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ZnS quantum dots derived a reagentless uric acid biosensor.

PubMed
Authors: Zhang F, Li C, Li X, Wang X, Wan Q, Xian Y, Jin L, Yamamoto K

Year

2006

Paper ID

12808

Status

Peer-reviewed

Abstract Read

~2 min

Abstract Words

118

Citations

N/A

Abstract

A reagentless amperometric uric acid biosensor based on zinc sulfide (ZnS) quantum dots (QDs) was firstly developed. It could detect uric acid without the presence of an electron mediator. The carboxyl group functionalized ZnS QDs were synthesized, and they were soluble biocompatible and conductive. ZnS QDs conjugates could provide increased enzyme binding sites, which may result in higher enzyme loading. Thus, the proposed uricase/ZnS QDs/l-cys biosensor exhibited higher amperometric response compared to the one without QDs (uricase/l-cys biosensor). In addition, there was little AA interference. It showed a linear dependence on the uric acid concentration ranging from 5.0x10(-6) to 2.0x10(-3)molL(-1) with a detection limit of 2.0x10(-6)molL(-1) at 3sigma.

Why This Paper Matters

  • This paper contributes to the Quantum Chemistry research area in the Quantum Articles archive.
  • It adds a 2006 reference point for readers tracking recent quantum research.
  • A reagentless amperometric uric acid biosensor based on zinc sulfide (ZnS) quantum dots (QDs) was firstly developed.

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