A Comparative Study on Various Spectrometries with Thin Layer Chromatography for Simultaneous Analysis of Drotaverine and Nifuroxazide in Capsules

• Ayad Magda Mohammed

  Analytical Chemistry Department, Faculty of Pharmacy, Zagazig University

• Youssef Nadia Fayek

  National Organization for Drug Control and Research (NODCAR), Egypt

• Abdellatif Hisham Ezzat

  Analytical Chemistry Department, Faculty of Pharmacy, Zagazig University

• Soliman Suzan Mahmod

  National Organization for Drug Control and Research (NODCAR), Egypt

書誌事項

タイトル別名

• Comparative Study on Various Spectrometries with Thin Layer Chromatography for Simultaneous Analysis of Drotaverine and Nifuroxazide in Capsules

抄録

Three spectrophotometric methods including Vierordt's method, derivative, ratio spectra derivative, and thin layer chromatography (TLC)-UV densitometric method were developed for simultaneous determination of drotaverine HCl (DRT) and nifuroxazide (NIF) in presence of its impurity, 4-hydroxybenzohydrazide (4-HBH). In Vierordt's method, (E_{1 cm}^1%) values were calculated at 227 and 368 nm in the zero-order spectra of DRT and NIF. By derivative spectrophotometry, the zero-crossing method, drotaverine HCl was determined using the second derivative at 245 nm and the third derivative at 238 nm, while nifuroxazide was determined using the first derivative at 399 nm and the second derivative at 411 nm. The ratio spectra derivative spectrophotometry is basedon the measure of the amplitude at 459 nm for DRT and at 416 nm for NIF in the first derivative of the ratio spectra. Calibration graphs of the three spectrophotometric methods were plotted in the range 1—10 μg/ml of DRT and 2—20 μg/ml of NIF. TLC-UV densitometric method was achieved on silica gel plates using ethyl acetate : methanol : ammonia 33% (10 : 1 : 0.1 v/v/v) as the mobile phase. The Rf values were 0.74, 0.50, 0.30±0.01 for DRT, NIF and 4-HBH, respectively. On the fluorescent plates, the spots were located by fluorescence quenching and the densitometrical area were measured at 308 and 287 nm with linear range 0.2—4 μg/spot and 0.6—12 μg/spot for DRT and NIF, respectively. The proposed methods have been successfully applied to the commercial pharmaceutical formulation without any interference of excipients. Mean recoveries, relative standard deviations and the results of the proposed methods were compared with those obtained by applying the alternate methods.

収録刊行物

• ＣＨＥＭＩＣＡＬ　＆　ＰＨＡＲＭＡＣＥＵＴＩＣＡＬ　ＢＵＬＬＥＴＩＮ

  ＣＨＥＭＩＣＡＬ　＆　ＰＨＡＲＭＡＣＥＵＴＩＣＡＬ　ＢＵＬＬＥＴＩＮ 54 (6), 807-813, 2006

  公益社団法人 日本薬学会

キーワード

• drotaverine
• nifuroxazide
• Vierordt's method
• derivative spectrophotometry
• ratio spectra derivative
• TLC-UV densitometry

詳細情報

• CRID: 1390282679147503232
• NII論文ID: 110004836382
• NII書誌ID: AA00602100
• DOI: 10.1248/cpb.54.807
• ISSN: 13475223
• ISSN: 00092363
• NDL書誌ID: 7920962
• Web Site: https://ndlsearch.ndl.go.jp/books/R000000004-I7920962
• Web Site: http://www.jstage.jst.go.jp/article/cpb/54/6/54_6_807/_pdf
• 本文言語コード: en
• データソース種別:
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  • NDL
  • Crossref
  • CiNii Articles
• 抄録ライセンスフラグ: 使用不可