Real-time monitoring of a controlled drug delivery system in vivo: construction of a near infrared fluorescence monomer conjugated with pH-responsive polymeric micelles

被引:17
作者
Chen, Li [1 ]
Chen, Bizheng [2 ]
Liu, Xiaodong [1 ]
Xu, Yujie [2 ]
Zhang, Lifen [1 ]
Cheng, Zhenping [1 ]
Zhu, Xiulin [1 ]
机构
[1] Soochow Univ, Suzhou Key Lab Macromol Design & Precis Synth, Jiangsu Key Lab Adv Funct Polymer Design & Applic, Dept Polymer Sci & Engn,Coll Chem Chem Engn & Mat, Suzhou 215123, Peoples R China
[2] Soochow Univ, Sch Radiat Med & Protect, Coll Med, Suzhou 215123, Peoples R China
基金
中国国家自然科学基金;
关键词
FRAGMENTATION CHAIN-TRANSFER; LIVING RADICAL POLYMERIZATION; REVERSIBLE-ADDITION; AGET ATRP; QUANTUM DOTS; NANOPARTICLES; NANOCOMPOSITE; NANOMATERIALS; COORDINATION; NANOCARRIERS;
D O I
10.1039/c6tb00315j
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Real-time monitoring of drug delivery systems has attracted growing interest for potential applications in biomedical therapy. Fluorescence imaging is a highly sensitive technique for illuminating the pathways of such systems. In this work, we designed and synthesized a new near infrared (NIR) fluorescent dye monomer (NFM). The NFM monomer was covalently attached to a pH-responsive amphiphilic block copolymer by reversible addition-fragmentation chain transfer (RAFT) copolymerization using hydrophilic poly(poly(ethylene glycol) methyl ether methacrylate) (PPEGMA) as the macro-RAFT agent and pH-responsive 2-(4-(dodecyloxy)phenyl)-1,3-dioxan-5-yl methacrylate (DBAM) and NFM as the comonomer, to synthesize the multifunctional amphiphilic block copolymer PPEGMA-b-P(DBAM-co-NFM) with NIR moieties and pH-sensitive groups. The PPEGMA-b-P(DBAM-co-NFM) could be self-assembled easily into stable micelles with doxorubicin (DOX) with an average diameter of 66 nm in water. The nano-size of the micelles is suitable for cycling through the body and carrying drugs to tumor sites safely via the enhanced permeability and retention (EPR) effect. Confocal laser scanning microscopy (CLSM) results indicated cells' uptake and the intracellular distribution. In vivo imaging of the micelles was observed in real time and the fluorescent signals clearly demonstrated the dynamic process of tumor treatment. This versatile and effective strategy is a potential tool for monitoring controlled drug delivery for tumor treatment.
引用
收藏
页码:3377 / 3386
页数:10
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