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用于测量肿瘤坏死因子α的血样的最佳采集方法

Optimal collection of blood samples for the measurement of tumor necrosis factor alpha.

作者信息

Exley A R, Cohen J

机构信息

Department of Bacteriology, Hammersmith Hospital, London, UK.

出版信息

Cytokine. 1990 Sep;2(5):353-6. doi: 10.1016/1043-4666(90)90065-2.

Abstract

We have examined how delayed separation of plasma from cells affects the recovery of recombinant human tumor necrosis factor alpha (rhTNF alpha) from whole blood. Storage of heparinized whole blood samples at room temperature for 1 hr results in a significant (p = 0.036) fall in recovery of plasma TNF alpha from 788 +/- 119 pg/mL to 472 +/- 77 pg/mL, measured by specific enzyme-linked immunosorbent assay (ELISA). Storage of whole blood samples at 4 degrees C for 1 hr reduces but does not prevent the fall in recovery of plasma TNF alpha: 725 +/- 82 pg/mL at time 0, 472 +/- 81 pg/mL after 1 hr, p = 0.038. Recovery of bioactive TNF alpha (cytotoxocity for L929 cells) after 1 hr at room temperature is also significantly reduced from 576 +/- 139 pg/mL to 450 +/- 154 pg/mL, p = 0.036. Studies with 125I-rhTNF alpha confirmed the fall in plasma activity and revealed a rapid commensurate increase in 125I-rhTNF alpha activity in the cell fractions. We recommend that clinical samples for the measurement of cytokines should be kept at 4 degrees C and separated rapidly (within half an hour) before storing the plasma at -70 degrees C.

摘要

我们研究了血浆与细胞延迟分离对从全血中回收重组人肿瘤坏死因子α(rhTNFα)的影响。将肝素化全血样本在室温下储存1小时,通过特异性酶联免疫吸附测定(ELISA)测量,血浆TNFα回收率从788±119 pg/mL显著下降(p = 0.036)至472±77 pg/mL。将全血样本在4℃下储存1小时可减少但不能阻止血浆TNFα回收率的下降:初始时为725±82 pg/mL,1小时后为472±81 pg/mL,p = 0.038。在室温下放置1小时后,生物活性TNFα(对L929细胞的细胞毒性)回收率也从576±139 pg/mL显著降低至450±154 pg/mL,p = 0.036。对125I-rhTNFα的研究证实了血浆活性的下降,并揭示了细胞组分中125I-rhTNFα活性迅速相应增加。我们建议,用于测量细胞因子的临床样本应保存在4℃,并在半小时内迅速分离,然后将血浆储存在-70℃。

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