Flow-injection spectrophotometric determination of vitamin B1 (thiamine) in multivitamin preparations

Clezio Aniceto, Airton Vicente Pereira, Cícero Oliveira Costa-Neto, Orlando Fatibello-Filho
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引用次数: 5

Abstract

A flow-injection (FI) spectrophotometric procedure is proposed for the determination of vitamin B1 (thiamine hydrochloride) in multivitamin preparations. Powdered sample, containing from 25 to 100 mg of multivitamin preparations, was previous dissolved in 0.1 mol L−1 hydrochloric acid, and a volume of 250 μL was injected directly into a carrier stream of 0.10% (w/v) potassium hexacyanoferrate(III) in 0.5 mol L−1 sodium hydroxide at a flow rate of 2.46 mL min−1 an FI system. The thiochrome produced in the oxidation of thiamine hydrochloride by potassium hexacyanoferrate(III) in alkaline solution was directly measured at 369 nm. Potassium hexacyanoferrate(III) in this concentration did not cause any interference.

Vitamin B1 was determined in three multivitamin preparations in the concentration range from 2.5 to 50.0 mg L−1 (calibration graph: A = −0.0132 + 0.0134 C, r = 0.9990, where A is the absorbance and C is the vitamin B1 concentration in mg L−1). Sucrose, glucose, fructose, lactose, citric acid, starch, vitamin B2, and vitamin B6 do not interfere, even in concentrations five times higher than vitamin B1. Only vitamin B12 causes interference, but this vitamin is not present in the multivitamin preparations used in this work. The detection limit was 1.0 mg L−1, and the recovery of vitamin B1 from three samples ranged from 97.5 to 105.0. The sampling rate was 41 h−1 and RSDs were less than 1% for solutions containing 10.0 and 30.0 mg L−1 vitamin B1 (n = 10). The results obtained for the determination of vitamin B1 in commercial preparations are in good agreement with those obtained by differential pulse polarography (r = 0.9999) and also with the label values (r = 0.9998). © 1999 John Wiley & Sons, Inc. Lab Robotics and Automation 11: 45–50, 1999

流动注射分光光度法测定复合维生素制剂中维生素B1(硫胺素)的含量
建立了流动注射分光光度法测定复合维生素制剂中维生素B1(盐酸硫胺素)含量的方法。将含有25 ~ 100 mg复合维生素制剂的粉状样品溶于0.1 mol L−1盐酸中,以0.5 mol L−1氢氧化钠为载体,以0.10% (w/v)六氰高铁酸钾(III)为载体,流速2.46 mL min−1,FI系统直接注入250 μL。在369 nm处直接测定了六氰高铁酸钾(III)在碱性溶液中氧化盐酸硫胺素生成的硫铬。六氰高铁酸钾(III)在该浓度下不产生任何干扰。测定了三种复合维生素制剂中维生素B1的浓度范围为2.5 ~ 50.0 mg L−1(校准图:A = - 0.0132 + 0.0134 C, r = 0.9990,其中A为吸光度,C为维生素B1浓度,单位为mg L−1)。蔗糖、葡萄糖、果糖、乳糖、柠檬酸、淀粉、维生素B2和维生素B6不受干扰,即使浓度比维生素B1高5倍。只有维生素B12会引起干扰,但这种维生素不存在于这项工作中使用的多种维生素制剂中。检出限为1.0 mg L−1,3个样品中维生素B1的回收率为97.5 ~ 105.0。对于含有10.0和30.0 mg L - 1维生素B1的溶液(n = 10),采样率为41 h−1,rsd < 1%。所得结果与差示脉冲极谱法测定的结果(r = 0.9999)和标签值(r = 0.9998)吻合良好。©1999 John Wiley &儿子,Inc。实验室机器人与自动化(11):45-50,1999
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