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司替戊醇对映异构体的HPLC法拆分及其含量测定

Chiral Separation and Determination of Stiripentol Enantiomers by HPLC
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摘要 建立了高效液相色谱法拆分并测定司替戊醇对映异构体。采用Chiralpak AY-H色谱柱,以正己烷∶异丙醇(90∶10)为流动相,检测波长270 nm。(R)、(S)-司替戊醇均在15.6-500?g/ml范围内线性关系良好。平均回收率为98.60%和99.84%,RSD为0.82%和0.72%。 An HPLC method was established for the enantiomeric separation and determination of stiripentol enantiomers. A Chiralpak AY-H column was used, with the mobile phase of n-hexane : isopropanol (90 : 10), at the detection wavelength of 270 nm. It was linear in the concentration range of 15.6-500 μg/ml for both (R)- and (S)- stiripentol. Their recoveries were 98.60 % and 99.84 %, with RSDs of 0.82 % and 0.72 %.
出处 《中国医药工业杂志》 CAS CSCD 北大核心 2016年第1期74-76,共3页 Chinese Journal of Pharmaceuticals
关键词 司替戊醇 手性拆分 对映异构体 高效液相色谱 测定 stiripentol chiral separation enantiomer HPLC determination
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参考文献4

  • 1Chiron C, Dulac O. The pharmacologic treatment of Dravetsyndrome [J]. Epilepsia, 2011, 52 (Suppl 2): 72—75.
  • 2杜玉民,张恺,方瑜.一种司替戊醇的制备方法,中国:102391242A [P]. 2012-03-28.
  • 3胡艾希,伍智林,叶姣.一种司替戊醇的制备方法:中国,201210200284.X[P].2012-06-18.
  • 4赵杰,张恺,华圆,程诚,杜玉民.司替戊醇的合成[J].中国医药工业杂志,2013,44(8):747-748. 被引量:1

二级参考文献6

  • 1C6olin R, Dugu6 J, Rouland JC, et al. Solid state studies on stiripentol: a novel anticonvulsant drug [J]. lnt J Pharm, 1991, 74(1): 77-82.
  • 2Arends HGPR, Zhang KY, Levy RH, et al. Stereoselective pharmacokinetics of stiripentol: an explanation for the development of tolerance to anticonvulsant effect EJ]. Epilepsy Res, 1994, 18 (2) : 91-96.
  • 3Vallet FMJ. 1- (3,4-Methylenedioxy-phenyl) -4,4-dimethyl- pent-l-en-3-ol: US, 3910959 [P]. 1975-10-07. (CA 1973, 79: 146216).
  • 4Madelmont JC, Dupuy JM, Rapp M, et al. Marquage par C et 3H du 4,4-dimethyl- 1- (methylendioxy-3,4 phenyl) - 1-pentene- 3-ol ou stiripentol t4C and 3H labelling of 4,4-dimethyl-1- (methylenedioxy-3,4-phenyl)-1-pentene-3-ol or stiripentol [J]. JLabelled CompdRadiopharm, 1992, 31 (11): 961-966.
  • 5Mohamed NAE, Aida AEA, Mohamed IA, et al. Design and synthesis of novel stiripentol analogues as potential anticonvulsants [J]. Eur J Med Chem, 2012, 47 (1) : 360-369.
  • 6Alvarez-Ibarra C, Perez MSA, Fernandez MJ, et al. Efficient Wittig-Horner and improved Claisen-Schmidt synthesis of acyclic x-enones with a 2-furyl or 3,4-methylenedioxyphenyl group at the 13-position [J]. J Chem Res (Miniprint), 1992, 10: 2674-2686.

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