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650 related items for PubMed ID: 22562819
1. A novel and rapid validated stability-indicating UPLC method of related substances for dorzolamide hydrochloride and timolol maleate in ophthalmic dosage form. Sharma N, Rao SS, Reddy AM. J Chromatogr Sci; 2012 Oct; 50(9):745-55. PubMed ID: 22562819 [Abstract] [Full Text] [Related]
2. Rapid and sensitive HPLC method for the simultaneous determination of dorzolamide hydrochloride and timolol maleate in eye drops with diode-array and UV detection. Erk N. Pharmazie; 2003 Jul; 58(7):491-3. PubMed ID: 12889534 [Abstract] [Full Text] [Related]
3. UPLC and LC-MS studies on degradation behavior of irinotecan hydrochloride and development of a validated stability-indicating ultra-performance liquid chromatographic method for determination of irinotecan hydrochloride and its impurities in pharmaceutical dosage forms. Kumar N, Sangeetha D, Reddy SP. J Chromatogr Sci; 2012 Oct; 50(9):810-9. PubMed ID: 22661461 [Abstract] [Full Text] [Related]
4. A validated stability-indicating UPLC method for desloratadine and its impurities in pharmaceutical dosage forms. Rao DD, Satyanarayana NV, Malleswara Reddy A, Sait SS, Chakole D, Mukkanti K. J Pharm Biomed Anal; 2010 Feb 05; 51(3):736-42. PubMed ID: 19815361 [Abstract] [Full Text] [Related]
5. Stability-indicating UPLC method for determination of Valsartan and their degradation products in active pharmaceutical ingredient and pharmaceutical dosage forms. Krishnaiah Ch, Reddy AR, Kumar R, Mukkanti K. J Pharm Biomed Anal; 2010 Nov 02; 53(3):483-9. PubMed ID: 20646890 [Abstract] [Full Text] [Related]
6. A novel reverse phase stability indicating RP-UPLC method for the quantitative determination of fifteen related substances in Ranolazine drug substance and drug product. Malati V, Reddy AR, Mukkanti K, Suryanarayana MV. Talanta; 2012 Aug 15; 97():563-73. PubMed ID: 22841123 [Abstract] [Full Text] [Related]
7. A validated stability indicating ultra performance liquid chromatographic method for determination of impurities in Esomeprazole magnesium gastro resistant tablets. Nalwade SU, Reddy VR, Rao DD, Morisetti NK. J Pharm Biomed Anal; 2012 Jan 05; 57():109-14. PubMed ID: 21920688 [Abstract] [Full Text] [Related]
8. A stability-indicating HPLC method for the determination of bazedoxifene acetate and its related substances in active pharmaceutical ingredient. Visweswara Rao K, Reddy KP, Kumari KS, Srinivas M. J Chromatogr Sci; 2013 Mar 05; 51(3):215-21. PubMed ID: 22865837 [Abstract] [Full Text] [Related]
9. Quality by design approach for the separation of naproxcinod and its related substances by fused core particle technology column. Inugala UR, Pothuraju NR, Vangala RR. J Chromatogr Sci; 2013 Mar 05; 51(5):453-9. PubMed ID: 23060406 [Abstract] [Full Text] [Related]
10. Development and validation of a stability-indicating RP-HPLC method for the simultaneous estimation of process related impurities and degradation products of rasagiline mesylate in pharmaceutical formulation. Reddy PS, Sudhakar Babu K, Kumar N. J Chromatogr Sci; 2013 Mar 05; 51(3):242-9. PubMed ID: 22988002 [Abstract] [Full Text] [Related]
11. Determination of duloxetine hydrochloride in the presence of process and degradation impurities by a validated stability-indicating RP-LC method. Raman NV, Harikrishna KA, Prasad AV, Reddy KR, Ramakrishna K. J Pharm Biomed Anal; 2010 Mar 11; 51(4):994-7. PubMed ID: 20005658 [Abstract] [Full Text] [Related]
12. Stability indicating LC method for rapid determination of related substances of O-desmethyl venlafaxine in active pharmaceutical ingredients and pharmaceutical formulations. Rao KV, Reddy KP, Kumar YR. J Chromatogr Sci; 2014 Mar 11; 52(10):1247-54. PubMed ID: 24474426 [Abstract] [Full Text] [Related]
13. Stability-indicating UPLC method for determining related substances and degradants in dronedarone. Pydimarry SP, Cholleti VK, Vangala RR. J Chromatogr Sci; 2014 Aug 11; 52(7):666-75. PubMed ID: 23863770 [Abstract] [Full Text] [Related]
14. Stability-indicating UPLC method for determination of Imatinib Mesylate and their degradation products in active pharmaceutical ingredient and pharmaceutical dosage forms. Nageswari A, Reddy KV, Mukkanti K. J Pharm Biomed Anal; 2012 Jul 11; 66():109-15. PubMed ID: 22502910 [Abstract] [Full Text] [Related]
15. Development and validation of a stability-indicating micellar liquid chromatographic method for the determination of timolol maleate in the presence of its degradation products. Rizk MS, Merey HA, Tawakkol SM, Sweilam MN. J Chromatogr Sci; 2015 Apr 11; 53(4):503-10. PubMed ID: 25013029 [Abstract] [Full Text] [Related]
16. A validated stability-indicating normal phase LC method for clopidogrel bisulfate and its impurities in bulk drug and pharmaceutical dosage form. Durga Rao D, Kalyanaraman L, Sait SS, Venkata Rao P. J Pharm Biomed Anal; 2010 May 01; 52(1):160-5. PubMed ID: 20074888 [Abstract] [Full Text] [Related]
17. Development and validation of a novel stability-indicating HPLC method for the quantitative determination of eleven related substances in ezetimibe drug substance and drug product. Luo Z, Deng Z, Liu Y, Wang G, Yang W, Hou C, Tang M, Yang R, Zhou H. Talanta; 2015 Jul 01; 139():67-74. PubMed ID: 25882410 [Abstract] [Full Text] [Related]
18. Development and validation of a stability-indicating RP-LC method for famciclovir. Raman NV, Harikrishna KA, Prasad AV, Ratnakar Reddy K, Ramakrishna K. J Pharm Biomed Anal; 2009 Dec 05; 50(5):797-802. PubMed ID: 19632799 [Abstract] [Full Text] [Related]
19. Simultaneous determination of dorzolomide and timolol in aqueous humor: a novel salting out liquid-liquid microextraction combined with HPLC. Mohamed AM, Abdel-Wadood HM, Mousa HS. Talanta; 2014 Dec 05; 130():495-505. PubMed ID: 25159439 [Abstract] [Full Text] [Related]
20. Development of stability-indicating UHPLC method for the quantitative determination of silodosin and its related substances. Shaik JV, Saladi S, Sait SS. J Chromatogr Sci; 2014 Aug 05; 52(7):646-53. PubMed ID: 23845884 [Abstract] [Full Text] [Related] Page: [Next] [New Search]