Nanogel carrier design for targeted drug delivery

被引:147
作者
Eckmann, D. M. [1 ]
Composto, R. J. [2 ]
Tsourkas, A. [3 ]
Muzykantov, V. R. [4 ]
机构
[1] Univ Penn, Dept Anesthesia & Crit Care, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Mat Sci & Engn, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Bioengn, Philadelphia, PA 19104 USA
[4] Univ Penn, Dept Pharmacol, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
GLUCOSE-RESPONSIVE MICROGELS; CROSS-LINKED NANOPARTICLES; CONTROLLED-RELEASE; HYDROGEL NANOPARTICLES; CYTOSOLIC DELIVERY; POLYMER MICELLES; EXTRACELLULAR PH; SOLID TUMORS; IRON-OXIDE; CORE;
D O I
10.1039/c4tb01141d
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
Polymer-based nanogel formulations offer features attractive for drug delivery, including ease of synthesis, controllable swelling and viscoelasticity as well as drug loading and release characteristics, passive and active targeting, and the ability to formulate nanogel carriers that can respond to biological stimuli. These unique features and low toxicity make the nanogels a favorable option for vascular drug targeting. In this review, we have addressed key chemical and biological aspects of nanogel drug carrier design. In particular, we have highlighted published studies of nanogel design, descriptions of nanogel functional characteristics and their behavior in biological models. These studies form a compendium of information that supports the scientific and clinical rationale for development of this carrier for targeted therapeutic interventions.
引用
收藏
页码:8085 / 8097
页数:13
相关论文
共 161 条
[41]   Ni-NTA-gold clusters target his-tagged proteins [J].
Hainfeld, JF ;
Liu, WQ ;
Halsey, CMR ;
Freimuth, P ;
Powell, RD .
JOURNAL OF STRUCTURAL BIOLOGY, 1999, 127 (02) :185-198
[42]   Understanding Ligand Distributions in Modified Particle and Particlelike Systems [J].
Hakem, Ilhem F. ;
Leech, Anna M. ;
Johnson, Jermaine D. ;
Donahue, Scott J. ;
Walker, Jeremy P. ;
Bockstaller, Michael R. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2010, 132 (46) :16593-16598
[43]   Nanogel-quantum dot hybrid nanoparticles for live cell imaging [J].
Hasegawa, U ;
Nomura, SIM ;
Kaul, SC ;
Hirano, T ;
Akiyoshi, K .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 331 (04) :917-921
[44]   Quantifying nanoparticle adhesion mediated by specific molecular interactions [J].
Haun, Jered B. ;
Hammer, Daniel A. .
LANGMUIR, 2008, 24 (16) :8821-8832
[45]   Osteoblastic Bone Formation Is Induced by Using Nanogel-Crosslinking Hydrogel as Novel Scaffold for Bone Growth Factor [J].
Hayashi, Chikako ;
Hasegawa, Urara ;
Saita, Yoshitomo ;
Hemmi, Hiroaki ;
Hayata, Tadayoshi ;
Nakashima, Kazuhisa ;
Ezura, Yoichi ;
Amagasa, Teruo ;
Akiyoshi, Kazunari ;
Noda, Masaki .
JOURNAL OF CELLULAR PHYSIOLOGY, 2009, 220 (01) :1-7
[46]   pH-sensitive nanogel possessing reactive PEG tethered chains on the surface [J].
Hayashi, H ;
Iijima, M ;
Kataoka, K ;
Nagasaki, Y .
MACROMOLECULES, 2004, 37 (14) :5389-5396
[47]   Both Core- and Shell-Cross-Linked Nanogels: Photoinduced Size Change, Intraparticle LCST, and Interparticle UCST Thermal Behaviors [J].
He, Jie ;
Yan, Bin ;
Tremblay, Luc ;
Zhao, Yue .
LANGMUIR, 2011, 27 (01) :436-444
[48]   Charge-switching, amphoteric glucose-responsive microgels with physiological swelling activity [J].
Hoare, Todd ;
Pelton, Robert .
BIOMACROMOLECULES, 2008, 9 (02) :733-740
[49]   Engineering glucose swelling responses in poly(N-isopropylacrylamide)-based microgels [J].
Hoare, Todd ;
Pelton, Robert .
MACROMOLECULES, 2007, 40 (03) :670-678
[50]   Light-Induced Temperature Transitions in Biodegradable Polymer and Nanorod Composites [J].
Hribar, Kolin C. ;
Metter, Robert B. ;
Ifkovits, Jamie L. ;
Troxler, Thomas ;
Burdick, Jason A. .
SMALL, 2009, 5 (16) :1830-1834