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1.
Int J Pharm ; 370(1-2): 167-74, 2009 Mar 31.
Artigo em Inglês | MEDLINE | ID: mdl-19100319

RESUMO

BMS-488043 is an HIV-attachment inhibitor that exhibited suboptimal oral bioavailability upon using conventional dosage forms prepared utilizing micronized crystalline drug substance. BMS-488043 is classified as a Biopharmaceutics Classification System (BCS) Class-II compound with a poor aqueous solubility of 0.04mg/mL and an acceptable permeability of 178nm/s in the Caco2 cell-line model. Two strategies were evaluated to potentially enhance the oral bioavailability of BMS-488043. The first strategy targeted particle size reduction through nanosizing the crystalline drug substance. The second strategy aimed at altering the drug's physical form by producing an amorphous drug. Both strategies provided an enhancement in oral bioavailability in dogs as compared to a conventional formulation containing the micronized crystalline drug substance. BMS-488043 oral bioavailability enhancement was approximately 5- and 9-folds for nanosizing and amorphous formulation approaches, respectively. The stability of the amorphous coprecipitated drug prepared at different compositions of BMS-488043/polyvinylpyrrolidone (PVP) was evaluated upon exposure to stressed stability conditions of temperature and humidity. The drastic effect of exposure to humidity on conversion of the amorphous drug to crystalline form was observed. Additionally, the dissolution behavior of coprecipitated drug was evaluated under discriminatory conditions of different pH values to optimize the BMS-488043/PVP composition and produce a stabilized, amorphous BMS-488043/PVP (40/60, w/w) spray-dried intermediate (SDI), which was formulated into an oral dosage form for further development and evaluation.


Assuntos
Composição de Medicamentos/métodos , Inibidores da Fusão de HIV/farmacocinética , Nanopartículas , Piperazinas/farmacocinética , Administração Oral , Animais , Disponibilidade Biológica , Química Farmacêutica , Cromatografia Líquida de Alta Pressão , Estudos Cross-Over , Cães , Sistemas de Liberação de Medicamentos , Estabilidade de Medicamentos , Feminino , Inibidores da Fusão de HIV/administração & dosagem , Inibidores da Fusão de HIV/química , Umidade , Indóis , Tamanho da Partícula , Transição de Fase , Piperazinas/administração & dosagem , Piperazinas/química , Povidona/química , Ácido Pirúvico , Solubilidade , Tecnologia Farmacêutica , Temperatura
2.
Zoology (Jena) ; 111(3): 218-30, 2008.
Artigo em Inglês | MEDLINE | ID: mdl-18328681

RESUMO

Within the salamander family Plethodontidae, five different clades have evolved high levels of enucleated red blood cells, which are extremely unusual among non-mammalian vertebrates. In each of these five clades, the salamanders have large genomes and miniaturized or attenuated body forms. Such a correlation suggests that the loss of nuclei in red blood cells may be related, in part, to the interaction between large genome size and small body size, which has been shown to have profound morphological consequences for the nervous and visual systems in plethodontids. Previous work has demonstrated that variation in both the level of enucleated cells and the size of the nuclear genome exists among species of the monophyletic plethodontid genus Batrachoseps. Here, we report extensive intraspecific variation in levels of enucleated red blood cells in 15 species and provide measurements of red blood cell size, nucleus size, and genome size for 13 species of Batrachoseps. We present a new phylogenetic hypothesis for the genus based on 6150bp of mitochondrial DNA sequence data from nine exemplar taxa and use it to examine the relationship between genome size and enucleated red blood cell morphology in a phylogenetic framework. Our analyses demonstrate positive direct correlations between genome size, nucleus size, and both nucleated and enucleated cell sizes within Batrachoseps, although only the relationship between genome size and nucleus size is significant when phylogenetically independent contrasts are used. In light of our results and broader studies of comparative hematology, we propose that high levels of enucleated, variably sized red blood cells in Batrachoseps may have evolved in response to rheological problems associated with the circulation of large red blood cells containing large, bulky nuclei in an attenuate organism.


Assuntos
Eritrócitos/fisiologia , Evolução Molecular , Variação Genética , Urodelos/sangue , Urodelos/genética , Animais , Tamanho Celular , Genoma , Filogenia , Especificidade da Espécie
3.
J Pharm Sci ; 94(7): 1598-607, 2005 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-15929069

RESUMO

Spray drying drug with excipients is usually associated with the preparation of microcrystalline or amorphous drug in order to improve bioavailability. It was found that BMS-347070, when spray-dried with Pluronic F127 from acetone or methylene chloride, was dispersed as nanosized crystalline drug within the water-soluble Pluronic matrix. The reduction in drug particle/crystallite size, coupled with wetting by the Pluronic, resulted in a fast-onset formulation with bioavailability comparable to that of a solubilized and a NanoCrystal formulation. For this system, it is theorized that the polyethylene oxide segments of Pluronic crystallize and that the polypropylene oxide segments remain amorphous, providing a size-restricted domain in which the COX-2 drug crystallizes. This results in improved bioavailability while limiting the potential risk of conversion of an amorphous drug to its crystalline state.


Assuntos
Inibidores de Ciclo-Oxigenase/farmacocinética , Furanos/farmacocinética , Mesilatos/farmacocinética , Prostaglandina-Endoperóxido Sintases/metabolismo , Disponibilidade Biológica , Varredura Diferencial de Calorimetria , Cromatografia Líquida de Alta Pressão , Ciclo-Oxigenase 2 , Inibidores de Ciclo-Oxigenase 2 , Inibidores de Ciclo-Oxigenase/química , Dessecação , Excipientes , Furanos/química , Mesilatos/química , Microscopia Eletrônica de Varredura , Microesferas , Tamanho da Partícula , Poloxâmero/química , Difração de Raios X
4.
Columbia J Law Soc Probl ; 37(3): 359-411, 2004.
Artigo em Inglês | MEDLINE | ID: mdl-16755693

RESUMO

The advent of the human genome sequence has focused research on understanding underlying genetic links to complex diseases such as cancer, asthma and heart disease. In the past few years, individual countries, such as Iceland, Estonia, Singapore and the United Kingdom, have created national databases of their citizens' DNA for comparative research. Most recently, an international consortium including Nigeria, Japan, China and the United States launched a $100 million project called the International HapMap to map the human genome according to haplotypes, blocks of DNA that contain genetic variation. Such population genetic databases present challenging ethical, social and legal issues, yet regulation of genetic information has developed sporadically, from region to region, without a consistent international standard. Without a clear understanding of the consequences of genetic research in terms of individual and community-wide discrimination and stigmatization, genetic databases raise concerns about the protection of genetic information. This Note provides a survey of the evolving landscape of population genetic databases as a legislative and public policy tool for national and international regulators. It compares different approaches to regulating the collection and use of population genetic databases in order to understand what areas of consensus are formulating a foundation for an international standard. As the first population genetics project that will span multiple countries for the collection of DNA, the International HapMap has the potential to become an influential standard for the protection of population genetic information. This Note highlights issues among the national databases and the HapMap project that raise ethical, social and legal concerns for the future and recommends further protections for both individual donors and community interests.


Assuntos
Bases de Dados Genéticas/ética , Bases de Dados Genéticas/legislação & jurisprudência , Genética Populacional , Haplótipos/genética , Internacionalidade , Acesso à Informação/legislação & jurisprudência , Bancos de Espécimes Biológicos/legislação & jurisprudência , Confidencialidade/legislação & jurisprudência , Revelação/legislação & jurisprudência , Estônia , Comitês de Ética em Pesquisa , Família , Projeto Genoma Humano , Humanos , Islândia , Consentimento Livre e Esclarecido/legislação & jurisprudência , Consentimento Presumido/legislação & jurisprudência , Recusa de Participação/legislação & jurisprudência , Singapura , Reino Unido
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