Development and optimization of a LC-MS/MS compatible method for quantification of losartan, hydrochlorothiazide and their impurities using AQbD approach and measurement uncertainty evaluation (2023)
- Authors:
- USP affiliated authors: LOURENÇO, FELIPE REBELLO - FCF ; ROCHA, ARIEL LUCAS - FCF
- Unidade: FCF
- DOI: 10.1016/j.talanta.2023.124481
- Subjects: ESPECTROMETRIA DE MASSAS; CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
ROCHA, Ariel Lucas e LOURENÇO, Felipe Rebello. Development and optimization of a LC-MS/MS compatible method for quantification of losartan, hydrochlorothiazide and their impurities using AQbD approach and measurement uncertainty evaluation. Talanta, v. 259, p. 1-14, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.talanta.2023.124481. Acesso em: 12 jan. 2026. -
APA
Rocha, A. L., & Lourenço, F. R. (2023). Development and optimization of a LC-MS/MS compatible method for quantification of losartan, hydrochlorothiazide and their impurities using AQbD approach and measurement uncertainty evaluation. Talanta, 259, 1-14. doi:10.1016/j.talanta.2023.124481 -
NLM
Rocha AL, Lourenço FR. Development and optimization of a LC-MS/MS compatible method for quantification of losartan, hydrochlorothiazide and their impurities using AQbD approach and measurement uncertainty evaluation [Internet]. Talanta. 2023 ; 259 1-14.[citado 2026 jan. 12 ] Available from: https://doi.org/10.1016/j.talanta.2023.124481 -
Vancouver
Rocha AL, Lourenço FR. Development and optimization of a LC-MS/MS compatible method for quantification of losartan, hydrochlorothiazide and their impurities using AQbD approach and measurement uncertainty evaluation [Internet]. Talanta. 2023 ; 259 1-14.[citado 2026 jan. 12 ] Available from: https://doi.org/10.1016/j.talanta.2023.124481 - Desenvolvimento de método cromatográfico compatível com LC-MS, indicativo de estabilidade para associação de losartana potássica e hidroclorotiazida em comprimidos pela abordagem Quality by Design e avaliação de incertezas
- Separation of neomycin b and c and its relative antimicrobial potency
- Uncertainty measurement of microbiological assay for apramycin soluble powder
- Measurement uncertainty of a UPLC stability indicating method for determination of linezolid in dosage forms
- Measurement uncertainty in the determination of linezolid by uv spectrophotometry
- Relationship assessment among content of aminoglycoside antibiotic components by HPLC and C13-NMR and their microbiological assay potencies
- Uncertainty evaluation for determining linezolid in injectable solution by UV spectrophotometry
- Measurement uncertainty of dissolution test of acetaminophen immediate release tablets using Monte Carlo simulations
- Using measurement uncertainty to assess the fitness for purpose of an HPLC analytical method in the pharmaceutical industry
- Development and validation of an uplc stability-indicating method for determination
Informações sobre o DOI: 10.1016/j.talanta.2023.124481 (Fonte: oaDOI API)
Download do texto completo
| Tipo | Nome | Link | |
|---|---|---|---|
 |
3134024.pdf |
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
