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Detection method based on real-time polymerase chain reaction for celery (Apium graveolens) in beverages and dehydrated soups

机译:基于实时聚合酶链反应的饮料和脱水汤中芹菜的检测方法

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摘要

According to European legislation, food ingredients with potential allergenic properties, including celery (Apium graveolens), have to be declared. In order to provide an appropriate detection method for specific matrices, a method based on real-time polymerase chain reaction (PCR) for celery in beverages and dehydrated soups was developed and validated. Three varieties of celery frequently processed in food production were used for artificial contamination of vegetable and fruit beverages as well as instant soups in order to prepare model samples. Detection limits of 2.8-9.2 pg celery DNA per sample (200 mg of food sample) for all three varieties were reached. Inclusivity and exclusivity of the real-time PCR system was 100 %. A practical detection limit of 10 mg center dot kg(-1) was determined for artificially contaminated beverages and soups. Real samples of fresh pressed vegetable and fruit juices with and without the celery component were analysed with identical results stated by the manufacturer.
机译:根据欧洲法规,必须声明具有潜在过敏特性的食品成分,包括芹菜(Apiumgravolens)。为了为特定基质提供合适的检测方法,开发并验证了一种基于实时聚合酶链反应(PCR)的饮料和脱水汤中芹菜的检测方法。食品生产中经常加工的三种芹菜品种被用于人为污染的蔬菜和水果饮料以及速溶汤汁,以制备模型样品。所有三个品种的每个样品(200 mg食品样品)的检出限为2.8-9.2 pg芹菜DNA。实时PCR系统的包含性和专有性为100%。确定了人为污染的饮料和汤料的实际检测极限为10 mg中心点kg(-1)。使用和不使用芹菜成分对新鲜压榨的蔬菜和果汁的真实样品进行了分析,制造商给出的结果相同。

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