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Volumn 57, Issue 5, 2009, Pages 534-541

Development of a validated RP-HPLC method for separation and determination of process-related impurities of omeprazole in bulk drugs

Author keywords

Omeprazole; Process related impurities; RP HPLC; Validation

Indexed keywords

2 [(3,5 DIMETHYLPYRIDIN 2 YL)METHYL]SULPHINYL 5 METHOXY 1H BENZIMIDAZOLE; 4 METHOXY 2 [[(5 METHOXY 1H BENZIMIDAZOL 2 YL)SULPHINYL]METHYL] 3,5 DIMETHYLPYRIDINE 1 OXIDE; 5 METHOXY 1H BENZIMIDAZOLE 2 THIOL; 5 METHOXY 2 [[(4 CHLORO 3,5 DIMETHYLPYRIDIN 2 YL)METHYL]SULPHINYL] 1H BENZIMIDAZOLE; BENZIMIDAZOLE DERIVATIVE; OMEPRAZOLE; OMEPRAZOLE SULFONE; UFIPRAZOLE; UNCLASSIFIED DRUG;

EID: 73349117471     PISSN: 00148237     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (15)

References (5)
  • 2
    • 42949149118 scopus 로고    scopus 로고
    • The HPLC assay of ondansetron hydrochloride and its impurities using a new stationary phase
    • Varvara A., Monciu C.M, Arama C., Popescu C. The HPLC assay of ondansetron hydrochloride and its impurities using a new stationary phase. Farmacia 2008; 56 (2):154-165.
    • (2008) Farmacia , vol.56 , Issue.2 , pp. 154-165
    • Varvara, A.1    Monciu, C.M.2    Arama, C.3    Popescu, C.4
  • 3
    • 40749162406 scopus 로고    scopus 로고
    • Reversed phase high performance liquid chromatography (RP-HPLC) determination of lisinopril and its degradation products in stability and compatibility studies
    • Constantinescu D., Curea E. Reversed phase high performance liquid chromatography (RP-HPLC) determination of lisinopril and its degradation products in stability and compatibility studies. Farmacia 2008; 56 (1) :50-56.
    • (2008) Farmacia , vol.56 , Issue.1 , pp. 50-56
    • Constantinescu, D.1    Curea, E.2
  • 4
    • 45949108485 scopus 로고    scopus 로고
    • Validation of HPLC-UV method for analysis of omeprazole in presence of its metabolites in human plasma
    • Iuga C., Moldovan M., Popa A., Leucuţa S.E. Validation of HPLC-UV method for analysis of omeprazole in presence of its metabolites in human plasma. Farmacia, 2008, 56 (3): 254-260.
    • (2008) Farmacia , vol.56 , Issue.3 , pp. 254-260
    • Iuga, C.1    Moldovan, M.2    Popa, A.3    Leucuţa, S.E.4
  • 5
    • 34250626476 scopus 로고    scopus 로고
    • Validation of chromatographic methods: Evaluation of detection and quantification limits in the determination of impurities in omeprazole
    • Ribani M, Collins CH, Bottoli CB. Validation of chromatographic methods: evaluation of detection and quantification limits in the determination of impurities in omeprazole. J Chromatogr A. 2007; (1156) 1-2:201-205.
    • (2007) J Chromatogr A , vol.1156
    • Ribani, M.1    Collins, C.H.2    Bottoli, C.B.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.