Melanin nanoparticles as an endogenous agent for efficient iron overload therapy

被引:21
|
作者
Yan, Junjie [1 ]
Ji, Yu [2 ,3 ]
Zhang, Pengjun [1 ]
Lu, Xiaomei [4 ,5 ]
Fan, Quli [2 ,3 ]
Pan, Donghui [1 ]
Yang, Runlin [1 ]
Xu, Yuping [1 ]
Wang, Lizhen [1 ]
Zhang, Lei [2 ,3 ]
Yang, Min [1 ]
机构
[1] Jiangsu Inst Nucl Med, Key Lab Nucl Med, Jiangsu Key Lab Mol Nucl Med, Minist Hlth, Wuxi 214063, Peoples R China
[2] Nanjing Univ Posts & Telecommun, Key Lab Organ Elect Informat Displays, Nanjing 210023, Jiangsu, Peoples R China
[3] Nanjing Univ Posts & Telecommun, Inst Adv Mat, Nanjing 210023, Jiangsu, Peoples R China
[4] Nanjing Tech Univ NanjingTech, Jiangsu Natl Synerget Innovat Ctr Adv Mat SICAM, KLOFE, Nanjing 211816, Jiangsu, Peoples R China
[5] Nanjing Tech Univ NanjingTech, Jiangsu Natl Synerget Innovat Ctr Adv Mat SICAM, IAM, Nanjing 211816, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
DEFERASIROX; CHEMISTRY; SYSTEM;
D O I
10.1039/c6tb01558a
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
Improving iron-chelating drugs for the safe and efficient therapy of iron overload disease is greatly challenging and highly desired. Endogenous iron chelators are perfect candidates because of their intrinsic biodegradability and biocompatibility, which avoid the severe side effects of the exogenous drugs currently present in clinical applications. Herein, for the first time, we have reported simply using melanin nanoparticles as an efficient natural nano-drug for iron overload therapy in living mice. Its native biocompatibility, biodegradability, high iron-capturing volume and long circulation time endow it with a lower required dosage quantity and frequency, but it accomplishes better therapeutic effects than the traditional drug deferoxamine (DFO).
引用
收藏
页码:7233 / 7240
页数:8
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