Rational Design of Nanogels for Overcoming the Biological Barriers in Various Administration Routes

被引:59
作者
Zhao, Qing [1 ]
Zhang, Siyu [1 ]
Wu, Fengchang [3 ]
Li, Dengyu [1 ]
Zhang, Xuejiao [1 ]
Chen, Wei [2 ]
Xing, Baoshan [4 ]
机构
[1] Chinese Acad Sci, Key Lab Pollut Ecol & Environm Engn, Inst Appl Ecol, Shenyang 110016, Peoples R China
[2] China Pharmaceut Univ, Dept Pharmaceut Engn, Sch Engn, Nanjing 211198, Peoples R China
[3] Chinese Res Inst Environm Sci, State Key Lab Environm Criteria & Risk Assessment, Beijing 100012, Peoples R China
[4] Univ Massachusetts, Stockbridge Sch Agr, Amherst, MA 01003 USA
基金
中国国家自然科学基金;
关键词
administration routes; biological barriers; drug delivery; nanogels; structure modulation;
D O I
10.1002/anie.201911048
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nanogels have been identified as outstanding nanocarrier candidates for drug delivery due to their desirable physiochemical properties and versatile applicability for diverse therapeutic molecules and imaging probes. One of the main challenges that hinder the clinical translation of nanogels is the low efficiency of drug delivery to the target sites because of the complex biological barriers during the in vivo journey. The purpose of this review is to examine and summarize the recent advances on the rational design and structural modulation of nanogels to overcome the barriers and challenges on the way to the site of action following various dosing modes. In particular, the functional moieties or domains have been incorporated in the nanogels, allowing them to spontaneously regulate their structure and physiochemical properties to cross one or more of the multifaceted barriers. In addition, the future perspectives are presented with regards to opportunities and challenges for the precise and efficient therapeutic use of nanogel formulations.
引用
收藏
页码:14760 / 14778
页数:19
相关论文
共 154 条
[1]   Developing the Potential Ophthalmic Applications of Pilocarpine Entrapped Into Polyvinylpyrrolidone-Poly(acrylic acid) Nanogel Dispersions Prepared By γ Radiation [J].
Abd El-Rehim, Hassan A. ;
Swilem, Ahmed E. ;
Klingner, Anke ;
Hegazy, El-Sayed A. ;
Hamed, Ashraf A. .
BIOMACROMOLECULES, 2013, 14 (03) :688-698
[2]  
[Anonymous], 2018, Angew. Chem., DOI DOI 10.1002/ANGE.201711242
[3]   Biomimetic Delivery with Micro- and Nanoparticles [J].
Balmert, Stephen C. ;
Little, Steven R. .
ADVANCED MATERIALS, 2012, 24 (28) :3757-3778
[4]   Principles of nanoparticle design for overcoming biological barriers to drug delivery [J].
Blanco, Elvin ;
Shen, Haifa ;
Ferrari, Mauro .
NATURE BIOTECHNOLOGY, 2015, 33 (09) :941-951
[5]   Synthesis and evaluation of mucoadhesive acryloyl-quaternized PDMAEMA nanogels for ocular drug delivery [J].
Brannigan, Ruairi P. ;
Khutoryanskiy, Vitaliy V. .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2017, 155 :538-543
[6]   Unravelling the stealth effect [J].
Butcher, Neville J. ;
Mortimer, Gysell M. ;
Minchin, Rodney F. .
NATURE NANOTECHNOLOGY, 2016, 11 (04) :310-311
[7]   Polymer nanogels: A versatile nanoscopic drug delivery platform [J].
Chacko, Reuben T. ;
Ventura, Judy ;
Zhuang, Jiaming ;
Thayumanavan, S. .
ADVANCED DRUG DELIVERY REVIEWS, 2012, 64 (09) :836-851
[8]   PLGA-lecithin-PEG core-shell nanoparticles for controlled drug delivery [J].
Chan, Juliana M. ;
Zhang, Liangfang ;
Yuet, Kai P. ;
Liao, Grace ;
Rhee, June-Wha ;
Langer, Robert ;
Farokhzad, Omid C. .
BIOMATERIALS, 2009, 30 (08) :1627-1634
[9]   Three-dimensional photopatterning of hydrogels using stereolithography for long-term cell encapsulation [J].
Chan, Vincent ;
Zorlutuna, Pinar ;
Jeong, Jae Hyun ;
Kong, Hyunjoon ;
Bashir, Rashid .
LAB ON A CHIP, 2010, 10 (16) :2062-2070
[10]   Saporin-loaded CD44 and EGFR dual-targeted nanogels for potent inhibition of metastatic breast cancer in vivo [J].
Chen, Jing ;
He, Hua ;
Deng, Chao ;
Yin, Lichen ;
Zhong, Zhiyuan .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2019, 560 :57-64