Morphology and internal structure control over PLA microspheres by compounding PLLA and PDLA and effects on drug release behavior

• Published in: Colloids and surfaces, B, Biointerfaces B, Biointerfaces, 2018-12, Vol.172, p.105-112
• Main Authors: Yu, Bowen, Meng, Lu, Fu, Sirui, Zhao, Zhiyu, Liu, Yuhang, Wang, Ke, Fu, Qiang
• Format: Article
• Language: English
• Subjects: Calorimetry, Differential Scanning; Crystallization; Drug Liberation; Microspheres; Morphology control; Polyesters - chemistry; Polylactide microspheres; Stereocomplex; Surface Properties; Temperature; X-Ray Diffraction
• ISSN: 0927-7765; 1873-4367
• DOI: 10.1016/j.colsurfb.2018.08.037

[Display omitted] •The morphology of PLA microspheres could be varied through the formation of PLA stereocomplex.•By simply changing the ratio of PLLA and PDLA in solution, the porosity of the microspheres could be varied.•The drug release rate of the PLLA/PDLA microspheres can be easily tuned from slow to fast with slight initial burst. The applications of Polylactide (PLA) microspheres in biomedical areas are greatly determined by the size, morphology and internal structure. Taking advantage of the formation of stereocomplex (SC) crystallites between poly(L-lactide) (PLLA) and poly(D-lactide) (PDLA), we propose a facile strategy to prepare PLA microspheres with tunable morphology and crystalline structure by compounding PLLA and PDLA. With increasing PDLA content, the crystallinity of SC-PLA rose gradually until the ratio of PLLA and PDLA reached 1:1 and then fell. Correspondingly, the morphology of the microspheres were varied (smooth, porous, golf-ball like, guava like) and higher crystallinity of SC-PLA would lead to a more coarse and porous structure. Finally, three typical kinds of Rifampicin-loaded microspheres with different ratio of PLLA and PDLA (7:3, 3:7, 10:0, sorted by porosity from high to low) were prepared and the release behavior was compared. At 30 h, the cumulative release of 7:3, 3:7 and 10:0 microspheres were 32.6%, 17.8% and 6.0% respectively, indicating that the release profiles were generally determined by the porosity of the microspheres. Our findings not only provide a new strategy to prepare PLA microspheres with controllable morphology but offer additional possibilities for the applications of SC-PLA products in biomedical area.