmacokinetics of olmesartan following oral administration of its prodrug, olmesartan medoxomil: in healthy volunteers and hypertensive patients, Clin. Pharmacokin., 44 (2005) 1329-1342.Search in Google Scholar

H. Nakamura, T. Inoue, N. Arakawa, Y. Shimizu, Y. Yoshigae, I. Fujimori, E.H. Nakamura, T. Inoue, N. Arakawa, Y. Shimizu, Y. Yoshigae, I. Fujimori, E. Shimakawa, T. Toyoshi and T. Yokoyama, Pharmacological and pharmacokinetic study of olmesartan medoxomil in animal diabetic retinopathy models, Eur. J. Pharmacol. 512 (2005) 239-246; DOI: 10.1016/j.ejphar.2005.02.047.10.1016/j.ejphar.2005.02.04715840410Search in Google Scholar

V.V. Vaidya, S.M. Roy, S.M. Yetal, S.S. Joshi and S.A. Parekh, LC-MS-MS determination of olmesartan in human plasma, Chromatographia 67 (2008) 147-150; DOI: 10.1365/s10337-007-0453-x.10.1365/s10337-007-0453-xSearch in Google Scholar

L. Dongyang, H. Pei, M. Nobuka, L. Xiaoming, L. Li and J. Ji, Quantitative determination of olmesartan in human plasma and urine by liquid chromatography coupled to tandem mass spectrometry, J. Chromatogr. B 856 (2007) 190-197; DOI: 10.1016/j.jchromb.2007.05.049.10.1016/j.jchromb.2007.05.04917602900Search in Google Scholar

N.J. Shah, B.N. Suhagia, R.R. Shah and N.M. Patel, Development and validation of a simultaneous HPTLC method for the estimation of olmesartan medoxomil and hydrochlorothiazide in tablet dosage form, Indian J. Pharm. Sci. 69 (2007) 834-836; DOI: 10.4103/0250-474X.39447.10.4103/0250-474X.39447Search in Google Scholar

C. Mustafa and A. Sacide, Development of a CZE method for the determination of olmesartan medoxomil in tablets, Chromatographia 66 (2007) 929-933; DOI: 10.1365/s10337-007-0424-2.10.1365/s10337-007-0424-2Search in Google Scholar

T. Murakami, H. Konno, N. Fukutsu, M. Onodera, T. Kawasaki and F. Kusu, Identification of a degradation product in stressed tablets of olmesartan medoxomil by the complementary use of HPLC hyphenated techniques, J. Pharm. Biomed. Anal. 47 (2008) 553-559; DOI: 10.1016/j.jpba.2008.02.021.10.1016/j.jpba.2008.02.02118394840Search in Google Scholar

International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use, ICH Harmonized Tripartite Guidelines, Validation of Analytical Procedure: Text and Methodology Q2 (R1), Current Step 4 version, ICH Geneva, Nov. 2005.Search in Google Scholar

G.W. Ewing, Instrumental Methods of Chemical Analysis, 5th ed., Lippincott-Raven, Philadelphia 1995, pp. 484-486.Search in Google Scholar

Z. Zhao, Q. Wang, E.W. Tsai, X.Z. Qin and D. Ip, Identification of losartan degradates in stressed tablets by LC-MS and LC-MS/MS, J. Pharm. Biomed. Anal. 20 (1999) 129-36; DOI: 10.1016/S0731-7085(99)00004-7.10.1016/S0731-7085(99)00004-7Search in Google Scholar

eISSN:
1846-9558
ISSN:
1330-0075
Lingua:
Inglese
Frequenza di pubblicazione:
4 volte all'anno
Argomenti della rivista:
Pharmacy, other