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首页> 外文期刊>Vox Sanguinis: International Journal of Blood Transfusion and Immunohaematology >In-vitro evaluation of the PALL Leukotrap Affinity Prion Reduction Filter as a secondary device following primary leucoreduction.
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In-vitro evaluation of the PALL Leukotrap Affinity Prion Reduction Filter as a secondary device following primary leucoreduction.

机译:体外评价笼罩Leukotrap亲和力朊病毒减少过滤器作为二次设备以下主要leucoreduction。

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Background and Objectives A filter (PRF1) designed to remove abnormal prion proteins from red-cell units has been developed. The purpose of this study was to evaluate the quality of red cells produced using this device. Materials and Methods Leucocyte-depleted red-cell units (CPD, CPD-A1 and CPD/SAGM) processed according to standard UK practices were filtered using PRF1. Filtered and control units were stored and sampled on day 1, day 7 and on the date of expiry and were tested using standard measures of red-cell quality. Results Filtered units were found to have significantly higher percentage haemolysis levels, lower haemoglobin levels and a smaller volume compared with controls. All results, however, were well within the permitted 0.8% haemolysis level at the end of storage and all units met the UK guidelines for haemoglobin and volume. The other test parameters measured showed no significant differences between the test and control units. Conclusions The PRF1 filter was found to be easy to use and resulted in red-cell units that met all relevant UK and European Guidelines.
机译:设计背景和目标一个过滤器(PRF1)删除从红细胞异常朊病毒蛋白质单位了。研究是对红细胞的质量进行评估用这个设备的。Leucocyte-depleted红细胞单位(CPD, CPD-A1和CPD / SAGM)根据英国标准处理实践是使用PRF1过滤。控制单元是存储和采样1天,第七天,到期日期和测试使用标准红细胞质量的措施。结果过滤单元被发现比例明显高于溶血血红蛋白水平较低的水平,和一个更小的量与控制。然而,在允许的0.8%红血球溶解级别的存储和所有单位遇到英国血红蛋白和指南体积。测试和之间没有显著差异控制单元。发现是易于使用和导致红细胞单位,符合所有相关的英国和欧洲指导方针。

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