TY - JOUR
T1 - Fluorometric determination of angiotensins in human plasma derivatized with 2,3-naphthalenedialdehyde
AU - Matsufuji, Hiroshi
AU - Matsui, Toshiro
AU - Oki, Tomoyuki
AU - Osajima, Yutaka
AU - Kawasaki, Terukazu
PY - 1995
Y1 - 1995
N2 - A fluorometric determination method for angiotensins (ANG I, II, III) in human plasma was developed with 2,3-naphthalenedialdehyde (NDA). Human plasma (10 ml) ultrafiltered with a Molucut L (< M.W. 5000) was put directly on a reversed-phase column for HPLC with an UV detector. The fractions containing each angiotensin were derivatized with 0.1 mM NDA in the presence of cyanide for 60 min at ambient temperature. The derivatized angiotensin (NDA-ANG) was injected onto the HPLC system with a fluorometric detector. Excitation and emission wavelengths were set at 420 nm and 490 nm, respectively. The peak areas of NDA-ANG were linearly related with the amount of angiotensin applied, and were highly reproducible (3.5%, n=5). The concentrations of ANG I, II and III in plasma, calculated from the respective calibration curve, were 315.8 pg/ml, 19.2pg/ml and <1.3pg/ml, respectively. The concentration of ANG II obtained by this fluorometric method coincided with that (22.6 pg/ml) by radioimmunoassay.
AB - A fluorometric determination method for angiotensins (ANG I, II, III) in human plasma was developed with 2,3-naphthalenedialdehyde (NDA). Human plasma (10 ml) ultrafiltered with a Molucut L (< M.W. 5000) was put directly on a reversed-phase column for HPLC with an UV detector. The fractions containing each angiotensin were derivatized with 0.1 mM NDA in the presence of cyanide for 60 min at ambient temperature. The derivatized angiotensin (NDA-ANG) was injected onto the HPLC system with a fluorometric detector. Excitation and emission wavelengths were set at 420 nm and 490 nm, respectively. The peak areas of NDA-ANG were linearly related with the amount of angiotensin applied, and were highly reproducible (3.5%, n=5). The concentrations of ANG I, II and III in plasma, calculated from the respective calibration curve, were 315.8 pg/ml, 19.2pg/ml and <1.3pg/ml, respectively. The concentration of ANG II obtained by this fluorometric method coincided with that (22.6 pg/ml) by radioimmunoassay.
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U2 - 10.2116/bunsekikagaku.44.783
DO - 10.2116/bunsekikagaku.44.783
M3 - Article
AN - SCOPUS:85008309260
SN - 0525-1931
VL - 44
SP - 783
EP - 788
JO - Bunseki Kagaku
JF - Bunseki Kagaku
IS - 10
ER -