Brito Rodrigo O, Marques Eduardo F, Silva Sandra G, do Vale Maria Luísa, Gomes Paula, Araújo Maria J, Rodriguez-Borges J Enrique, Infante Maria Rosa, Garcia Maria Teresa, Ribosa Isabel, Vinardell María Pilar, Mitjans Montserrat
Departmento de Química, Faculdade de Ciências, Centro de Investigação em Química, Universidade do Porto, Porto, Portugal.
Colloids Surf B Biointerfaces. 2009 Aug 1;72(1):80-7. doi: 10.1016/j.colsurfb.2009.03.017. Epub 2009 Apr 1.
The design of efficient liposomal systems for drug delivery is of considerable biomedical interest. In this context, vesicles prepared from cationic/anionic surfactants may offer several advantages, mainly due to their spontaneity in formation and long-term stability. There is also an impending need to produce less toxic, more biocompatible amphiphiles, while maintaining the desirable aggregation properties. In this work, we present data for acute toxicity to Daphnia magna (IC(50)), and potential ocular irritation (HC(50)) for some newly prepared ionic surfactants with dodecyl chains, derived from the amino acids tyrosine (Tyr), serine (Ser), hydroxyproline (Hyp) and lysine (Lys). The micellization behavior of the compounds, evaluated from surface tension measurements, is presented and compared to more conventional ionic amphiphiles. Two types of spontaneouly formed catanionic vesicles, composed either by a dodecyltrimethylammonium bromide (DTAB)/Lys-derivative and or Ser-/Lys-derivative mixture, have also been tested for their ecotoxicity and hemolytic potential. All the micelle-forming surfactants as well as the vesicle-containing mixtures are found to have lower ecotoxicity than the reference surfactant DTAB. Moreover, the results from hemolysis and hemoglobin denaturation tests show that the Tyr- and Lys-derivatives are moderately irritant, whereas the Hyp- and Ser- ones are just slightly irritant. Even more significantly, the vesicle-containing mixtures exhibit lower hemolytic activity than the neat surfactants, a positive result for their potential use in liposomal formulations.
设计高效的脂质体药物递送系统具有重大的生物医学意义。在此背景下,由阳离子/阴离子表面活性剂制备的囊泡可能具有多种优势,主要因其形成的自发性和长期稳定性。同时,迫切需要生产毒性更低、生物相容性更高的两亲分子,同时保持理想的聚集特性。在这项工作中,我们给出了一些新制备的带有十二烷基链的离子型表面活性剂对大型溞的急性毒性(IC(50))以及潜在眼刺激性(HC(50))的数据,这些表面活性剂衍生自氨基酸酪氨酸(Tyr)、丝氨酸(Ser)、羟脯氨酸(Hyp)和赖氨酸(Lys)。通过表面张力测量评估了这些化合物的胶束化行为,并与更传统的离子型两亲分子进行了比较。还测试了两种自发形成的阴阳离子囊泡,一种由十二烷基三甲基溴化铵(DTAB)/赖氨酸衍生物组成,另一种由丝氨酸/赖氨酸衍生物混合物组成,评估了它们的生态毒性和溶血潜力。结果发现,所有形成胶束的表面活性剂以及含囊泡的混合物的生态毒性均低于参比表面活性剂DTAB。此外,溶血和血红蛋白变性试验结果表明,酪氨酸和赖氨酸衍生物有中度刺激性,而羟脯氨酸和丝氨酸衍生物只有轻微刺激性。更显著的是,含囊泡的混合物的溶血活性低于纯表面活性剂,这对于它们在脂质体制剂中的潜在应用来说是个积极结果。