Cutaneous delivery of 8-methoxypsoralen from liposomal and niosomal carriers

This work describes the preparation, characterization and properties of niosomal and liposomal carriers for the topical application of 8- metho.xypsoraten (8-MOP). lunge multilamellar (MLV) and sonicated unilamellar (UV) vesicular systems were prepared from either non-ionic surfactant octylklecyl polyglucoside (Oramix CGI 10) or hydrogenated soy phosphatidylcholine (Phospholipon 9011), cholesterol and a positive or negative charge inducer. The formulations were characterized using transmission electron microscopy (TEM) and Cryo-TEM, dynamic light scattering, incorporation efficiency and diffusion experiments through a silicone membrane. The effects of the vesicular incorporation on the 8-MOP diffusion through and into the skin were investigated in vitro using newborn pig skin. Statistical analysis of the data showed that alt the vesicular carriers increased the total 8-MOP permeation through the skin when compared to a control hydroalcoholic solution. Moreover, the amount of drug delivered into the skin was affected by the size and surface charge of the vesicles. Indeed, sonicated, positively charged octvl/decyl polyglucoside niosomes showed the greatest accumulation of 8-MOP in the skin (epidermis and dermis). These results suggest that our niosomes and liposomes may be suitable carriers in an 8-MOP cutaneous target.