TY - JOUR
T1 - The use of countercurrent chromatography in the separation of nonpolar lipid compounds
AU - Vetter, Walter
AU - Hammann, Simon
AU - Müller, Marco
AU - Englert, Michael
AU - Huang, Yining
PY - 2017/6/9
Y1 - 2017/6/9
N2 - Isolation of lipophilic compounds by countercurrent chromatography (CCC) is a challenge because biphasic solvent systems in which these compounds distribute evenly are difficult to obtain. In this article we present novel applications of lipid compound isolation from natural sources. Conjugated linolenic acids (CLnAs, log KOW ∼7) were isolated from pomegranate oil using a solvent system consisting of n-heptane/methanol/water 100:91:9 (v/v/v). The CLnA fraction was free of other fatty acids but consisted of different isomers which were not resolved from each other. In the less polar range (log KOW ∼12), three tocotrienols (α-, γ- and δ-tocotrienol) were isolated from a vitamin E capsule produced from palm oil by using the solvent system n-hexane/acetonitrile/benzotrifluoride (BTF) at a ratio of 10:6.5:3.5 (v/v/v). Between 36 and 65 mg of each of the three tocotrienols were obtained in one injection with purities >97%. Advantages and disadvantages of the “BTF system” are discussed by comparing the phase composition with the simple n-hexane/acetonitrile system and by the fractionation of phytosterols (log KOW ∼9.5) from rapeseed oil.
AB - Isolation of lipophilic compounds by countercurrent chromatography (CCC) is a challenge because biphasic solvent systems in which these compounds distribute evenly are difficult to obtain. In this article we present novel applications of lipid compound isolation from natural sources. Conjugated linolenic acids (CLnAs, log KOW ∼7) were isolated from pomegranate oil using a solvent system consisting of n-heptane/methanol/water 100:91:9 (v/v/v). The CLnA fraction was free of other fatty acids but consisted of different isomers which were not resolved from each other. In the less polar range (log KOW ∼12), three tocotrienols (α-, γ- and δ-tocotrienol) were isolated from a vitamin E capsule produced from palm oil by using the solvent system n-hexane/acetonitrile/benzotrifluoride (BTF) at a ratio of 10:6.5:3.5 (v/v/v). Between 36 and 65 mg of each of the three tocotrienols were obtained in one injection with purities >97%. Advantages and disadvantages of the “BTF system” are discussed by comparing the phase composition with the simple n-hexane/acetonitrile system and by the fractionation of phytosterols (log KOW ∼9.5) from rapeseed oil.
KW - BTF system
KW - Conugated linolenic acids
KW - Countercurrent chromatography
KW - Lipid compounds
KW - Tocotrienols
UR - http://www.scopus.com/inward/record.url?scp=85018676952&partnerID=8YFLogxK
U2 - 10.1016/j.chroma.2017.04.035
DO - 10.1016/j.chroma.2017.04.035
M3 - Article (Academic Journal)
C2 - 28456359
AN - SCOPUS:85018676952
SN - 0021-9673
VL - 1501
SP - 51
EP - 60
JO - Journal of Chromatography A
JF - Journal of Chromatography A
ER -