315 related articles for article (PubMed ID: 25060753)
1. Stability-indicating liquid chromatographic method for determination of saxagliptin and structure elucidation of the major degradation products using LC-MS.
Abdel-Ghany MF; Abdel-Aziz O; Ayad MF; Tadros MM
J Chromatogr Sci; 2015 Apr; 53(4):554-64. PubMed ID: 25060753
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Development of validated stability indicating assay method for simultaneous estimation of metformin hydrochloride and vildagliptin by RP-HPLC.
Satheeshkumar N; Pradeepkumar M; Shanthikumar S; Rao VJ
Drug Res (Stuttg); 2014 Mar; 64(3):124-9. PubMed ID: 24081820
[TBL] [Abstract][Full Text] [Related]
4. Preparation and characterization of two new forced degradation products of letrozole and development of a stability-indicating RP-LC method for its determination.
Elkady EF; Fouad MA
Pak J Pharm Sci; 2015 Nov; 28(6):2041-51. PubMed ID: 26639498
[TBL] [Abstract][Full Text] [Related]
5. Stability-indicating LC-UV method for the determination of eszopiclone and degradation impurities in tablet dosage form.
Shaikh K; Patil A; Gite S
J Chromatogr Sci; 2014 Apr; 52(4):293-7. PubMed ID: 23552846
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Development of stability-indicating UHPLC method for the quantitative determination of silodosin and its related substances.
Shaik JV; Saladi S; Sait SS
J Chromatogr Sci; 2014 Aug; 52(7):646-53. PubMed ID: 23845884
[TBL] [Abstract][Full Text] [Related]
8. A validated stability-indicating liquid chromatographic method for the determination of retapamulin in topical dosage form.
Nalwade S; Reddy VR
J Chromatogr Sci; 2014 Mar; 52(3):238-45. PubMed ID: 23510782
[TBL] [Abstract][Full Text] [Related]
9. Stability-indicating RP-LC method for determination of azilsartan medoxomil and chlorthalidone in pharmaceutical dosage forms: application to degradation kinetics.
Ebeid WM; Elkady EF; El-Zaher AA; El-Bagary RI; Patonay G
Anal Bioanal Chem; 2014 Oct; 406(26):6701-12. PubMed ID: 25190009
[TBL] [Abstract][Full Text] [Related]
10. LC-MS-MS Characterization of Forced Degradation Products of Fidarestat, a Novel Aldose Reductase Inhibitor: Development and Validation of a Stability-Indicating RP-HPLC Method.
Talluri MV; Khatoon L; Kalariya PD; Chavan BB; Ragampeta S
J Chromatogr Sci; 2015 Oct; 53(9):1588-96. PubMed ID: 26014964
[TBL] [Abstract][Full Text] [Related]
11. A rapid and sensitive LC-MS/MS assay for the determination of saxagliptin and its active metabolite 5-hydroxy saxagliptin in human plasma and its application to a pharmacokinetic study.
Batta N; Pilli NR; Derangula VR; Vurimindi HB; Damaramadugu R; Yejella RP
Drug Res (Stuttg); 2015 Mar; 65(3):133-40. PubMed ID: 24941084
[TBL] [Abstract][Full Text] [Related]
12. Validated Stability Indicating High Performance Liquid Chromatographic Determination of Lesinurad.
Attia KAM; El-Abasawi NM; El-Olemy A; Abdelazim AH
J Chromatogr Sci; 2018 Apr; 56(4):358-366. PubMed ID: 29474515
[TBL] [Abstract][Full Text] [Related]
13. Stability-indicating RP-LC method for the determination of vildagliptin and mass spectrometry detection for a main degradation product.
Barden AT; Salamon B; Schapoval EE; Steppe M
J Chromatogr Sci; 2012 May; 50(5):426-32. PubMed ID: 22511486
[TBL] [Abstract][Full Text] [Related]
14. Novel liquid chromatographic methods for the determination of varenicline tartrate.
El-Bagary RI; Abo-Talib NF; Mohamed MA
Talanta; 2016; 146():83-92. PubMed ID: 26695238
[TBL] [Abstract][Full Text] [Related]
15. Development and validation of a stability-indicating RP-HPLC method for the determination of febuxostat (a xanthine oxidase inhibitor).
Mukthinuthalapati MA; Bandaru SP; Bukkapatnam V; Mohapatro C
J Chromatogr Sci; 2013; 51(10):931-8. PubMed ID: 23204011
[TBL] [Abstract][Full Text] [Related]
16. Forced degradation study to develop and validate stability-indicating RP-LC method for the determination of ciclesonide in bulk drug and metered dose inhalers.
Elkady EF; Fouad MA
Talanta; 2011 Dec; 87():222-9. PubMed ID: 22099671
[TBL] [Abstract][Full Text] [Related]
17. Selective determination of diclazuril in the presence of its degradation products.
Rezk MR
J Chromatogr Sci; 2015 Feb; 53(2):302-6. PubMed ID: 25002681
[TBL] [Abstract][Full Text] [Related]
18. Development of a stability-indicating LC method for determination of a synthetic chalcone derivative in a nanoemulsion dosage form and identification of the main photodegradation product by LC-MS.
Mattos CB; Deponti VB; Barreto F; Simões CM; Andrighetti-Frohner CR; Nunes RJ; Steindel M; Teixeira HF; Koester LS
J Pharm Biomed Anal; 2012 Nov; 70():652-6. PubMed ID: 22884784
[TBL] [Abstract][Full Text] [Related]
19. Development and Validation of Rapid Stability-Indicating RP-HPLC-DAD Method for the Quantification of Lapatinib and Mass Spectrometry Analysis of Degraded Products.
Saadat E; Dehghan Kelishady P; Ravar F; Kobarfard F; Dorkoosh FA
J Chromatogr Sci; 2015 Jul; 53(6):932-9. PubMed ID: 25491314
[TBL] [Abstract][Full Text] [Related]
20. 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; 52(1):142-8. PubMed ID: 20053517
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
