首页> 外文期刊>Chromatographia >Separation of natural food pigments in saponified and un-saponified paprika oleoresin by ultra high performance supercritical fluid chromatography (UHPSFC)
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Separation of natural food pigments in saponified and un-saponified paprika oleoresin by ultra high performance supercritical fluid chromatography (UHPSFC)

机译:超高效超临界流体色谱法(UHPSFC)分离皂化和未皂化辣椒粉中的天然食品色素

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摘要

The natural pigments in paprika were rapidly and efficiently separated by ultra high performance supercritical fluid chromatography. The separation of both un-saponified and saponified mixtures of paprika oleoresin were optimized, with run times of 10.6 min. Three different C18 columns, a cyano, silica and diol column, all 3 × 100 mm, with 1.8 μm particles were compared. The best separation for the un-saponified sample was found with an SB-C18 column, while the saponified samples were best separated on a bare silica, RX-Sil column. A SB-CN column allowed near optimum separation of both the unsaponified, and saponified samples, with similar run times. The best mobile phase was carbon dioxide (CO_2) modified with isopropyl alcohol (IPA), with a composition gradient. Fingerprints of several commercial pepper products indicated that one appeared to be colored with artificial dyes, while the color of a chili powder may have been enhanced with a paprika extract. Spectra, using CO_2 with IPA as modifier, produced a single maximum at 453 nm, which appears to represent up to a 30 nm solvatochromic shift from the maxima in most organic solvents. Acetonitrile (ACN) as modifier produced spectra with two maxima and a similar solvatochromic shift. These results appear to be the first on saponified paprika oleoresin samples using SFC. It is also the first detailed report on the separation of un-saponified samples. The results are up to six times faster than comparable results by HPLC. It appears that SFC is a viable, superior alternative to HPLC for the analysis of this important commercial product, without using ACN, or chlorinated solvents.
机译:辣椒粉中的天然色素通过超高效超临界流体色谱法快速有效地分离。优化了辣椒粉中未皂化和皂化混合物的分离,运行时间为10.6分钟。比较了三种不同的C18色谱柱(氰基,二氧化硅和二醇色谱柱),色谱柱均为3×100 mm,粒径为1.8μm。对于未皂化的样品,最好用SB-C18色谱柱进行分离,而最好用裸露的二氧化硅RX-Sil色谱柱对皂化的样品进行分离。 SB-CN色谱柱可以以相似的运行时间对未皂化和皂化样品进行近乎最佳的分离。最好的流动相是用异丙醇(IPA)改性的二氧化碳(CO_2),其组成梯度。几种商品胡椒产品的指纹显示,其中一种似乎用人造染料着色,而辣椒粉的颜色可能已被辣椒粉提取物所增强。使用带有IPA作为改性剂的CO_2的光谱在453 nm处产生了一个最大值,这似乎代表了在大多数有机溶剂中从最大值起直至30 nm的溶剂化色移。乙腈(ACN)作为改性剂产生的光谱具有两个最大值和相似的溶剂化色移。这些结果似乎是使用SFC对皂化辣椒粉油树脂样品进行的第一个结果。这也是关于未皂化样品分离的第一份详细报告。结果比HPLC的可比结果快六倍。看起来,在不使用ACN或氯化溶剂的情况下,SFC是分析该重要商业产品的可行且优于HPLC的替代品。

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