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高效液相色谱法测定卡西酮 被引量:3

Detecting cathinone with HPLC
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摘要 目的建立卡西酮的高效液相色谱检测方法。方法采用UPLC-DAD分析方法。分析柱:Agilent ZorbaxSB-Phenyl柱(250mm×4.6mm,5μm),流动相为三氟乙酸(pH 3.5)∶乙腈为85∶15,流速0.2mL/min,检测波长254nm。结果卡西酮在0.5~1 000μg/mL浓度范围内线性关系良好R2=0.999 4,日内与日间保留时间和峰面积的标准偏差(RSD)均<1.06%,检出限为0.068μg/mL,平均回收率95.9%。结论本方法峰形好,分离度好,线性范围良好,回收率高,适用于刑事案件中卡西酮的定性定量分析。 Objective To establish a method for detecting cathinone with HPLC. Methods Using UPLC- DAD detection. The analytical column was Agilent Zorbax@ SB-Phenyl column (250mm x 4.6mm, 5 μm ) , and the mobile phase is trifluoracetic acid (pH 3.5 ) :acetonitrile = 85:15, at a flow rate of 0. 2mL/min, with 254nm as the detection wavelength. Results This method has good linearity with the real value at the range from 0. 5 to 1 0001xg/mL, R2 = 0. 999 4. Both intra-day and inter-day precisions expressed by relative standard deviations of retention time and peak area were less than 1.06%. The detectable limit was 0. 068 μg/ mL. Average recovery was 95.9%. Conclusion This method has good peak shape, less mobile phase, good separation, good linearity and high recovery. This method was suitable for qualitative and quantitative analysis.
作者 常颖 高利生
出处 《中国法医学杂志》 CSCD 2012年第5期389-390,共2页 Chinese Journal of Forensic Medicine
关键词 法医毒物分析 高效液相色谱 卡西酮 定性 定量 forensic toxicological analysis HPLC cathinone qualitative quantitative
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参考文献2

  • 1Kelly J P. Cathinone derivatives : a review of their chemistry, pharmacology and toxicology [ J ]. Drug Test Anal, 2011, 3(7-8) : 439-453.
  • 2Goshgarian A M, Benford D M, Caplan J P . Bath salt abuse : neuropsychiatric effects of cathinone derivatives [ J ]. Psvchosomatics, 2011.52 (6) : 593-594.

同被引文献20

  • 1李宏森,黄克建,林翠梧,蒙念,潘智文.顶空固相微萃取与气质联用快速检测尿液中苯丙胺、甲基苯丙胺、MDA和MDMA[J].广西大学学报(自然科学版),2007,32(3):266-269. 被引量:15
  • 2Kelly J P. Cathinone derivatives : a review of their chemistry, pharmacology and toxicology[J]. Drug Test Anal, 2011,3 (7-8) : 439-453.
  • 3Goshgarian A M, Benford D M, Caplan J P. Bath salt abuse: neuropsyehiatrie effects of cathinone derivatives [J]. Psyehosomaties, 2011, 52(6): 593-594.
  • 4Diekson, A.J., Vorce, S.P., Levine, B., et ol. Multiple- drug toxicity caused by the eoadministration of 4-methyl- metheathinone (mephedrone) and heroin[J]. Journal of Ana- lytical Toxicology, 2010, 34(3): 162-168.
  • 5Wood, D.M., Davies, S., Puehnarewicz, M., et al. Recre- ational use of mephedrone (4-methylmetheathinone, 4- MMC ) with associated sympathomimetie toxicity[J]. Journal of Medical Toxicology, 2010, 6(3): 327-330.
  • 6Dominika G., Piotr A., Agnieszka S., et al. Analysis of 4- MEC in biological and non-biological material-Three case reports[J]. Forensic Science International, 2013,228 (1-3) : 11-15.
  • 7Brandt, S.D., Freeman, S., Sumnall, H.R., et al. Analysis of NRG 'legal highs' in the UK: Identification and formation of novel cathinones[J]. Journal of Medical Toxicology, 2010, (6) :327-330.
  • 8Camilleri A., Johnston M., Brennan M., et ol. Chemical anal- ysis of four capsules containing the controlled substance ana- logues 4 -methylmetheathinone, 2 -fluorometham phetamine, alpha-phthalimidopropiophenone and N-ethylcathinone [J]. Forensic Science International, 2010, ( 197 ) : 59-66.
  • 9C.R. Maheux, C.R. Copeland, M.M. Pollard. Characterisation of three methcathinone analogs: 4-methylmethcathinone, methylone, and bk-MBDB[J]. Microgram Journal, 2010, (7) : 42-49.
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