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Podophyllotoxin-loaded solid lipid nanoparticles for epidermal targeting

机译:载鬼臼毒素的固体脂质纳米粒用于表皮靶向

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The purpose of this study was to evaluate solid lipid nanoparticles as the topical carrier for epidermal targeting of podophyllotoxin (POD). The high pressure homogenization was employed to prepare drug-loaded solid lipid nanoparticles. The POD-loaded SLN stabilized by 0.5% poloxamer 188 and 1.5% soybean lecithin (P-SLN) and 2% polysorbate 80 (T-SLN) was characterized by photon correlation spectroscopy (PCS). P-SLN showed an average diameter of 73.4 nm and a zeta potential of -48.36 mV The imaging of AFM indicated that the P-SLN had a spherical shape. DSC and X-ray diffraction analysis showed that POD was dispersed in SLN in an amorphous state. The in vitro permeation study showed that P-SLN increased the accumulative amount of POD in porcine skin 3.48 times over 0.15% tincture. But T-SLN with a diameter of 123.1 nm and a zeta potential of -17.4 mV did not show a high accumulative amount of POD when compared with P-SLN, though both P-SLN and T-SLN could avoid the systemic uptake of POD. Because of the fluorescence property of POD, fluorescence microscopy imaging was employed to visualize the penetration of POD into skin from SLN. The penetration of POD from P-SLN seemed to follow two pathways along the stratum corneum and hair follicle route. The imaging revealed that P-SLN had a strong localization of POD within epidermis. The penetration of P-SLN with low particle size into stratum corneum along the skin surface 'furrow' and the consequent controlled release of POD might lead to the epidermal targeting. P-SLN provides a good epidermal targeting effect and may be a promising carrier for topical delivery of POD. (c) 2005 Elsevier B.V. All rights reserved.
机译:这项研究的目的是评估固态脂质纳米颗粒作为表皮靶向鬼臼毒素(POD)的局部载体。高压均质化用于制备载有药物的固体脂质纳米颗粒。用光子相关光谱法(PCS)对通过0.5%泊洛沙姆188和1.5%大豆卵磷脂(P-SLN)和2%聚山梨酯80(T-SLN)稳定的POD负载的SLN进行了表征。 P-SLN的平均直径为73.4 nm,ζ电位为-48.36mV。AFM成像表明P-SLN具有球形。 DSC和X射线衍射分析表明POD以无定形状态分散在SLN中。体外渗透研究表明,P-SLN比0.15%的cture剂使猪皮肤中POD的累积量增加了3.48倍。但是,与P-SLN相比,直径为123.1 nm且zeta电位为-17.4 mV的T-SLN并未显示出高的POD累积量,尽管P-SLN和T-SLN都可以避免系统吸收POD 。由于POD的荧光特性,因此采用荧光显微镜成像来可视化POD从SLN渗入皮肤的过程。 P-SLN的POD渗透似乎沿着角质层和毛囊途径的两个途径。成像显示,P-SLN在表皮中具有强烈的POD定位。低粒径的P-SLN沿皮肤表面“犁沟”渗透到角质层中,随后POD的受控释放可能导致表皮靶向。 P-SLN具有良好的表皮靶向作用,可能是POD局部递送的有希望的载体。 (c)2005 Elsevier B.V.保留所有权利。

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