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[负载生育酚磷酸酯的磷脂纳米粒的皮肤渗透特性表征与评价]

[Characterization and Evaluation of Skin Permeation of Tocopheryl Phosphoric Acid-loaded Phospholipid Nanoparticles].

作者信息

Uchino Tomonobu, Miyazaki Yasunori, Fujii Ako, Kagawa Yoshiyuki

机构信息

Department of Clinical Pharmaceutics, School of Pharmaceutical Sciences, University of Shizuoka.

出版信息

Yakugaku Zasshi. 2017;137(8):979-986. doi: 10.1248/yakushi.17-00014.

Abstract

Tocopheryl phosphoric acid (TPA, a hydrophilic vitamin E derivative) loaded liposome and glycerin containing phospholipid nanoparticles (GPLNP) were prepared using the film rehydration and extrusion method. Nanoparticle formulations were evaluated for size, zeta potential, and in vitro permeation across hairless mouse skin, and P NMR spectral analysis was performed. The prepared formulations were stable for 2 weeks, and their mean nanoparticle size varied between 90 and 140 nm. Although glycerin did not affect the particle size of the empty (no TPA) system, TPA-loading resulted in the reduction of particle size and conferred a negative charge. The P NMR spectral analysis showed that the presence of glycerin in the formulation changed the nanoparticle structure from a bilayer to a nonbilayer. Moreover, it was suggested that TPA molecules interacted with phospholipid by entrapping nanoparticles in the formulations. TPA did not permeate across the hairless mouse skin after 48 h. However, the TPA concentration in the hairless mouse skin after permeation study increased in the nanoparticle systems and the 30% GPLNP formulation was the best formulation for the accelerated TPA permeation in the hairless mouse skin. These results demonstrate that 30% GPLNP improved TPA permeation in the hairless mouse skin model. And it was strongly suggested that glycerin has an important role for changing the structure of nanoparticles and enhancing the skin permeation of TPA.

摘要

采用薄膜水化和挤压法制备了负载生育酚磷酸酯(TPA,一种亲水性维生素E衍生物)的脂质体和含甘油的磷脂纳米粒(GPLNP)。对纳米粒制剂进行了粒径、zeta电位以及在无毛小鼠皮肤上的体外渗透评估,并进行了磷核磁共振光谱分析。所制备的制剂在2周内稳定,其平均纳米粒粒径在90至140纳米之间变化。虽然甘油不影响空载体(无TPA)系统的粒径,但负载TPA会导致粒径减小并赋予负电荷。磷核磁共振光谱分析表明,制剂中甘油的存在将纳米粒结构从双层变为非双层。此外,提示TPA分子通过包裹制剂中的纳米粒与磷脂相互作用。48小时后TPA未渗透过无毛小鼠皮肤。然而,渗透研究后无毛小鼠皮肤中的TPA浓度在纳米粒系统中有所增加,30%GPLNP制剂是无毛小鼠皮肤中加速TPA渗透的最佳制剂。这些结果表明,30%GPLNP改善了TPA在无毛小鼠皮肤模型中的渗透。并且强烈提示甘油在改变纳米粒结构和增强TPA的皮肤渗透方面具有重要作用。

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