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1.
Drug Dev Ind Pharm ; 33(7): 755-65, 2007 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-17654024

RESUMO

Many new molecular entities targeted for pharmaceutical applications face serious development challenges because of poor water solubility. Although particle engineering technologies such as controlled precipitation have been shown to enhance aqueous dissolution and bioavailability of poorly water soluble active pharmaceutical ingredients, the data available are the results of laboratory-scale experiments. These technologies must be evaluated at larger scale to ensure that the property enhancement is scalable and that the modified drugs can be processed on conventional equipment. In experiments using ketoconazole as the model drug, the controlled precipitation process was shown to produce kg-scale modified drug powder with enhanced dissolution comparable to that of lab-scale powder. Ketoconazole was demonstrated to be stable throughout the controlled precipitation process, with a residual methanol level below the ICH limit. The modified crystalline powder can be formulated, and then compressed using conventional high-speed tableting equipment, and the resulting tablets showed bioavailability more than double that of commercial tablets. When appropriately protected from moisture, both the modified powder and tablets prepared from the modified powder showed no change in dissolution performance for at least 6 months following storage at accelerated conditions and for at least 18 months following storage at room temperature.


Assuntos
Antifúngicos/química , Antifúngicos/farmacocinética , Cetoconazol/química , Cetoconazol/farmacocinética , Animais , Disponibilidade Biológica , Precipitação Química , Estudos Cross-Over , Cães , Estabilidade de Medicamentos , Armazenamento de Medicamentos , Técnicas In Vitro , Masculino , Metanol/análise , Microscopia Eletrônica de Varredura , Tamanho da Partícula , Pós/química , Distribuição Aleatória , Solubilidade , Solventes/análise , Comprimidos/química , Tecnologia Farmacêutica , Difração de Raios X
2.
Eur J Pharm Biopharm ; 65(1): 57-67, 2007 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-16987642

RESUMO

An ultra-rapid freezing (URF) technology has been developed to produce high surface area powders composed of solid solutions of an active pharmaceutical ingredient (API) and a polymer stabilizer. A solution of API and polymer excipient(s) is spread on a cold solid surface to form a thin film that freezes in 50 ms to 1s. This study provides an understanding of how the solvent's physical properties and the thin film geometry influence the freezing rate and consequently the final physico-chemical properties of URF-processed powders. Theoretical calculations of heat transfer rates are shown to be in agreement with infrared images with 10ms resolution. Danazol (DAN)/polyvinylpyrrolidone (PVP) powders, produced from both acetonitrile (ACN) and tert-butanol (T-BUT) as the solvent, were amorphous with high surface areas (approximately 28-30 m2/g) and enhanced dissolution rates. However, differences in surface morphology were observed and attributed to the cooling rate (film thickness) as predicted by the model. Relative to spray-freezing processes that use liquid nitrogen, URF also offers fast heat transfer rates as a result of the intimate contact between the solution and cold solid surface, but without the complexity of cryogen evaporation (Leidenfrost effect). The ability to produce amorphous high surface area powders with submicron primary particles with a simple ultra-rapid freezing process is of practical interest in particle engineering to increase dissolution rates, and ultimately bioavailability.


Assuntos
Excipientes/química , Liofilização/métodos , Solventes/química , Tecnologia Farmacêutica , Acetonitrilas/química , Química Farmacêutica , Cristalografia por Raios X , Danazol/química , Cinética , Microscopia Eletrônica de Varredura , Modelos Químicos , Tamanho da Partícula , Povidona/química , Pós , Solubilidade , Temperatura , Termografia , Fatores de Tempo , Água/química , terc-Butil Álcool/química
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