Alston Steven M, Solen Kenneth A, Broderick Adam H, Sukavaneshvar Sivaprasad, Mohammad S Fazal
Chemical Engineering Department, Brigham Young University, Provo, UT 84602, USA.
Transl Res. 2007 Apr;149(4):187-95. doi: 10.1016/j.trsl.2006.08.004.
Fibrin-based sealants are commonly employed to arrest bleeding after surgery. Usually, fibrinogen obtained from pooled human plasma is used to prepare sealants, with attendant risk of blood-borne infections. Availability of autologous fibrinogen would eliminate this risk. To prepare autologous fibrin sealant, fibrinogen was precipitated from human plasma using protamine. Under optimal conditions (10-mg/mL protamine and 22 degrees C), 96 +/- 4% of clottable fibrinogen was recovered by a simple and inexpensive technique. Nearly 50% of the plasma factor XIII was also recovered with the fibrinogen. Using bovine thrombin, the fibrinogen was clotted (1) in a specially designed mold to measure tensile strength and (2) in a lap joint between 2 aortic vessel strips to measure adhesion strength. Tensile and adhesion strengths increased with increasing fibrinogen concentration, and they were increased by the addition of calcium chloride. The addition of aprotinin and -aminocaproic acid to the fibrinogen concentrate before clotting had no effect on the mechanical properties of the clots. After adding thrombin to sealant containing 15-mg/mL fibrinogen, maximum tensile strength was achieved in 1-5 min, and maximum adhesion strength was reached in 5-15 min. For the sealant with 30-60-mg/mL fibrinogen and added calcium, the tensile strength was equivalent to that of the commercial fibrin sealant Tisseel. The adhesion strength of sealant with 30-60-mg/mL fibrinogen exceeded the adhesive strength of Tisseel under identical conditions. Autologous fibrin sealant is an attractive alternative to commercial sealants. It can be readily prepared from 5-mL plasma or more and exhibits mechanical properties equivalent to those of the leading commercial sealant.
纤维蛋白基密封剂常用于手术后止血。通常,从混合人血浆中获得的纤维蛋白原用于制备密封剂,存在血源感染的风险。自体纤维蛋白原的可用性将消除这种风险。为了制备自体纤维蛋白密封剂,使用鱼精蛋白从人血浆中沉淀纤维蛋白原。在最佳条件下(10mg/mL鱼精蛋白和22摄氏度),通过简单且廉价的技术可回收96±4%的可凝结纤维蛋白原。近50%的血浆因子XIII也与纤维蛋白原一起被回收。使用牛凝血酶,将纤维蛋白原(1)在专门设计的模具中凝结以测量拉伸强度,(2)在两条主动脉血管条之间的搭接处凝结以测量粘附强度。拉伸强度和粘附强度随纤维蛋白原浓度的增加而增加,并且通过添加氯化钙而提高。在凝结前向纤维蛋白原浓缩物中添加抑肽酶和ε-氨基己酸对凝块的机械性能没有影响。向含有15mg/mL纤维蛋白原的密封剂中加入凝血酶后,在1-5分钟内达到最大拉伸强度,在5-15分钟内达到最大粘附强度。对于含有30-60mg/mL纤维蛋白原并添加钙的密封剂,其拉伸强度与商业纤维蛋白密封剂Tisseel相当。在相同条件下,含有30-60mg/mL纤维蛋白原的密封剂的粘附强度超过了Tisseel的粘附强度。自体纤维蛋白密封剂是商业密封剂的一种有吸引力的替代品。它可以很容易地从5mL或更多的血浆中制备出来,并且其机械性能与领先的商业密封剂相当。