Bioeliminable Nanohydrogels for Drug Delivery

被引:70
作者
Gao, De [1 ]
Xu, Hao [2 ]
Philbert, Martin A. [2 ]
Kopelman, Raoul [1 ]
机构
[1] Univ Michigan, Dept Chem, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Environm Hlth Sci, Ann Arbor, MI 48109 USA
关键词
D O I
10.1021/nl8017274
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
One of the most significant obstacles for systematic delivery of nanopayloads is the foreign particle clearance by the mononuclear phagocyte system (MPS). The majority of biocompatible nanopayloads with charged groups on their surface cannot fully evade the clearance by MPS during systemic circulation. For safe and effective targeted nanodrug delivery in vivo, we describe a novel approach for evading the macrophage clearance. We demonstrate that neutral and hydrophilic materials can effectively evade the macrophage uptake and also quickly degrade into bioeliminable fragments. We show that there is no opsonization effect and no toxic effect on living cells. In addition, the payloads are stable in an aqueous environment, and they can release drugs in a cellular environment. These results suggest that the unique properties of this kind of payloads may make them useful for designing new drug delivery systems.
引用
收藏
页码:3320 / 3324
页数:5
相关论文
共 27 条
[1]   Drug delivery systems: Entering the mainstream [J].
Allen, TM ;
Cullis, PR .
SCIENCE, 2004, 303 (5665) :1818-1822
[2]   Biodegradation and biocompatibility of PLA and PLGA microspheres [J].
Anderson, JM ;
Shive, MS .
ADVANCED DRUG DELIVERY REVIEWS, 1997, 28 (01) :5-24
[3]   Optochemical nanosensor PEBBLEs: photonic explorers for bioanalysis with biologically localized embedding [J].
Buck, SM ;
Koo, YEL ;
Park, E ;
Xu, H ;
Philbert, MA ;
Brasuel, MA ;
Kopelman, R .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2004, 8 (05) :540-546
[4]   FATE OF N-(2-HYDROXYPROPYL)METHACRYLAMIDE COPOLYMERS WITH PENDENT GALACTOSAMINE RESIDUES AFTER INTRAVENOUS ADMINISTRATION TO RATS [J].
DUNCAN, R ;
SEYMOUR, LCW ;
SCARLETT, L ;
LLOYD, JB ;
REJMANOVA, P ;
KOPECEK, J .
BIOCHIMICA ET BIOPHYSICA ACTA, 1986, 880 (01) :62-71
[5]   The dawning era of polymer therapeutics [J].
Duncan, R .
NATURE REVIEWS DRUG DISCOVERY, 2003, 2 (05) :347-360
[6]   Polymer conjugates as anticancer nanomedicines [J].
Duncan, Ruth .
NATURE REVIEWS CANCER, 2006, 6 (09) :688-701
[7]   Control of polymer structure by a chain-transfer reaction in the radical polymerization of acrylamide by β-mercaptopropionic acid and 1,2,6-hexanetriol trithioglycolate [J].
Endo, K ;
Sawada, T .
COLLOID AND POLYMER SCIENCE, 2001, 279 (11) :1058-1063
[8]   Cancer nanotechnology: Opportunities and challenges [J].
Ferrari, M .
NATURE REVIEWS CANCER, 2005, 5 (03) :161-171
[9]   Visual evidence of acidic environment within degrading poly(lactic-co-glycolic acid) (PLGA) microspheres [J].
Fu, K ;
Pack, DW ;
Klibanov, AM ;
Langer, R .
PHARMACEUTICAL RESEARCH, 2000, 17 (01) :100-106
[10]   Nanoparticles for two-photon photodynamic therapy in living cells [J].
Gao, De ;
Agayan, Rodney R. ;
Xu, Hao ;
Philbert, Martin A. ;
Kopelman, Raoul .
NANO LETTERS, 2006, 6 (11) :2383-2386