沙振方, 孙文基, 高海. C型甲苯咪唑的红外光谱定量测定J. 药学学报, 1989, 24(12): 932-936.
引用本文: 沙振方, 孙文基, 高海. C型甲苯咪唑的红外光谱定量测定J. 药学学报, 1989, 24(12): 932-936.
ZF Sha, WJ Sun , H Gao, . INFRARED SPECTROMETRY DETERMINATION OF POLYMORPHIC FORM C IN MEBENDAZOLEJ. Acta Pharmaceutica Sinica, 1989, 24(12): 932-936.
Citation: ZF Sha, WJ Sun , H Gao, . INFRARED SPECTROMETRY DETERMINATION OF POLYMORPHIC FORM C IN MEBENDAZOLEJ. Acta Pharmaceutica Sinica, 1989, 24(12): 932-936.

C型甲苯咪唑的红外光谱定量测定

INFRARED SPECTROMETRY DETERMINATION OF POLYMORPHIC FORM C IN MEBENDAZOLE

  • 摘要: 本文用红外光谱法测定了甲苯咪唑中晶型C的含量。取高铁氰化钾细粉(6mg)为内标物,与样品细粉(30mg)在0.25ml液体石蜡中仔细研磨均匀。将糊状物放入0.1mm铅片隔开的KBr窗片之间,分别于800~850cm-1和2050~2150cm-1以吸收度的方式扫描谱图。最后以834和842cm-1,2114和2140cm-1吸收度之差按内标法计算甲苯咪唑C型晶型的百分含量。该法对甲苯咪唑原料和片剂都适用,操作简便、专属性高,结果满意。

     

    Abstract: Mebendazole displays polymorphism. There are three polymor phic forms (A, B and C) which were identified by means of IR and X-ray diffraction techniques.Procedures have been worked out to determine the amount of the polymorphic form C in pure mebendazole and in tablets. The sample (30 mg) and internal standard (K3Fe(CN)6, 6 mg) were mulled in 0.25ml of mineral oil and placed between KBr plates separated by a 0.1 mm lead spacer. The spectra were recorded by the absorbance mode between 850~800cm-1 and 2150~2050 cm-1. Both of the base lines are the horizontal line from 2140 cm-1 peak valley and from 842 cm-1 peak valley.The values of theabsorbance difference were measured at 834 and 842 cm-1, 2114 and 2140 cm-1 respectively. The percent content of the polymorphic form C was calculated by the method of internal standard. This analytical approach is simple and the results are satisfactory.

     

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