Drug Excipient Interaction Study with Polymorphic Forms of Tibolone
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
20/10/2012
20/10/2012
2010
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Resumo |
Powder mixtures (1:1) of tibolone polymorphic forms I (monoclinic) and II (triclinic) and excipients have been prepared and compacted. The samples were stored at 50 degrees C and 90% RH for one month and subsequently were evaluated using differential scanning calorimetry (DSC) and high-performance liquid chromatography (HPLC). The results indicate that during the compaction, the applied pressure reduced the chemical stability of tibolone in both polymorph forms. The triclinic form was more chemically unstable, both pure and in contact with excipients, than the monoclinic form. Lactose monohydrate was shown to reduce chemical degradation for both forms. Ascorbyl palmitate was shown to affect the tibolone stability differently depending on the polymorphic form used. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq) Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Fundacao de Amparo Pesquisa do Estado de Sao Paulo (FAPESP) |
Identificador |
LATIN AMERICAN JOURNAL OF PHARMACY, v.29, n.3, p.472-476, 2010 0326-2383 |
Idioma(s) |
eng |
Publicador |
COLEGIO FARMACEUTICOS PROVINCIA DE BUENOS AIRES |
Relação |
Latin American Journal of Pharmacy |
Direitos |
closedAccess Copyright COLEGIO FARMACEUTICOS PROVINCIA DE BUENOS AIRES |
Palavras-Chave | #Drug-excipient interaction #Polymorphism of drugs #Solid-state characterization #Thermal analysis #Pharmacology & Pharmacy |
Tipo |
article original article publishedVersion |