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一次性微流控芯片中全血中革兰氏阳性和革兰氏阴性菌的细胞裂解和 DNA 提取。

Cell lysis and DNA extraction of gram-positive and gram-negative bacteria from whole blood in a disposable microfluidic chip.

机构信息

Department of Biomedical Engineering, Boston University, Boston, MA 02115, USA.

出版信息

Lab Chip. 2009 Oct 7;9(19):2811-7. doi: 10.1039/b905065p. Epub 2009 Jun 29.

Abstract

Sepsis caused by gram positive and gram negative bacteria is the leading cause of death in noncoronary ICUs and the tenth leading cause of death in the United States. We have developed a microfluidic sample preparation platform for rapid on-chip detection of infectious organisms for point-of-care diagnostics. The microfluidic chips are made of a robust thermoplastic and can be easily multiplexed for high throughput applications. Bacteria are lysed on-chip via hybrid chemical/mechanical method. Once lysed, the bacterial DNA is isolated using a microscale silica bead/polymer composite solid-phase-extraction (SPE) column. Lysis was confirmed using off-chip real time PCR. We isolated and detected both gram-negative (Escherichia coli) and gram-positive (Bacillussubtilis and Enterococcus faecalis) bacterial genomic DNA from microliter scale spiked whole human blood samples. The system performs better for gram-negative bacteria than it does for gram-positive bacteria, with limits of detection at 10(2) CFU/ml and 10(3)-10(4) CFU/ml, respectively. Total extraction times are less than one hour and can be further decreased by altering the channel geometry and pumping configuration.

摘要

革兰氏阳性菌和革兰氏阴性菌引起的败血症是非冠心病 ICU 患者死亡的主要原因,也是美国第十大死亡原因。我们开发了一种用于即时检测诊断的微生物芯片制备平台,用于快速检测传染性病原体。该微流控芯片由坚固的热塑性塑料制成,可以轻松地进行多重化以实现高通量应用。细菌通过混合化学/机械方法在芯片上裂解。一旦裂解,使用微尺度硅珠/聚合物复合固相萃取(SPE)柱分离细菌 DNA。通过离片实时 PCR 确认裂解。我们从微升级加标全血样本中分离并检测了革兰氏阴性(大肠杆菌)和革兰氏阳性(枯草芽孢杆菌和粪肠球菌)细菌的基因组 DNA。该系统对革兰氏阴性菌的检测效果优于革兰氏阳性菌,检测限分别为 10(2) CFU/ml 和 10(3)-10(4) CFU/ml。总提取时间不到一个小时,通过改变通道几何形状和泵送配置可以进一步缩短提取时间。

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