Fabrication, modeling and optimization of lyophilized advanced platelet rich fibrin in combination with collagen-chitosan as a guided bone regeneration membrane

被引:19
作者
Ansarizadeh, Mohamadhasan [1 ]
Mashayekhan, Shohreh [1 ]
Saadatmand, Maryam [1 ]
机构
[1] Sharif Univ Technol, Dept Chem & Petr Engn, Tehran, Iran
关键词
Collagen membrane; Advanced platelet rich fibrin; Response surface methodology; GROWTH-FACTORS; A-PRF; DEGRADATION; PLASMA; EXTRACTION; SCAFFOLDS; DIFFERENTIATION; ANTIBACTERIAL; POROSITY; DEFECTS;
D O I
10.1016/j.ijbiomac.2018.12.078
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
In this study, lyophilized advanced platelet rich fibrin (A-PRF) was used in combination with collagen-chitosan membrane for the first time to combine advantages of both collagen and A-PRF membranes. Response surface methodology (RSM) was used to design the experimental condition and to correlate the effects of parameters, including chitosan/collagen (chit/col) weight ratio and A-PRF concentration on Young's modulus, mesenchymal stem cell (MSCs) viability and degradation rate of the membranes. Results showed that Young's modulus of the membranes was intensified by increasing chit/col weight ratio and decreasing A-PRF concentration from 3 to 8 MPa. Cell viability of MSCs was improved by both increasing chit/col weight ratio and A-PRF concentration. Moreover, as chit/col weight ratio increased from 0 to 4 and A-PRF concentration decreased from 5 to 0, degradation rate of the membranes decreased from 90 to 20% after four weeks incubation. Finally, based on Design Expert Software calculation for minimizing the degradation rate and maximizing both Young's modulus and cell viability, the values of chit/col weight ratio and A-PRF concentration were suggested to be 4 and 0.58 mg/ml, respectively. Alkaline phosphatase (ALP) activity analysis showed that the addition of A-PRF caused higher osteogenic differentiation. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:383 / 391
页数:9
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