Pregled bibliografske jedinice broj: 817944
Forced degradation of nepafenac: development and validation of stability indicating UHPLC method
Forced degradation of nepafenac: development and validation of stability indicating UHPLC method // Journal of pharmaceutical and biomedical analysis, 123 (2016), 42-52 doi:10.1016/j.jpba.2016.02.003 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 817944 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Forced degradation of nepafenac: development and validation of stability indicating UHPLC method
Autori
Runje, Mislav ; Babić, Sandra ; Meštrović, Ernest ; Nekola, Irena ; Dujmić-Vučinić, Željka ; Vojčić, Nina
Izvornik
Journal of pharmaceutical and biomedical analysis (0731-7085) 123
(2016);
42-52
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
Nepafenac ; Forced degradation ; Stability indicating study ; Ultra high performance liquid chromatography ; Degradation products ; Mass spectrometry
Sažetak
This paper presents stability study of the nonsteroidal anti-inflammatory drug (NSAID) nepafenac. In order to investigate stability of nepafenac, it was subjected to forced degradation under different stress conditions: acid and base hydrolysis, oxidation, humidity, heat and light. A novel stability indicating reverse phase ultra high performance liquid chromatographic (UHPLC) method coupled to ultraviolet detector has been developed to separate nepafenac and all related compounds (2-aminobenzophenone, Cl-thionepafenac, thionepafenac, Cl-nepafenac, hydroxy-nepafenac, and cyclic-nepafenac). Efficient chromatographic separation was achieved on a Waters Acquity BEH C18 stationary phase with a gradient elution. Quantification was carried out at 235 nm at a flow rate of 0.6 mL/min−1. The resolution between nepafenac and six potential impurities is found to be greater than 2.0. The developed methodwas validated with respect to specificity, LOD, LOQ, linearity, precision, accuracy and robustness. The r2 values for nepafenac and six potential impurities were all greater than 0.999. The developed method is capable to detect impurities of nepafenac at a level of 0.005% with respect to test concentration of 1.0 mg/mL. Significant degradation is observed in acid, base and oxidative degradation conditions and degradation products (DPs) were identified using mass spectrometry analysis ; two of them were foundto be a known process related impurities (hydroxy- and cyclic-nepafenac) whereas four degradation products were identified as new degradation impurities. The forced degradation samples were assayed against a qualified reference standard and the mass balance was found to be close to 99.5%.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Ustanove:
Fakultet kemijskog inženjerstva i tehnologije, Zagreb,
PLIVA HRVATSKA d.o.o.
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE
Uključenost u ostale bibliografske baze podataka::
- CA Search (Chemical Abstracts)