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用于局部给药的负载番茄红素的纳米结构脂质载体制剂的物理化学特性

Physicochemical characterization of lycopene-loaded nanostructured lipid carrier formulations for topical administration.

作者信息

Okonogi Siriporn, Riangjanapatee Pornthida

机构信息

Department of Pharmaceutical Sciences, Faculty of Pharmacy, Chiang Mai University, Chiang Mai 50200, Thailand.

National Nanotechnology Center, National Science and Technology Development Agency (NSTDA), Pathum Thani 12120, Thailand.

出版信息

Int J Pharm. 2015 Jan 30;478(2):726-35. doi: 10.1016/j.ijpharm.2014.12.002. Epub 2014 Dec 3.

Abstract

Nanostructured lipid carriers (NLC) are interesting delivery systems for enhancing the penetration of an active substance through the skin after topical administration. In the present study, lycopene was loaded into NLC, composed of Eumulgin(®) SG, orange wax and rice bran oil, using high pressure homogenization (HPH). Photon correlation spectroscopy analysis showed that the lycopene-loaded NLC had a size of 150-160nm with a relatively small size distribution (PdI<0.15). The entrapment efficiency of lycopene was found to be 100±0% for all formulations. An in vitro release study of lycopene showed a biphasic release profile: a relatively fast release during the first 6h followed by a sustained release during the next 18h. An in vitro occlusion test showed that the occlusive properties of NLC increased with increasing lycopene loading. A free radical scavenging activity test of the NLC loaded with 50mg% lycopene showed a Trolox equivalent antioxidant capacity value of 36.6±0.4μM Trolox/mg NLC which is higher than that of the NLC base (26.6±0.1μM Trolox/mg NLC). The concentration of 50% antioxidant activity (IC50) of the lycopene-loaded NLC was 14.1±0.6mg/mL, and lower than that of the formulation without lycopene (17.7±0.4mg/mL). The particle size, size distribution, and zeta potential of lycopene-loaded NLC stored at different temperatures of 4, 30, 40°C for 120 days did not change in time, demonstrating an excellent colloidal stability of the systems. Chemical stability data indicated that the utilization of NLC increased the stability of lycopene and it was found that the degradation of lycopene was retarded when stored at low temperatures. In conclusion, NLC are attractive systems for the cutaneous delivery of lycopene.

摘要

纳米结构脂质载体(NLC)是一种有趣的给药系统,用于增强活性物质经皮局部给药后的透皮能力。在本研究中,采用高压均质法(HPH)将番茄红素负载到由聚氧乙烯脂肪酸酯(®)SG、橙蜡和米糠油组成的NLC中。光子相关光谱分析表明,负载番茄红素的NLC粒径为150 - 160nm,粒径分布相对较窄(多分散指数PdI < 0.15)。所有制剂中番茄红素的包封率均为100±0%。番茄红素的体外释放研究显示出双相释放曲线:在前6小时内释放相对较快,随后在接下来的18小时内持续释放。体外封闭试验表明,NLC的封闭性能随番茄红素负载量的增加而增强。对负载50mg%番茄红素的NLC进行自由基清除活性测试,结果显示其Trolox等效抗氧化能力值为36.6±0.4μM Trolox/mg NLC,高于NLC基质(26.6±0.1μM Trolox/mg NLC)。负载番茄红素的NLC的50%抗氧化活性浓度(IC50)为14.1±0.6mg/mL,低于不含番茄红素的制剂(17.7±0.4mg/mL)。负载番茄红素的NLC在4、30、40°C不同温度下储存120天,其粒径、粒径分布和zeta电位均未随时间变化,表明该体系具有优异的胶体稳定性。化学稳定性数据表明,NLC的应用提高了番茄红素的稳定性,并且发现低温储存时番茄红素的降解受到抑制。总之,NLC是用于番茄红素经皮给药的有吸引力的体系。

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