Gupta Rakesh, Kashyap Nishi, Rai Beena
Physical Science Research Area, TCS Research, Tata Research Development and Design Centre, 54B, Hadapsar, Pune, India.
Department of Chemical Engineering, Indian Institute of Technology Delhi, New Delhi, India.
Phys Chem Chem Phys. 2017 Mar 15;19(11):7537-7545. doi: 10.1039/c6cp08775b.
Transdermal delivery, where the skin acts as the route for local or systemic distribution, presents a lot of advantages over conventional routes such as oral and intravenous and intramuscular injections. However, the delivery of large biomolecules like proteins through the skin is challenging due to their size and structural properties. A molecular level understanding of their transport across the skin barrier is desirable to design successful formulations. We have employed constrained and unconstrained coarse grained molecular dynamics simulation techniques to obtain the molecular mechanism of penetration of the horseradish peroxidase (HRP) protein into the skin, in the presence and absence of gold nanoparticles (AuNPs). Unconstrained simulations show that HRP, when considered individually, was not able to breach the skin barrier, while in the presence of AuNPs, it first binds to the AuNPs and then breaches the barrier. The constrained simulations revealed that there was a free energy barrier for HRP to permeate inside the skin lipid layer when taken alone, while in the presence of gold nanoparticles, no barrier was found. Our study opens up the field of computational modeling based design of nanoparticle carriers for a given protein's transdermal delivery.
经皮给药是指皮肤作为局部或全身给药的途径,与口服、静脉注射和肌肉注射等传统给药途径相比具有诸多优势。然而,由于蛋白质等大分子的大小和结构特性,通过皮肤递送它们具有挑战性。为了设计出成功的制剂,需要从分子水平了解它们穿过皮肤屏障的过程。我们采用了受限和非受限粗粒度分子动力学模拟技术,以获得在有和没有金纳米颗粒(AuNP)的情况下,辣根过氧化物酶(HRP)蛋白渗透到皮肤中的分子机制。非受限模拟表明,单独考虑时,HRP无法突破皮肤屏障,而在有AuNP的情况下,它首先与AuNP结合,然后突破屏障。受限模拟显示,单独的HRP渗透到皮肤脂质层内部时存在自由能屏障,而在有金纳米颗粒的情况下,则没有发现屏障。我们的研究开辟了基于计算建模设计用于特定蛋白质经皮递送的纳米颗粒载体的领域。