Unique Oxygen Analyzer Combining a Dual Emission Probe and a Low-Cost Solid-State Ratiometric Fluorometer

Author:

Kostov Yordan1,Van Houten Kelly A.1,Harms Peter1,Pilato Robert S.1,Rao Govind1

Affiliation:

1. Medical Biotechnology Center, University of Maryland Biotechnology Institute, 725W. Lombard St., Baltimore, Maryland 21201 (Y.K., P.H., G.R.); Department of Chemical and Biochemical Engineering, University of Maryland, Baltimore County, 1000 Hilltop Circle, Baltimore, Maryland (G.R.); University of Maryland, Department of Chemistry and Biochemistry, College Park, Maryland 20742 (K.V.); and LUMET, 1808 Briggs Chaney Rd. Silver Spring, Maryland 20905 (R.S.P.)

Abstract

A new oxygen analyzer combining a polymer-encapsulated dual-emission probe and a diode-based ratiometric fluorometer is described. The ratiometric fluorometer was configured to measure the relative fluorescence and phosphorescence intensity of the short-lived singlet and long-lived oxygen-quenchable triplet of [(dppe)Pt{S2C2(CH2CH2–N–2-pyridinium)}](BPh4), where dppe is 1,2- bis(diphenylphosphino)ethane. This luminescent dye was immobilized at 0.3% by weight in cellulose acetate/75% triethylcitrate and cast into a 0.5 mm-thick film. The dye molecule was excited with a blue light-emitting diode (LED) and the singlet and triplet emissions monitored by individual photodiodes at 570 and 680 nm, respectively. Oxygen can be accurately measured without interference from nonanalyte-induced intensity changes by monitoring the relative output of the two photodiodes. The output of the device was linear with oxygen concentration. The PO2(1/2) from the ratio-adapted Stern–Volmer plot was 9.6% oxygen (≈73 torr), offering a dynamic range of 0–90% O2. The device is stable and the oxygen measurements reproducible. Intentional photobleaching of ≈20% of the sensor dye had little effect upon the reproducibility of the oxygen measurements.

Publisher

SAGE Publications

Subject

Spectroscopy,Instrumentation

Reference56 articles.

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