Recently, nano- and micro-particulate systems have been widely utilized to deliver pharmaceutical compounds to achieve enhanced therapeutic effects and reduced side effects. Poly (DL-lactide-co-glycolide) (PLGA), as one of the biodegradable polyesters, has been widely used to fabricate particulate systems because of advantages including controlled and sustained release, biodegradability, and biocompatibility. However, PLGA is known for low encapsulation efficiency (%) and insufficient controlled release of water-soluble drugs. It would result in fluctuation in the plasma levels and unexpected side effects of drugs. Therefore, the purpose of this work was to develop microcapsules loaded with alginate-coated chitosan that can increase the encapsulation efficiency of the hydrophilic drug while exhibiting a controlled and sustained release profile with reduced initial burst release. The encapsulation of nanoparticles in PLGA microcapsules was done by the emulsion solvent evaporation method. The encapsulation of nanoparticles in PLGA microcapsules was confirmed by scanning electron microscopy and confocal microscopy. The release profile of hydrophilic drugs can further be altered by the chitosan coating. The chitosan coating onto alginate exhibited a less initial burst release and sustained release of the hydrophilic drug. In addition, the encapsulation of alginate nanoparticles and alginate nanoparticles coated with chitosan in PLGA microcapsules was shown to enhance the encapsulation efficiency of a hydrophilic drug. Based on the results, this delivery system could be a promising platform for the high encapsulation efficiency and sustained release with reduced initial burst release of the hydrophilic drug. 相似文献
Vertically aligned polymer nanopillar arrays on substrates are receiving increasing interest as functional surfaces for a broad range of applications. However, methods for preparing polymeric nanopillar arrays have poor controllability of dimensional parameters and are limited to few polymers. Here, a new method to prepare freestanding biodegradable nanopillar arrays on different substrates, including flexible sheets, by plasma etching with polystyrene‐block‐poly(acrylic acid) (PS‐PAA) block copolymer (BCP) micelles encapsulating Au nanoparticles (AuNP@PS‐PAA) is reported. The adsorption density of the AuNP@PS‐PAA micelles is controlled by the pH of the micelle solutions, affecting electrostatic interaction with the polyelectrolyte layers formed on a poly(lactic‐co‐glycolic acid) (PLGA) film coated on the substrates; thus, density‐controlled PLGA nanopillar arrays are prepared using the micelle array as an etching mask during plasma etching. The height of the PLGA nanopillars is controlled by adjusting the plasma etching time, achieving high aspect ratios (>10) on inch‐sized substrates. This new platform combining bottom‐up (controlling absorption of BCP micelles used as etching mask) and top‐down (plasma etching for nanopillar formation) approaches can be applied to prepare nanopillar arrays on substrates using different soft materials including biodegradable polymers.
