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中国药学(英文版) ›› 2016, Vol. 25 ›› Issue (12): 876-881.DOI: 10.5246/jcps.2016.12.098

• 【研究论文】 • 上一篇    下一篇

Spectrophotometric and spectrofluorimetric methods for the determination of ropinirole content in pharmaceutical dosage forms

Effat Souri*, Milad Torabadi, Maliheh Barazandeh Tehrani   

  1. Department of Medicinal Chemistry, Faculty of Pharmacy and Drug Design and Development Research Center, Tehran University of Medical Sciences, Tehran 14155-6451, Iran
  • 收稿日期:2016-09-15 修回日期:2016-10-21 出版日期:2016-12-21 发布日期:2016-10-30
  • 通讯作者: Tel.: +98-21-66959065, Fax: +98-21-66461178, E-mail: souri@sina.tums.ac.ir

Spectrophotometric and spectrofluorimetric methods for the determination of ropinirole content in pharmaceutical dosage forms

Effat Souri*, Milad Torabadi, Maliheh Barazandeh Tehrani   

  1. Department of Medicinal Chemistry, Faculty of Pharmacy and Drug Design and Development Research Center, Tehran University of Medical Sciences, Tehran 14155-6451, Iran
  • Received:2016-09-15 Revised:2016-10-21 Online:2016-12-21 Published:2016-10-30
  • Contact: Tel.: +98-21-66959065, Fax: +98-21-66461178, E-mail: souri@sina.tums.ac.ir

摘要:

Two simple and rapid spectrofluorimetric and spectrophotometric methods were described for the determination of ropinirole hydrochloride content in pharmaceutical dosage forms. Both methods are based on the reaction of ropinirole hydrochloride and eosin Y in aqueous medium at pH 4.0. Quenching of the fluorescence intensity of eosin Y at 540 nm upon excitation at 350 nm was used for the determination of ropinirole hydrochloride levels after ion-pair complex formation. Also, the absorbance increase of eosin Y at 546 nm after ion-pair complex formation was used for spectrophotometric measurements. Both methods showed linear relationships between the fluorescence quenching or absorbance increase and ropinirole concentration in the range of 6–150 µg/mL and 50–500 µg/mL for spectrofluorimetric and spectrophotometric methods, respectively. As no organic solvents were used in these two methods, they could be categorized as green analytical methods. Both methods were accurate (Error<1.2%) and precise (CV<1.9%), as shown by statistical analysis results. Both methods were used for determination of ropinirole hydrochloride content in pharmaceutical dosage forms without any significant interference from associated impurities.

关键词: Ropinirole, Spectrophotometry, Spectrofluorimetry, Eosin Y, Ion-pair complex

Abstract:

Two simple and rapid spectrofluorimetric and spectrophotometric methods were described for the determination of ropinirole hydrochloride content in pharmaceutical dosage forms. Both methods are based on the reaction of ropinirole hydrochloride and eosin Y in aqueous medium at pH 4.0. Quenching of the fluorescence intensity of eosin Y at 540 nm upon excitation at 350 nm was used for the determination of ropinirole hydrochloride levels after ion-pair complex formation. Also, the absorbance increase of eosin Y at 546 nm after ion-pair complex formation was used for spectrophotometric measurements. Both methods showed linear relationships between the fluorescence quenching or absorbance increase and ropinirole concentration in the range of 6–150 µg/mL and 50–500 µg/mL for spectrofluorimetric and spectrophotometric methods, respectively. As no organic solvents were used in these two methods, they could be categorized as green analytical methods. Both methods were accurate (Error<1.2%) and precise (CV<1.9%), as shown by statistical analysis results. Both methods were used for determination of ropinirole hydrochloride content in pharmaceutical dosage forms without any significant interference from associated impurities.

Key words: Ropinirole, Spectrophotometry, Spectrofluorimetry, Eosin Y, Ion-pair complex

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