Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros

Base de dados
Ano de publicação
Tipo de documento
Intervalo de ano de publicação
1.
Ann Pharm Fr ; 75(1): 17-29, 2017 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-27659414

RESUMO

There is currently only one monoclonal antibody for which there is a biosimilar: infliximab, which was released onto the French market in 2015. The SPC for the biosimilar (Remsima®) are superimposable on those of the original, including 24-hour stability at both 4 and 25°C. The aim of our study was to determine the stability of this biosimilar during one month at 4 and 25°C. Three different batches at two concentrations (0.7mg/mL or 1.6mg/mL) were used. Physicochemical stability was evaluated by the following methods: turbidity, UV spectrometry, DLS, ion chromatography (CEX), gel exclusion chromatography (SEC), and light microscopy. The analyses were performed in triplicate. All methods used have been demonstrated to be valid for measuring antibody stability. There were no signs of physicochemical instability after seven days (on D7) of storage at 4 or 25°C. From D15, we observed slight changes by ion (percentage distribution of the different isoforms) and gel exclusion chromatography (percentage distribution of different polymers, i.e. dimers, oligomers). However, the areas under the curves were unchanged, and the proportions of polymers remained lower than 0.5%. Tertiary structure analysis also showed a change from D15. All observed changes are consistent with progressive oligomerization by hydrophobic interactions. In conclusion, the reconstituted biosimilar is stable for seven days at 4 and 25°C. Gradual oligomerization is observed from D15 but appears to be less than 0.5%, suggesting instability, albeit very limited, in the longer term; the practical consequences of this remain to be evaluated.


Assuntos
Anticorpos Monoclonais/análise , Medicamentos Biossimilares/análise , Infliximab/análise , Estabilidade de Medicamentos , Armazenamento de Medicamentos , Luz , Nefelometria e Turbidimetria , Espalhamento de Radiação , Espectrofotometria Ultravioleta , Temperatura
2.
Ann Pharm Fr ; 74(2): 129-36, 2016 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-26601885

RESUMO

The topological pressure-temperature phase diagram for the dimorphism of spiperone, a potent neuroleptic drug, has been constructed using literature data and improved crystal structures obtained with new crystallographic data from single-crystal X-ray diffraction at various temperatures. It is inferred that form II, which is the more dense form and exhibits the lower melting temperature, becomes the more stable phase under pressure. Under ambient conditions, form I is more stable.


Assuntos
Antipsicóticos/química , Espiperona/química , Cristalização , Modelos Moleculares , Temperatura , Termodinâmica , Difração de Raios X
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA