College of Science, China University of Petroleum (East China) , Qingdao, 266580, P. R. China.
Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), College of Chemistry and Molecular Sciences, Wuhan University , Wuhan 430072, P. R. China.
ACS Appl Mater Interfaces. 2017 Mar 22;9(11):9416-9425. doi: 10.1021/acsami.6b16831. Epub 2017 Mar 7.
Enrichment and purification of bacteria from complex matrices are crucial for their detection and investigation, in which magnetic separation techniques have recently show great application advantages. However, currently used magnetic particles all have their own limitations: Magnetic microparticles exhibit poor binding capacity with targets, while magnetic nanoparticles suffer slow magnetic response and high loss rate during treatment process. Herein, we used a highly controllable layer-by-layer assembly method to fabricate quick-response magnetic nanospheres (MNs), and with Salmonella typhimurium as a model, we successfully achieve their rapid and efficient enrichment. The MNs combined the advantages of magnetic microparticles and nanoparticles. On the one hand, the MNs had a fast magnetic response, and almost 100% of the MNs could be recovered by 1 min attraction with a simple magnetic scaffold. Hence, using antibody conjugated MNs (immunomagnetic nanospheres, IMNs) to capture bacteria hardly generated loss and did not need complex separation tools or techniques. On the other hand, the IMNs showed much excellent capture capacity. With 20 min interaction, almost all of the target bacteria could be captured, and even only one bacterium existing in the samples was not missed, comparing with the immunomagnetic microparticles which could only capture less than 50% of the bacteria. Besides, the IMNs could achieve the same efficient enrichment in complex matrices, such as milk, fetal bovine serum, and urine, demonstrating their good stability, strong anti-interference ability, and low nonspecific adsorption. In addition, the isolated bacteria could be directly used for culture, polymerase chain reaction (PCR) analyses, and fluorescence immunoassay without a release process, which suggested our IMNs-based enrichment strategy could be conveniently coupled with the downstream identification and analysis techniques. Thus, the MNs provided by this work showed great superiority in bacteria enrichment, which would be a promising tool for bacteria detection and investigation.
从复杂基质中富集和纯化细菌对于它们的检测和研究至关重要,在这方面,磁性分离技术最近显示出了巨大的应用优势。然而,目前使用的磁性颗粒都有各自的局限性:磁性微球与目标的结合能力较差,而磁性纳米颗粒在处理过程中表现出缓慢的磁响应和高损失率。在此,我们使用一种高度可控的层层组装方法来制备快速响应的磁性纳米球(MNs),并以鼠伤寒沙门氏菌为模型,成功地实现了它们的快速高效富集。MNs 结合了磁性微球和纳米颗粒的优点。一方面,MNs 具有快速的磁响应,通过简单的磁支架 1 分钟的吸引,几乎 100%的 MNs 可以被回收。因此,使用抗体偶联的 MNs(免疫磁性纳米球,IMNs)来捕获细菌几乎不会产生损失,也不需要复杂的分离工具或技术。另一方面,IMNs 表现出了优异的捕获能力。经过 20 分钟的相互作用,几乎可以捕获所有的目标细菌,即使在样品中只有一个细菌存在也不会错过,而免疫磁性微球只能捕获不到 50%的细菌。此外,IMNs 可以在复杂基质中实现相同的高效富集,如牛奶、胎牛血清和尿液,证明了它们良好的稳定性、强抗干扰能力和低非特异性吸附。此外,分离得到的细菌无需释放过程即可直接用于培养、聚合酶链反应(PCR)分析和荧光免疫分析,这表明我们基于 IMNs 的富集策略可以方便地与下游的鉴定和分析技术相结合。因此,本工作提供的 MNs 在细菌富集方面表现出了巨大的优势,有望成为细菌检测和研究的一种有前途的工具。