BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

117 related articles for article (PubMed ID: 36126752)

  • 1. Validated stability indicating chromatographic method for determination of baricitinib and its degradation products in their tablet dosage form: Implementation to content uniformity and in vitro dissolution studies.
    Mohamed MA
    Ann Pharm Fr; 2023 Mar; 81(2):267-283. PubMed ID: 36126752
    [TBL] [Abstract][Full Text] [Related]  

  • 2. An Effective Chromatographic Method for Simultaneous Quantification of Antidiabetic Drugs Alogliptin Benzoate and Pioglitazone HCl in Their Tablet Dosage Form: Implementation to In vitro Dissolution Studies and Uniformity of Dosage Unit.
    Mohamed MA
    J Chromatogr Sci; 2023 Oct; 61(8):705-716. PubMed ID: 35876214
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Chromatographic Techniques for Assessment of Bisoprolol Fumarate and Perindopril Arginine in Solid Formulations under Various Stress Conditions and Application to Six Sigma, Content Uniformity, and Comparative Dissolution Approaches.
    Mahmoud OA; Omran AA; Binsaleh AY; Almalki MA; Mohamed MA
    J AOAC Int; 2023 Sep; 106(5):1165-1179. PubMed ID: 37341634
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Simultaneous determination of emtricitabine, tenofovir alafenamide fumarate and dolutegravir sodium by validated stability-indicating RP-HPLC-DAD method.
    Rathod SM; Patel NC; Patel PU
    Ann Pharm Fr; 2023 Jan; 81(1):94-106. PubMed ID: 36037931
    [TBL] [Abstract][Full Text] [Related]  

  • 5. RP-HPLC method development and validation for quantification of daclatasvir dihydrochloride and its application to pharmaceutical dosage form.
    Hussain Shah SS; Nasiri MI; Sarwar H; Ali A; S Naqvi SB; Anwer S; Kashif M
    Pak J Pharm Sci; 2021 May; 34(3):951-956. PubMed ID: 34602418
    [TBL] [Abstract][Full Text] [Related]  

  • 6. QbD-Based Development and Validation of Novel Stability-Indicating Method for the Assay and Dissolution of Garenoxacin in Garenoxacin Tablets.
    Azhakesan A; Kuppusamy S
    J AOAC Int; 2022 Mar; 105(2):370-378. PubMed ID: 34894249
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A simple stability indicating RP-HPLC-DAD method for concurrent analysis of Tenofovir Disoproxil Fumarate, Doravirine and Lamivudine in pure blend and their combined film coated tablets.
    Godela R; Gummadi S
    Ann Pharm Fr; 2021 Nov; 79(6):640-651. PubMed ID: 34019910
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Green analytical chromatographic assay method for quantitation of cyclobenzaprine in tablets, spiked human urine and in-vitro dissolution test.
    Walash MI; El Abass Mohamed SA
    Ann Pharm Fr; 2019 Sep; 77(5):418-425. PubMed ID: 31296331
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Development and validation of a stability-Indicating RP-HPLC method for simultaneous estimation of sofosbuvir and velpatasvir in fixed dose combination tablets and plasma.
    Mehmood Y; Khan IU; Shahzad Y; Khalid SH; Irfan M; Asghar S; Yousaf AM; Hussain T; Khalid I
    Pak J Pharm Sci; 2019 Jul; 32(4(Supplementary)):1835-1842. PubMed ID: 31680080
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Development and Validation of a Stability-indicating UPLC-DAD Method for the Simultaneous Determination of Ivermectin and Praziquantel in Pharmaceutical Tablets and Dissolution Media.
    Ibrahim A; Wang F; Gary Hollenbeck R; Martinez MN; Fahmy R; Hoag SW
    AAPS PharmSciTech; 2023 Oct; 24(7):211. PubMed ID: 37821763
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. DEVELOPMENT AND VALIDATION OF HPLC ANALYTICAL METHODS USED-FOR DETERMINATION OF ASSAY, CONTENT UNIFORMITY AND DISSOLUTION OF IMMEDIATE RELEASE CANDESARTAN CILEXETIL 32 MG TABLETS.
    Yuce M; Capan Y
    Acta Pol Pharm; 2017 Mar; 74(2):357-367. PubMed ID: 29624240
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Simultaneous Estimation of Escitalopram and Clonazepam in Tablet Dosage Forms Using HPLC-DAD Method and Optimization of Chromatographic Conditions by Box-Behnken Design.
    Foudah AI; Alshehri S; Shakeel F; Alqarni MH; Aljarba TM; Alam P
    Molecules; 2022 Jun; 27(13):. PubMed ID: 35807458
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Development and validation of a versatile HPLC-DAD method for simultaneous determination of the antiviral drugs daclatasvir, ledipasvir, sofosbuvir and ribavirin in presence of seven potential impurities. Application to assay of dosage forms and dissolution studies.
    Baker MM; Hammad SF; Belal TS
    Drug Dev Ind Pharm; 2019 Jul; 45(7):1111-1119. PubMed ID: 30929537
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Development and validation of a stability-indicating column high-performance liquid chromatographic assay method for determination of nebivolol in tablet formulation.
    Kachhadia PK; Doshi AS; Joshi HS
    J AOAC Int; 2008; 91(3):557-61. PubMed ID: 18567301
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A Stability-indicating HPLC Method for Assay of Lercanidipine Hydrochloride in Tablets and for Determining Content Uniformity.
    Kaila HO; Ambasana MA; Thakkar RS; Saravaia HT; Shah AK
    Indian J Pharm Sci; 2010 May; 72(3):381-4. PubMed ID: 21188053
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A reversed-phase-high performance liquid chromatography method for simultaneous determination of paracetamol, caffeine, drotaverine HCl and their related impurities with dissolution profiling of their tablets and greenness profile assessment.
    Tawfik SA; El-Ragehy NA; Hegazy MA; Sedik GA
    Biomed Chromatogr; 2023 Feb; 37(2):e5539. PubMed ID: 36287616
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Simultaneous Determination of Impurities of Atazanavir and Ritonavir in Tablet Dosage Form by Using Reversed-Phase Ultra Performance Liquid Chromatographic Method.
    Mantripragada MKVVN; Rao SV; Nutulapati VVS; Mantena BPV
    J Chromatogr Sci; 2018 Mar; 56(3):270-284. PubMed ID: 29300835
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Validated specific HPLC-DAD method for simultaneous estimation of paracetamol and chlorzoxazone in the presence of five of their degradation products and toxic impurities.
    El-Yazbi AF; Guirguis KM; Bedair MM; Belal TS
    Drug Dev Ind Pharm; 2020 Nov; 46(11):1853-1861. PubMed ID: 32894703
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.