TY - JOUR
T1 - Capillary electrophoresis with a UV light-emitting diode source for chemical monitoring of native and derivatized fluorescent compounds
AU - Hapuarachchi, Suminda
AU - Janaway, Gordon A.
AU - Aspinwall, Craig A.
PY - 2006/10
Y1 - 2006/10
N2 - We report the utilization of a high power UV light-emitting diode for fluorescence detection (UV-LED-IF) in CE separations. CE-UV-LED-IF allows analysis of a range of environmentally and biologically important compounds, including PAHs and biogenic amines, including neurotransmitters, amino acids, proteins, and peptides, that have been derivatized with UV-excited fluorogenic labels, e.g., o-phthalic dicarbox-aldehyde/ β-mercaptoethanol (OPA/β-ME). The 365 nm UV-LED was used as a stable, low cost source for detection of UV-excited fluorescent compounds. UV-LED-IF was used with both zonal CE separations and MEKC. Native fluorescence detection of PAHs was accomplished with detection limits ranging from 10 nM to 1.3 μM. Detection limits for OPA/ β-ME-labeled glutamic acid and aspartic acid were 11 and 10 nM, respectively, for off-line labeling, and 47 and 47 nM, respectively, for on-line labeling, comparable to UV-laser-based systems. Analysis of OPA/ β-ME-labeled proteins and peptides was performed with 28 and 47 nM detection limits for BSA and myoglobin, respectively.
AB - We report the utilization of a high power UV light-emitting diode for fluorescence detection (UV-LED-IF) in CE separations. CE-UV-LED-IF allows analysis of a range of environmentally and biologically important compounds, including PAHs and biogenic amines, including neurotransmitters, amino acids, proteins, and peptides, that have been derivatized with UV-excited fluorogenic labels, e.g., o-phthalic dicarbox-aldehyde/ β-mercaptoethanol (OPA/β-ME). The 365 nm UV-LED was used as a stable, low cost source for detection of UV-excited fluorescent compounds. UV-LED-IF was used with both zonal CE separations and MEKC. Native fluorescence detection of PAHs was accomplished with detection limits ranging from 10 nM to 1.3 μM. Detection limits for OPA/ β-ME-labeled glutamic acid and aspartic acid were 11 and 10 nM, respectively, for off-line labeling, and 47 and 47 nM, respectively, for on-line labeling, comparable to UV-laser-based systems. Analysis of OPA/ β-ME-labeled proteins and peptides was performed with 28 and 47 nM detection limits for BSA and myoglobin, respectively.
KW - Amino acids
KW - Capillary electrophoresis
KW - Chemical monitoring
KW - Fluorescent detection
KW - Light-emitting diode
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UR - http://www.scopus.com/inward/citedby.url?scp=33750579610&partnerID=8YFLogxK
U2 - 10.1002/elps.200600232
DO - 10.1002/elps.200600232
M3 - Article
C2 - 16983640
AN - SCOPUS:33750579610
SN - 0173-0835
VL - 27
SP - 4052
EP - 4059
JO - ELECTROPHORESIS
JF - ELECTROPHORESIS
IS - 20
ER -