Unique oxygen analyzer combining a dual emission probe and a low-cost solid-state ratiometric fluorometer

被引:27
作者
Kostov, Y
Van Houten, KA
Harms, P
Pilato, RS
Rao, G
机构
[1] Univ Maryland, Inst Biotechnol, Ctr Med Biotechnol, Baltimore, MD 21201 USA
[2] Univ Maryland Baltimore Cty, Dept Chem & Biochem Engn, Baltimore, MD 21228 USA
[3] Univ Maryland, Dept Chem & Biochem, College Pk, MD 20742 USA
[4] LUMET, Silver Spring, MD 20905 USA
关键词
oxygen analyzer; ratiometric sensor; low-cost fluorimeter;
D O I
10.1366/0003702001950238
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
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 (approximate to 73 torr), offering a dynamic range of 0-90% O-2. The device is stable and the oxygen measurements reproducible. Intentional photobleaching of approximate to 20% of the sensor dye had little effect upon the reproducibility of the oxygen measurements.
引用
收藏
页码:864 / 868
页数:5
相关论文
共 56 条
[1]   DETERMINATION OF OXYGEN CONCENTRATIONS BY LUMINESCENCE QUENCHING OF A POLYMER-IMMOBILIZED TRANSITION-METAL COMPLEX [J].
BACON, JR ;
DEMAS, JN .
ANALYTICAL CHEMISTRY, 1987, 59 (23) :2780-2785
[2]   SENSING OXYGEN THROUGH SKIN USING A RED DIODE-LASER AND FLUORESCENCE LIFETIMES [J].
BAMBOT, SB ;
RAO, G ;
ROMAULD, M ;
CARTER, GM ;
SIPIOR, J ;
TERPETCHNIG, E ;
LAKOWICZ, JR .
BIOSENSORS & BIOELECTRONICS, 1995, 10 (6-7) :643-652
[3]   PHASE FLUOROMETRIC STERILIZABLE OPTICAL OXYGEN SENSOR [J].
BAMBOT, SB ;
HOLAVANAHALI, R ;
LAKOWICZ, JR ;
CARTER, GM ;
RAO, G .
BIOTECHNOLOGY AND BIOENGINEERING, 1994, 43 (11) :1139-1145
[4]  
BAMBOT SB, 1995, TRENDS BIOTECHNOL, V13, P83
[5]   Ratiometric and fluorescence lifetime-based biosensors incorporating cytochrome c′ and the detection of extra- and intracellular macrophage nitric oxide [J].
Barker, SLR ;
Clark, HA ;
Swallen, SF ;
Kopelman, R ;
Tsang, AW ;
Swanson, JA .
ANALYTICAL CHEMISTRY, 1999, 71 (09) :1767-1772
[6]   PHOTOPHYSICS AND PHOTOCHEMISTRY OF OXYGEN SENSORS BASED ON LUMINESCENT TRANSITION-METAL COMPLEXES [J].
CARRAWAY, ER ;
DEMAS, JN ;
DEGRAFF, BA ;
BACON, JR .
ANALYTICAL CHEMISTRY, 1991, 63 (04) :337-342
[7]   Radioluminescent light source for optical oxygen sensors [J].
Chuang, H ;
Arnold, MA .
ANALYTICAL CHEMISTRY, 1997, 69 (10) :1899-1903
[8]   Linear calibration function for optical oxygen sensors based on quenching of ruthenium fluorescence [J].
Chuang, H ;
Arnold, MA .
ANALYTICA CHIMICA ACTA, 1998, 368 (1-2) :83-89
[9]  
CLARK LC, 1956, T AM SOC ART INT ORG, V2, P41
[10]   MODELING OF LUMINESCENCE QUENCHING-BASED SENSORS - COMPARISON OF MULTISITE AND NONLINEAR GAS SOLUBILITY MODELS [J].
DEMAS, JN ;
DEGRAFF, BA ;
XU, WY .
ANALYTICAL CHEMISTRY, 1995, 67 (08) :1377-1380