Construction and biocompatibility of a thin type I/II collagen composite scaffold

• Published in: Cell and tissue banking 2018-03, Vol.19 (1), p.47-59
• Main Authors: Han, Long, Zhang, Zhong-wen, Wang, Bo-he, Wen, Zhen-kun
• Format: Article
• Language: English
• Subjects: Absorption; Biocompatibility; Biomedical and Life Sciences; Biomedicine; Carbodiimide; Cartilage (articular); Cell Biology; Chondrocytes; Collagen; Collagen (type I); Collagen (type II); Collagenase; Composite materials; Compression; Compressive strength; Construction; Cross-linking; Electron microscopy; Femur; Gel electrophoresis; Injuries; Knee; Lesions; Life Sciences; Scanning electron microscopy; Sodium; Sodium lauryl sulfate; Tissue engineering; Transplant Surgery; Ultraviolet absorption; Vacuum
• ISSN: 1389-9333; 1573-6814
• DOI: 10.1007/s10561-017-9653-2

Articular cartilage injury is a common type of damage observed in clinical practice. A matrix-induced autologous chondrocyte implant was developed to repair articular cartilage as an advancement on the autologous chondrocyte implant procedure. Here, we establish a thin double layer of collagen as a novel and effective bioscaffold for the regeneration of cartilaginous lesions. We created a collagen membrane with double layers using a cover slip, a cover slip, and the collagen was then freeze-dried under vacuum. Carbodiimide as a crosslinking agent was used to obtain a relatively stable collagen construction. The thickness of the knee joint cartilage from grown rabbits was measured from a frozen section. Both type I and type II collagens were characterized using Sodium dodecylsulfate/polyacrylamide gel electrophoresis (SDS-PAGE) and ultraviolet absorption peaks. The aperture size of the scaffold was observed using a scanning electron microscope (SEM). The degradation of the scaffolds in vitro was tested through digestion using collagenase solution. The mechanical capacity of the scaffolds was assessed under dynamic compression. The influence of the scaffold on chondrocyte proliferation was assessed using the methyl thiazolyl tetrazolium (MTT) colourimetric assay and scanning electron microscopy. The frozen sections of the rabbit femoral condyle showed that the thickness of the weight-bearing area of the articular cartilage was less than 1 mm. The results of the SDS-PAGE and ultraviolet absorption peaks of the collagens were in agreement with the standard photographs in the references. SEM showed that the aperture size of the cross-linked scaffold was 82.14 ± 15.70 μm. The in vitro degradation studies indicated that Carbodiimide cross-linking can effectively enhance the biostability of the scaffolds. The Carbodiimide cross-linking protocol resulted in a mean value for the samples that ranged from 8.72 to 15.95 MPa for the compressive strength. The results of the MTT demonstrated that the scaffold had promoted chondrocyte proliferation and SEM observations showed that the scaffold was a good adhesive and growth material for chondrocytes. Thin type I/II collagen composite scaffold can meet the demands of cartilage tissue engineering and have good biocompatibility.