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机构地区:[1]四川大学华西公共卫生学院卫生检验教研室,四川成都610041
出 处:《分析测试学报》2010年第4期386-389,393,共5页Journal of Instrumental Analysis
基 金:国家科技支撑计划资助项目(2006BAD27B02)
摘 要:建立了功能食品和饮品中牛磺酸的高效毛细管电泳陕速分析方法。以邻苯二甲醛(OPA)为衍生剂进行柱前衍生,采用45mmol/L(pH9.5)的硼砂缓冲溶液为运行缓冲溶液,熔融石英毛细管(50cm×50μm,有效长度41cm,未涂层)为分离柱;柱上紫外睑测波长:335nm,分离电压19kV,电泳温度20℃,重力进样,进样时间10s。牛磺酸的质量浓度在5.0~100.0mg/L范围内呈良好线性关系(r〉0.999),检出限(S/N=3)为1.6mg/L,迁移时问和峰面积的相对标准偏差(n=7)分别为2.4%和3.8%。用该法测定了功能食品、乳制饮品和饮料等样品中的牛磺酸,相对标准偏差为0.7%~3.7%,加标回收率为93%~111%。A new method for the rapid quantification of taurine in functional food and beverage samples by capillary eleetrophoresis with ultraviolet detection was developed. The sample solution was derivatized with o-phthaldialdehyde (OPA) , and separated by high performance capillary electrophoresis (HPCE). The experimental parameters were as follows: separation column: an uncoated fused-sili- ca capillary(50 cm ×50 μm, and 41 cm effective length) ; running buffer: 45 mmol/L sodium tetraborate(pH 9.5) ; running voltage: 19 kV; temperature: 20 ℃ ; sampling time: 10 s; detection wavelength: 335 nm. The method showed a good linearity within the concentration range of 5.0 - 100. 0 mg/L( r 〉 0. 999). The detection limit( S/N = 3 ) was 1.6 mg/L. The RSDs ( n = 7 ) of migration times and peak areas for taurine standards were 2. 4% and 3.8%, respectively. Satisfactory results were obtained for analysis of functional foods, dairy drinks and beverages with recoveries of 93%- 111% and RSDs of 0. 7% -3.7% .
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