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A method to measure thrombin activity in a mixture of fibrinogen and thrombin powders

机译:一种测定纤维蛋白原和凝血酶粉末混合物中凝血酶活性的方法

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摘要

Thrombin and fibrinogen powders are the active components of advanced surgical hemostasis products including the EVARREST Fibrin Sealant Patch. Measuring the enzymatic activity of thrombin in the presence of fibrinogen is challenging, as hydration of the powders in a neutral aqueous environment will cause the enzyme to rapidly react with the fibrinogen to form a fibrin clot, which in turn binds and entraps the enzyme thus preventing subsequent measurement of thrombin activity. A novel approach has been developed to overcome this challenge. After isolation of the mixture of powders, an alkaline carbonate solution is used to solubilize the proteins, while reversibly inhibiting the activity of thrombin and preventing clot formation. Once the powders have been fully solubilized, thrombin activity can be restored by neutralization in a buffered fibrinogen solution resulting in fibrin clot formulation. The rate of clot formation can be quantified in a coagulometer to determine the thrombin activity of the original powder. Samples coated with powders containing fibrinogen and varying amounts of thrombin were tested using the method described herein. The results demonstrated that the method could consistently measure the activity of (alpha) thrombin in the presence of fibrinogen over a broad range of thrombin activity levels. The test was successfully validated according to International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use Guidelines and thus is suitable for use as part of a commercial manufacturing process. A method has been developed that enables thrombin activity to be measured in a mixture of fibrinogen and thrombin powders.
机译:凝血酶和纤维蛋白原粉是包括EVARREST纤维蛋白密封胶在内的先进外科止血产品的活性成分。在纤维蛋白原存在的情况下测量凝血酶的酶活性具有挑战性,因为粉末在中性水性环境中的水合会导致酶与纤维蛋白原快速反应形成纤维蛋白凝块,进而凝结并截留酶,从而防止随后测量凝血酶活性。已经开发出一种新颖的方法来克服这一挑战。分离粉末混合物后,使用碱性碳酸盐溶液溶解蛋白质,同时可逆地抑制凝血酶的活性并防止血凝块形成。粉末完全溶解后,可通过在缓冲的纤维蛋白原溶液中进行中和来恢复凝血酶活性,从而形成纤维蛋白凝块。凝块形成的速率可以在血凝仪中定量以确定原始粉末的凝血酶活性。使用本文所述的方法测试涂覆有含有纤维蛋白原和变化量的凝血酶的粉末的样品。结果表明,该方法可以在纤维蛋白原存在的情况下,在很宽的凝血酶活性水平范围内连续测量α凝血酶的活性。该测试已根据国际药品注册人用技术要求统一准则指南成功验证,因此适合用作商业生产过程的一部分。已经开发出一种能够在纤维蛋白原和凝血酶粉末的混合物中测量凝血酶活性的方法。

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