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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

133 related articles for article (PubMed ID: 23781463)

  • 61. A Stability Indicating Method for the Determination of the Antioxidant Sodium Bisulfite in Pharmaceutical Formulation by RP-HPLC Technique.
    Trivedi HK; Patel MC
    Sci Pharm; 2011; 79(4):909-20. PubMed ID: 22145114
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Quantification of halobetasol propionate and its impurities present in topical dosage forms by stability-indicating LC method.
    Nalwade S; Reddy VR; Kulkarni D; Todamal S
    J Chromatogr Sci; 2015 Jan; 53(1):127-34. PubMed ID: 24784115
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Development and Validation of a Stability-Indicating LC-Method for the Simultaneous Estimation of Levodropropizine, Chloropheniramine, Methylparaben, Propylparaben, and Levodropropizine Impurities.
    Kumar PA; Raju TV; Thirupathi D; Kumar R; Shree J
    Sci Pharm; 2013; 81(1):139-50. PubMed ID: 23641334
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Development and validation of a repharsed phase- HPLC method for simultaneous determination of rosiglitazone and glimepiride in combined dosage forms and human plasma.
    El-Enany NM; Abdelal AA; Belal FF; Itoh YI; Nakamura MN
    Chem Cent J; 2012 Jan; 6(1):9. PubMed ID: 22277722
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Validated LC Method for the Estimation of Voriconazole in Bulk and Formulation.
    Patel CN; Dave JB; Patel JV; Panigrahi B
    Indian J Pharm Sci; 2009 Nov; 71(6):699-702. PubMed ID: 20376229
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Method Development and Validation of a Stability-Indicating RP-HPLC Method for the Quantitative Analysis of Dronedarone Hydrochloride in Pharmaceutical Tablets.
    Dabhi B; Jadeja Y; Patel M; Jebaliya H; Karia D; Shah A
    Sci Pharm; 2013; 81(1):115-22. PubMed ID: 23641332
    [TBL] [Abstract][Full Text] [Related]  

  • 67. A validated stability-indicating liquid chromatographic method for determination of degradation impurities and diastereomers in voriconazole tablets.
    Shaikh KA; Patil AT
    Sci Pharm; 2012; 80(4):879-88. PubMed ID: 23264937
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Development and validation of a stability indicating UPLC method for determination of ticlopidine hydrochloride in its tablet formulation.
    Ram V; Kher G; Dubal K; Dodiya B; Joshi H
    Saudi Pharm J; 2011 Jul; 19(3):159-64. PubMed ID: 23960754
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Sensitive method for the quantitative determination of risperidone in tablet dosage form by high-performance liquid chromatography using chlordiazepoxide as internal standard.
    Ashour S; Kattan N
    Int J Biomed Sci; 2013 Jun; 9(2):91-7. PubMed ID: 23847459
    [TBL] [Abstract][Full Text] [Related]  

  • 70. The Validation of a Simple, Robust, Stability-Indicating RP-HPLC Method for the Simultaneous Detection of Lamivudine, Tenofovir Disoproxil Fumarate, and Dolutegravir Sodium in Bulk Material and Pharmaceutical Formulations.
    Omoteso OA; Milne M; Aucamp M
    Int J Anal Chem; 2022; 2022():3510277. PubMed ID: 35154325
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Validated Reverse Phase-High-Performance Liquid Chromatography Method for Estimation of Fisetin in Self-Nanoemulsifying Drug Delivery System.
    Kumar R; Kumar R; Khursheed R; Awasthi A; Ramanunny AK; Kaur J; Khurana N; Singh SK; Khurana S; Pandey NK; Kapoor B; Sharma N
    Assay Drug Dev Technol; 2020; 18(6):274-281. PubMed ID: 32608988
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Stability-indicating liquid chromatographic method for the determination of Letrozole in pharmaceutical formulations.
    Annapurna MM; Mohapatro C; Narendra A
    J Pharm Anal; 2012 Aug; 2(4):298-305. PubMed ID: 29403757
    [TBL] [Abstract][Full Text] [Related]  

  • 73. A developed and validated stability-indicating reverse-phase high performance liquid chromatographic method for determination of cefdinir in the presence of its degradation products as per International Conference on Harmonization guidelines.
    Hamrapurkar P; Patil P; Phale M; Gandhi M; Pawar S
    Pharm Methods; 2011 Jan; 2(1):15-20. PubMed ID: 23781424
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Complexity in estimation of esomeprazole and its related impurities' stability in various stress conditions in low-dose aspirin and esomeprazole magnesium capsules.
    Reddy PS; Hotha KK; Sait S
    Sci Pharm; 2013; 81(2):475-92. PubMed ID: 23833714
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Development and validation of HPLC method for the determination of pregabalin in capsules.
    Kasawar GB; Farooqui MN
    Indian J Pharm Sci; 2010 Jul; 72(4):517-9. PubMed ID: 21218069
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Determination of Cefadroxil in Tablet/Capsule formulations by a validated Reverse Phase High Performance Liquid Chromatographic method.
    Rahim N; Naqvi SB; Shakeel S; Iffat W; Muhammad IN
    Pak J Pharm Sci; 2015 Jul; 28(4):1345-9. PubMed ID: 26142506
    [TBL] [Abstract][Full Text] [Related]  

  • 77. A Study of Method Development, Validation, and Forced Degradation for Simultaneous Quantification of Paracetamol and Ibuprofen in Pharmaceutical Dosage Form by RP-HPLC Method.
    Jahan MS; Islam MJ; Begum R; Kayesh R; Rahman A
    Anal Chem Insights; 2014; 9():75-81. PubMed ID: 25452691
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Development and validation of RP-HPLC method for estimation of ethacridine lactate in bulk and in pharmaceutical formulation.
    Jain PS; Jivani HN; Khatal RN; Surana SJ
    Pharm Methods; 2011 Apr; 2(2):112-6. PubMed ID: 23781440
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Development and validation of RP-HPLC method for simultaneous determination of cefpodoxime proxetil and H2 receptor antagonists in pharmaceutical dosage forms.
    Hassan S; Iqbal S; Zaheer E; Hassan A; Hamid S; Ali M; Akram A; Maroof SZ; Abedin S; Khan SJ
    Pak J Pharm Sci; 2019 Mar; 32(2 (Supplementary)):839-844. PubMed ID: 31103980
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Development and validation of HPLC method for the determination of alpha-tocopherol in human erythrocytes for clinical applications.
    Solichová D; Korecká L; Svobodová I; Musil F; Bláha V; Zdánský P; Zadák Z
    Anal Bioanal Chem; 2003 Jun; 376(4):444-7. PubMed ID: 12719955
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.