Issue 21, 2016

Direct water-phase synthesis of lead sulfide quantum dots encapsulated by β-lactoglobulin for in vivo second near infrared window imaging with reduced toxicity

Abstract

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 β-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.

Graphical abstract: Direct water-phase synthesis of lead sulfide quantum dots encapsulated by β-lactoglobulin for in vivo second near infrared window imaging with reduced toxicity

Supplementary files

Article information

Article type
Communication
Submitted
06 Jan 2016
Accepted
11 Feb 2016
First published
11 Feb 2016

Chem. Commun., 2016,52, 4025-4028

Direct water-phase synthesis of lead sulfide quantum dots encapsulated by β-lactoglobulin for in vivo second near infrared window imaging with reduced toxicity

J. Chen, Y. Kong, W. Wang, H. Fang, Y. Wo, D. Zhou, Z. Wu, Y. Li and S. Chen, Chem. Commun., 2016, 52, 4025 DOI: 10.1039/C6CC00099A

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