Department of Chemical Engineering, Pohang University of Science and Technology, Pohang 790-784 (Korea).
Division of Bioengineering, Incheon National University, Incheon 406-772 (Korea).
Angew Chem Int Ed Engl. 2015 Jun 15;54(25):7318-22. doi: 10.1002/anie.201501748. Epub 2015 May 12.
A novel bioinspired strategy for protein nanoparticle (NP) synthesis to achieve pH-responsive drug release exploits the pH-dependent changes in the coordination stoichiometry of iron(III)-3,4-dihydroxyphenylalanine (DOPA) complexes, which play a major cross-linking role in mussel byssal threads. Doxorubicin-loaded polymeric NPs that are based on Fe(III)-DOPA complexation were thus synthesized with a DOPA-modified recombinant mussel adhesive protein through a co-electrospraying process. The release of doxorubicin was found to be predominantly governed by a change in the structure of the Fe(III)-DOPA complexes induced by an acidic pH value. It was also demonstrated that the fabricated NPs exhibited effective cytotoxicity towards cancer cells through efficient cellular uptake and cytosolic release. Therefore, it is anticipated that Fe(III)-DOPA complexation can be successfully utilized as a new design principle for pH-responsive NPs for diverse controlled drug-delivery applications.
一种新颖的仿生策略被用于合成蛋白质纳米颗粒(NP)以实现 pH 响应性药物释放,该策略利用了铁(III)-3,4-二羟基苯丙氨酸(DOPA)配合物的配位化学计量比在贻贝足丝中发挥主要交联作用时的 pH 依赖性变化。通过共静电纺丝过程,用 DOPA 修饰的重组贻贝黏附蛋白合成了基于 Fe(III)-DOPA 络合的载多柔比星聚合物 NPs。发现多柔比星的释放主要受酸性 pH 值引起的 Fe(III)-DOPA 配合物结构变化所控制。还证明了所制备的 NPs 通过有效的细胞摄取和细胞质释放,对癌细胞表现出有效的细胞毒性。因此,预计 Fe(III)-DOPA 络合可以成功用作用于各种控制药物递送应用的 pH 响应性 NPs 的新设计原理。