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采用体外核磁共振协议的多中心试验。欧洲经济共同体联合研究项目。

Multi-center trial with an in vitro NMR protocol. EEC Concerted Research Project.

作者信息

Mathur-De Vré R, Binet J, Bovée W M, Foster M A

机构信息

Institut d'Hygiene et d'Epidemiologie, Brussels, Belgium.

出版信息

Magn Reson Imaging. 1988 Mar-Apr;6(2):185-94. doi: 10.1016/0730-725x(88)90449-3.

Abstract

The EEC Protocol for in vitro measurement of T1 and T2 presented in paper II of this series was tested in 15 centers on a variety of instruments. This article discusses the results of this protocol trial using biological samples (rat liver and thigh muscle) and two reference gel samples. Each reference gel was prepared as a single batch, dispensed into appropriate sample tubes and sent to all participants. Details of instrument types and operating conditions are given, along with measurement frequencies and temperatures and the results of precision testing. The relaxation time measurements from the gels for the trial are compared with temperature and frequency effects examined in independent centers under similar conditions. The relaxation time values for biological tissues are examined in the light of the scatter of such values in the general literature. To check the effects of data analysis methods on relaxation times, full relaxation data for one reference sample was provided by each group. This was re-analyzed in three centers using different methods; these results are compared with the values calculated by each group using its own method. In general, the results from different groups show good consistency with the reference values. The use of this Protocol has helped reduce scatter in results from biological samples and has provided information for improvement of individual operating conditions and improvement of the protocol to its final form.

摘要

本系列论文第二篇中介绍的用于体外测量T1和T2的欧洲经济共同体(EEC)方案,在15个中心使用各种仪器进行了测试。本文讨论了使用生物样本(大鼠肝脏和大腿肌肉)以及两种参考凝胶样本进行该方案试验的结果。每种参考凝胶均作为单一批次制备,分装到合适的样本管中,并发送给所有参与者。文中给出了仪器类型和操作条件的详细信息,以及测量频率、温度和精密度测试结果。将试验中凝胶的弛豫时间测量结果与在类似条件下独立中心研究的温度和频率效应进行比较。根据一般文献中此类值的离散情况,对生物组织的弛豫时间值进行研究。为检查数据分析方法对弛豫时间的影响,每个小组提供了一个参考样本的完整弛豫数据。在三个中心使用不同方法对其进行重新分析;将这些结果与每个小组使用自身方法计算的值进行比较。总体而言,不同小组的结果与参考值显示出良好的一致性。该方案的使用有助于减少生物样本结果的离散性,并为改善个体操作条件以及将方案完善至最终形式提供了信息。

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