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使用早熟染色体凝聚试验进行辐射剂量测定,构建6兆伏直线加速器X射线的剂量反应曲线。

Construction of dose response curve for 6 MV LINAC X-rays using Premature Chromosome Condensation assay for radiation dosimetry.

作者信息

Meenakshi C, Venkatachalam P, Chandrasekaran S, Venkatraman B

机构信息

Human Genetics Department, Sri Ramachandra Institute of Higher Education and Research, Chennai, Tamilnadu, India.

Human Genetics Department, Sri Ramachandra Institute of Higher Education and Research, Chennai, Tamilnadu, India.

出版信息

Appl Radiat Isot. 2021 Jul;173:109729. doi: 10.1016/j.apradiso.2021.109729. Epub 2021 Apr 18.

Abstract

Quantification of chromosomal aberrations in the exposed personnel blood samples is considered as a 'gold standard' and sensitive biomarker in biological dosimetry. Despite technological developments, culture of cells for 48-52 h remains an unmet need in case of triage biodosimetry. Moreover, it is difficult to get sufficient number of metaphase spreads for scoring after high doses of exposures. The technique which causes condensation of chromatin before mitosis using biological or chemical agent is named as Premature Chromosome Condensation (PCC) assay. This assay is considered as an alternative to chromosome aberration assay, particularly at high acute doses of low and high LET radiation. To establish the PCC assay, blood samples were collected from healthy non-smoking individuals (n = 3) and exposed to various doses (0-20 Gy) of 6 MV X-rays at a dose rate of 5.6 Gy/min, using a high energy Linear accelerator (LINAC). Irradiated blood samples were subjected to Calyculin-A induced PCC. About 500 cells or more than 100 Ring Chromosomes (RC) were scored at each dose. Dicentric chromosomes (DC) and acentric fragments were also scored at each dose; the number of chromosomal aberrations in G1, M, G2/M and M/A phase of cell cycle were recorded and the frequency was used to construct the dose response curve. A dose dependent increase in RC and DC frequency were observed with a slope of 0.049 ± 0.002 and 0.30 ± 0.02 respectively. This study is first of its kind to construct a dose response curve for LINAC X-rays using a PCC assay.

摘要

对受照人员血液样本中的染色体畸变进行定量分析,被视为生物剂量测定中的“金标准”和敏感生物标志物。尽管技术不断发展,但在进行分流生物剂量测定时,培养细胞48 - 52小时的需求仍未得到满足。此外,在高剂量照射后,很难获得足够数量的中期分裂相进行评分。利用生物或化学试剂在有丝分裂前使染色质浓缩的技术,被称为早熟染色体浓缩(PCC)试验。该试验被认为是染色体畸变试验的一种替代方法,特别是在低线性能量传递(LET)和高线性能量传递辐射的高急性剂量情况下。为建立PCC试验,从健康非吸烟个体(n = 3)采集血液样本,使用高能直线加速器(LINAC),以5.6 Gy/min的剂量率,使其暴露于不同剂量(0 - 20 Gy)的6 MV X射线下。对辐照后的血液样本进行Calyculin - A诱导的PCC处理。在每个剂量下对约500个细胞或100多个环状染色体(RC)进行评分。在每个剂量下还对双着丝粒染色体(DC)和无着丝粒片段进行评分;记录细胞周期G1、M、G2/M和M/A期的染色体畸变数量,并使用该频率构建剂量反应曲线。观察到RC和DC频率呈剂量依赖性增加,斜率分别为0.049±0.002和0.30±0.02。本研究首次使用PCC试验构建了LINAC X射线的剂量反应曲线。

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