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测定小鼠血清样本中的雌二醇:商业雌二醇免疫分析方法的评估。

Estimation of estradiol in mouse serum samples: evaluation of commercial estradiol immunoassays.

机构信息

Ligand Assay and Analysis Core Facility, University of Virginia Center for Research in Reproduction, Charlottesville, Virginia 22908, USA.

出版信息

Endocrinology. 2011 Nov;152(11):4443-7. doi: 10.1210/en.2011-1501. Epub 2011 Sep 20.

Abstract

The University of Virginia Center for Research in Reproduction Ligand Core performed an evaluation of nine commercial estradiol (E2) immunoassays for use with mouse serum. The evaluation had two components. 1) Recovery Studies: a mouse pool was spiked with E2 concentrations across the assay range, and percent recovery and parallelism to the assay standard curve were determined. 2) Correlation Studies: serum pools were collected from intact females, ovariectomized (OVX) and OVX-E2 treated mice and E2 assayed, then measured by gas chromatography/tandem mass spectrometry (GC/MSMS) for comparison to a gold standard method. Recovery results showed that E2 recovery from spiked mouse pools varied greatly (from <18% to >640%) among kits tested. However, three kits (DiaSorin Radioimmunoassay, Siemens Double Antibody RIA, and CalBiotech Enzyme Immunoassay) showed reasonable recoveries and parallelism. Data collected from the Correlation Study showed that values from intact, OVX and OVX-E2-treated mouse pools varied by several fold vs. GC/MSMS for most of the kits tested. The DiaSorin RIA and CalBiotech Enzyme Immunoassay Kits showed the best correlation to GC/MSMS. Unfortunately, while this evaluation was ongoing, the DiaSorin Kit was discontinued. In summary, the CalBiotech Kit was the only available assay tested that demonstrated good E2 parallelism to the assay standard curve and accuracy vs. a gold standard method (i.e. GC/MSMS). Also of note, the CalBiotech assay is sensitive and requires minimal sample volume. Therefore, based on these findings the CalBiotech E2 assay has been implemented for use in mouse serum samples within the Ligand Core.

摘要

弗吉尼亚大学研究生殖配体核心中心对九种商业雌二醇 (E2) 免疫分析试剂盒进行了评估,以用于检测小鼠血清。该评估包括两个部分。1)回收研究:用 E2 浓度跨越检测范围的小鼠池进行加标,确定回收率和与检测标准曲线的平行度。2)相关研究:从完整雌性、卵巢切除(OVX)和 OVX-E2 处理的小鼠中收集血清池,并进行 E2 检测,然后通过气相色谱/串联质谱(GC/MSMS)进行测量,与金标准方法进行比较。回收结果表明,在所测试的试剂盒中,E2 从加标小鼠池中的回收率差异很大(<18%至>640%)。然而,有三种试剂盒(DiaSorin 放射免疫分析、Siemens 双抗体 RIA 和 CalBiotech 酶免疫分析)显示出合理的回收率和平行度。相关性研究收集的数据表明,对于大多数测试的试剂盒,完整、OVX 和 OVX-E2 处理的小鼠池中的值与 GC/MSMS 相比差异了数倍。DiaSorin RIA 和 CalBiotech 酶免疫分析试剂盒与 GC/MSMS 的相关性最好。不幸的是,在进行此评估的同时,DiaSorin 试剂盒已停产。总之,在测试的可用试剂盒中,CalBiotech 试剂盒是唯一表现出与检测标准曲线良好的 E2 平行性和与金标准方法(即 GC/MSMS)准确性的试剂盒。值得注意的是,CalBiotech 测定法具有很高的灵敏度,并且需要最小的样本量。因此,基于这些发现,CalBiotech E2 测定法已在 Ligand Core 中用于检测小鼠血清样品。

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