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[基于标记基因的强心丸生物活性一致性评价]

[Bioactive consistency evaluation of cardiotonic pill using marker genes].

作者信息

Sun Wan-yang, Tong Ling, Li Dong-xiang, Bi Kai-shun

出版信息

Yao Xue Xue Bao. 2016 Aug;51(8):1290-6.

Abstract

The study is aimed to develop a method in evaluation of the bioactive consistency of cardiotonic pill (CP). HepG2 cell line was employed as a biological detector. After treated with CP for 24 h, gene chip and qRT-PCR were used to select m RNAs that can represent the bioactivity of CP. Then similarity between different batches of CP were calculated based on expression levels of marker genes to evaluate the bioactive consistency of CP. Marker genes were selected according to the criteria as follows: 1 fold change < 0.67 or > 1.5; 2 potential relevance to curative effects; 3 extensive involvement in the cellular functions and clustering analysis categories; 4 dose-dependent effect. A total of 10 genes were selected as bioactive markers of CP. Angular cosine was calculated to evaluate the similarity between two samples. The method was validated using intra-day precision and inter-day precision. Using angular cosine similarity, the intra-day and inter-day precision were 0.4% and 0.6%, respectively. The similarities of 6 batches of CDPs ranged from 0.992 to 0.999, and 1 batch of Compound Danshen Tablet was 0.534. The established method is specific and accurate, and provides comprehensive and objective evaluation of bioactive quality of CDPs. It can also benefit the bioactive consistency evaluation of other compounds in traditional Chinese medicines.

摘要

本研究旨在建立一种评价强心丸(CP)生物活性一致性的方法。采用HepG2细胞系作为生物检测器。用CP处理24小时后,使用基因芯片和qRT-PCR筛选能够代表CP生物活性的mRNA。然后根据标记基因的表达水平计算不同批次CP之间的相似度,以评价CP的生物活性一致性。标记基因根据以下标准选择:1. 变化倍数<0.67或>1.5;2. 与疗效潜在相关;3. 广泛参与细胞功能和聚类分析类别;4. 剂量依赖性效应。共选择10个基因作为CP的生物活性标记物。计算角余弦以评估两个样品之间的相似度。该方法通过日内精密度和日间精密度进行验证。使用角余弦相似度,日内和日间精密度分别为0.4%和0.6%。6批次CP的相似度范围为0.992至0.999,1批次复方丹参片的相似度为0.534。所建立的方法具有特异性和准确性,为CP的生物活性质量提供了全面客观地评价。它也有助于中药中其他化合物的生物活性一致性评价。

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