Biomaterials & Tissue Engineering Laboratory, Department of Nanobiomedical Science & WCU Research Center, Dankook University, Cheonan, South Korea.
J Mater Sci Mater Med. 2012 May;23(5):1271-9. doi: 10.1007/s10856-012-4588-4. Epub 2012 Mar 2.
Here we prepared three-dimensional (3D) porous-structured biodegradable polymer scaffolds for tissue regeneration using room temperature ionic liquids (RTILs) as a novel porogen, and addressed their biological properties, including in vitro cell growth and differentiation and in vivo tissue compatibility. RTIL based on 1-butyl-3-methylimidazolium ([bmim]) bearing hydrophilic anion Cl was introduced within the polymer structure to provide a pore network. A mixture of poly(lactic acid) (PLA) with RTIL dissolved in an organic solvent formed a bi-continuous network during the drying process. Selective dissolution of the RTIL phase was facilitated in ethanol, which resulted in a porous network of the polymer phase with complete removal of the RTIL. The RTILs-assisted porous scaffolds showed a typical open-channeled network with pore sizes over 100 μm and porosities of about 86-94%. For the biocompatibility assessments of the scaffolds, mesenchymal stem cells (MSCs) derived from rat bone marrow were seeded onto the PLA scaffold, and the cell proliferation and osteoblastic differentiation behaviors were examined. Results showed a typical on-going increase in the cell population with a level comparable to that observed on the tissue culture plastic control, indicating good cell compatibility. When cultured in an osteogenic medium, the alkaline phosphatase (ALP) activity of the cells on the PLA scaffolds was stimulated to increase with time from 7 to 14 days, in a similar manner to that on the control. Moreover, the expression of genes related to osteoblasts, including collagen type I, osteocalcin and bone sialoprotein, was stimulated on the 3D PLA scaffold during culture for up to 14 days, with levels higher than those on the control, suggesting the developed scaffold provided a 3D matrix condition for osteogenesis. An in vivo pilot study conducted subcutaneously in rat for 4 weeks revealed good tissue compatibility of the scaffold, with the ingrowth of cells and formation of collageneous tissue around and deep within the pores of the scaffold and no significant inflammatory reaction. Taken together, this novel method of using RTILs as a pore generator is considered to be useful in the development of biocompatible porous polymer scaffolds for tissue regeneration.
在这里,我们使用室温离子液体(RTILs)作为新型造孔剂制备了用于组织再生的三维(3D)多孔结构可生物降解聚合物支架,并研究了它们的生物学特性,包括体外细胞生长和分化以及体内组织相容性。在聚合物结构中引入了基于 1-丁基-3-甲基咪唑 ([bmim]) 的带亲水阴离子 Cl 的 RTIL,以提供孔网络。聚乳酸(PLA)与 RTIL 的混合物溶解在有机溶剂中,在干燥过程中形成双连续网络。在乙醇中促进 RTIL 相的选择性溶解,导致聚合物相的多孔网络形成,RTIL 完全去除。RTIL 辅助多孔支架显示出典型的开放式通道网络,孔径超过 100μm,孔隙率约为 86-94%。为了评估支架的生物相容性,将大鼠骨髓来源的间充质干细胞(MSCs)接种到 PLA 支架上,并检测细胞增殖和成骨细胞分化行为。结果表明,细胞群体呈典型的持续增加,水平与组织培养塑料对照观察到的水平相当,表明细胞相容性良好。当在成骨培养基中培养时,PLA 支架上细胞的碱性磷酸酶(ALP)活性随时间从 7 天增加到 14 天,与对照相似。此外,在培养的 14 天内,3D PLA 支架上与成骨细胞相关的基因,包括胶原 I、骨钙素和骨涎蛋白的表达被刺激,水平高于对照,表明所开发的支架为成骨提供了三维基质条件。在大鼠皮下进行的为期 4 周的体内初步研究表明,支架具有良好的组织相容性,细胞向内生长,并在支架的孔内和深处形成胶原组织,没有明显的炎症反应。总之,使用 RTILs 作为造孔剂的这种新方法被认为有助于开发用于组织再生的生物相容多孔聚合物支架。