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首页> 外文期刊>The Open Conference Proceedings Journal >The Role of Deformable Liposome Characteristics on Skin Permeability ofMeloxicam: Optimal Transfersome as Transdermal Delivery Carriers
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The Role of Deformable Liposome Characteristics on Skin Permeability ofMeloxicam: Optimal Transfersome as Transdermal Delivery Carriers

机译:可变形脂质体特征对美洛昔康皮肤渗透性的作用:最佳传递体作为透皮传递载体。

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The role of deformable liposomes characteristics on skin permeability has evoked considerable interest, sincethe articles reporting the effectiveness of transfersomes for skin delivery were increasingly published. Several reportsfocus on the effect of formulation factor which directly affected the transfersome’s skin permeability. However, the effectof formulation factors was not fully understood as the contradictory results. To clarify this problem, the reliable statisticaltechniques, excellent experimental design and systematical variation were used in this study. Transfersomes loadedmeloxicam containing controlled amount of phosphatidylcholine (PC), cholesterol (Chol), type of surfactant (hydrophilicpart, lipophilic part ) were prepared and investigated for the physicochemical characteristics (e.g., size, size distribution,charge, elasticity, drug content, morphology) and skin permeability. The results indicated that the transfersome containing10% cholesterol, 29% cetylpyridinium chloride (cationic surfactant) with 16 carbons chain length and 10% meloxicamwas the optimal formulation for meloxicam transdermal delivery carrier. The skin permeation of meloxicam in noveltransfersome formulation was higher than classical transfersomes, conventional liposomes and meloxicam saturatedsuspension. Thus, our finding provided important fundamental information for developing novel deformable liposomesfor transdermal drug delivery, especially transfersomes containing surfactant systems.
机译:可变形脂质体特征对皮肤渗透性的作用引起了人们的极大兴趣,因为越来越多地报道了传递体对皮肤递送的有效性的文章。几份报告集中于直接影响传递体的皮肤渗透性的配方因子的作用。但是,配方因素的影响并没有被完全理解为矛盾的结果。为了澄清这个问题,本研究使用可靠的统计技术,出色的实验设计和系统的变异性。制备载有控制量的磷脂酰胆碱(PC),胆固醇(Chol),表面活性剂类型(亲水性部分,亲脂性部分)的载有美洛昔康的传递体,并研究其理化特性(例如大小,大小分布,电荷,弹性,药物含量,形态)和皮肤渗透性。结果表明,包含10%胆固醇,29%十六烷基氯化吡啶鎓(阳离子表面活性剂),碳链长度为16和10%美洛昔康的传递体是美洛昔康透皮递送载体的最佳配方。美洛昔康在新型转移体制剂中的皮肤渗透率高于经典的转移体,常规脂质体和美洛昔康饱和混悬液。因此,我们的发现为开发用于透皮药物递送的新型可变形脂质体,特别是含有表面活性剂系统的脂质体提供了重要的基础信息。

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