Zhang Chenzhen, He Tengfei, Vedadghavami Armin, Bajpayee Ambika G
Department of Bioengineering, Northeastern University, Boston, MA, 02115, USA.
Department of Mechanical Engineering, Northeastern University, Boston, MA, 02115, USA.
MethodsX. 2020 Apr 22;7:100882. doi: 10.1016/j.mex.2020.100882. eCollection 2020.
Here we describe methods for synthesizing a cationic, multi-arm Avidin (mAv) nano-construct that has a wide range of applications in drug delivery and imaging of negatively charged tissues. We use Avidin-biotin technology that gives the flexibility for conjugating biotinylated Dexamethasone to mAv by simple mixing at room temperature. We also describe methods to control hydrolysis rates of ester linkers to enable sustained (and tunable) drug release rates in therapeutic doses.•Multi-arm structure provides multiple sites for covalent conjugation of drugs•Use of Avidin-biotin reaction gives multi-arm nano-construct a modular design enabling conjugation and delivery of similar sized biotinylated drugs.
在此,我们描述了合成一种阳离子多臂抗生物素蛋白(mAv)纳米结构的方法,该结构在带负电荷组织的药物递送和成像方面有广泛应用。我们采用抗生物素蛋白-生物素技术,通过在室温下简单混合,可灵活地将生物素化地塞米松与mAv偶联。我们还描述了控制酯连接子水解速率的方法,以实现治疗剂量下持续(且可调)的药物释放速率。
•多臂结构为药物的共价偶联提供多个位点
•抗生物素蛋白-生物素反应的应用赋予多臂纳米结构模块化设计,使其能够偶联和递送大小相似的生物素化药物。