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http://dx.doi.org/10.3746/jkfn.2009.38.3.359

Determination of Niacin in Infant Formula by Solid-phase Clean-up and HPLC with Photodiode Array Detector  

Hong, Jee-Eun (Center for Food and Drug Analysis, Gyeongin Regional Food & Drug Adminstration)
Kim, Mi-Ran (Center for Food and Drug Analysis, Gyeongin Regional Food & Drug Adminstration)
Cheon, Sang-Hee (Center for Food and Drug Analysis, Gyeongin Regional Food & Drug Adminstration)
Chai, Jung-Young (Center for Food and Drug Analysis, Gyeongin Regional Food & Drug Adminstration)
Park, Eun-Ryong (Center for Food and Drug Analysis, Gyeongin Regional Food & Drug Adminstration)
Mun, Chun-Sun (Center for Food and Drug Analysis, Gyeongin Regional Food & Drug Adminstration)
Gwak, In-Shin (Food Safety Evaluation Department, Korea Regional Food & Drug Adminstration)
Kim, Ok-Hee (Center for Food and Drug Analysis, Gyeongin Regional Food & Drug Adminstration)
Lee, Kwang-Ho (Food Safety Evaluation Department, Korea Regional Food & Drug Adminstration)
Publication Information
Journal of the Korean Society of Food Science and Nutrition / v.38, no.3, 2009 , pp. 359-363 More about this Journal
Abstract
This study was performed to establish a rapid and simple analytical method for niacin (nicotinic acid and nicotinamide) using HPLC. A pretreatment method for the extraction and clean-up of niacin in infant formula sample and an instrumental condition for HPLC were optimized. Niacin was extracted by 5 mM hexanesulfonate with ultrasonication for 30 min. For the clean-up of the sample, the extract was applied to a HLB cartridge, and then niacin was eluted from the cartridge using 5 mL of 80% methanol after washing with 5 mL of n-hexane. The total recoveries were $83{\sim}104%$ and relative standard deviation were in the range of $1.5{\sim}3.5%$ during the extraction and clean-up process. Niacin was determined by gradient elution with sodium hexanesulfonate/methanol buffer as a mobile phase and a photodiode array detector (260 nm). It showed a high linearity between the content of niacin and the peak area ($r^2$=1.000) in the range of $0.02{\sim}10.0$ mg/L of nicotinic acid and nicotinamide. The detection limit was 0.02 mg/L (0.2 mg/kg in the sample). The method was successfully applied for the determination of niacin in infant formula. Total niacin contents were in the range of $53.5{\sim}140.3$ mg/kg.
Keywords
niacin; HPLC; solid phase extraction; infant formula;
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