首页> 外文期刊>Drug delivery letters >Nanopotentiation of Propolis for Revocation of Enzyme Imbalance in UVB Cnduced Cutaneous Toxicity in Murine Model: a Preliminary Study for Chemoprotection of Skin Cancer
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Nanopotentiation of Propolis for Revocation of Enzyme Imbalance in UVB Cnduced Cutaneous Toxicity in Murine Model: a Preliminary Study for Chemoprotection of Skin Cancer

机译:蜂胶的纳米增强作用可消除小鼠模型中UVB诱导的皮肤毒性中的酶失衡:皮肤癌化学保护作用的初步研究。

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Indian Propolis, a resin-like substance obtained from plants and modified by bees is a blend of various natural components and a potential candidate for topical application for chemoprevention of skin cancer. In the present study, the potential role of propolis loaded ethosomal transgel for the chemoprevention of skin cancer was investigated. Ethosomal vesicular systems were optimized by varying the proportions of lecithin and ethanol taking vesicle size, polydispersity index (PDI) and entrapment efficiency as dependent variables. The vesicles were found to be unilamellar spherical shaped entities with size varying from 100 nm to 300 nm and entrapment efficiency in a range of 48% to 84%. The permeation and extent of penetration of the optimized formulation were evaluated by Franz diffusion cell and Confocal scanning laser microscopy (CSLM) respectively. It showed a sustained mode of release and remarkable penetration capacity of vesicles (133um) as compared to hydroethanolic solution of the drug. Histopathological evaluation of the formulation treated skin revealed the interaction of vesicles with the skin which was further supported by FTIR analysis reflecting the mechanism of vesicle permeation via skin. Propolis loaded ethosomal vesicles were then incorporated into carbopol gel and characterized using a texture profile analyzer. The optimized gel so obtained was then finally evaluated for its chemo preventive activity by exposing Swiss albino mice to UVB radiation. The study indicated the possible use of propolis for the prevention of skin cancer through a deep-rooted delivery via ethosomal system eventually circumventing the problem of poor penetrability of topical preparations.
机译:印度蜂胶是一种从植物中获得并经过蜜蜂修饰的树脂样物质,是多种天然成分的混合物,是局部化学疗法预防皮肤癌的潜在候选者。在本研究中,研究了装载蜂胶的内体转凝胶对皮肤癌的化学预防的潜在作用。以囊泡大小,多分散指数(PDI)和包封效率为因变量,通过改变卵磷脂和乙醇的比例来优化酶体囊泡系统。发现该囊泡是单层球形实体,其尺寸在100nm至300nm之间变化并且包封效率在48%至84%的范围内。分别通过Franz扩散池和共聚焦扫描激光显微镜(CSLM)评估了优化配方的渗透性和渗透程度。与药物的氢乙醇溶液相比,它显示出持续的释放模式和显着的囊泡渗透能力(133um)。制剂处理的皮肤的组织病理学评价显示了囊泡与皮肤的相互作用,这由FTIR分析进一步支持,反映了囊泡经由皮肤渗透的机制。然后将装载有蜂胶的内体囊泡掺入卡波姆凝胶中,并使用质地分布分析仪进行表征。然后,通过将瑞士白化病小鼠暴露于UVB辐射中,最终评估由此获得的优化凝胶的化学预防活性。该研究表明蜂胶可以通过经由酶体系统的深层递送来预防皮肤癌,从而最终避免了局部制剂渗透性差的问题。

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