Centre for Nano and Material Sciences, Jain Global Campus, Jain University, Bangalore 562112, India; Pilot Plant Development and Training Institute, King Mongkut's University of Technology Thonburi, Bangkhuntien-Chaitalay Road, Thakam, Bangkok 10150, Thailand.
Centre for Nano and Material Sciences, Jain Global Campus, Jain University, Bangalore 562112, India.
J Photochem Photobiol B. 2020 Mar;204:111799. doi: 10.1016/j.jphotobiol.2020.111799. Epub 2020 Jan 20.
CdSe/CdS core shelled quantum dots (QDs) were prepared by colloidal synthesis using a binary ligand system and a non-coordinating, reusable solvent n-octadecane (nOD). Both the synthesis of CdSe and CdSe/CdS core shelled quantum dots were achieved by hot injection technique at much lower temperatures than reported earlier. The use of binary ligand facilitated enough nucleation and growth. Red shift in absorption spectra, an enhanced crystallite and particle size is evidenced by XRD and TEM respectively, confirming the formation of core shell structure of CdSe/CdS. The synthesized core shells exhibited high fluorescence intensity, long term stability and good mono dispersion, making it a potential material for bio-imaging and sensing. Core shell QDs were modified with mercapto propionic acid (MPA) to impart aqueous solubility. Studies on cytotoxicity of shelled QDs reveal good bio compatibility with a very minimum toxicity of IC = 20 μg/L. These QDs were used for sensing E. coli. Ordinary glass slide, modified using plasma etching is surface modified through APTES aiding conjugation of antibodies. Anti- E. coli polyclonal antibody on glass matrix (slide) and antibody conjugated QDs were used for detection of E. coli in a typical sandwich model. The excellent optical transparency of glass and high emission of QDs lead to detection of E.coli with a limit of detection of 50 CFU/mL.
CdSe/CdS 核壳量子点(QDs)通过胶体合成制备,使用二元配体系统和非配位、可重复使用的溶剂正十八烷(nOD)。CdSe 和 CdSe/CdS 核壳量子点的合成均通过热注射技术在比以前报道的更低的温度下实现。二元配体的使用促进了足够的成核和生长。吸收光谱的红移、XRD 和 TEM 分别证实了晶体和颗粒尺寸的增强,证明了 CdSe/CdS 核壳结构的形成。合成的核壳表现出高荧光强度、长期稳定性和良好的单分散性,使其成为生物成像和传感的潜在材料。核壳 QDs 用巯基丙酸(MPA)修饰以赋予水溶性。壳层 QDs 的细胞毒性研究表明具有良好的生物相容性,IC=20μg/L 时毒性最小。这些 QDs 用于检测大肠杆菌。普通载玻片通过等离子体蚀刻进行表面修饰,通过 APTES 辅助抗体缀合。玻璃基质(载玻片)上的抗大肠杆菌多克隆抗体和抗体偶联的 QDs 用于典型的三明治模式检测大肠杆菌。玻璃的优异光学透明度和 QDs 的高发射率导致可以检测到 50 CFU/mL 的大肠杆菌。