TY - JOUR
T1 - In-capillary derivatization with fluorescamine for the rapid determination of adamantane drugs by capillary electrophoresis with UV detection
AU - Prapatpong, Pornpan
AU - Nuchtavorn, Nantana
AU - Macka, Mirek
AU - Suntornsuk, Leena
N1 - Publisher Copyright:
© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2018/10
Y1 - 2018/10
N2 - In-capillary derivatization using fluorescamine as the labeling reagent was proposed to enhance the detectability of adamantine drugs (memantine, amantadine and rimantadine) by spectrophotometric detection. Fluorescamine and the drugs were delivered to the capillary electrophoresis instrument at a ratio of 10:1 by zone injection. The derivatization reaction occurred following the application of voltage (20 kV). The derivatized products, hydrolyzed- fluorescamine and excess fluorescamine were separated in 7 min using 100 mM borate buffer (pH 10.0) containing 0.1% w/v of Brij®-35 and 20% v/v of acetonitrile. Validation data showed good linearity (r2 > 0.98), precision (%RSDs < 3.4), and accuracy (recoveries ranging from 98.0 to 102.0%). The detection and quantitation limits are in the range of 6.0–8.5 and 18–25 μM, respectively. The validation data is comparable to reported methods, however, the current method offers better precision with enhanced sensitivity (up to six times). Applications of the method show percent labeled amounts found in the studied samples within 100.6–109.3%, which complied with the United States Pharmacopeia limit (90.0–110.0%). The method was simple, rapid and, automated, which required no extra instrumentation or skillful operators.
AB - In-capillary derivatization using fluorescamine as the labeling reagent was proposed to enhance the detectability of adamantine drugs (memantine, amantadine and rimantadine) by spectrophotometric detection. Fluorescamine and the drugs were delivered to the capillary electrophoresis instrument at a ratio of 10:1 by zone injection. The derivatization reaction occurred following the application of voltage (20 kV). The derivatized products, hydrolyzed- fluorescamine and excess fluorescamine were separated in 7 min using 100 mM borate buffer (pH 10.0) containing 0.1% w/v of Brij®-35 and 20% v/v of acetonitrile. Validation data showed good linearity (r2 > 0.98), precision (%RSDs < 3.4), and accuracy (recoveries ranging from 98.0 to 102.0%). The detection and quantitation limits are in the range of 6.0–8.5 and 18–25 μM, respectively. The validation data is comparable to reported methods, however, the current method offers better precision with enhanced sensitivity (up to six times). Applications of the method show percent labeled amounts found in the studied samples within 100.6–109.3%, which complied with the United States Pharmacopeia limit (90.0–110.0%). The method was simple, rapid and, automated, which required no extra instrumentation or skillful operators.
KW - adamantine
KW - fluorescamine
KW - in-capillary derivatization
KW - memantine
KW - rimantadine
UR - https://www.scopus.com/pages/publications/85052483468
U2 - 10.1002/jssc.201800591
DO - 10.1002/jssc.201800591
M3 - Article
C2 - 30063122
AN - SCOPUS:85052483468
SN - 1615-9306
VL - 41
SP - 3764
EP - 3771
JO - Journal of Separation Science
JF - Journal of Separation Science
IS - 19
ER -