Department of Bioscience and Biotechnology, National Taiwan Ocean University, Keelung 20224, Taiwan.
J Mater Chem B. 2020 Apr 29;8(16):3506-3512. doi: 10.1039/c9tb02468a.
In this study, we have developed a rapid and cost-effective method employing platinum ion (Pt4+)-capped fluorescent carbon quantum dots (CQDs) coupled with loop-mediated isothermal amplification (LAMP) to detect dual MRSA genes. We synthesized nitrogen- and chlorine-co-doped fluorescent CQDs (CQDSPDs) from spermidine trihydrochloride via a simple one-step pyrolysis. The CQDSPDs capped with Pt4+ ions through the cooperative coordination of the amine and chlorine groups on the surface of CQDs facilitated the double-stranded DNA (dsDNA)-induced fluorescence quenching of CQDs, and enabled the construction of the CQDSPDs/Pt4+ probe for the detection of as few as 10 copies of the MRSA gene (mecA and femA). The sensitivity and specificity of the CQDSPDs/Pt4+ probe for MRSA detection in clinical specimens (n = 24) were 94% and 86%, respectively. Our results reveal that the CQDSPDs/Pt4+ probe has great potential for the diagnosis of antibiotic-resistant superbugs with high sensitivity, specificity, and agreement.
在这项研究中,我们开发了一种快速且经济有效的方法,使用铂离子(Pt4+)封端的荧光碳量子点(CQDs)与环介导等温扩增(LAMP)相结合来检测双重 MRSA 基因。我们从 spermidine trihydrochloride 通过简单的一步热解合成了氮和氯共掺杂的荧光 CQDs(CQDSPDs)。通过 CQDs 表面上的胺和氯基团的协同配位,Pt4+离子封端的 CQDSPDs 促进了 CQDs 的双链 DNA(dsDNA)诱导的荧光猝灭,从而构建了 CQDSPDs/Pt4+探针,用于检测低至 10 个拷贝的 MRSA 基因(mecA 和 femA)。CQDSPDs/Pt4+探针对临床标本(n=24)中 MRSA 的检测灵敏度和特异性分别为 94%和 86%。我们的结果表明,CQDSPDs/Pt4+探针具有高灵敏度、特异性和一致性,非常有潜力用于诊断抗生素耐药性超级细菌。