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1.
Mol Pharm ; 7(1): 227-36, 2010 Feb 01.
Artigo em Inglês | MEDLINE | ID: mdl-19874003

RESUMO

Surface functionalized mesoporous silicon (pSi) microparticles are reported as a solid dispersion carrier for improving dissolution and enhancing the orally administered pharmacokinetics (fasted rat model) of indomethacin (IMC), employed as a model poorly soluble BCS type II drug. IMC was loaded via immersion/solvent evaporation onto the thermally oxidized pSi particles, which provide a stable hydrophilic matrix with a nanoporous structure. The solid state properties of IMC loaded pSi were characterized by Fourier transform infrared spectroscopy, X-ray powder diffraction, differential scanning calorimetry and thermogravimetric analysis. IMC molecules are encapsulated in a noncrystalline state due to geometric confinement in the nanopores; stability of the noncrystalline state has been demonstrated for several months under accelerated storage conditions. The pSi carrier facilitates accelerated immediate release of IMC and enhanced oral delivery performance in comparison with crystalline indomethacin and Indocid i.e. a 4-times reduction on T(max), a 200% increase on C(max) and a significant increase in bioavailability. The in vitro-in vivo correlation is discussed based on the noncompartment model and gives insight into the delivery mechanism for the pSi carrier.


Assuntos
Sistemas de Liberação de Medicamentos , Indometacina/administração & dosagem , Silício , Absorção , Administração Oral , Animais , Disponibilidade Biológica , Varredura Diferencial de Calorimetria , Técnicas In Vitro , Indometacina/química , Indometacina/farmacocinética , Masculino , Microscopia Eletrônica de Varredura , Tamanho da Partícula , Difração de Pó , Ratos , Ratos Sprague-Dawley , Solubilidade , Espectroscopia de Infravermelho com Transformada de Fourier , Termogravimetria , Água
2.
Expert Opin Drug Deliv ; 4(2): 101-10, 2007 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-17335408

RESUMO

Nanostructuring materials can radically change their properties. Two interesting examples highlighted here are nanoscale porosity inducing biodegradability, and nanoscale confinement affecting the physical form of an entrapped drug. Mesoporous silicon is under increasing study for drug-delivery applications, and is the topic of this review. The authors focus on those properties of most relevance to this application, as well as those recent studies published on small molecule and peptide/protein delivery.


Assuntos
Sistemas de Liberação de Medicamentos/métodos , Nanoestruturas/química , Nanotecnologia/métodos , Preparações Farmacêuticas/química , Silício/química , Química Farmacêutica , Composição de Medicamentos/métodos , Teste de Materiais , Peptídeos , Porosidade , Proteínas , Semicondutores
3.
Nanoscale Res Lett ; 7(1): 407, 2012 Jul 20.
Artigo em Inglês | MEDLINE | ID: mdl-22818086

RESUMO

Unlike the trace minerals iron, copper and zinc, the semiconductor silicon has not had its organoleptic properties assessed. Nanostructured silicon provides the nutrient orthosilicic acid through hydrolysis in the gastrointestinal tract and is a candidate for oral silicon supplements. Mesoporous silicon, a nanostructured material, is being assessed for both oral drug and nutrient delivery. Here we use taste panels to determine the taste threshold and taste descriptors of both solid and mesoporous silicon in water and chewing gum base.Comparisons are made with a metal salt (copper sulphate) and porous silica. We believe such data will provide useful benchmarks for likely consumer acceptability of silicon supplemented foodstuffs and beverages.

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