共 39 条
Optimization of a Plasma Rich in Growth Factors Membrane for the Treatment of Inflammatory Ocular Diseases
被引:5
作者:

Anitua, Eduardo
论文数: 0 引用数: 0
h-index: 0
机构:
Biotechnol Inst BTI, Regenerat Med Lab, Vitoria 01007, Spain Biotechnol Inst BTI, Regenerat Med Lab, Vitoria 01007, Spain

de la Fuente, Maria
论文数: 0 引用数: 0
h-index: 0
机构:
Biotechnol Inst BTI, Regenerat Med Lab, Vitoria 01007, Spain Biotechnol Inst BTI, Regenerat Med Lab, Vitoria 01007, Spain

Merayo-Lloves, Jesus
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Oviedo, Fdn Invest Oftalmol, Inst Oftalmol Fernandez Vega, Oviedo 33012, Spain Biotechnol Inst BTI, Regenerat Med Lab, Vitoria 01007, Spain

Muruzabal, Francisco
论文数: 0 引用数: 0
h-index: 0
机构:
Biotechnol Inst BTI, Regenerat Med Lab, Vitoria 01007, Spain Biotechnol Inst BTI, Regenerat Med Lab, Vitoria 01007, Spain
机构:
[1] Biotechnol Inst BTI, Regenerat Med Lab, Vitoria 01007, Spain
[2] Univ Oviedo, Fdn Invest Oftalmol, Inst Oftalmol Fernandez Vega, Oviedo 33012, Spain
来源:
BIOENGINEERING-BASEL
|
2022年
/
9卷
/
10期
关键词:
plasma rich in growth factors;
platelet rich plasma;
PRP;
ocular surface diseases;
autoimmune diseases;
complement system;
heat inactivation;
fibrin membrane;
D O I:
10.3390/bioengineering9100508
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
The main purpose of the present study is to develop an immunosafe fibrin membrane obtained by plasma rich in growth factors technology (is-mPRGF) with improved mechanical properties that could be applied in patients with inflammatory ocular diseases. Blood was drawn from three healthy donors and centrifuged, and the collected PRGF was activated and distributed into two groups: (i) mPRGF: a PRGF membrane maintained at 37 degrees C for 30 min; (ii) IS5+30: mPRGF incubated at 37 degrees C for 5 min and then incubated at 56 degrees C for 30 min. The content of both membranes was analyzed for several growth factors such as IgE and the complement activation, as well as biological activity on different ocular surface cells. Furthermore, the physical and mechanical characterizations were also evaluated. IS5+30 completely reduced the complement activity and decreased the IgE while preserving the concentration of the main growth factors. IS5+30 induced similar biological activity regarding mPRGF on the different ocular surface cells analyzed. Furthermore, no significant differences in release kinetics or fibrin degradation were observed between both membranes. Summarizing, IS5+30 totally reduces complement activity while preserving the concentration of most growth factors and their biological activity. Furthermore, the physical and mechanical properties of the fibrin membrane are preserved after heat inactivation.
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