Duddu S P, Mehvar R, Grant D J
Department of Pharmaceutics, College of Pharmacy, University of Minnesota, Minneapolis 55455.
Pharm Res. 1991 Nov;8(11):1430-3. doi: 10.1023/a:1015813509816.
An HPLC method has been developed for the separation of four stereoisomers of ephedrine using precolumn derivatization with S(+)-1-(1-naphthyl)-ethyl isocyanate. The formed derivatives are subsequently separated on a normal-phase column and are detected at a UV wavelength of 220 nm. This method was used to quantitate the differences in the enantiomeric impurity of various samples of (+)-pseudoephedrine. The reported method can differentiate between samples of (+)-pseudoephedrine which differ in their enantiomeric impurity by as little as 0.02%. Possible racemization of (+)-pseudoephedrine in aqueous solutions was also studied. Samples of (+)-pseudoephedrine from various suppliers and, indeed, different lots from the same supplier, differed significantly in their degree of enantiomeric impurity.
已开发出一种高效液相色谱(HPLC)方法,用于分离麻黄碱的四种立体异构体,该方法采用S(+)-1-(1-萘基)-乙基异氰酸酯进行柱前衍生化。随后,形成的衍生物在正相柱上进行分离,并在220 nm的紫外波长下进行检测。该方法用于定量不同样品中(+)-伪麻黄碱对映体杂质的差异。所报道的方法能够区分对映体杂质差异低至0.02%的(+)-伪麻黄碱样品。同时还研究了(+)-伪麻黄碱在水溶液中可能的消旋化情况。来自不同供应商的(+)-伪麻黄碱样品,以及同一供应商不同批次的样品,其对映体杂质程度存在显著差异。