Fluorescence of indocyanine green in blood: intensity dependence on concentration and stabilization with sodium polyaspartate

被引:80
作者
Maarek, JMI
Holschneider, DP
Harimoto, J
机构
[1] Univ So Calif, Dept Biomed Engn, Los Angeles, CA 90089 USA
[2] Univ So Calif, Keck Sch Med, Dept Neurol, Dept Psychiat & Behav Sci, Los Angeles, CA USA
[3] Univ So Calif, Keck Sch Med, Greater Los Angeles VA Hlth Care Ctr, Los Angeles, CA USA
关键词
indocyanine green; fluorescence; sodium polyaspartate; dye stability; blood; mathematical model;
D O I
10.1016/S1011-1344(01)00264-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Indocyanine green (ICG) has been widely used in cardiovascular, hepatic, and ophthalmologic studies. Application of this fluorescent dye has been handicapped by its poor stability in solution and by the complex dependence of its fluorescence intensity on concentration. Noncovalent interactions between ICG and sodium polyaspartate (PASP) stabilize ICG fluorescence in aqueous solution, but the effect of PASP on ICG fluorescence in blood has not been described. The current study had two main goals: first, to characterize in vitro in blood the relationship between fluorescence intensity and concentration of ICG-PASP (ICG) and the stability of this relationship over time; second, to test a new phenomenological model describing the dependence of ICG fluorescence on concentration. Freshly-prepared ICG and ICG-PASP solutions produced the same fluorescence intensity over a wide range of concentrations (0.0005-0.1271 mg/ml). The peak fluorescence of ICG was reduced by 11% after 10 h and by 72% at 7 days. In contrast, the peak fluorescence intensity of ICG-PASP solutions was nearly unchanged for up to 14 days. The dependence of the fluorescence intensity on concentration was accurately represented by our model that accounted for the generation of fluorescence following light absorption, and for the reabsorption of the emitted fluorescence by ICG. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:157 / 164
页数:8
相关论文
共 27 条
[1]  
BAKER KJ, 1966, P SOC EXP BIOL MED, V122, P957
[2]   FLUORESCENCE PROPERTIES OF INDOCYANINE GREEN AS RELATED TO ANGIOGRAPHY [J].
BENSON, RC ;
KUES, HA .
PHYSICS IN MEDICINE AND BIOLOGY, 1978, 23 (01) :159-163
[3]  
BJORNSSON OG, 1983, J CLIN CHEM CLIN BIO, V21, P453
[4]   A REVIEW OF THE OPTICAL-PROPERTIES OF BIOLOGICAL TISSUES [J].
CHEONG, WF ;
PRAHL, SA ;
WELCH, AJ .
IEEE JOURNAL OF QUANTUM ELECTRONICS, 1990, 26 (12) :2166-2185
[5]   Fluorescence properties and metabolic features of indocyanine green (ICG) as related to angiography [J].
Desmettre, T ;
Devoisselle, JM ;
Mordon, S .
SURVEY OF OPHTHALMOLOGY, 2000, 45 (01) :15-27
[6]   NONINVASIVE FLUORESCENCE DETECTION OF HEPATIC AND RENAL FUNCTION [J].
Dorshow, Richard B. ;
Bugaj, Joseph E. ;
Burleigh, B. Daniel ;
Duncan, James R. ;
Johnson, Michael A. ;
Jones, William B. .
JOURNAL OF BIOMEDICAL OPTICS, 1998, 3 (03) :340-345
[7]   ASSESSMENT OF MICROCIRCULATION OF AN AXIAL SKIN FLAP USING INDOCYANINE GREEN FLUORESCENCE ANGIOGRAPHY [J].
EREN, S ;
RUBBEN, A ;
KREIN, R ;
LARKIN, G ;
HETTICH, R .
PLASTIC AND RECONSTRUCTIVE SURGERY, 1995, 96 (07) :1636-1649
[8]   MONTE-CARLO MODELING OF LIGHT-PROPAGATION IN HIGHLY SCATTERING TISSUES .1. MODEL PREDICTIONS AND COMPARISON WITH DIFFUSION-THEORY [J].
FLOCK, ST ;
PATTERSON, MS ;
WILSON, BC ;
WYMAN, DR .
IEEE TRANSACTIONS ON BIOMEDICAL ENGINEERING, 1989, 36 (12) :1162-1168
[9]   STABILITY STUDIES ON INDOCYANINE GREEN DYE [J].
GATHJE, J ;
STEUER, RR ;
NICHOLES, KR .
JOURNAL OF APPLIED PHYSIOLOGY, 1970, 29 (02) :181-&
[10]  
HOLLINS B, 1987, CLIN CHEM, V33, P765