Chen Jinghua, Zhang Jing, Zhuang Qian, Zhang Shaobo, Lin Xinhua
Department of Pharmaceutical Analysis, Faculty of Pharmacy, Fujian Medical University, Fuzhou 350004, PR China.
Talanta. 2007 Jul 31;72(5):1805-10. doi: 10.1016/j.talanta.2007.02.022. Epub 2007 Feb 21.
A very sensitive electroanalytical method was employed to determine bergenin in phosphate buffer with a pH of 6.0, bergenin was accumulated at a 4-(2-pyridylazo)-resorcinol (PAR) polymer film modified glassy carbon electrode (GCE) surface under the condition of open-circuit. In the following anodic sweep from -0.4 to 0.8 V, bergenin adsorbed at the PAR polymer film modified electrode surface, was oxidized and yielded a sensitive oxidation peak at 0.595V. Due to its unique structure and extraordinary properties, the PAR polymer film shows higher accumulation efficiency toward bergenin compared with a bare GCE. Hence, the amount of bergenin at the PAR polymer film modified GCE surface increases significantly, and finally the oxidation peak current improves greatly. The experimental conditions, such as supporting electrolyte, pH value, accumulation time and scan rate, were optimized for the measurement of bergenin, and a sensitive electroanalytical method was proposed for bergenin determination. The oxidation peak current varies linearly with the concentration of bergenin over the range of 2.0x10(-7) to 1.2x10(-5)mol/L, and the detection limit is 2.0x10(-8)mol/L after 3 min open-circuit accumulation. The relative standard deviation of the same electrode in 10 successive scans is 1.8% for 1.0x10(-6)mol/L bergenin and 2.1% for interelectrodes, indicating excellent reproducibility. This new method was successfully demonstrated with bergenin tablets and diluted urine.
采用一种非常灵敏的电分析方法,在pH为6.0的磷酸盐缓冲液中测定岩白菜素。在开路条件下,岩白菜素在4-(2-吡啶偶氮)-间苯二酚(PAR)聚合物膜修饰玻碳电极(GCE)表面富集。在随后从-0.4至0.8 V的阳极扫描中,吸附在PAR聚合物膜修饰电极表面的岩白菜素被氧化,并在0.595 V处产生一个灵敏的氧化峰。由于其独特的结构和非凡的性质,PAR聚合物膜对岩白菜素的富集效率比裸玻碳电极更高。因此,PAR聚合物膜修饰玻碳电极表面的岩白菜素量显著增加,最终氧化峰电流大幅提高。对岩白菜素测定的实验条件,如支持电解质、pH值、富集时间和扫描速率进行了优化,并提出了一种灵敏的岩白菜素电分析测定方法。在2.0×10⁻⁷至1.2×10⁻⁵mol/L范围内,氧化峰电流与岩白菜素浓度呈线性关系,开路富集3分钟后检测限为2.0×10⁻⁸mol/L。对于1.0×10⁻⁶mol/L岩白菜素,同一电极在10次连续扫描中的相对标准偏差为1.8%,电极间相对标准偏差为2.1%,表明重现性良好。该新方法已成功应用于岩白菜素片剂和稀释尿液的检测。