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生物材料在动态流动环中的体外血栓形成性测试:测试样品长度和数量的影响。

In Vitro Thrombogenicity Testing of Biomaterials in a Dynamic Flow Loop: Effects of Length and Quantity of Test Samples.

作者信息

Jamiolkowski Megan A, Golding Madelyn D, Malinauskas Richard A, Lu Qijin

机构信息

U.S. Food and Drug Administration, Silver Spring, MD 20993.

出版信息

J Med Device. 2023 Sep 1;17(3):031003. doi: 10.1115/1.4062863. Epub 2023 Jul 25.

Abstract

The results of in vitro dynamic thrombogenicity testing of biomaterials and medical devices can be significantly impacted by test conditions. To develop and standardize a robust dynamic in vitro thrombogenicity tool, the key test parameters need to be appropriately evaluated and optimized. We used a flow loop test system previously developed in our laboratory to investigate the effects of sample length and the number of samples per test loop on the thrombogenicity results. Porcine blood heparinized to a donor-specific target concentration was recirculated at room temperature through polyvinyl chloride (PVC) tubing loops containing test materials for 1 h at 200 mL/min. Four test materials (polytetrafluoroethylene (PTFE), latex, PVC, and silicone) with various thrombotic potentials in two sample lengths (12 and 18 cm) were examined. For the 12-cm long materials, two different test configurations (one and two samples per loop) were compared. Thrombogenicity was assessed through percent thrombus surface coverage, thrombus weight, and platelet count reduction in the blood. The test system was able to effectively differentiate the thrombogenicity profile of the materials (latex > silicone > PVC ≥ PTFE) at all test configurations. Increasing test sample length by 50% did not significantly impact the test results as both 12 and 18 cm sample lengths were shown to equally differentiate thrombotic potentials between the materials. The addition of a second test sample to each loop did not increase the test sensitivity and may produce confounding results, and thus a single test sample per loop is recommended.

摘要

生物材料和医疗器械的体外动态血栓形成性测试结果会受到测试条件的显著影响。为了开发并标准化一个强大的体外动态血栓形成性工具,关键测试参数需要得到适当评估和优化。我们使用了先前在我们实验室开发的流动环路测试系统,来研究样品长度和每个测试环路中样品数量对血栓形成性结果的影响。将猪血液肝素化至供体特异性目标浓度,在室温下以200毫升/分钟的流速通过含有测试材料的聚氯乙烯(PVC)管环路循环1小时。对四种具有不同血栓形成潜力的测试材料(聚四氟乙烯(PTFE)、乳胶、PVC和硅酮)在两种样品长度(12厘米和18厘米)下进行了检测。对于12厘米长的材料,比较了两种不同的测试配置(每个环路一个和两个样品)。通过血栓表面覆盖率、血栓重量和血液中血小板计数减少来评估血栓形成性。该测试系统能够在所有测试配置下有效区分材料的血栓形成性概况(乳胶>硅酮>PVC≥PTFE)。将测试样品长度增加50%对测试结果没有显著影响,因为12厘米和18厘米的样品长度都能同样区分材料之间的血栓形成潜力。向每个环路添加第二个测试样品并没有提高测试灵敏度,且可能产生混杂结果,因此建议每个环路使用单个测试样品。

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