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

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

By: Ritesh Sharma and  Shyam Pancholi  
Open Access
|Mar 2010

References

  1. FDA, Draft Guidance for Industry: Stability Testing of Drug Substances and Drug Products, FDA, Rockville 1998.
  2. 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.
  3. 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.
  4. 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.
  5. 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.fd16220064
  6. 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-S14.10.1097/00004872-200106001-0000211451212
  7. G.T. Warner and B. Jarvis, Olmesartan medoxomil, Drugs 62 (2002) 1345-1353.10.2165/00003495-200262090-0000512076183
  8. 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/s10337-007-0304-9
  9. 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.
  10. 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.2005.02.04715840410
  11. 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-x
  12. 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.2007.05.04917602900
  13. 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.39447
  14. 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/s10337-007-0424-2
  15. 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.2008.02.02118394840
  16. 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.
  17. G.W. Ewing, Instrumental Methods of Chemical Analysis, 5th ed., Lippincott-Raven, Philadelphia 1995, pp. 484-486.
  18. 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)00004-7
DOI: https://doi.org/10.2478/v10007-010-0010-2 | Journal eISSN: 1846-9558 | Journal ISSN: 1330-0075
Language: English
Page range: 13 - 24
Published on: Mar 13, 2010
Published by: Croatian Pharmaceutical Society
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year
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© 2010 Ritesh Sharma, Shyam Pancholi, published by Croatian Pharmaceutical Society
This work is licensed under the Creative Commons License.

Volume 60 (2010): Issue 1 (March 2010)