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Influence of ceramide 2 on in vitro skin permeation and retention of 5-ALA and its ester derivatives, for Photodynamic Therapy

机译:神经酰胺2对光动力疗法对5-ALA及其酯衍生物的体外皮肤渗透和保留的影响

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摘要

Photodynamic therapy (PDT) based on topical 5-aminolevulinic acid (5-ALA), an endogenous precursor of protoporphyrin, is an interesting approach for the treatment of skin cancer. However, 5-ALA is a hydrophilic molecule and such a characteristic limits its appropriate cutaneous penetration and retention. In this way, more lipophilic molecules, such as esterified 5-ALA derivatives, have been under investigation in order to improve the skin penetration of this molecule. Drug formulation can also alter 5-ALA skin penetration. Therefore, the aim of this work was to study the influence of ceramide 2 - the main lipid of the SC- on the cutaneous delivery of 5-ALA and its ester derivatives in vitro, using Franz diffusion cell. The skin permeation of all studied drugs was decreased in the presence of ceramide, representing a desirable characteristic in order to avoid the risk of systemic side effects. Nevertheless, the SC and [epidermis + dermis] retention after 16 h has also been decreased in the presence of ceramide, as compared to control. In conclusion, ceramide was not a good adjuvant, meaning that research of other vehicles could be useful to improve cutaneous delivery of 5-ALA.
机译:基于局部5-氨基乙酰丙酸(5-ALA)(原卟啉的内源性前体)的光动力疗法(PDT)是一种治疗皮肤癌的有趣方法。然而,5-ALA是亲水分子,并且这种特性限制了其适当的皮肤渗透和保留。以这种方式,已经研究了更多的亲脂性分子,例如酯化的5-ALA衍生物,以改善该分子的皮肤渗透性。药物制剂还可以改变5-ALA皮肤渗透率。因此,这项工作的目的是使用Franz扩散池研究神经酰胺2(SC的主要脂质)对5-ALA及其酯衍生物的体外皮肤递送的影响。在神经酰胺的存在下,所有研究药物的皮肤渗透性均降低,这是一种理想的特性,以避免发生全身性副作用的风险。然而,与对照相比,在存在神经酰胺的情况下,在16小时后的SC和[表皮+真皮]保留也降低了。总之,神经酰胺不是很好的佐剂,这意味着对其他媒介物的研究可能对改善5-ALA的皮肤递送有用。

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