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原位显色研究镥双辛基取代酞菁与选定生物辅因子的相互作用。

In situ chemichromic studies of interactions between a lutetium bis-octaalkyl-substituted phthalocyanine and selected biological cofactors.

机构信息

The Wolfson Centre for Materials Processing, Brunel University, Uxbridge, Middlesex UB8 3PH, UK.

出版信息

J R Soc Interface. 2012 Jan 7;9(66):183-9. doi: 10.1098/rsif.2010.0726. Epub 2011 Jun 15.

Abstract

Spin-coated films, approximately 100 nm thick, of a newly synthesized bis[octakis(octyl)phthalocyaninato] lutetium(III) complex on ultrasonically cleaned glass substrates exhibit pronounced chemichromic behaviour with potential application in healthcare. In situ kinetic optical absorption spectroscopic measurements show that the phthalocyanine Q-band is red shifted by 60 nm upon oxidation arising from exposure to bromine vapour. Recovery to the original state is achieved by the treatment of the oxidized films with nicotinamide adenine dinucleotide and l-ascorbic acid (vitamin C) in an aqueous solution containing 1.5 M lithium perchlorate. The neutralization process is found to be governed by first-order kinetics. The linear increase of the reduction rate with increasing concentration of cofactors provides a basis for calibration of analyte concentrations ranging from 3.5 mM down to 0.03 mM.

摘要

旋涂于超声清洗玻璃基底上的约 100nm 厚的新型双[辛基(辛基)酞菁]镥(III)配合物薄膜具有明显的化学变色行为,在医疗保健方面具有潜在应用。原位动力学光学吸收光谱测量表明,酞菁 Q 带在暴露于溴蒸气时发生 60nm 的红移,这是由于氧化引起的。通过在含有 1.5 M 高氯酸锂的水溶液中用烟酰胺腺嘌呤二核苷酸和 l-抗坏血酸(维生素 C)处理氧化膜,可以恢复到原始状态。发现中性化过程受一级动力学控制。随着辅因子浓度的增加,还原速率的线性增加为分析物浓度从 3.5mM 降至 0.03mM 的校准提供了基础。

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