Department of Pharmacy, College of Pharmacy, Ewha Womans University, Seodaemun-gu, Seoul 120-750, Korea.
J Biomed Mater Res B Appl Biomater. 2010 Oct;95(1):150-60. doi: 10.1002/jbm.b.31695.
Poly(L-lactic acid) (PLLA) microfibrous scaffolds with three-dimensional (3D) structures were fabricated using an electrospinning technique with a subsequent mechanical expansion process. To achieve a 3D fibrous structure, the fusion at the contact points of the as-spun PLLA microfibers was avoided using an appropriate binary solvent system of methylene chloride and acetone. The solvent composition was optimized based on the solvent power, volatility, and viscosity (methylene chloride:acetone = 9:1 volume ratio). The final 3D structure of the electrospun scaffolds was obtained after mechanical expansion of the electrospun microfibrous mats. The pore sizes of the scaffolds were controlled by varying the degree of expansion of the nonbonded microfibrous mats, and they were in the range of several microns up to 400 μm. The 3D scaffolds were examined for their morphological properties and their potential use for the proliferation of osteoblasts. Generally recognized electrospun 2D nanofibrous membranes were also tested in order to compare the cell behaviors using different scaffold geometries. The 3D scaffolds demonstrated a high level of osteoblast proliferation (1.8-fold higher than nanofibrous membranes in a week). The osteoblasts actively penetrated the inside of the 3D scaffold and showed a spatial cell distribution, as confirmed by SEM and H&E staining, while a monolayer formed in the case of the 2D nanofibrous membranes with limited cell infiltration. In vivo results further showed that 3D electrospun microfibrous matrices were a favorable substrate for cell infiltration and bone formation after 2 and 4 weeks, using a rabbit calvarial defect model. In this study, the 3D microfibrous PLLA scaffolds fabricated using electrospinning techniques might be an innovative addition to tissue engineering applications.
聚(L-乳酸)(PLLA)具有三维(3D)结构的微纤维支架是通过静电纺丝技术和随后的机械膨胀过程制造的。为了获得 3D 纤维结构,避免使用合适的二甲基亚砜和丙酮混合溶剂系统使纺丝 PLLA 微纤维在接触点融合。根据溶剂的溶解力、挥发性和粘度(二甲基亚砜:丙酮=9:1 体积比)优化溶剂组成。在对静电纺微纤维垫进行机械膨胀后,获得最终的 3D 电纺支架结构。支架的孔径通过改变未结合微纤维垫的膨胀程度来控制,其范围从几微米到 400μm。对 3D 支架的形态特性及其对成骨细胞增殖的潜在用途进行了研究。还测试了公认的 3D 支架,以比较使用不同支架几何形状的细胞行为。3D 支架表现出高水平的成骨细胞增殖(在一周内比纳米纤维膜高 1.8 倍)。成骨细胞积极地渗透到 3D 支架的内部,并表现出空间细胞分布,这通过 SEM 和 H&E 染色得到证实,而在 2D 纳米纤维膜的情况下形成单层,细胞渗透有限。体内结果进一步表明,在使用兔颅骨缺损模型的 2 和 4 周后,3D 静电纺丝微纤维基质是细胞渗透和骨形成的有利基质。在这项研究中,使用静电纺丝技术制造的 3D 微纤维 PLLA 支架可能是组织工程应用的创新补充。