• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to project page

1990 Fiscal Year Final Research Report Summary

Discrimination and Simultaneous Determination of Analogs by Derivative Spectrum Method

Research Project

Project/Area Number 63571027
Research Category

Grant-in-Aid for General Scientific Research (C)

Allocation TypeSingle-year Grants
Research Field Physical pharmacy
Research InstitutionTeikyo University

Principal Investigator

IWATSURU Motoharu  Teikyo University, Pharmaceutics, Professor, 薬学部, 教授 (50050448)

Co-Investigator(Kenkyū-buntansha) AOYAMA Kazu  Teikyo University, Pharmaceutics, Assistant, 薬学部, 助手 (50167798)
SHIMIZU Kiyoshi  Teikyo University, Pharmaceutics, Assistant, 薬学部, 助手 (80119586)
Project Period (FY) 1988 – 1989
KeywordsDerivative spectrum / UV absorption / Paraben / Surfactant / Sodium lauryl sulfate / Shift of wavelength / Simultaneous determination / Products analysis
Research Abstract

As the preservatives, such as methylparaben, ethylparaben, propylparaben, and butylparaben, have similar absorption spectrum which show maximum at 253-254 nm, it is not possible to discriminate them by absorption spectrum only. The addition of surfactant into their aqueous solution caused the shift of the wavelength of maximum absortion. This solubilization phenomena made it possible to measure the partition parameter of the preservative between aqueous and micellar phase. The parameter values of alkylparabens in sodium lauryl sulfate solution were in the order of butyl->propyl->ethyl->methylparaben at all temperatures where experiment were done. This means that the longer the acylchain of alkylparaben, the more can be solubilized into micellar phase. This ended up greater shift length and bigger partition parameter values. The same results were observed not in sodium lauryl sulfate solution, but also in cetyltrimethylammonium bromide solution, Tween 20 solution, and octaethyleneglycol-n-dodecylether solution. Thus the discrimination of alkylparabens were attained through the measurement of partition parameter.
It was confirmed that the shift length of the mixed parabens depended on the molar ratio of its constituents. This made it possible to determine the concentration of parabens only knowing the magnitude of shift length and total absorptivity at given (maximum) wavelength. This method can be applied to any systems where absorption shift occurs as long as surfactant can cause the shift. It is a great advantage, once the calibration curve are set, then we need only the shift length and absorptivity to calculate the concentration of each components. This method can be more useful where so many samples should be handled in shorter time such as products analysis.

  • Research Products

    (4 results)

All Other

All Publications (4 results)

  • [Publications] K. Shimizu, C. Imada and M. Iwatsuru: "Measurement of the Distribution Parameter in Solubilized Systems. III. Measurement of the Distribution Parameter of Drugs Which Show Blue Shift in the Surfactant Solution and Its Utilization to Discrimination" Chem. Pharm. Bull.

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Y. Motoyama, K. Shimizu and M. Iwatsuru: "Simultaneous Determination of Parabens in Aqueous Solution by FDAS Method" Chem. Pharm. Bull.

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] K. Shimizu, C. Imada and M. Iwatsuru: "Measurement of the Distribution Parameter in Solubilized Systems. III. Measurement of the Distribution Parameter of Drugs Which Show Blue Shift in the Surfactant Solution and Its Utilization to Discrimination" Chem. Pharm. Bull.

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Y. Moroyama, K. Shimizu and M. Iwatsuru: "Simultaneous Determination of Parabens in Aqueous Solution by FDAS Method" Chem. Pharm. Bull.

    • Description
      「研究成果報告書概要(欧文)」より

URL: 

Published: 1993-08-12  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi