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用于化妆品抗老化应用的载有七肽的固体脂质纳米粒。

Heptapeptide-loaded solid lipid nanoparticles for cosmetic anti-aging applications.

作者信息

Suter Franz, Schmid Daniel, Wandrey Franziska, Zülli Fred

机构信息

Mibelle Biochemistry, Bolimattstrasse 1, CH 5033 Buchs, Switzerland.

Mibelle Biochemistry, Bolimattstrasse 1, CH 5033 Buchs, Switzerland.

出版信息

Eur J Pharm Biopharm. 2016 Nov;108:304-309. doi: 10.1016/j.ejpb.2016.06.014. Epub 2016 Jun 23.

Abstract

The cosmetic industry requires more and more expensive actives and ingredients such as retinol, coenzyme Q10, proteins, peptides and biotechnologically produced molecules. In this study, we demonstrate the development of a cost effective formulation of a nanostructured lipid carrier (NLC) or solid lipid nanoparticles (SLN) improving peptide delivery into skin. NLC or SLN are very suitable vehicles for the delivery of active ingredients into skin. The SLN, produced by using hot high pressure homogenization method combine advantages such as physical stability, protection of incorporated labile actives and controlled release. By the used method we dispersed the amorphous heptapeptide DEETGEF in shea butter and homogenized this pre-dispersion at 60°C together with the water phase using a Microfluidizer at 1000bar. The analysis of the obtained SLN-P7 showed a particle size of 173nm, incorporated peptide of 0.014%, entrapment efficiency of 90.8%, melting peak (DSC) of the core lipid of 27°C and a zeta potential of -54mV. By an ex vivo study with skin explants we could stimulate NQO1 (NAD(P)H quinone oxidoreductase), HMOX1 (Heme oxygenase-1) and PRDX1 (Peroxiredoxin-1) genes all of which are cell protecting enzymes. In a multicellular protection against UV induced stress study with skin explants we detected the formation of sun burn cells and the number and morphology of Langerhans cells. The application of our SLN-P7 formulation on skin explants led to a significant and dose dependent protection against UV irradiation. In the clinical suction blister study, irradiation with UVA light for two hours after final product application led to a statistically significant increase of the 8-OhdG (8-hydroxy-2'-deoxyguanosine) concentration in the human epidermis. The skin treated with our verum formulation showed a statistically significant 20% decrease in DNA damage compared to placebo. In conclusion, it was demonstrated that SLN technology enabled peptide delivery into skin allowing it to perform protective functions.

摘要

化妆品行业对越来越昂贵的活性成分和原料的需求不断增加,比如视黄醇、辅酶Q10、蛋白质、肽以及生物技术生产的分子。在本研究中,我们展示了一种具有成本效益的纳米结构脂质载体(NLC)或固体脂质纳米粒(SLN)配方的开发,该配方可改善肽向皮肤中的递送。NLC或SLN是将活性成分递送至皮肤的非常合适的载体。通过使用热高压均质法生产的SLN兼具多种优点,如物理稳定性、保护包裹其中的不稳定活性成分以及控释。通过我们所采用的方法,我们将无定形七肽DEETGEF分散在乳木果油中,并在60°C下使用微流体均质器在1000巴的压力下将这种预分散液与水相一起均质化。对所得的SLN-P7的分析显示,其粒径为173nm,包裹的肽含量为0.014%,包封率为90.8%,核心脂质的熔点峰(差示扫描量热法)为27°C,ζ电位为-54mV。通过对皮肤外植体进行的体外研究,我们能够刺激NQO1(NAD(P)H醌氧化还原酶)、HMOX1(血红素加氧酶-1)和PRDX1(过氧化物酶1)基因,这些都是细胞保护酶。在一项针对皮肤外植体的多细胞抗紫外线诱导应激研究中,我们检测了晒伤细胞的形成以及朗格汉斯细胞的数量和形态。将我们的SLN-P7配方应用于皮肤外植体可产生显著的、剂量依赖性的抗紫外线辐射保护作用。在临床吸疱研究中,在最终产品应用后用UVA光照射两小时导致人表皮中8-OhdG(8-羟基-2'-脱氧鸟苷)浓度有统计学意义的增加。与安慰剂相比,用我们的真品配方处理的皮肤显示DNA损伤有统计学意义的20%的降低。总之,已证明SLN技术能够将肽递送至皮肤,使其发挥保护功能。

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