Synthesis of Cd-free InP/ZnS Quantum Dots Suitable for Biomedical Applications

Matthew A. Ellis; Giovanna Grandinetti; Katye M. Fichter

doi:10.3791/53684

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화학

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바이오 메디컬 응용 프로그램에 적합 InP를 /의 ZnS 양자점 CD-자유의 합성

Synthesis of Cd-free InP/ZnS Quantum Dots Suitable for Biomedical Applications

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Synthesis of Cd-free InP/ZnS Quantum Dots Suitable for Biomedical Applications

바이오 메디컬 응용 프로그램에 적합 InP를 /의 ZnS 양자점 CD-자유의 합성

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13,554 Views

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10:56 min

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February 06, 2016

DOI:

10.3791/53684-v

DOI:

10.3791/53684-v

•

10:56 min

February 06, 2016

•

7 Views

Matthew A. Ellis¹, Giovanna Grandinetti², Katye M. Fichter¹

¹Department of Chemistry,Missouri State University, ²Center for Molecular Microscopy, Leidos Biomedical Research, Inc.,Frederick National Laboratory for Cancer Research

내레이션 대본

Summary

In this protocol, the synthesis of Cd-free InP/ZnS quantum dots (QDs) is detailed. InP-based QDs are gaining popularity due to the toxicity of Cd²⁺ ions that may be released through nanoparticle degradation. After synthesis, QDs are solubilized in water using an amphiphilic polymer for use in biomedical applications.