http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
고체상 정제 및 HPLC/PDA에 의한 영유아식 중 나이아신의 분석
홍지은(Jee Eun Hong),김미란(Miran Kim),천상희(Sanghee Cheon),채정영(Jungyoung Chai),박은령(Eun Ryong Park),문춘선(Chun Sun Mun),곽인신(In-Shin Gwak),김옥희(Ok-Hee Kim),이광호(Kwang Ho Lee) 한국식품영양과학회 2009 한국식품영양과학회지 Vol.38 No.3
영유아식 중 나이아신의 기기분석법을 개발하고 영ㆍ유아식 중의 나이아신의 함량을 조사하였다. 니코틴산 및 니코틴아미드에 대해 액체 추출 및 고체상 정제과정을 통해 전처리한 후 HPLC로 분석할 경우 83~104% 범위의 회수율과 1.5~3.5% 범위의 재현성을 나타내었다. 또한 260 ㎚의 파장에서 분석할 경우 0.02~10 ㎎/L 범위에서 검량선의 직선성이 1.0000 수준으로 매우 높게 나타났으며 영유아식 중의 검출한계는 0.2 ㎎/㎏ 수준으로 나타났다. 총 50건의 영ㆍ유아식에 대해 나이아신 함량을 모니터링한 결과 53.5~140.3 ㎎/㎏ 수준으로 나타났으며 3회 반복시험 시의 상대표준편차는 0.6~5.5% 범위로 나타나 본 방법이 나이아신 분석에 유용한 방법임을 확인하였다. 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 83~104% and relative standard deviation were in the range of 1.5~3.5% 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 ㎚). It showed a high linearity between the content of niacin and the peak area (r²=1.000) in the range of 0.02~10.0 ㎎/L of nicotinic acid and nicotinamide. The detection limit was 0.02 ㎎/L (0.2 ㎎/㎏ in the sample). The method was successfully applied for the determination of niacin in infant formula. Total niacin contents were in the range of 53.5~140.3 ㎎/㎏.
RPLC/DAD를 이용한 Polycyclic Aromatic Hydrocarbon류의 분석에 관한 연구(I)
이원,홍지은,박송자,표희수,Lee, Won,Hong, Jee-Eun,Park, Song-Ja,Pyo, Hee Soo 한국분석과학회 1997 분석과학 Vol.10 No.5
Benzo(a)pyrene을 비롯한 16종의 polycyclic aromatic hydrocarbon(PAHs)과 4종의 nitro-PAHs를 reversed-phase liquid chromatography/diode array detection (RPLC/DAD)를 이용하여 기울기용리법으로 분리하고, PAH류의 머무름거동에 영향을 미치는 인자들, 즉 탄소수, F인자, L/B ratio, 물에 대한 용해도 및 방해수소원자쌍의 수와 시료의 머무름과의 상관관계를 고찰하였다. 대부분의 PAH류는 탄소원자수와 F값이 커질수록 logk'이 증가하는 사실을 확인하였다. 그리고 몇 가지 이성체들과 nitro-PAH류들은 용해도가 크고, L/B값이 작으며, 방해수소원자쌍의 수가 많을수록 먼저 용리됨을 확인하였다. 각 PAH류의 검출한계는 100~500ng/mL 범위로 나타났으며, 실제 물시료에 대한 검출한계(method detection limit, MDL)는 0.1~0.5ng/mL 범위였다. The retention behaviors of 16 PAHs and 4 nitro-PAHs were studied with several parameters involved numbers of carbon atoms, F factor, aqueous solubility, L/B ratio, and numbers of interfering hydrogen atom pairs on the chemical structures of PAHs by using reversed-phase liquid chromatography/diode array detection method (RPLC/DAD) and gradient elution method. It was obtain that the log k' for most of PAHs with increasing the number of carbon and the F factor in their molecules. Chromatographic retention of PAH isomers and nitro-PAHs were examined with aqueous solubility, L/B ratio and number of interfering hydrogen atom pairs. As a result of comparison with these factors and retention times, it was found that those solutes having larger aqueous solubilities and greater L/B ratios were retained longer on stationary phase. This tendency was also occured in the molecules having the more number of interfering hydrogen atom pairs. Detection limits of PAHs which were obtained with three times measurements by RPLC/DAD were in the range of 100~500ng/mL and method detection limit(MDL) for water sample were in the range of 0.1~0.5ng/mL.