Multi-Stimuli Responsive Self-Assembled Nanostructures Useful for Colon Drug Delivery

被引:13
作者
Yadav, Santosh [1 ]
Deka, Smriti R. [1 ]
Tiwari, Kunjlata [1 ]
Sharma, Ashwani K. [1 ]
Kumar, Pradeep [1 ]
机构
[1] Inst Genom & Integrat Biol, CSIR, Nucle Acids Res Lab, Delhi Univ Campus, Delhi 110007, India
关键词
Azobenzene; drug delivery; nanostructures; PEG; self-assembly; stimuli-sensitive; MESOPOROUS SILICA NANOPARTICLES; BUILDING-BLOCKS; BIOMEDICAL APPLICATIONS; POLYMER MICELLES; RELEASE; CANCER; HYDROGELS; THERAPY; SYSTEMS; DESIGN;
D O I
10.1109/TNB.2017.2757958
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Self-assembled nanoformulations have been finding various applications in biomedical sciences. Here, we have designed and synthesized a small molecule-based amphiphilic conjugate of azobenzene, Azo-PEG-OMe, which self-assembles into nanostructures in an aqueous environment. The formation of nanostructures was evidenced by light scattering and electron microscopic analyses, which revealed the size of the so formed nanostructures similar to 199 and similar to 42 nm, respectively. Responsiveness of these nanostructures to various stimuli was demonstrated by enzyme and UV-Vis light exposure, pH and chemical reductant, sodium dithionite. Morphological alterations in the nanostructures on exposure to these stimuli were recorded and subsequently, these nanostructures were demonstrated as efficient carrier of drugs by entrapping an antiprotozoan drug, ornidazole, with similar to 82% entrapment efficiency. Under influence of different stimuli (light, pH, and enzyme), the drug release behavior displayed good response to each stimulus implying that the projected nanostructures could be used as efficient drug delivery system. Response to azoreductase enzyme further established that the formulation can be used for site specific drug delivery particularly useful for colonic drug delivery.
引用
收藏
页码:764 / 772
页数:9
相关论文
共 63 条
[11]   Stimuli-responsive polymers for anti-cancer drug delivery [J].
Cheng, Weiren ;
Gu, Liuqun ;
Ren, Wei ;
Liu, Ye .
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS, 2014, 45 :600-608
[12]   Enzyme-Induced and Tumor-Targeted Drug Delivery System Based on Multifunctional Mesoporous Silica Nanoparticles [J].
Cheng, Yin-Jia ;
Luo, Guo-Feng ;
Zhu, Jing-Yi ;
Xu, Xiao-Ding ;
Zeng, Xuan ;
Cheng, Dong-Bing ;
Li, You-Mei ;
Wu, Yan ;
Zhang, Xian-Zheng ;
Zhuo, Ren-Xi ;
He, Feng .
ACS APPLIED MATERIALS & INTERFACES, 2015, 7 (17) :9078-9087
[13]   Enzyme-responsive nanoparticles for drug release and diagnostics [J].
de la Rica, Roberto ;
Aili, Daniel ;
Stevens, Molly M. .
ADVANCED DRUG DELIVERY REVIEWS, 2012, 64 (11) :967-978
[14]   Supramolecular Hydrogelators and Hydrogels: From Soft Matter to Molecular Biomaterials [J].
Du, Xuewen ;
Zhou, Jie ;
Shi, Junfeng ;
Xu, Bing .
CHEMICAL REVIEWS, 2015, 115 (24) :13165-13307
[15]   Self-assembly of short peptides to form hydrogels: Design of building blocks, physical properties and technological applications [J].
Fichman, Galit ;
Gazit, Ehud .
ACTA BIOMATERIALIA, 2014, 10 (04) :1671-1682
[16]  
Fleige E., ADV DRUG DEL REV, V64, P866
[17]   Efficient catalytic reduction of azo dyes by N,N-dimethylformamide mediated by viologen [J].
Gao, Gui-Qi ;
Xu, An-Wu .
NEW JOURNAL OF CHEMISTRY, 2014, 38 (10) :4661-4665
[18]   Drug Release from Electric-Field-Responsive Nanoparticles [J].
Ge, Jun ;
Neofytou, Evgenios ;
Cahill, Thomas J., III ;
Beygui, Ramin E. ;
Zare, Richard N. .
ACS NANO, 2012, 6 (01) :227-233
[19]   A Lipase-Responsive Vehicle Using Amphipathic Polymer Synthesized with the Lipase as Catalyst [J].
Ge, Jun ;
Lu, Diannan ;
Yang, Cheng ;
Liu, Zheng .
MACROMOLECULAR RAPID COMMUNICATIONS, 2011, 32 (06) :546-550
[20]   Photo-responsive block copolymer micelles: design and behavior [J].
Gohy, Jean-Francois ;
Zhao, Yue .
CHEMICAL SOCIETY REVIEWS, 2013, 42 (17) :7117-7129