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T-prep24的开发与性能评估:一种基于硅胶磁珠的新型自动化核酸提取系统

Development and Performance Evaluation of T-prep24: A Novel Automated Nucleic Acid Extraction System Based on Silica Magnetic Beads.

作者信息

Park Jung Ho, Kwak Naeun, Kim Dokyun, Chae Jong-Chan, Jeong Seok Hoon

机构信息

Division of Biotechnology, Jeonbuk National University, Iksan 54596, Republic of Korea.

BioPark Diagnostics Inc., Seoul 01809, Republic of Korea.

出版信息

Diagnostics (Basel). 2025 Jun 16;15(12):1528. doi: 10.3390/diagnostics15121528.

Abstract

Rapid molecular detection of infectious pathogen with high sensitivity and specificity has become increasingly important in clinical microbiology laboratories. The need to develop domestically produced nucleic acid extraction equipment has grown since COVID-19 pandemic in South Korea. In this study, we developed a new magnetic bead-based automated nucleic acid extraction system, T-Prep24 system, and the performance of the new system was evaluated with many clinical specimens. A total of 180 respiratory specimens were collected, and nucleic acids were extracted using three different systems, the T-Prep24 system, TANBead system, and Qiagen system. The quality and concentration of extracted nucleic acid were evaluated by spectrophotometer and Qubit fluorometer. Qualitative determination for SARS-CoV-2 was performed by PowerChek SARS-CoV-2 Real-time PCR kit. The median concentration of nucleic acid extracted by T-Prep24 system and measured by a fluorescence-based method was 0.685 ng/µL (first to third interquartile range, 0.258-1.493 ng/µL), which was lower than that of nucleic acid extracted by TANBead system (median value, 0.985 ng/µL; first to third interquartile range, 0.610-1.583 ng/µL; < 0.001), and that of nucleic acid extracted by Qiagen system (median value, 4.710 ng/µL; first to third interquartile range, 3.783-5.810 ng/µL; < 0.001). The Cq values of PCR assays using nucleic acid extracted by T-prep24 showed minimal systematic bias (slope = 1.015) when compared with those using nucleic acid extracted by TANBead, but significant proportional constant bias (slope = 0.907) when compared with those using nucleic acid extracted by Qiagen. The results of PCR assays using nucleic acid extracted by the T-Prep24 system were identical to those of PCR assays using nucleic acid extracted by TANBead system, and two discrepant results were identified when comparing with those by the Qiagen system. T-Prep24 system is a reliable and effective tool for nucleic acid extraction in clinical settings. Future investigations should be carried out to widen the applicability to a range of pathogens and sample types.

摘要

在临床微生物学实验室中,对感染性病原体进行快速、高灵敏度和高特异性的分子检测变得越来越重要。自韩国爆发新冠疫情以来,开发国产核酸提取设备的需求日益增长。在本研究中,我们开发了一种基于磁珠的新型自动化核酸提取系统——T-Prep24系统,并使用多种临床标本对该新系统的性能进行了评估。共收集了180份呼吸道标本,并使用三种不同的系统——T-Prep24系统、TANBead系统和Qiagen系统提取核酸。通过分光光度计和Qubit荧光计评估提取核酸的质量和浓度。使用PowerChek SARS-CoV-2实时荧光定量PCR试剂盒对新型冠状病毒进行定性测定。采用基于荧光的方法测量,T-Prep24系统提取的核酸中位数浓度为0.685 ng/µL(第一至第三四分位数范围,0.258 - 1.493 ng/µL),低于TANBead系统提取的核酸浓度(中位数为0.985 ng/µL;第一至第三四分位数范围,0.610 - 1.583 ng/µL;P < 0.001),也低于Qiagen系统提取的核酸浓度(中位数为4.710 ng/µL;第一至第三四分位数范围,3.783 - 5.810 ng/µL;P < 0.001)。与使用TANBead系统提取的核酸相比,使用T-Prep24系统提取的核酸进行PCR检测的Cq值显示出最小的系统偏差(斜率 = 1.015),但与使用Qiagen系统提取的核酸相比,存在显著的比例常数偏差(斜率 = 0.907)。使用T-Prep24系统提取的核酸进行PCR检测的结果与使用TANBead系统提取的核酸进行PCR检测的结果相同,与Qiagen系统相比,发现有两个结果不一致。T-Prep24系统是临床环境中核酸提取的可靠有效工具。未来应开展进一步研究,以扩大其对一系列病原体和样本类型的适用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/073e/12191882/ea5c310a6e02/diagnostics-15-01528-g001.jpg

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