BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

337 related articles for article (PubMed ID: 25705547)

  • 1. Stability-Indicating RP-HPLC Method for Simultaneous Estimation of Enrofloxacin and Its Degradation Products in Tablet Dosage Forms.
    Chakravarthy VA; Sailaja BB; Kumar AP
    J Anal Methods Chem; 2015; 2015():735145. PubMed ID: 25705547
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Development and validation of stability indicating the RP-HPLC method for the estimation of related compounds of guaifenesin in pharmaceutical dosage forms.
    Reddy SP; Babu KS; Kumar N; Sekhar YV
    Pharm Methods; 2011 Oct; 2(4):229-34. PubMed ID: 23781462
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 139():67-74. PubMed ID: 25882410
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A validated stability-indicating liquid chromatographic method for determination of process related impurities and degradation behavior of Irbesartan in solid oral dosage.
    Goswami N
    J Adv Pharm Technol Res; 2014 Jan; 5(1):33-40. PubMed ID: 24695518
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Development and validation of a reversed-phase HPLC method for simultaneous analysis of butylhydroxyanisol, simvastatin and its impurities in tablet dosage forms.
    El Karbane M; Azougagh M; Amood A L-Kamarany M; Bouchafra H; Cherrah Y; Bouklouze A
    Ann Pharm Fr; 2014 Jul; 72(4):244-55. PubMed ID: 24997886
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Development and Validation of a Stability-Indicating RP-HPLC Method for the Determination of Process-Related Impurities and Degradation Products of Rabeprazole Sodium in Pharmaceutical Formulation.
    Kumar N; Sangeetha D
    Sci Pharm; 2013; 81(3):697-711. PubMed ID: 24106668
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Impurity profile of macitentan in tablet dosage form using a stability-indicating high performance liquid chromatography method and forced degradation study].
    Lakka NS; Kuppan C; Rangasamy P
    Se Pu; 2019 Jan; 37(1):100-110. PubMed ID: 30693716
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Developing and validation of impurity and the simultaneous quantity determination methods for tablet forms containing Ciprofloxacin HCl and Ornidazole.
    Tunca AK; Karakaya D; Bulbul S
    Pak J Pharm Sci; 2020 May; 33(3):1105-1114. PubMed ID: 33191235
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A Validated RP-HPLC Stability Method for the Estimation of Chlorthalidone and Its Process-Related Impurities in an API and Tablet Formulation.
    Kharat C; Shirsat VA; Kodgule YM; Kodgule M
    Int J Anal Chem; 2020; 2020():3593805. PubMed ID: 32328101
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Development of validated stability-indicating chromatographic method for the determination of fexofenadine hydrochloride and its related impurities in pharmaceutical tablets.
    Maher HM; Sultan MA; Olah IV
    Chem Cent J; 2011 Dec; 5(1):76. PubMed ID: 22136482
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Development and Validation of a Stability-Indicating RP-HPLC Method for the Quantitative Analysis of Anagrelide Hydrochloride.
    Pujeri SS; Khader AM; Seetharamappa J
    Sci Pharm; 2012; 80(3):567-79. PubMed ID: 23008806
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Development of a Stability-Indicating RP-HPLC Method for the Determination of Rupatadine and its Degradation Products in Solid Oral Dosage Form.
    Trivedi HK; Patel MC
    Sci Pharm; 2012; 80(4):889-902. PubMed ID: 23264938
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A Validated Stability-Indicating HPLC Method for Simultaneous Determination of Amoxicillin and Enrofloxacin Combination in an Injectable Suspension.
    Batrawi N; Wahdan S; Al-Rimawi F
    Sci Pharm; 2017 Feb; 85(1):. PubMed ID: 28212319
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Validated Stability-Indicating RP-HPLC Method for the Estimation of Degradation Behaviour of Organic Peroxide and Third-Generation Synthetic Retinoids in Topical Pharmaceutical Dosage Formulation.
    Roy C; Panigrahi L; Chakrabarty J
    Sci Pharm; 2015; 83(2):321-38. PubMed ID: 26839821
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Stability-indicating HPLC method development and validation for simultaneous estimation of metformin, dapagliflozin, and saxagliptin in bulk drug and pharmaceutical dosage form.
    Vankalapati KR; Alegete P; Boodida S
    Biomed Chromatogr; 2022 Jul; 36(7):e5384. PubMed ID: 35434817
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Development and Validation of a Stability-Indicating RP-HPLC Method for the Estimation of Drotaverine Impurities in API and Pharmaceutical Formulation.
    Thummala VR; Tharlapu SS; Rekulapalli VK; Ivaturi MR; Nittala SR
    Sci Pharm; 2014; 82(1):99-115. PubMed ID: 24634845
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A Validated Stability-Indicating RP-UPLC Method for Simultaneous Determination of Desloratadine and Sodium Benzoate in Oral Liquid Pharmaceutical Formulations.
    Kumar N; Sangeetha D; Reddy PS; Prakash L
    Sci Pharm; 2012; 80(1):153-65. PubMed ID: 22396911
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.