Development of Extraction and Gas Chromatography Analytical Methodology for Cyanogenic Glycosides in Flaxseed (Linum usitatissimum)

Abstract

Abstract The development of well-characterized rapid methodology for the extraction and gas chromatographic analysis of the cyanogenic glycosides linustatin and neolinustatin from flaxseed (Linum usitatissimum L.) is reported. Two quantitation methods using phenyl-β-d-glucopyranoside as an internal standard are described: direct quantitation using linustatin and neolinustatin external standard curves standard curve slope variabilities of 2.6 and 5.7% relative standard deviation (RSD), respectively, over 7 days or by use of methyl-α-d-glucopyranoside as a surrogate external standard, with conversion factors to convert to linustatin and neolinustatin concentration 1.109 ± 0.015 (SD) mg linustatin/mg methyl-α-d-glucopyranoside and 1.180 ± 0.067 (SD) mg neolinustatin/mg methyl-α-d-glucopyranoside. The former method is direct, thereby contributing less uncertainty to the method, and the latter adds a small degree of uncertainty coupled with considerable cost savings. Limits of detection for all standards were in the low- to sub-nanogram level and were 10-100 times lower than the lower limit of quantitation (LOQ). Repeatability precision was performed on 2 separate days at the lower and upper LOQs, with the RSD in peak response being 1% or lower in all cases. Extraction methods were evaluated for their ability to extract linustatin and neolinustatin from flaxseed using several combinations of aqueous ethanol, and recoveries were determined against the highest yielding method. Recoveries were as low as 82%, indicating that optimized extraction methodology is critical for the accuracy of results.