| Literature DB >> 29495833 |
Osamu Wakao1, Ken Satou2, Ayano Nakamura3, Ken Sumiyoshi2, Masanori Shirokawa2, Chikaaki Mizokuchi2, Kunihiro Shiota2, Masatoshi Maeki4, Akihiko Ishida4, Hirofumi Tani4, Koji Shigemura2, Akihide Hibara5, Manabu Tokeshi4.
Abstract
Fluorescence polarization (FP) offers easy operation and rapid processing, making it implementable in molecular interaction analysis. Previously we have developed a unique FP measurement system using a liquid crystal (LC) layer and an image sensor. The system is based on a principle of synchronized detection between the switching rate of the LC layer and the sampling rate of the CCD. The FP system realized simultaneous multiple sample detection; however, the measurement precision was lower than that of the conventional FP apparatus. The main drawbacks were low light transmittance of the LC layer and insufficient synchronization between the LC layer and CCD. In this paper, we developed a new FP analyzer based on LC-CCD synchronization detection. By using a newly designed LC with high transmittance and improving synchronization, the performance of the system has been dramatically improved. Additionally, we reduced the cost by using an inexpensive CCD and an LED as the excitation source. Simultaneous FP immunoassay of multiple samples of prostaglandin E2 was performed. The error rate of the FP system is reduced from 16.9% to 3.9%, as comparable to the commercial conventional FP system.Entities:
Year: 2018 PMID: 29495833 DOI: 10.1063/1.5017081
Source DB: PubMed Journal: Rev Sci Instrum ISSN: 0034-6748 Impact factor: 1.523