关键词: Chitin quantitation in food raw materials by HPLC—C18-DAD with off-line derivatization Chitosan Crab Cricket Crustaceans DAD Diode-array detector FLD Fluorescence detector Fungi Insects Liquid chromatography Lobster Mealworm Mushroom PDA Reverse phase Shrimp Tenebrio molitor

来  源:   DOI:10.1016/j.mex.2024.102729   PDF(Pubmed)

Abstract:
This HPLC method is suitable for chitin quantitation (reported as glucosamine) in food raw materials like insects (mealworm larvae, crickets), shrimps, mushrooms and fungi in a research (non-routine) laboratory using a C18 column with HPLC system <600 bar with UV detection capability (at 265 nm). To remove interferences, the sample is defatted (Soxhlet) and deproteinized (by alkali) prior to acid hydrolysis in 6 M HCl. A five-point linear calibration (5-100 µg/mL) is used. The use of fluorescence detection (λex = 260 nm, λem = 350 nm) is also possible with this method [1].•18 min HPLC run time•LOD = 0.05 µg/mL and LOQ = 5 µg/mL.
摘要:
此HPLC方法适用于昆虫(粉虫幼虫,板球),虾,研究(非常规)实验室中的蘑菇和真菌,使用C18色谱柱,HPLC系统<600bar,具有UV检测能力(265nm)。要消除干扰,将样品脱脂(索氏)并脱蛋白(通过碱),然后在6MHCl中进行酸水解。使用五点线性校准(5-100μg/mL)。使用荧光检测(λex=260nm,λem=350nm)也可以用这种方法[1]。•18分钟HPLC运行时间•LOD=0.05μg/mL和LOQ=5μg/mL。
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