UV-Spectrophotometric Determination of Glucosamine Hydrochloride in Its Drug Capsule
摘 要
基于盐酸氨基葡萄糖(GSM)与镍(Ⅱ)在碱性介质中生成配合物,在波长219 nm处有其最大吸收的现象作了进一步验证。将此反应用于紫外-可见分光光度法测定其药物胶囊中GSM含量。测定时,将一颗GSM胶囊中的药物颗粒取出称重后(每颗药物中GSM的质量的标示量为0.24 g)溶于水中并定容至250 mL。取此溶液5.00 mL置于50 mL容量瓶中,相继顺序加入0.10 mol·L-1氢氧化钠溶液10 mL和1.0×10-2mol·L-1硫酸镍溶液2.00 mL,用0.10 mol·L-1氢氧化钠溶液定容,在20℃水浴中反应15 min。在波长219 nm处测量其吸光度。GSM的浓度在6.00×10-4~4.00×10-3mol·L-1内与其相应的吸光度呈线性关系,其检出限(3S/N)为4.10×10-5mol·L-1。以GSM胶囊样品溶液为基体,按标准加入法在4个浓度水平上进行回收试验,测得回收率为80.0%~110%。测定值的相对标准偏差(n=5)均小于0.2%。按此方法对药物实样进行分析,测得其GSM浓度为7.26×10-4mol·L-1,换算成胶囊中GSM的质量为0.238 6 g,与其标示值相符。
Abstract
Based on the phenomenon of coordination of glucosamine hydrochloride (GSM) with Ni2+ in alkaline medium to form a coordination complex having its absorption maximum at 219 nm, further research was done to work out a method for UV-spectrophotometric determination of GSM in its drug capsule. In the determination, the drug particles of GSM in a capsule were taken, weighed (ca. 0.24 g as labelled), dissolved and made its volume to 250 mL with water. An aliquot of 5.00 mL of this solution was taken and placed in a 50 mL volumetric flask, 10 mL of 0.10 mol·L-1 sodium hydroxide solution and 2.00 mL of 1.0×10-2mol·L-1 nickel sulfate solution were added successively and volume of the solution was made up to 50 mL with 0.10 mol·L-1 sodium hydroxide solution. Then the solution was placed into a water bath keeping at constant temperature of 20℃ for 15 min for completion of the coordination reaction. Absorbance of the solution was then measured at 219 nm. Linear relationship between values of absorbance measured and the respective concentrations of GSM was obtained in the range from 6.00×10-4 to 4.00×10-3mol·L-1; the detection limit (3S/N) found was 4.10×10-5mol·L-1. On the base of GSM taken from a capsule, recovery was tested by addition of GSM standard solution at 4 concentration levels, giving results of recovery in the range of 80.0%-110% and values of RSDs (n=5) less than 0.2%. A substantial drug capsule was analyzed by this method, the concentration of GSM found was 7.26×10-4mol·L-1, which was equivalent to a mass of 0.238 6 g in the capsule by conversion calculation. This value was found in consistency with the labelled value.
中图分类号 O657.32 DOI 10.11973/lhjy-hx202003016
所属栏目 工作简报
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收稿日期 2019/7/17
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备注刘欣,教授,硕士,主要从事食品分析方面的研究工作,liuxin197207@126.com
引用该论文: LIU Xin,WANG Yuqing,LI Yongge,LIU Chunyu. UV-Spectrophotometric Determination of Glucosamine Hydrochloride in Its Drug Capsule[J]. Physical Testing and Chemical Analysis part B:Chemical Analysis, 2020, 56(3): 340~343
刘欣,王誉清,李咏歌,刘春雨. 紫外-可见分光光度法测定药物胶囊中盐酸氨基葡萄糖[J]. 理化检验-化学分册, 2020, 56(3): 340~343
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【3】冷艳霞,孙璐,邸欣,等.盐酸氨基葡萄糖片的相对生物利用度及其生物等效性评价[J].沈阳药科大学学报, 2006,23(1):6-9.
【4】JEONG D H, ULLAH H M A, GOO M J, et al. Effects of oral glucosamine hydrochloride and mucopolysaccharide protein in a rabbit model of osteoarthritis[J]. International Journal of Rheumatic Diseases, 2018,21(3):620-628.
【5】CHAN P S, CARON J P, ROSA G J M, et al. Glucosamine and chondroitin sulfate regulate gene expression and synthesis of nitric oxide and prostaglandin E2 in articular cartilage explants[J]. Osteoarthritis and Cartilage, 2005,13(5):387-394.
【6】万慧芳,万欢,汪华杰.盐酸氨基葡萄糖反相高效液相色谱法含量测定方法研究[J].南昌大学学报(医学版), 2010,50(5):104-105.
【7】陈璥.关于一种重要保健葡萄糖衍生物的探讨[J].淀粉与淀粉糖, 2006,12(4):31-33.
【8】赵海珍,姚丽娜.中药保健品中D-氨基葡萄糖盐酸盐含量测定[J].黑龙江医药, 2008,21(5):27-28.
【9】陈金东,李蔚.滴定分析法和分光光度法测定保健食品中D-氨基葡萄糖盐酸盐含量的研究[J].中国卫生检验杂志, 2002,12(2):143-144.
【10】吴学军,金鹏飞,朱峰,等.高效液相色谱法快速测定盐酸氨基葡萄糖胶囊的含量[J].医药导报, 2011,30(8):1085-1087.
【11】刘利萍,章非凡,张阳,等.HPLC测定盐酸氨基葡萄糖的柱前衍生化条件的响应面优化[J].营养学报, 2013,35(4):387-390.
【12】沈丹丹,曾杰,王玥,等.HPLC测定盐酸氨基葡萄糖有关物质与含量[J].中国药学杂志, 2017,52(4):314-318.
【13】甘宾宾,刘展华,黎少豪.HPLC法测定保健食品中盐酸氨基葡萄糖含量的研究[J].中国食品卫生杂志, 2011,23(6):531-533.
【14】王太亮,王子秦.HPLC-ELSD法测定氨糖美辛肠溶胶囊中盐酸氨基葡萄糖及相关物质[J].中国生化药物杂志, 2016,36(6):194-196.
【15】卢素格,王爱月,张榕杰.高效液相色谱测定保健食品中盐酸氨基葡萄糖含量[J].中国卫生工程学, 2011,10(6):499-500.
【16】郑家概,王飞,农云军,等氨基葡萄糖盐酸盐含量的HPLC柱前衍生法测定[J].分析测试学报, 2009,28(9):1081-1083.
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