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Preparation of molecularly imprinted polymer sensor for blood level measurement of intravenous anesthetic.

Research Project

Project/Area Number 16591549
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Anesthesiology/Resuscitation studies
Research InstitutionUniversity of Miyazaki

Principal Investigator

IBUSUKI Shoichiro  University of Miyazaki, Department of medicine, Instructor, 医学部, 講師 (70315381)

Co-Investigator(Kenkyū-buntansha) SHIRASAKA Tetsuro  University of Miyazaki, Department of medicine, Instructor, 医学部, 講師 (00274788)
Project Period (FY) 2004 – 2005
Project Status Completed (Fiscal Year 2005)
Budget Amount *help
¥3,400,000 (Direct Cost: ¥3,400,000)
Fiscal Year 2005: ¥1,500,000 (Direct Cost: ¥1,500,000)
Fiscal Year 2004: ¥1,900,000 (Direct Cost: ¥1,900,000)
Keywordsmolecularly imprinted polymer / propofol / quartz crystal microbalance / blood level / methacrylic acid / ethacrylic acid
Research Abstract

The purpose of this research was preparation of a sensor for blood level measurement of intravenous anesthetic such as propofol. The molecularly imprinted polymers (MIPs) were employed as a propofol sensitive layer, and quartz crystal microbalances (QCM) were employed to determine the propofol concentration.
In 2004, for practice of membrane preparation, the propofol selective MIPs were polymerized on the surface of slide glasses. Propofol (template), methacrylic acid (MAA, functional monomer), ethylene glyacol dimethacrylate (EGDMA, cross-linker) and 2,2'-Azobis(2.4-dimethyl valeronitrile) (initiator) were measured 1 : 6.5 : 8.5 : 0.4 (mol ratio, respectively) and dissolved in hexane. The mixture solution was painted thinly on the surface of slide glass and polymerized at 40℃ for 48 hours. It was very difficult to make the MIP into flat and thin layer. In 2005, we tried to improve the MIP layer preparation. The method of MIP polymerization was changed to precipitation polymerization to make MIP into microspheres. The MIP microspheres were binded onto slide glass or quartz crystal with PVC. However, it was still difficult to make MIP microspheres into flat/thin layer. Therefor, the property of MIP-QCM system could not be estimated. Additional improvement was needed

Report

(3 results)
  • 2005 Annual Research Report   Final Research Report Summary
  • 2004 Annual Research Report

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Published: 2004-04-01   Modified: 2016-04-21  

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