LAUSR

BACKGROUND Propylene chlorohydrins (PCH) are formed as byproducts in the reaction between starch and propylene oxide (PO). For hydroxypropylated starch (HP-starch) applications in food, JECFA set the maximum allowed total propylene chlorohydrin (PHC-t) residues level at 1 mg/kg. OBJECTIVE To develop an improved analytical method for the determination of the PCH-t content in starches in the low mg/kg range to replace the outdated JECFA method. METHOD A new GC-MS method that utilizes aqueous methanol as extraction medium for PCH. The GC-MS system is equipped with a programmable temperature vaporization injector and Stabilwax-DA column using helium as carrier gas. The quantitative detection is achieved in the selected ion monitoring mode. RESULTS This single laboratory validation (SLV) study showed good linear calibrations for both 1-chloro-2-propanol (PCH-1) and 2-chloro-1-propanol (PCH-2) in the concentration range of 0.5-4 mg/kg in dry starch. The lower limit of quantitation of PCH-1 and PCH-2 was 0.2-0.3 mg/kg in dry starch, the relative standard deviation reproducibility (RSDR) at the concentration level of 1-2 mg/kg in dry starch was 3-5%, and the recovery values for both PCH-1 and PCH-2 were in the range of 78-112% at a concentration level of about 0.6 mg/kg in dry starch.Compared with the current, outdated JECFA method, the new GC-MS method is more sustainable, less laborious and therefore more economical. The analytical capacity of the new method is 4-5 times higher than the analytical capacity of the old JECFA method. CONCLUSION The GC-MS method is fit for a Multi Laboratory Trial (MLT). HIGHLIGHT Based on the results of this SLV and the MLT (will be published in a second paper), the Joint FAO/WHO Expert Committee on Food Additives has recently decided to replace the outdated GC-FID JECFA method for the new GC-MS method for the determination of PCH-t content in starches.