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1.浙江海洋大学食品与药学学院,浙江 舟山 316022
2.舟山市食品药品检验检测研究院,浙江 舟山 316021
Published:30 April 2023,
Received:26 September 2022,
Revised:10 March 2023,
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倪东宇,王琼芬,张梦奇等.盐酸氨基葡萄糖片中5-HMF的含量测定及形成动力学研究 Δ[J].中国药房,2023,34(08):950-954.
NI Dongyu,WANG Qiongfen,ZHANG Mengqi,et al.Content determination of 5-HMF in glucosamine hydrochloride tablets and formation kinetics study[J].ZHONGGUO YAOFANG,2023,34(08):950-954.
倪东宇,王琼芬,张梦奇等.盐酸氨基葡萄糖片中5-HMF的含量测定及形成动力学研究 Δ[J].中国药房,2023,34(08):950-954. DOI: 10.6039/j.issn.1001-0408.2023.08.11.
NI Dongyu,WANG Qiongfen,ZHANG Mengqi,et al.Content determination of 5-HMF in glucosamine hydrochloride tablets and formation kinetics study[J].ZHONGGUO YAOFANG,2023,34(08):950-954. DOI: 10.6039/j.issn.1001-0408.2023.08.11.
目的
2
建立测定盐酸氨基葡萄糖片中5-羟甲基糠醛(5-HMF)含量的方法,分析其含量变化规律及影响因素。
方法
2
采用高效液相色谱法对5-HMF进行定量测定,以Shim-pack GIST C
18
-AQ为色谱柱,0.1%磷酸溶液-甲醇(90∶10,
V
/
V
)为流动相,柱温为30 ℃,检测波长为284 nm,流速为1.0 mL/min,进样量为20 μL。通过不同温度反应动力学实验分析5-HMF含量与反应温度、反应时间的相关性,建立其形成动力学模型。
结果
2
5-HMF检测质量浓度的线性范围为0.057~5.698 μg/mL(
r
=0.999 9);检测限为5.70 ng/mL,定量限为17.09 ng/mL;精密度、重复性和稳定性(24 h)试验的RSD均小于1.0%(
n
=6);加样回收率为99.38%~99.73%(RSD=0.53%,
n
=9)。8批样品含量为4.10~35.13 μg/g。反应动力学实验数据拟合结果显示,随着反应温度升高、反应时间延长,样品中5-HMF含量越高。50、60、70、80 ℃下,5-HMF含量与反应时间均呈线性关系,符合零级动力学模型,反应速率常数分别为6.789、7.715、8.815、11.430。
结论
2
所建含量测定方法专属性强、灵敏度高、准确度好;反应温度和反应时间是影响盐酸氨基葡萄糖片中5-HMF形成的重要因素,其含量变化规律符合零级动力学模型。
OBJECTIVE
2
To establish the method for the content determination of 5-hydroxymethylfurfural (5-HMF) in glucosamine hydrochloride tablets, and to analyze its regularity and influential factors.
METHODS
2
Quantitative analysis of 5-HMF was performed using high-performance liquid chromatography. The analysis was conducted on Shim-pack GIST C
18
-AQ column with mobile phase consisted of 0.1% phosphoric acid solution-methanol (90∶10,
V
/
V
) at the flow rate of 1.0 mL/min. The column temperature was 30 ℃, and detection wavelength was 284 nm. The injection volume was 20 μL. Reaction kinetics test of different temperatures was adopted to analyze the relationship of 5-HMF content with reaction temperature and reaction time, and utilized to build its formation kinetic model.
RESULTS
2
The linger range of 5-HMF was 0.057-5.698 μg/mL (
r
=0.999 9). The limits of detection and quantitation were 5.70 and 17.09 ng/mL; RSDs of precision, repeatability and stability (24 h) tests were all lower than 1.0% (
n
=6). The average recoveries ranged from 99.38% to 99.73%(RSD=0.53%,
n
=9). The contents of the 5-HMF in 8 batches of samples ranged 4.10-35.13 μg/g. Results of data fitting in reaction kinetics test showed that the higher reaction temperature and the longer reaction time, the higher 5-HMF content in the sample. At 50, 60, 70 and 80 ℃, the relationship between the content of 5-HMF and the reaction time was linear, in accordance with a zero-order kinetic model. The reaction rate constants were 6.789, 7.715, 8.815 and 11.430, respectively.
CONCLUSIONS
2
The established method has strong specificity, high sensitivity, and good accuracy; the reaction temperature and reaction time are important influential factors for the formation of 5-HMF in glucosamine hydrochloride tables. The change rule of its content conforms to the zero-order kinetic model.
盐酸氨基葡萄糖片5-羟甲基糠醛高效液相色谱法含量测定形成动力学
5-hydroxymethylfurfuralHPLCcontent determinationformation kinetics
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