134 related articles for article (PubMed ID: 36416121)
41. Analysis of Tolfenamic Acid using a Simple, Rapid, and Stability-indicating Validated HPLC Method.
Kazi SH; Sheraz MA; Musharraf SG; Ahmed S; Bano R; Haq FU; Anwar Z; Ali R
Antiinflamm Antiallergy Agents Med Chem; 2024; 23(1):52-70. PubMed ID: 37291774
[TBL] [Abstract][Full Text] [Related]
42. A new, rapid, stability-indicating UPLC method for separation and determination of impurities in amlodipine besylate, valsartan and hydrochlorothiazide in their combined tablet dosage form.
Vojta J; Jedlička A; Coufal P; Janečková L
J Pharm Biomed Anal; 2015 May; 109():36-44. PubMed ID: 25756663
[TBL] [Abstract][Full Text] [Related]
43. RP-HPLC Method for the Simultaneous Determination of a Quaternary Mixture of Propyphenazone, Flavoxate HCl and Two of Their Official Impurities with Dissolution Profiling of Their Tablets.
El-Ragehy NA; Ramadan NK; Ragab MT; El-Zeany BA
J AOAC Int; 2020 Jul; 103(4):958-965. PubMed ID: 33241355
[TBL] [Abstract][Full Text] [Related]
44. Unique Quality by Design Approach for Developing HPLC and LC-MS Method for Estimation of Process and Degradation Impurities in Pibrentasvir, Antiviral Agent for Hepatitis C.
Vemuri DK; Akshinthala P; Konduru N; Kowtharapu LP; Katari NK; Jonnalagadda SB; Gundla R
ACS Omega; 2022 Dec; 7(51):47650-47661. PubMed ID: 36591161
[TBL] [Abstract][Full Text] [Related]
45. A validated, stability-indicating HPLC method for the determination of dexamethasone related substances on dexamethasone-coated drug-eluting stents.
Chen Q; Zielinski D; Chen J; Koski A; Werst D; Nowak S
J Pharm Biomed Anal; 2008 Nov; 48(3):732-8. PubMed ID: 18722070
[TBL] [Abstract][Full Text] [Related]
46. Development and validation of a simple and sensitive HPLC method for the determination of related substances in regorafenib tablets.
Li S; Jiang M; Li M; Hu P; Xu M; Shu C
Anal Sci; 2022 Mar; 38(3):591-599. PubMed ID: 35286636
[TBL] [Abstract][Full Text] [Related]
47. Development of an efficient stability-indicating LC-MS/MS method for the analysis of selexipag and characterization of its degradation products.
Amara Babu NLA; Koganti K; Palakeeti B; Srinivas KSV; Rao KP
Biomed Chromatogr; 2021 Oct; 35(10):e5178. PubMed ID: 33998014
[TBL] [Abstract][Full Text] [Related]
48. 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]
49. Development of RP UPLC-TOF/MS, stability indicating method for omeprazole and its related substances by applying two level factorial design; and identification and synthesis of non-pharmacopoeial impurities.
Jadhav SB; Kumar CK; Bandichhor R; Bhosale PN
J Pharm Biomed Anal; 2016 Jan; 118():370-379. PubMed ID: 26600119
[TBL] [Abstract][Full Text] [Related]
50. Development and validation of a stability-indicating high performance liquid chromatographic (HPLC) method for the determination of related substances of micafungin sodium in drug substances.
Zhu S; Meng X; Su X; Luo Y; Sun Z
Int J Mol Sci; 2013 Oct; 14(11):21202-14. PubMed ID: 24284389
[TBL] [Abstract][Full Text] [Related]
51. 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]
52. Development and validation of a stability-indicating RP-HPLC method for the simultaneous estimation of process related impurities and degradation products of rasagiline mesylate in pharmaceutical formulation.
Reddy PS; Sudhakar Babu K; Kumar N
J Chromatogr Sci; 2013 Mar; 51(3):242-9. PubMed ID: 22988002
[TBL] [Abstract][Full Text] [Related]
53. Development and Validation of a RP-HPLC Method for Determination of Related Substances and Degradants in Entacapone.
Purnachand D; Veerareddy A; Ramadevi B; Kameswarrao ChV; Madhusudhanreddy B
J Chromatogr Sci; 2016 Sep; 54(8):1310-23. PubMed ID: 27165569
[TBL] [Abstract][Full Text] [Related]
54. LC and LC-MS/MS study of forced decomposition behavior of anastrozole and establishment of validated stability-indicating analytical method for impurities estimation in low dose anastrozole tablets.
Reddy YR; Nandan SR; Bharathi DV; Nagaraju B; Reddy SS; Ravindranath LK; Rao VS
J Pharm Biomed Anal; 2009 Oct; 50(3):397-404. PubMed ID: 19541446
[TBL] [Abstract][Full Text] [Related]
55. Development and validation of a stability-indicating RP-HPLC method for the identification, determination of related substances and assay of dimethyl fumarate in drug substance.
Kommareddy S; Nigam RS; Kumar S
Ann Pharm Fr; 2021 Mar; 79(2):179-193. PubMed ID: 33091397
[TBL] [Abstract][Full Text] [Related]
56. Optimization of separation and determination of moxifloxacin and its related substances by RP-HPLC.
Djurdjevic P; Ciric A; Djurdjevic A; Stankov MJ
J Pharm Biomed Anal; 2009 Sep; 50(2):117-26. PubMed ID: 19464135
[TBL] [Abstract][Full Text] [Related]
57. Rapid Development and Validation of Improved Reversed-Phase High-performance Liquid Chromatography Method for the Quantification of Mangiferin, a Polyphenol Xanthone Glycoside in
Naveen P; Lingaraju HB; Prasad KS
Pharmacognosy Res; 2017; 9(2):215-219. PubMed ID: 28539748
[TBL] [Abstract][Full Text] [Related]
58. Development and validation of a HPLC method for the determination of sertraline and three non-chiral related impurities.
Ferrarini A; Huidobro AL; Pellati F; Barbas C
J Pharm Biomed Anal; 2010 Oct; 53(2):122-9. PubMed ID: 20138727
[TBL] [Abstract][Full Text] [Related]
59. Degradation pathways and impurity profiling of the anticancer drug apalutamide by HPLC and LC-MS/MS and separation of impurities using Design of Experiments.
Lakka NS; Kuppan C; Vadagam N; Reddamoni SY; Muthusamy C
Biomed Chromatogr; 2023 Feb; 37(2):e5549. PubMed ID: 36409057
[TBL] [Abstract][Full Text] [Related]
60. Development and validation of stability-indicating -HPLC method for the determination of related substances in novel nitroimidazole antituberculosis drug pretomanid: Robustness study by Design-Expert and application to stability studies.
Surapuraju PKR; Juturu RR
Biomed Chromatogr; 2022 Dec; 36(12):e5498. PubMed ID: 36065902
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]