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采用邻苯二甲醛衍生化的在线柱后高效液相色谱法测定大米和小麦中水解葡萄糖神经酰胺中的鞘氨醇碱。

Determination of sphingoid bases from hydrolyzed glucosylceramide in rice and wheat by online post-column high-performance liquid chromatography with O-phthalaldehyde derivatization.

作者信息

Goto Hirofumi, Nishikawa Keiko, Shionoya Noriko, Taniguchi Makoto, Igarashi Tomoji

机构信息

Japan Food Research Laboratories, Nagoya Branch, Nagoya, Japan.

出版信息

J Oleo Sci. 2012;61(12):681-8. doi: 10.5650/jos.61.681.

DOI:10.5650/jos.61.681
PMID:23196868
Abstract

We developed a determination method for sphingoid bases using online post-column high-performance liquid chromatography (HPLC) with O-phthalaldehyde (OPA) derivatization. Good separation was achieved using a reversed-phase column and eluting with 50% acetonitrile containing formic acid and heptafluorobutyric acid. Using these conditions, an excellent linearity (R² > 0.999) was achieved using standard solutions of sphinganine (d18:0), sphingosine (d18:1(4t)), 4-hydroxy-sphinganine (t18:0), glucosylsphingosine (glc-d18:1(4t)), and galactosylsphingosine (gal-d18:1(4t)). Plant glucosylceramides were hydrolyzed with 1 M aqueous HCl in methanol for 18 h at 90°C, followed by extraction of sphingoid bases with diethyl ether in preparation for analysis using the proposed HPLC conditions. The glc-d18:1(4t) standard was also hydrolyzed and analyzed by HPLC using the same procedure, and the d18:1(4t) peak obtained from the hydrolyzed glc-d18:1(4t) standard was used as a reference for calculation. We also confirmed the applicability of this method to the analysis of sphingoid bases in rice and wheat, obtaining relative standard deviations of 8.0% for rice and 4.6% for wheat. The recoveries of spiked rice and wheat samples were 104% and 106%, respectively. Our proposed method enables the straightforward determination of sphingoid bases without expensive facilities, employing fluorescence detection of OPA derivatives.

摘要

我们开发了一种使用在线柱后高效液相色谱(HPLC)结合邻苯二甲醛(OPA)衍生化来测定鞘氨醇碱的方法。使用反相柱并以含有甲酸和七氟丁酸的50%乙腈洗脱,实现了良好的分离。在这些条件下,使用鞘氨醇(d18:0)、鞘氨醇(d18:1(4t))、4-羟基鞘氨醇(t18:0)、葡萄糖基鞘氨醇(glc-d18:1(4t))和半乳糖基鞘氨醇(gal-d18:1(4t))的标准溶液获得了出色的线性(R²>0.999)。植物葡萄糖神经酰胺在90°C下用1M盐酸甲醇水溶液水解18小时,然后用乙醚萃取鞘氨醇碱,以准备使用所提出的HPLC条件进行分析。glc-d18:1(4t)标准品也按照相同程序进行水解并用HPLC分析,从水解后的glc-d18:1(4t)标准品获得的d18:1(4t)峰用作计算参考。我们还证实了该方法对水稻和小麦中鞘氨醇碱分析的适用性,水稻的相对标准偏差为8.0%,小麦为4.6%。加标水稻和小麦样品的回收率分别为104%和106%。我们提出的方法能够在无需昂贵设备的情况下直接测定鞘氨醇碱,采用OPA衍生物的荧光检测。

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