BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

134 related articles for article (PubMed ID: 36416121)

  • 21. 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]  

  • 22. 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]  

  • 23. Development and validation of a stability-indicating HPLC method for determination of voriconazole and its related substances.
    Gu P; Li Y
    J Chromatogr Sci; 2009 Aug; 47(7):594-8. PubMed ID: 19772734
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Development and validation of a stability-indicating, single HPLC method for sacubitril-valsartan and their stereoisomers and identification of forced degradation products using LC-MS/MS.
    Vijaykumar C; Kumar YR; Aparna P; Rao PSP
    Biomed Chromatogr; 2023 Feb; 37(2):e5550. PubMed ID: 36410774
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Validated stability-indicating RP-HPLC method for the determination of rimonabant in a pharmaceutical dosage form.
    Hurtado FK; Ravanello A; Arend MZ; Wrasse M; Dalmora SL; Rolim CM
    J AOAC Int; 2010; 93(3):869-75. PubMed ID: 20629389
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Development of RP-HPLC, Stability Indicating Method for Degradation Products of Linagliptin in Presence of Metformin HCl by Applying 2 Level Factorial Design; and Identification of Impurity-VII, VIII and IX and Synthesis of Impurity-VII.
    Jadhav SB; Reddy PS; Narayanan KL; Bhosale PN
    Sci Pharm; 2017 Jun; 85(3):. PubMed ID: 28653975
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A rapid stability-indicating, fused-core HPLC method for simultaneous determination of β-artemether and lumefantrine in anti-malarial fixed dose combination products.
    Suleman S; Vandercruyssen K; Wynendaele E; D'Hondt M; Bracke N; Duchateau L; Burvenich C; Peremans K; De Spiegeleer B
    Malar J; 2013 Apr; 12():145. PubMed ID: 23631682
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [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]  

  • 30. A rapid RP-HPLC stability-indicating method development and validation of moxifloxacin hydrochloride-related substances in finished dosage forms.
    Vankalapati KR; Algete P; Boodida S
    Biomed Chromatogr; 2021 Nov; 35(11):e5192. PubMed ID: 34110029
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Reversed-phase ultra-performance liquid chromatographic method development and validation for determination of impurities related to torsemide tablets.
    Patel HB; Mohan A; Joshi HS
    J AOAC Int; 2011; 94(1):143-9. PubMed ID: 21391491
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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; 50(5):710-7. PubMed ID: 19632800
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Assay of afoxolaner and determination of its related substances in commercial bulk batches of afoxolaner by reversed-phase HPLC method based on a short octadecyl column.
    Padivitage N; Adhikari S; Rustum AM
    J Chromatogr B Analyt Technol Biomed Life Sci; 2021 Nov; 1184():122984. PubMed ID: 34644667
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Validated stability-indicating HPLC-UV method for simultaneous determination of glipizide and four impurities.
    Gupta S; Bansal G
    J AOAC Int; 2011; 94(2):523-30. PubMed ID: 21563686
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Development of a stability- indicating HPLC method for simultaneous determination of ten related substances in vonoprazan fumarate drug substance.
    Luo Z; Liu A; Liu Y; Wang G; Chen X; Wang H; Li M; Zhang H; Qiu Y; Zhai H
    J Pharm Biomed Anal; 2018 Feb; 149():133-142. PubMed ID: 29112902
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Fast RP-HPLC Method for the Determination of Bisoprolol.
    Panainte AD; Vieriu M; Ţântaru G; Apostu M; Bibire N
    Rev Med Chir Soc Med Nat Iasi; 2016; 120(3):720-6. PubMed ID: 30152661
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A Stability Indicating Method Development and Validation for Separation of Process Related Impurities and Characterization of Unknown Impurities of Tyrosine Kinase Inhibitor Ibrutinib Using QbD Approach by RP-HPLC, NMR Spectroscopy and ESI-MS.
    Gopireddy RR; Maruthapillai A; Mahapatra S
    J Chromatogr Sci; 2021 Sep; 59(9):830-846. PubMed ID: 33420506
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Development of an effective novel validated stability-indicating HPLC method for the resolution of brivaracetam stereoisomeric impurities.
    Baksam V; N S; Pocha VR; Chakka VB; Ummadi RR; Kumar P
    Chirality; 2020 Sep; 32(9):1208-1219. PubMed ID: 32656914
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Stability-Indicating RP-HPLC Method for the Estimation of Process-Related Impurities and Degradation Products in Fesoterodine Fumarate by Using a Mass Spectrometric Compatible Mobile Phase.
    Kumar N; Sangeetha D; Kalyanraman L
    J Chromatogr Sci; 2021 Jan; 59(2):154-164. PubMed ID: 33190158
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Development and validation of a stability-indicating RP-HPL C-CAD method for gabapentin and its related impurities in presence of degradation products.
    Ragham PK; Chandrasekhar KB
    J Pharm Biomed Anal; 2016 Jun; 125():122-9. PubMed ID: 27018505
    [TBL] [Abstract][Full Text] [Related]  

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