| Literature DB >> 22063006 |
Moritz Beck-Broichsitter1, Christoph Schweiger, Thomas Schmehl, Tobias Gessler, Werner Seeger, Thomas Kissel.
Abstract
Numerous studies have addressed the controlled pulmonary drug delivery properties of colloidal particles. However, only scant information on the potential of spray-drying for submicron particle preparation is available. By exploiting the advantages of spray-drying, the characteristics of submicron particles can be optimized to meet the requirements necessary for lung application. Submicron particles were prepared from organic poly(d,l-lactide-co-glycolide) (PLGA) solutions, and composite particles were spray-dried from aqueous PLGA nanosuspensions. The feed concentration, as well as the spray-mesh diameter influenced the resulting particle sizes. Nanoparticles were virtually unaffected after spray-drying. The aerodynamic characteristics of both particle species revealed aerosol particle sizes suitable for deposition in the deep lungs (≤4μm). While the entrapped drug was released within ~90min from the composite particles, extensive drug retardation (~480min) was observed for PLGA particles spray-dried from organic solution. These results suggest that nanospray-drying is a convenient method to prepare submicron, controlled drug delivery vehicles useful for pulmonary application potentially allowing access to alveolar tissue. Copyright ÂEntities:
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Year: 2011 PMID: 22063006 DOI: 10.1016/j.jconrel.2011.10.030
Source DB: PubMed Journal: J Control Release ISSN: 0168-3659 Impact factor: 9.776