Pore formation mechanism of porous poly(DL-lactic acid) matrix membrane

被引:41
|
作者
Phaechamud, Thawatchai [1 ]
Chitrattha, Sasiprapa [1 ]
机构
[1] Silpakorn Univ, Fac Pharm, Dept Pharmaceut Technol, Nakhon Pathom 73000, Thailand
关键词
Pore formation; Mechanism; Porous membrane; Poly(DL-lactic acid); POLY(LACTIC ACID); PHASE-SEPARATION; SCAFFOLDS; PEG; SOLVENT; TRANSPLANTATION; NANOFIBERS; NONSOLVENT; BLEND; FILM;
D O I
10.1016/j.msec.2016.01.014
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Porous PLA structure has been widely used in cell transplantation, drug carrier and wound dressing. The porous structure can be controlled depending on the choice of the polymer, solvent, nonsolvent and preparation parameters. In this study, the porous PIA matrix membranes were prepared by adding PEG 400 in PIA solution using dichloromethane (DCM) as solvent prior to casting. The influence of other liquids as co-solvent on pore formation and the structural change during membrane formation were evaluated. The co-solvents affected both porous topography and mechanical properties of PIA membrane. The porous matrix were produced when the non-solvent of PLA was used as co-solvent. Cryo-SEM micrographs revealed that PEG 400 still remained in the PIA porous matrix membrane. From the tracking of the structural change during film formation, the PIA-PEG solution changed into porous structure by liquid liquid phase separation and solidification processes, respectively. Thermogravimetric analysis revealed that PLA-PEG in DCM solution exhibited the two-step of weight loss, the first step occurred from DCM evaporation and the second step occurred from the degradation of PLA-PEG matrix. The liquid-liquid phase separation and solidification started when the amount of DCM was higher than PEG 400 for 2.67 folds and DCM amount was equal to that of PEG 400, respectively. These results could clarify the pore formation mechanism of porous PLA membrane and will be useful for the further investigation and application. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:744 / 752
页数:9
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