Label-Free Fluorescent Poly(amidoamine) Dendrimer for Traceable and Controlled Drug Delivery

被引:25
|
作者
Wang, Guoying [1 ,2 ]
Fu, Libing [1 ,2 ]
Walker, Adam [1 ,5 ]
Chen, Xianfeng [6 ]
Lovejoy, David B. [1 ]
Hao, Mingcong [2 ]
Lee, Albert [1 ]
Chung, Roger [1 ]
Rizos, Helen [1 ]
Irvine, Mal [1 ]
Zheng, Meng [2 ]
Liu, Xiuhua [3 ]
Lu, Yiqing [2 ,4 ]
Shi, Bingyang [1 ,2 ]
机构
[1] Macquarie Univ, Fac Med & Hlth Sci, Dept Biomed Sci, Sydney, NSW 2109, Australia
[2] Henan Univ, Henan Macquarie Univ Joint Ctr Biomed Innovat, Kaifeng 475001, Peoples R China
[3] Henan Univ, Sch Chem Engn, Kaifeng 475001, Peoples R China
[4] Macquarie Univ, Fac Sci & Engn, Dept Phys & Astron, Sydney, NSW 2109, Australia
[5] Univ Queensland, Queensland Brain Inst, St Lucia, Qld 4072, Australia
[6] Univ Edinburgh, Inst Bioengn, Sch Engn, Kings Bldg,Mayfield Rd, Edinburgh EH9 3JL, Midlothian, Scotland
基金
中国国家自然科学基金; 澳大利亚国家健康与医学研究理事会;
关键词
PAMAM DENDRIMERS; DOXORUBICIN; RELEASE; INHIBITION; POLYMERS; PLATFORM; CARRIER; DOX;
D O I
10.1021/acs.biomac.9b00494
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Poly(amidoamine) dendrimer (PAMAM) is well-known for its high efficiency as a drug delivery vehicle. However, the intrinsic cytotoxicity and lack of a detectable signal to facilitate tracking have impeded its practical applications. Herein, we have developed a novel label-free fluorescent and biocompatible PAMAM derivative by simple surface modification of PAMAM using acetaldehyde. The modified PAMAM possessed a strong green fluorescence, which was generated by the C=N bonds of the resulting Schiff Bases via n-pi* transition, while the intrinsic cytotoxicity of PAMAM was simultaneously ameliorated. Through further PEGylation, the fluorescent PAMAM demonstrated excellent intracellular tracking in human melanoma SKMEL28 cells. In addition, our PEGylated fluorescent PAMAM derivative achieved enhanced loading and delivery efficiency of the anticancer drug doxorubicin (DOX) compared to the original PAMAM. Importantly, the accelerated kinetics of DOX-encapsulated fluorescent PAMAM nanocomposites in an acidic environment facilitated intracellular drug release, which demonstrated comparable cytotoxicity to that of the free-form doxorubicin hydrochloride (DOX"FIC1) against melanoma cells. Overall, our label free fluorescent PAMAM derivative offers a new opportunity of traceable and controlled delivery for DOX and other drugs of potential clinical importance.
引用
收藏
页码:2148 / 2158
页数:11
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