Lu L, Garcia C A, Mikos A G
Department of Chemical Engineering, Rice University, Houston, Texas 77005-1892, USA.
J Biomed Mater Res. 1999 Aug;46(2):236-44. doi: 10.1002/(sici)1097-4636(199908)46:2<236::aid-jbm13>3.0.co;2-f.
This study was designed to investigate the in vitro degradation of thin poly(DL-lactic-co-glycolic acid) (PLGA) films for applications in retinal pigment epithelium transplantation and guided tissue regeneration. PLGA films of copolymer ratios of 75:25 and 50:50 were manufactured with thickness levels of 10 microm (thin) and 100 microm (thick). Degradation of the films occurred during sample processing, and thin films with a higher surface area to volume ratio degraded faster. Sample weight loss, molecular weight loss, dimensional, and morphological changes were analyzed over a 10-week period of degradation in 0.2 M of phosphate-buffered saline (PBS), pH 7.4, at 37 degrees C. All PLGA films degraded by heterogeneous bulk degradation. Sample weights remained relatively constant for the first several weeks and then decreased dramatically. The molecular weights of PLGA films decreased immediately upon placement in PBS and continued to decrease throughout the time course. PLGA 50:50 films degraded faster than 75:25 films due to their higher content of hydrophilic glycolic units. The results also demonstrated that thick films degrade faster than corresponding thin films with the same composition. This was attributed to the greater extent of the autocatalytic effect, which further was confirmed by heterogeneous gel permeation chromatograms. These studies suggest that the degradation rate of thin films can be engineered by varying film thicknesses.
本研究旨在调查用于视网膜色素上皮移植和引导组织再生的聚(DL-乳酸-乙醇酸)(PLGA)薄膜的体外降解情况。制备了共聚物比例为75:25和50:50的PLGA薄膜,厚度分别为10微米(薄)和100微米(厚)。薄膜在样品处理过程中发生降解,表面积与体积比更高的薄膜降解更快。在37℃、pH值为7.4的0.2M磷酸盐缓冲盐水(PBS)中进行为期10周的降解过程中,分析了样品的重量损失、分子量损失、尺寸变化和形态变化。所有PLGA薄膜均通过非均相本体降解方式降解。样品重量在最初几周相对保持恒定,然后急剧下降。PLGA薄膜的分子量在放入PBS后立即下降,并在整个时间段内持续下降。PLGA 50:50薄膜由于其亲水性乙醇酸单元含量较高,降解速度比75:25薄膜快。结果还表明,相同组成的厚膜比相应的薄膜降解更快。这归因于自催化作用的程度更大,这通过非均相凝胶渗透色谱图进一步得到证实。这些研究表明,可以通过改变薄膜厚度来设计薄膜的降解速率。