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用于放射免疫分析的样本中促红细胞生成素稳定性的评估。

Evaluation of the stability of human erythropoietin in samples for radioimmunoassay.

作者信息

Eckardt K U, Kurtz A, Hirth P, Scigalla P, Wieczorek L, Bauer C

机构信息

Physiologisches Institut der Universität Zürich.

出版信息

Klin Wochenschr. 1988 Mar 15;66(6):241-5. doi: 10.1007/BF01748163.

Abstract

Radioimmunoassays for erythropoietin are limited so far to a few specialized laboratories and this requires transport and storage of samples. We therefore tested the stability of immunoreactive erythropoietin in serum and plasma samples obtained from a uremic and a nonuremic anemic patient. No significant change in the concentration of immunoreactive erythropoietin was found in either serum or plasma samples for up to 14 days of storage. This type of stability was observed no matter whether the samples were stored at room temperature, 4 degrees C, or -20 degrees C. There was no difference between the estimates of erythropoietin in serum and heparinized plasma. Validity of the radioimmunoassay used in this study was demonstrated by parallelism of dilution curves of test specimens and the 2nd International Reference Preparation for erythropoietin and by a close correlation between the immunoreactivity and the bioactivity of the hormone, as assessed in the same samples by the exhypoxic polycythemic mouse bioassay. In conclusion the data obtained clearly indicate that the necessity of storage and transport of clinical samples does not limit the practicability of the radioimmunoassay for erythropoietin.

摘要

目前,促红细胞生成素的放射免疫测定仅限于少数专业实验室,这就需要对样本进行运输和储存。因此,我们检测了从一名尿毒症贫血患者和一名非尿毒症贫血患者采集的血清和血浆样本中免疫反应性促红细胞生成素的稳定性。在储存长达14天的血清或血浆样本中,未发现免疫反应性促红细胞生成素浓度有显著变化。无论样本是储存在室温、4℃还是-20℃,均观察到这种稳定性。血清和肝素化血浆中促红细胞生成素的测定结果没有差异。本研究中使用的放射免疫测定的有效性通过测试标本与促红细胞生成素第二国际参考制剂的稀释曲线平行以及通过低氧性红细胞增多症小鼠生物测定法在相同样本中评估的激素免疫反应性与生物活性之间的密切相关性得到证明。总之,所获得的数据清楚地表明,临床样本储存和运输的必要性并不限制促红细胞生成素放射免疫测定的实用性。

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