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1.
Artigo em Inglês | MEDLINE | ID: mdl-19963916

RESUMO

The ElectroNanospray process (Nanocopoeia, Inc) transforms drugs and polymers into many nanoscale material states including powders, liquids, encapsulated particles, and coatings. This enabling technology platform allows application of polymers and drugs to the surface of medical devices such as coronary stents in a single-stage process. Modification of ElectroNanospray process parameters resulted in surface coatings with rich morphologies ranging in appearance from smooth and heterogeneous to highly porous and rough (open matrix). The traditional approach of measuring percent release over time by HPLC shows that the drug release profiles change significantly with coating morphology. In this study, we employed high resolution imaging techniques such as SEM, Atomic Force Microscopy (AFM) and Confocal Raman Microscopy to elucidate the drug release process on these coatings in situ, indicating a correlation of release kinetics with coating morphology.


Assuntos
Materiais Revestidos Biocompatíveis/química , Nanocápsulas/química , Nanocápsulas/ultraestrutura , Preparações Farmacêuticas/química , Polímeros/química , Difusão , Composição de Medicamentos/métodos , Teste de Materiais , Propriedades de Superfície
2.
Langmuir ; 25(10): 5442-5, 2009 May 19.
Artigo em Inglês | MEDLINE | ID: mdl-19432489

RESUMO

Drug release from therapeutic biomedical films such as drug-polymer composite coatings on drug eluting stents is a highly complex and poorly understood process. The dynamics of drug release and the evolution of surface morphology during release have direct impact on the performance of the device. This information is not easily accessible, and there have been few systematic studies to investigate drug release from biomedical coatings in real time. In this study, the complementary analytical techniques of confocal Raman microscopy, in-liquid atomic force microscopy, scanning electron microscopy, and high performance liquid chromatography were used to examine real-time mobilization and release of the drug rapamycin from polyisobutylene-block-polystyrene thin films, during immersion in buffered saline for 12 h. Each technique was found to have distinct limitations in either temporal or spatial resolution; in combination, however, the overlapping techniques provided a level of detail that is not available using any single approach.


Assuntos
Antibióticos Antineoplásicos/química , Materiais Revestidos Biocompatíveis/química , Preparações de Ação Retardada/química , Membranas Artificiais , Modelos Químicos , Sirolimo/química , Microscopia de Força Atômica , Microscopia Confocal , Microscopia Eletrônica de Varredura , Polienos/química , Polímeros/química , Poliestirenos/química
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