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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

631 related items for PubMed ID: 18162355

  • 1. Isolation and characterization of process related impurities and degradation products of bicalutamide and development of RP-HPLC method for impurity profile study.
    Nageswara Rao R, Narasa Raju A, Narsimha R.
    J Pharm Biomed Anal; 2008 Feb 13; 46(3):505-19. PubMed ID: 18162355
    [Abstract] [Full Text] [Related]

  • 2. Isolation and characterization of degradation products of citalopram and process-related impurities using RP-HPLC.
    Rao RN, Raju AN, Narsimha R.
    J Sep Sci; 2008 Jun 13; 31(10):1729-38. PubMed ID: 18481321
    [Abstract] [Full Text] [Related]

  • 3. A validated stability-indicating RP-HPLC method for levofloxacin in the presence of degradation products, its process related impurities and identification of oxidative degradant.
    Lalitha Devi M, Chandrasekhar KB.
    J Pharm Biomed Anal; 2009 Dec 05; 50(5):710-7. PubMed ID: 19632800
    [Abstract] [Full Text] [Related]

  • 4. Development of a validated RP-LC/ESI-MS-MS method for separation, identification and determination of related substances of tamsulosin in bulk drugs and formulations.
    Nageswara Rao R, Kumar Talluri MV, Narasa Raju A, Shinde DD, Ramanjaneyulu GS.
    J Pharm Biomed Anal; 2008 Jan 07; 46(1):94-103. PubMed ID: 17951020
    [Abstract] [Full Text] [Related]

  • 5. Development and validation of stability-indicating HPLC and UPLC methods for the determination of bicalutamide.
    Nanduri VV, Adapa VS, Kura RR.
    J Chromatogr Sci; 2012 Apr 07; 50(4):316-23. PubMed ID: 22407342
    [Abstract] [Full Text] [Related]

  • 6. Gradient RP-HPLC method for the determination of potential impurities in atazanavir sulfate.
    Chitturi SR, Somannavar YS, Peruri BG, Nallapati S, Sharma HK, Budidet SR, Handa VK, Vurimindi HB.
    J Pharm Biomed Anal; 2011 Apr 28; 55(1):31-47. PubMed ID: 21316175
    [Abstract] [Full Text] [Related]

  • 7. Forced degradation and impurity profiling: recent trends in analytical perspectives.
    Jain D, Basniwal PK.
    J Pharm Biomed Anal; 2013 Dec 28; 86():11-35. PubMed ID: 23969330
    [Abstract] [Full Text] [Related]

  • 8. LC and LC-MS/MS study of forced decomposition behavior of anastrozole and establishment of validated stability-indicating analytical method for impurities estimation in low dose anastrozole tablets.
    Reddy YR, Nandan SR, Bharathi DV, Nagaraju B, Reddy SS, Ravindranath LK, Rao VS.
    J Pharm Biomed Anal; 2009 Oct 15; 50(3):397-404. PubMed ID: 19541446
    [Abstract] [Full Text] [Related]

  • 9. An improved and validated LC method for resolution of bicalutamide enantiomers using amylose tris-(3,5-dimethylphenylcarbamate) as a chiral stationary phase.
    Nageswara Rao R, Narasa Raju A, Nagaraju D.
    J Pharm Biomed Anal; 2006 Sep 26; 42(3):347-53. PubMed ID: 16750608
    [Abstract] [Full Text] [Related]

  • 10. Development and validation of a simple and sensitive high performance liquid chromatographic method for the simultaneous determination of anastrozole, bicalutamide, tamoxifen, and their synthetic impurities.
    Gomes FP, Garcia PL.
    Talanta; 2012 Nov 15; 101():495-503. PubMed ID: 23158354
    [Abstract] [Full Text] [Related]

  • 11. Isolation and characterization of process related impurities of olanzapine using HPLC and ESI-MS/MS.
    Rao RN, Raju AN, Narsimha R, Babu GR.
    J Sep Sci; 2008 Jan 15; 31(1):107-18. PubMed ID: 18080239
    [Abstract] [Full Text] [Related]

  • 12. A validated stability-indicating LC method for acetazolamide in the presence of degradation products and its process-related impurities.
    Srinivasu P, Subbarao DV, Vegesna RV, Sudhakar Babu K.
    J Pharm Biomed Anal; 2010 May 01; 52(1):142-8. PubMed ID: 20053517
    [Abstract] [Full Text] [Related]

  • 13. Development and validation of a highly sensitive LC-MS/MS-ESI method for the determination of bicalutamide in mouse plasma: application to a pharmacokinetic study.
    Sharma K, Pawar GV, Giri S, Rajagopal S, Mullangi R.
    Biomed Chromatogr; 2012 Dec 01; 26(12):1589-95. PubMed ID: 22495777
    [Abstract] [Full Text] [Related]

  • 14. LC determination of glimepiride and its related impurities.
    Khan MA, Sinha S, Vartak S, Bhartiya A, Kumar S.
    J Pharm Biomed Anal; 2005 Oct 04; 39(5):928-43. PubMed ID: 16040224
    [Abstract] [Full Text] [Related]

  • 15. Simultaneous separation and determination of coenzyme Q(10) and its process related impurities by NARP-HPLC and atmospheric pressure chemical ionization-mass spectrometry (APCI-MS).
    Nageswara Rao R, Kumar Talluri MV, Shinde DD.
    J Pharm Biomed Anal; 2008 Jun 09; 47(2):230-7. PubMed ID: 18243624
    [Abstract] [Full Text] [Related]

  • 16. Development and validation of a stability indicating assay of doxofylline by RP-HPLC: ESI-MS/MS, ¹H and ¹³C NMR spectroscopic characterization of degradation products and process related impurities.
    Rao RN, Naidu ChG, Prasad KG, Santhakumar B, Saida S.
    J Pharm Biomed Anal; 2013 May 05; 78-79():92-9. PubMed ID: 23466440
    [Abstract] [Full Text] [Related]

  • 17. Development and validation of a liquid chromatographic method for determination of related-substances of mosapride citrate in bulk drugs and pharmaceuticals.
    Nageswara Rao R, Nagaraju D, Alvi SN, Bhirud SB.
    J Pharm Biomed Anal; 2004 Nov 19; 36(4):759-67. PubMed ID: 15533668
    [Abstract] [Full Text] [Related]

  • 18. Separation and characterization of synthetic impurities of triclabendazole by reversed-phase high-performance liquid chromatography/electrospray ionization mass spectrometry.
    Zhou H, Tai Y, Sun C, Pan Y.
    J Pharm Biomed Anal; 2005 Feb 07; 37(1):97-107. PubMed ID: 15664748
    [Abstract] [Full Text] [Related]

  • 19. Validated stability-indicating HPLC method for the determination of dimethyl-4,4'-dimethoxy-5,6,5',6'-dimethylene dioxybiphenyl-2,2'-dicarboxylate (DDB) and its degradation products.
    Hadad GM.
    J Pharm Biomed Anal; 2008 Aug 05; 47(4-5):695-703. PubMed ID: 18403161
    [Abstract] [Full Text] [Related]

  • 20. High performance liquid chromatography method for the pharmacokinetic study of bicalutamide SMEDDS and suspension formulations after oral administration to rats.
    Singh AK, Chaurasiya A, Jain GK, Awasthi A, Asati D, Mishra G, Khar RK, Mukherjee R.
    Talanta; 2009 Jun 15; 78(4-5):1310-4. PubMed ID: 19362193
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 32.