Pedersen Mona H, Holzhauser Thomas, Bisson Caroline, Conti Amedeo, Jensen Louise B, Skov Per S, Bindslev-Jensen Carsten, Brinch Ditte S, Poulsen Lars K
Laboratory of Medical Allergology, Copenhagen University Hospital, Denmark.
Mol Nutr Food Res. 2008 Dec;52(12):1486-96. doi: 10.1002/mnfr.200700394.
Soybean containing products are widely consumed, thus reliable methods for detection of soy in foods are needed in order to make appropriate risk assessment studies to adequately protect soy allergic patients. Six methods were compared using eight food products with a declared content of soy: a direct sandwich ELISA based on polyclonal rabbit antibody (ab) to raw soy flakes, a commercial and an in-house competitive ELISA both based on ab to denatured, 'renatured' soy protein, an enzyme-allergosorbent test (EAST) inhibition based on two sera from soy allergic patients, histamine release (HR) using basophils passively sensitized with patient serum and a PCR method detecting soy DNA. Eight food products were selected as model foods to test the performance of the methods. There was an overall good agreement between the methods in terms of ranks of soy content but not the quantity. The sandwich ELISA aimed at native soy proteins had the lowest detection limit of 0.05 ppm, but only identified soy in 5/8 products, and generally in lower amounts compared to other methods. The competitive ELISA had a higher detection limit of 21 ppm, but seemed more successful in detecting processed soy. Only HR, EAST inhibition and PCR detected soy in all eight products. In spite of a general good correlation in terms of ranks of soy content, more than a single method may be necessary to confirm the presence of soy in foods.
含大豆产品被广泛食用,因此需要可靠的食品中大豆检测方法,以便进行适当的风险评估研究,充分保护大豆过敏患者。使用八种宣称含有大豆的食品对六种方法进行了比较:一种基于兔抗生大豆片多克隆抗体(ab)的直接夹心酶联免疫吸附测定(ELISA)、一种基于抗变性“复性”大豆蛋白抗体的商业ELISA和一种内部竞争ELISA、一种基于两名大豆过敏患者血清的酶过敏原吸附试验(EAST)抑制法、一种使用患者血清被动致敏嗜碱性粒细胞的组胺释放(HR)法以及一种检测大豆DNA的聚合酶链反应(PCR)方法。选择了八种食品作为模型食品来测试这些方法的性能。就大豆含量的排名而言,这些方法总体上有较好的一致性,但数量上并非如此。针对天然大豆蛋白的夹心ELISA检测限最低,为0.05 ppm,但仅在8种产品中的5种中检测到大豆,且与其他方法相比,检测到的量通常较少。竞争ELISA的检测限较高,为21 ppm,但在检测加工大豆方面似乎更成功。只有HR、EAST抑制法和PCR在所有八种产品中都检测到了大豆。尽管在大豆含量排名方面总体相关性良好,但可能需要不止一种方法来确认食品中大豆的存在。