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Direct electrochemical reduction of graphene oxide and its application to determination of l-tryptophan and l-tyrosine
. [Display omitted] ► Electrochemically reduced graphene oxide (ERGO) was prepared by potentiostatic method. ► ERGO have highly catalytic activity towards the l-tryptophane and l-tyrosine. ► ERGO was used for determination of l-tryptophane and l-tyrosine. Directly electrochemically reduced graphene...
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Published in: | Colloids and surfaces, B, Biointerfaces B, Biointerfaces, 2013-01, Vol.101 (1), p.183-188 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | . [Display omitted]
► Electrochemically reduced graphene oxide (ERGO) was prepared by potentiostatic method. ► ERGO have highly catalytic activity towards the l-tryptophane and l-tyrosine. ► ERGO was used for determination of l-tryptophane and l-tyrosine.
Directly electrochemically reduced graphene oxide (ERGO) was obtained by potentiostatic reduction of exfoliated graphene oxide sheets on a glassy carbon electrode (GCE). The ERGO-modified electrode (ERGO/GCE) displayed greatly improved voltammetric response to the amino acids l-tryptophane (Trp) and l-tyrosine (Tyr) compared with the chemically reduced graphene oxide (CRGO) modified electrode. The ERGO/GCE separated the voltammetric responses of ascorbic acid (AA) and uric acid (UA) from that of Trp and Tyr. It eliminated the interference from AA and UA. The electrode showed good reproducibility and was used to determine Trp and Tyr with linear ranges of 0.2–40.0μmolL−1and 0.5–80.0μmolL−1, detection limits of 0.1μmolL−1 and 0.2μmolL−1, respectively. |
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ISSN: | 0927-7765 1873-4367 |
DOI: | 10.1016/j.colsurfb.2012.06.007 |