利用电化学聚合法将金和L-半胱氨酸修饰于玻碳电极表面,制成了金掺杂聚L-半胱氨酸修饰电极,研究了多巴胺（DA）在该修饰电极上的电化学行为。实验结果表明,在p H 5.0的磷酸盐缓冲溶液中,多巴胺在修饰电极上产生一对明显的氧化还原峰,且...利用电化学聚合法将金和L-半胱氨酸修饰于玻碳电极表面,制成了金掺杂聚L-半胱氨酸修饰电极,研究了多巴胺（DA）在该修饰电极上的电化学行为。实验结果表明,在p H 5.0的磷酸盐缓冲溶液中,多巴胺在修饰电极上产生一对明显的氧化还原峰,且氧化峰电流与其浓度在2.0×10-6~3.0×10-4mol/L范围内呈良好的线性关系,方法检出限为2.08×10-7mol/L。该修饰电极用于实际样品中DA的测定,回收率达98.4%。展开更多
Aim To determine nucleic acid （DNA） using Nanometer-sized L-cysteine-capped CdS particles by resonance light scattering （RLS） method. Methods The nano-particles synthesized by a colloidal aqueous method were water...Aim To determine nucleic acid （DNA） using Nanometer-sized L-cysteine-capped CdS particles by resonance light scattering （RLS） method. Methods The nano-particles synthesized by a colloidal aqueous method were water-soluble, stable, and highly luminescent. The RLS of L-Cys-CdS particles were greatly quenched by DNA in Tris-HCl solutions. The intensity of RLS at 344 nm was proportional to the concentration of DNA. Results The linearity range of the calibration curve was 0. 01 - 1.0 μg·mL^-1 for calf thymus DNA and 0. 04 - 1.5 μg· mL^-1 for salmon sperm DNA. The detection limits （3 δ） were 8 ng·mL^-1 for calf thymus DNA and 10 ng·mL^-1 for salmon sperm DNA. Conclusion This method is simple, sensitive, and capable of avoiding the use of toxic dyes.展开更多
文摘利用电化学聚合法将金和L-半胱氨酸修饰于玻碳电极表面,制成了金掺杂聚L-半胱氨酸修饰电极,研究了多巴胺（DA）在该修饰电极上的电化学行为。实验结果表明,在p H 5.0的磷酸盐缓冲溶液中,多巴胺在修饰电极上产生一对明显的氧化还原峰,且氧化峰电流与其浓度在2.0×10-6~3.0×10-4mol/L范围内呈良好的线性关系,方法检出限为2.08×10-7mol/L。该修饰电极用于实际样品中DA的测定,回收率达98.4%。
基金National Natural Science Foundation of China(30370404).
文摘Aim To determine nucleic acid （DNA） using Nanometer-sized L-cysteine-capped CdS particles by resonance light scattering （RLS） method. Methods The nano-particles synthesized by a colloidal aqueous method were water-soluble, stable, and highly luminescent. The RLS of L-Cys-CdS particles were greatly quenched by DNA in Tris-HCl solutions. The intensity of RLS at 344 nm was proportional to the concentration of DNA. Results The linearity range of the calibration curve was 0. 01 - 1.0 μg·mL^-1 for calf thymus DNA and 0. 04 - 1.5 μg· mL^-1 for salmon sperm DNA. The detection limits （3 δ） were 8 ng·mL^-1 for calf thymus DNA and 10 ng·mL^-1 for salmon sperm DNA. Conclusion This method is simple, sensitive, and capable of avoiding the use of toxic dyes.
