TY - JOUR
T1 - Near infrared dyes as lifetime solvatochromic probes for micropolarity measurements of biological systems
AU - Berezin, Mikhail Y.
AU - Lee, Hyeran
AU - Akers, Walter
AU - Achilefu, Samuel
N1 - Funding Information:
This research was supported in part by National Institutes of Health grants R01 CA109754, R01 EB1430, 1 U01 HL080729, and U54 CA119342.
PY - 2007/10
Y1 - 2007/10
N2 - The polarity of biological mediums controls a host of physiological processes such as digestion, signaling, transportation, metabolism, and excretion. With the recent widespread use of near-infrared (NIR) fluorescent dyes for biological imaging of cells and living organisms, reporting medium polarity with these dyes would provide invaluable functional information in addition to conventional optical imaging parameters. Here, we report a new approach to determine polarities of macro- and microsystems for in vitro and potential in vivo applications using NIR polymethine molecular probes. Unlike the poor solvatochromic response of NIR dyes in solvents with diverse polarity, their fluorescence lifetimes are highly sensitive, increasing by a factor of up to 8 on moving from polar to nonpolar mediums. We also established a correlation between fluorescence lifetime and solvent orientation polarizability and developed a lifetime polarity index for determining the polarity of complex systems, including micelles and albumin binding sites. Because of the importance of medium polarity in molecular, cellular, and biochemical processes and the significance of reduced autofluorescence and deep tissue penetration of light in the NIR region, the findings reported herein represent an important advance toward using NIR molecular probes to measure the polarity of complex biological systems in vitro and in vivo.
AB - The polarity of biological mediums controls a host of physiological processes such as digestion, signaling, transportation, metabolism, and excretion. With the recent widespread use of near-infrared (NIR) fluorescent dyes for biological imaging of cells and living organisms, reporting medium polarity with these dyes would provide invaluable functional information in addition to conventional optical imaging parameters. Here, we report a new approach to determine polarities of macro- and microsystems for in vitro and potential in vivo applications using NIR polymethine molecular probes. Unlike the poor solvatochromic response of NIR dyes in solvents with diverse polarity, their fluorescence lifetimes are highly sensitive, increasing by a factor of up to 8 on moving from polar to nonpolar mediums. We also established a correlation between fluorescence lifetime and solvent orientation polarizability and developed a lifetime polarity index for determining the polarity of complex systems, including micelles and albumin binding sites. Because of the importance of medium polarity in molecular, cellular, and biochemical processes and the significance of reduced autofluorescence and deep tissue penetration of light in the NIR region, the findings reported herein represent an important advance toward using NIR molecular probes to measure the polarity of complex biological systems in vitro and in vivo.
UR - http://www.scopus.com/inward/record.url?scp=35348984824&partnerID=8YFLogxK
U2 - 10.1529/biophysj.107.111609
DO - 10.1529/biophysj.107.111609
M3 - Article
C2 - 17573433
AN - SCOPUS:35348984824
SN - 0006-3495
VL - 93
SP - 2892
EP - 2899
JO - Biophysical Journal
JF - Biophysical Journal
IS - 8
ER -