Direct water-phase synthesis of lead sulfide quantum dots encapsulated by β-lactoglobulin for in vivo second near infrared window imaging with reduced toxicity
Direct water-phase synthesis of lead sulfide quantum dots encapsulated by β-lactoglobulin for in vivo second near infrared window imaging with reduced toxicity
复制标题
直接水相合成β-乳球蛋白封装的硫化铅量子点,用于体内第二近红外窗口成像,毒性降低
DOI:
10.1039/c6cc00099a
复制
发表时间:
2016-01-01
影响因子:
4.9
通讯作者:
Chen, Shiyi
中科院分区:
文献类型:
--
作者:
Chen, Jun;Kong, Yifei;Chen, Shiyi
Compared to conventional fluorescence imaging in the visible (400-700 nm) and NIR-I regions (700-900 nm), optical fluorescence imaging in the second near infrared window (NIR-II, 1000-1400 nm) offers reduced photon scattering, deeper tissue penetration and lower auto-fluorescence. Despite excellent imaging capabilities, current NIR-II probes have not yet reached their full potential due to weak quantum yield, low water solubility and suboptimal biocompatibility. To address these problems, we report herein a new NIR-II fluorescent PbS quantum dots (QDs) that are fabricated in water using beta-lactoglobulin (LG) as a biological template. The LG-PbS QDs exhibit satisfactory dispersibility, relatively high quantum yield and favorable biocompatibility, and therefore are suitable for high-resolution in vivo imaging applications.