Development and optimization of stability-indicating method of ethinylestradiol, levonorgestrel, and their main impurities using quality by design approach (2023)
- Authors:
- Autor USP: LOURENÇO, FELIPE REBELLO - FCF
- Unidade: FCF
- DOI: 10.1016/j.jpba.2022.115208
- Subjects: CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA; MÉTODO DE MONTE CARLO; FÁRMACOS (SISTEMA REPRODUTOR)
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título: Journal of Pharmaceutical and Biomedical Analysis
- ISSN: 0731-7085
- Volume/Número/Paginação/Ano: v. 225, p. 1-14 art. 115208, 2023
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
SILVA, Fernando Antunes da e LOURENÇO, Felipe Rebello e CALIXTO, Leandro Augusto. Development and optimization of stability-indicating method of ethinylestradiol, levonorgestrel, and their main impurities using quality by design approach. Journal of Pharmaceutical and Biomedical Analysis, v. 225, p. 1-14 art. 115208, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2022.115208. Acesso em: 14 fev. 2026. -
APA
Silva, F. A. da, Lourenço, F. R., & Calixto, L. A. (2023). Development and optimization of stability-indicating method of ethinylestradiol, levonorgestrel, and their main impurities using quality by design approach. Journal of Pharmaceutical and Biomedical Analysis, 225, 1-14 art. 115208. doi:10.1016/j.jpba.2022.115208 -
NLM
Silva FA da, Lourenço FR, Calixto LA. Development and optimization of stability-indicating method of ethinylestradiol, levonorgestrel, and their main impurities using quality by design approach [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2023 ; 225 1-14 art. 115208.[citado 2026 fev. 14 ] Available from: https://doi.org/10.1016/j.jpba.2022.115208 -
Vancouver
Silva FA da, Lourenço FR, Calixto LA. Development and optimization of stability-indicating method of ethinylestradiol, levonorgestrel, and their main impurities using quality by design approach [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2023 ; 225 1-14 art. 115208.[citado 2026 fev. 14 ] Available from: https://doi.org/10.1016/j.jpba.2022.115208 - Setting multivariate and correlated acceptance limits for assessing the conformity of items
- Doseamento microbiológico de gentamicina por difusão em agar-proposta de delineamento experimental
- Frequentist approach for estimation of false decision risks in conformity assessment based on measurement uncertainty of liquid chromatography analytical procedures
- Application of measurement uncertainty on conformity assessment in pharmaceutical drug products
- Top-down evaluation of the matrix effects in microbial enumeration test uncertainty
- Development and optimization of a stability-indicating chromatographic method for verapamil hydrochloride and its impurities in tablets using an analytical quality by design (AQbD) approach
- Reduced incubation time for inhibition zone formation based on diffusion and growth mechanism elucidation
- Measurement uncertainty in pharmaceutical analysis and its application
- In vitro therapeutic equivalence of ciprofloxacin ophthalmic drugs based on measurement uncertainty and Monte Carlo simulations
- Physicochemical characterization of a lycopene-loaded mesoporous silica nanoparticle formulation
Informações sobre o DOI: 10.1016/j.jpba.2022.115208 (Fonte: oaDOI API)
Download do texto completo
| Tipo | Nome | Link | |
|---|---|---|---|
 |
3116382.pdf |
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
