McManus Michael C, Boland Eugene D, Koo Harry P, Barnes Catherine P, Pawlowski Kristin J, Wnek Gary E, Simpson David G, Bowlin Gary L
Department of Surgery, Virginia Commonwealth University, Richmond, 23298-0230, USA.
Acta Biomater. 2006 Jan;2(1):19-28. doi: 10.1016/j.actbio.2005.09.008. Epub 2005 Nov 22.
Fibrin and fibrinogen have a well-established track record in tissue engineering due to their innate ability to induce improved cellular interaction and subsequent scaffold remodeling compared to synthetic scaffolds. Use of fibrinogen as a primary scaffold component, however, has been limited by traditional processing techniques that render scaffolds with insufficient mechanical properties. The goal of this study was to demonstrate, based on mechanical properties, that electrospun fibrinogen overcomes these limitations and can be successful as a tissue engineering scaffold or wound dressing. Electrospun fibrinogen scaffolds were characterized for fiber diameter and pore area and subsequently tested for uniaxial mechanical properties while dry and hydrated. In addition, uniaxial mechanical testing was conducted on scaffolds treated to regulate scaffold degradation in serum-containing media by supplementing the media with aprotinin or cross-linking the scaffolds with glutaraldehyde vapor. A linear relationship between electrospinning solution concentration and measured fiber diameter was seen; fiber diameters ranged from 120 to 610 nm over electrospinning concentrations of 80 to 140 mg/ml fibrinogen, respectively. Pore areas ranged from 1.3 microm(2) to 13 microm(2) over the same fibrinogen concentrations. Aprotinin in the culture media inhibited scaffold degradation in a predictable fashion, but glutaraldehyde vapor fixation produced less reliable results as evidenced by mechanical property testing. In conclusion, the mechanical characteristics of electrospun fibrinogen strongly support its potential use as a tissue engineering scaffold or wound dressing.
与合成支架相比,纤维蛋白和纤维蛋白原在组织工程领域有着良好的记录,因为它们具有诱导改善细胞相互作用以及随后支架重塑的内在能力。然而,将纤维蛋白原用作主要支架成分受到传统加工技术的限制,这些技术使支架的机械性能不足。本研究的目的是基于机械性能证明,电纺纤维蛋白原克服了这些限制,并且可以成功用作组织工程支架或伤口敷料。对电纺纤维蛋白原支架进行纤维直径和孔隙面积表征,随后在干燥和水合状态下测试其单轴机械性能。此外,通过在含血清培养基中添加抑肽酶或用戊二醛蒸汽交联支架来处理支架,以调节支架在含血清培养基中的降解,并对其进行单轴机械测试。观察到电纺溶液浓度与测得的纤维直径之间存在线性关系;在80至140mg/ml纤维蛋白原的电纺浓度范围内,纤维直径分别为120至610nm。在相同的纤维蛋白原浓度范围内,孔隙面积为1.3平方微米至13平方微米。培养基中的抑肽酶以可预测的方式抑制支架降解,但戊二醛蒸汽固定产生的结果不太可靠,机械性能测试证明了这一点。总之,电纺纤维蛋白原的机械特性有力地支持了其作为组织工程支架或伤口敷料的潜在用途。