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反相高效液相色谱法测定医药中间体2-乙氧羰基环戊酮

Determination of Ethyl 2-oxocyclopentanecarboxylate by Reversed Phase High Performance Liquid Chromatograph
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摘要 建立了一种用反相高效液相色谱法(RP-HPLC)测定医药中间体2-乙氧羰基环戊酮的方法。选用Kromasil C18(250mm×4.6mm,5μm)色谱柱,以甲醇-水(60∶40,V∶V)为流动相,流速为0.6mL/min,紫外检测波长为253nm,对药物中2-乙氧羰基环戊酮的含量进行测定。实验表明,2-乙氧羰基环戊酮在6~300μg/mL的浓度范围内,峰高与浓度呈良好的线性关系,线性方程为Y=13.873X-70.839,线性相关系数R2=0.9992,RSD=3.30%,回收率为98.02%~101.22%。最低检测限为0.08μg/mL。本法操作简单、灵敏度高,可准确快速地测定药物中2-乙氧羰基环戊酮的含量。 A method for the determination of ethyl 2-oxocylopentanecaroxylate by reversed phase high performance liquid chromatography is developed. Kromasil C18 (250 mm ×4.6 mm, 5 μm) is chosen as chromatographic column. Methanol-water (60: 40, V: V) at flow-rate of 0.6 mL/min is mobile phase with UV detection wave at 253 nm. The relationship between peak height and concentration in the range from 6 to 300 μg/mL show good linearity. RSD is 3.30%. The detection limit is 0.08μg/mL. The recovery of samples are 98.02% - 101.22%. It indicates that the proposed method is sensitive reliable and can be? applied in analysis of medical materials.
出处 《东华理工大学学报(自然科学版)》 CAS 2008年第4期374-376,共3页 Journal of East China University of Technology(Natural Science)
基金 江西省教育厅科学技术研究项目(赣教技字[2007]231号)
关键词 反相高效液相色谱 2-乙氧羰基环戊酮 医药中间体 reversed phase high performance liquid chromatograph ethyl 2-oxocyclopentanecarboxylate phar- maceutical intermediate
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参考文献1

  • 1[13]Gramen,MahoneT A D.2001.M~nt of nicotine in hair by of reversed-phase high-performance liquid chromatography with electro chemical[J].J.Chromatogr,B,753:179-187.

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