摘要
The star-shaped poly( l -lactide) (s-PLLA) was synthesized via ring-opening polymerization of l -lactide, with xylitol as a multifunctional initiator and stannous octoate as a catalyst. The structures of s-PLLA were characterized by 1 H NMR spectroscopy, while the molecular weight ( M w ) and polydispersity index were determined by gel permeation chromatography. Bovine serum albumin (BSA) loaded s-PLLA microspheres were fabricated by a water–oil–water ( W 1 / O / W 2 ) double-emulsion solvent evaporation method. The morphology, drug encapsulation efficiency (EE), and in vitro release behavior of the prepared microspheres were studied in detail. Results indicated that the average diameters of s-PLLA microspheres could be controlled between 7 and 15 µm by varying the s-PLLA’s concentration or M w , and the drug encapsulation efficiency of BSA-loaded microspheres were 10–42%. The in vitro study shows that the BSA-loaded microspheres prepared by high molecular weight s-PLLA had a slow cumulative release behavior in phosphate buffer saline (PBS, pH 7.4) and the release process followed the Baker–Lonsdale equation. Present work supposes that the synthesized s-PLLA is a good candidate for drug delivery.
危险品化学品经营许可证(带存储)