Bioinspired Core–Shell Nanoparticles for Hydrophobic Drug Delivery. Issue 40 (19th August 2019)

• Record Type: Journal Article
• Authors: Yang, Guangze; Liu, Yun; Wang, Haofei; Wilson, Russell; Hui, Yue; Yu, Lei; Wibowo, David; Zhang, Cheng; Whittaker, Andrew K.; Middelberg, Anton P. J.; Zhao, Chun‐Xia
• Is Part Of: Angewandte Chemie international edition. Volume 58:Issue 40(2019)
• Page Start: 14357
• Page End: 14364
• Publication Date: 2019-08-19
• Subjects: biomimetic synthesis -- cancer -- drug delivery -- nanoparticles -- peptides; Chemistry -- Periodicals; 540
• DOI: 10.1002/anie.201908357
• Languages: English
• ISSNs: 1433-7851

Abstract

Abstract: A large range of nanoparticles have been developed to encapsulate hydrophobic drugs. However, drug loading is usually less than 10 % or even 1 %. Now, core–shell nanoparticles are fabricated having exceptionally high drug loading up to 65 % (drug weight/the total weight of drug‐loaded nanoparticles) and high encapsulation efficiencies (>99 %) based on modular biomolecule templating. Bifunctional amphiphilic peptides are designed to not only stabilize hydrophobic drug nanoparticles but also induce biosilicification at the nanodrug particle surface thus forming drug‐core silica–shell nanocomposites. This platform technology is highly versatile for encapsulating various hydrophobic cargos. Furthermore, the high drug loading nanoparticles lead to better in vitro cytotoxic effects and in vivo suppression of tumor growth, highlighting the significance of using high drug‐loading nanoparticles. Abstract : Difunctional amphiphilic peptides were designed to not only stabilize hydrophobic drug nanoparticles but also induce biosilicification at the drug particle surface to maintain the long‐term stability of the nano‐drug. The drug‐core silica–shell nanocomposites have exceptionally high drug loading (up to 65 % w/w) and encapsulation efficiencies (>99 %).