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用于组织工程的具有原位成孔功能的可注射聚乳酸-乙醇酸共聚物支架。

Injectable poly(lactic-co-glycolic) acid scaffolds with in situ pore formation for tissue engineering.

作者信息

Krebs Melissa D, Sutter Kathleen A, Lin Angela S P, Guldberg Robert E, Alsberg Eben

机构信息

Biomedical Engineering, Case Western Reserve University, Cleveland, OH, USA.

出版信息

Acta Biomater. 2009 Oct;5(8):2847-59. doi: 10.1016/j.actbio.2009.04.035. Epub 2009 May 4.

Abstract

Appropriate porosity is an important biomaterial design criterion for scaffolds used in tissue engineering applications as it can permit increased cell adhesion, migration, proliferation and extracellular matrix production within the scaffold at a tissue defect site. Tissue engineering scaffolds can either be injected in a minimally invasive manner or implanted through surgical procedures. Many injectable scaffolds are hydrogel-based; these materials often possess nanoscale porosity, which is suboptimal for cell migration and proliferation. Solid scaffolds with engineered micron-scale porosity are widely used, but these scaffolds are usually pre-formed and then must be implanted. Here we report on the development of a solid, injectable, biomaterial scaffold that solidifies in situ via phase inversion with microporous, interconnected architecture on the surface and within the bulk. This injectable system utilizes the biodegradable polymer poly(lactic-co-glycolic acid), a nontoxic FDA-approved solvent, and biocompatible porogens. Various scaffold formulations are examined in terms of morphology, porosity, degradation, elastic modulus, and ability to support cellular adhesion and growth. Furthermore, the ability to form a microporous architecture upon injection in vivo is verified. This technology is a promising noninvasive approach for in vivo formation of porous biodegradable scaffolds.

摘要

合适的孔隙率是组织工程应用中支架材料的一个重要生物材料设计标准,因为它能在组织缺损部位的支架内促进细胞黏附、迁移、增殖以及细胞外基质的产生。组织工程支架既可以通过微创方式注射,也可以通过外科手术植入。许多可注射支架是以水凝胶为基础的;这些材料通常具有纳米级孔隙率,这对于细胞迁移和增殖来说并不理想。具有工程化微米级孔隙率的固体支架被广泛使用,但这些支架通常是预先成型的,然后必须进行植入。在此,我们报告一种固体、可注射生物材料支架的研发情况,该支架通过相转变原位固化,在表面和内部具有微孔相互连通的结构。这种可注射系统利用了可生物降解的聚乳酸-羟基乙酸共聚物、一种无毒且经美国食品药品监督管理局批准的溶剂以及生物相容性致孔剂。对各种支架配方在形态、孔隙率、降解、弹性模量以及支持细胞黏附和生长的能力方面进行了研究。此外,还验证了在体内注射时形成微孔结构的能力。这项技术是一种很有前景的用于在体内形成多孔可生物降解支架的非侵入性方法。

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