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首页> 外文期刊>Chemistry: A European journal >Design of original bioactive formulations based on sugar-surfactanton-steroidal anti-inflammatory catanionic self-assemblies: A new way of dermal drug delivery
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Design of original bioactive formulations based on sugar-surfactanton-steroidal anti-inflammatory catanionic self-assemblies: A new way of dermal drug delivery

机译:基于糖表面活性剂/非甾体类消炎性阳离子自组装的原始生物活性制剂的设计:一种新型的皮肤药物递送方式

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摘要

A new kind of catanionic assembly was developed that associates a sugar-based surfactant with a non-steroidal anti-inflammatory drug (NSAID). Three different assemblies using indomethacin, ibuprofen and ketoprofen as NSAIDs were easily obtained in water by an acid-base reaction. These assemblies formed new amphiphilic entities because of electrostatic and hydrophobic effects in water and led to the spontaneous formation of vesicles. These catanionic vesicles were then tested as potential NSAID delivery systems for dermatological application. The anti-inflammatory activity was evaluated in vivo, and this study clearly showed an improved therapeutic effect for NSAIDs that were formulated as catanionic vesicles. These vesicles ensured a slower diffusion of the NSAID through the skin. This release probably increased the time of retention of the NSAID in the targeted strata of the skin. Thus, the present study suggests that this catanionic bioactive formulation could be a promising dermal delivery system for NSAIDs in the course of skin inflammation treatment.
机译:开发了一种新型的阳离子组件,该组件将糖基表面活性剂与非甾体抗炎药(NSAID)结合在一起。使用吲哚美辛,布洛芬和酮洛芬作为NSAID的三种不同组装物,可以通过酸碱反应在水中轻松获得。这些组装体由于在水中的静电和疏水作用而形成新的两亲实体,并导致囊泡的自发形成。然后将这些阳离子小泡作为潜在的NSAID递送系统进行皮肤病学测试。在体内评估了抗炎活性,这项研究清楚地表明了配制为阳离子小泡的NSAIDs的治疗效果有所改善。这些囊泡确保了NSAID在皮肤中的扩散较慢。这种释放可能会增加NSAID在皮肤目标层中的保留时间。因此,本研究表明该阳离子生物活性制剂在皮肤炎症治疗过程中可能是用于NSAID的有希望的皮肤递送系统。

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