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Enantioselective Determination of Chlorpheniramine in Various Formulations by HPLC using $Carboxymethyl-{eta}-cyclodextrin$ as a Chiral Additive
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  • Enantioselective Determination of Chlorpheniramine in Various Formulations by HPLC using $Carboxymethyl-{eta}-cyclodextrin$ as a Chiral Additive
  • Enantioselective Determination of Chlorpheniramine in Various Formulations by HPLC using $Carboxymethyl-{eta}-cyclodextrin$ as a Chiral Additive
저자명
Chen. Quan Cheng,Jeong. Su-Jin,Hwang. Gwi-Seo,Kim. Kyeong-Ho,Kang. Jong-Seong
간행물명
Archives of pharmacal research : a publication of the Pharmaceutical Society of Korea
권/호정보
2008년|31권 4호|pp.523-529 (7 pages)
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대한약학회
파일정보
정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

A chiral mobile phase HPLC method is described for chiral separation and determination of chlorpheniramine (CP) enantiomers in various commercial preparations. Chromatographic separation was achieved on a conventional ODS column with a mixture of aqueous sodium phosphate (5 mM) containing 0.5 mM $carboxymethyl-{eta}-cyclodextrin$, methanol and, triethylamine (73:25:2, v/v/v, pH 4.3) as the mobile phase. The flow rate of isocratic elution was 0,24 mL/min and peaks were detected at 224 nm. The method was applied to nine commercial CP preparations in six dosage forms and CP enantiomers were well separated without any disturbance of other ingredients or impurities present. The results showed that only one preparation was d-CP and the others were dl-CP preparations. The contents of all the preparations were found to be in the range of 97%-104% of labeled contents. This method was economical and convenient, affording sufficient accuracy, precision and reproducibility, as well as sensitivity and selectivity.