Arslan Azizoglu Gulcin, Tuncay Tanriverdi Sakine, Aydin Kose Fadime, Ballar Kirmizibayrak Petek, Ozer Ozgen
Department of Pharmaceutical Technology, Faculty of Pharmacy, Ege University, Izmir, Turkey.
Department of Biochemistry, Faculty of Pharmacy, Ege University, Izmir, Turkey.
AAPS PharmSciTech. 2017 Nov;18(8):2987-2998. doi: 10.1208/s12249-017-0786-1. Epub 2017 May 10.
Incorporation of antioxidants into sunscreens is a logical approach, yet co-delivery of them with UV filters is a challenge. Here, we purposed a combination therapy, in which the chemical UV filter, octyl methoxycinnamate, was accumulated on upper skin while the antioxidant, melatonin, can penetrate deeper layers to show its effects. Melatonin-loaded elastic niosomes and octyl methoxycinnamate Pickering emulsion were prepared separately. Lyophilized elastic niosomes were dispersed into the Pickering emulsion to prepare the proposed combination formulation. The characterization studies of the formulations revealed that elastic niosomes can be prepared with tunable nanometer sizes, whereas Pickering emulsions can encapsulate the UV filter in micrometer-sized droplets. Melatonin-loaded elastic niosomes prepared with Tween80/Span80 mixture were 146 nm with a PI of 0.438, and 58.42% entrapment efficiency was achieved. The mean diameter size of the combination formulation was 27.8 μm. Ex vivo permeation studies revealed that 7.40% of octyl methoxycinnamate and 58% of melatonin were permeated through the rat skin while 27.6% octyl methoxycinnamate and 37% of melatonin accumulated in the skin after 24 h. Cell culture studies with real-time cell analyzer showed that the proposed formulation consist of melatonin-loaded elastic niosomes and octyl methoxycinnamate Pickering emulsion had no negative effect on the cell proliferation and viability. According to α,α-diphenyl-β-picrylhydrazyl free radical scavenging method, the proposed formulation showed as high antioxidant activity as melatonin itself. It is concluded that the proposed formulation would be a promising dual therapy for UV-induced skin damage with co-delivery strategy.
将抗氧化剂添加到防晒霜中是一种合理的方法,然而将它们与紫外线过滤剂共同递送却是一项挑战。在此,我们提出了一种联合疗法,其中化学紫外线过滤剂甲氧基肉桂酸辛酯积聚在皮肤上层,而抗氧化剂褪黑素则可渗透到更深层发挥作用。分别制备了负载褪黑素的弹性非离子表面活性剂囊泡和甲氧基肉桂酸辛酯皮克林乳液。将冻干的弹性非离子表面活性剂囊泡分散到皮克林乳液中,制备出所提议的联合制剂。制剂的表征研究表明,弹性非离子表面活性剂囊泡可以制备成具有可调纳米尺寸的产品,而皮克林乳液可以将紫外线过滤剂包裹在微米级液滴中。用吐温80/司盘80混合物制备的负载褪黑素的弹性非离子表面活性剂囊泡直径为146纳米,多分散指数为0.438,包封率达到58.42%。联合制剂的平均直径大小为27.8微米。体外渗透研究表明,24小时后,7.40%的甲氧基肉桂酸辛酯和58%的褪黑素透过大鼠皮肤,同时有27.6%的甲氧基肉桂酸辛酯和37%的褪黑素积聚在皮肤中。使用实时细胞分析仪进行的细胞培养研究表明,所提议的由负载褪黑素的弹性非离子表面活性剂囊泡和甲氧基肉桂酸辛酯皮克林乳液组成的制剂对细胞增殖和活力没有负面影响。根据α,α-二苯基-β-苦基肼自由基清除法,所提议的制剂表现出与褪黑素本身一样高的抗氧化活性。结论是,所提议的制剂采用共同递送策略,将有望成为治疗紫外线引起的皮肤损伤的双重疗法。