Angelini G, Rigano L, Foti C, Vena G A, Grandolfo M
Department of Dermatology, University of Bari, Italy.
Contact Dermatitis. 1996 Apr;34(4):248-52. doi: 10.1111/j.1600-0536.1996.tb02194.x.
Since finding that all subjects with contact allergy to cocamidopropylbetaine give positive reactions to 3-dimethylaminopropylamine (DMPA), we wished to verify whether sensitization to other industrially-used tensioactives might also be due to content of DMPA as an impurity. We also investigated the possible "carrier action" that tensioactives might exert on minimal quantities of DMPA. Finally, we analyzed the relationship between the structure of DMPA and other chemically-correlated molecules and their sensitizing potential, with particular reference to the structure of alkylamidopropylbetaines. For this purpose, in 34 patients with contact allergy to DMPA, we tested: (i) DMPA in concentrations below the threshold limit in water and in different tensioactives; (ii) substances that employ DMPA as a reagent in their synthesis; (iii) substances similar to DMPA as regards chemically reactive groups. The study showed that: (i) DMPA remains as a quantitatively detectable impurity in all tensioactives employing it in their synthesis; (ii) some common anionic (SLES) and non-ionic (polysorbate 20) tensioactives enhance the risk of sensitization from very low doses of DMPA, presumably due to a "carrier effect;" (iii) the sensitizing chemical structures in DMPA and related molecules are the primary amine and the tertiary (dimethyl-substituted) amine groups, when separated by either 2 or 3 carbon atoms; (iv) no sensitizing action can be attributed to the functional groups present in alkylamidopropylbetaine molecules.
自从发现所有对椰油酰胺丙基甜菜碱有接触性过敏的受试者对3-二甲基氨基丙胺(DMPA)均呈阳性反应后,我们希望验证对其他工业用表面活性剂的致敏作用是否也可能归因于作为杂质的DMPA含量。我们还研究了表面活性剂对极少量DMPA可能产生的“载体作用”。最后,我们分析了DMPA与其他化学相关分子的结构及其致敏潜力之间的关系,尤其参考了烷基酰胺丙基甜菜碱的结构。为此,我们对34名对DMPA有接触性过敏的患者进行了测试:(i)测试水中以及不同表面活性剂中浓度低于阈限值的DMPA;(ii)在合成过程中使用DMPA作为试剂的物质;(iii)在化学反应基团方面与DMPA相似的物质。研究表明:(i)在所有在合成过程中使用DMPA的表面活性剂中,DMPA均作为一种可定量检测的杂质存在;(ii)一些常见的阴离子表面活性剂(月桂醇聚醚硫酸酯钠)和非离子表面活性剂(聚山梨醇酯20)会增加极低剂量DMPA致敏的风险,可能是由于“载体效应”;(iii)当被2个或3个碳原子隔开时,DMPA及相关分子中的致敏化学结构是伯胺和叔(二甲基取代)胺基团;(iv)烷基酰胺丙基甜菜碱分子中存在的官能团无致敏作用。