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作 者:Ying Xia Wang Yong Nian Ni Serge Kokot
机构地区:[1]State Key Laboratory of Food Science and Technology, Nanchang University, Nanchang 330047, China [2]Department of Chemistry, Nanchang University, Nanchang 330031, China [3]School of Physical and Chemical Sciences, Queensland University of Technology, Brisbane, QId 4001, Australia
出 处:《Chinese Chemical Letters》2010年第8期963-967,共5页中国化学快报(英文版)
基 金:the financial support by the State Key Laboratory of Food Science and Technology of Nanchang University(Nos.SKLF-MB-200807 and SKLF-TS-200819)
摘 要:The interactions of carbofuran and DNA were studied using voltammetry and fluorescence spectroscopy.The formation of carbofuran-DNA makes the current peak of DNA decreased by voltammetry method.The binding number(n) and constant(Ka) for complex carbofuran-DNA were calculated to be 1.06±0.04 and 0.11±0.03mol^-1 L,respectively by fluorescence measurement.Chemometrics approach,such as singular value decomposition(SVD) was used to evaluate the number of spectral species in the drug-DNA binding process.And the pure spectra and concentration profiles in the kinetic system were clearly deduced by multivariate curve resolution alternating least squares(MCR-ALS) with the initial estimates by evolving factor analysis(EFA).The interactions of carbofuran and DNA were studied using voltammetry and fluorescence spectroscopy.The formation of carbofuran-DNA makes the current peak of DNA decreased by voltammetry method.The binding number(n) and constant(Ka) for complex carbofuran-DNA were calculated to be 1.06±0.04 and 0.11±0.03mol^-1 L,respectively by fluorescence measurement.Chemometrics approach,such as singular value decomposition(SVD) was used to evaluate the number of spectral species in the drug-DNA binding process.And the pure spectra and concentration profiles in the kinetic system were clearly deduced by multivariate curve resolution alternating least squares(MCR-ALS) with the initial estimates by evolving factor analysis(EFA).
关 键 词:CARBOFURAN DNA VOLTAMMETRY CHEMOMETRICS
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