Stimuli-Responsive Graphene Nanohybrids for Biomedical Applications

被引:9
作者
Patel, Dinesh K. [1 ]
Seo, Yu-Ri [2 ]
Lim, Ki-Taek [1 ,2 ]
机构
[1] Kangwon Natl Univ, Inst Forest Sci, Chunchon 24341, South Korea
[2] Kangwon Natl Univ, Dept Biosyst Engn, Coll Agr & Life Sci, Chunchon 24341, South Korea
基金
新加坡国家研究基金会;
关键词
POLYMERS;
D O I
10.1155/2019/9831853
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Stimuli-responsive materials, also known as smart materials, can change their structure and, consequently, original behavior in response to external or internal stimuli. This is due to the change in the interactions between the various functional groups. Graphene, which is a single layer of carbon atoms with a hexagonal morphology and has excellent physiochemical properties with a high surface area, is frequently used in materials science for various applications. Numerous surface functionalizations are possible for the graphene structure with different functional groups, which can be used to alter the properties of native materials. Graphene-based hybrids exhibit significant improvements in their native properties. Since functionalized graphene contains several reactive groups, the behavior of such hybrid materials can be easily tuned by changing the external conditions, which is very useful in biomedical applications. Enhanced cell proliferation and differentiation of stem cells was reported on the surfaces of graphene-based hybrids with negligible cytotoxicity. In addition, pH or light-induced drug delivery with a controlled release rate was observed for such nanohybrids. Besides, notable improvements in antimicrobial activity were observed for nanohybrids, which demonstrated their potential for biomedical applications. This review describes the physiochemical properties of graphene and graphene-based hybrid materials for stimuli-responsive drug delivery, tissue engineering, and antimicrobial applications.
引用
收藏
页数:18
相关论文
共 50 条
[21]   Switching "on'' and "off'' the adhesion in stimuli-responsive elastomers [J].
Kaiser, S. ;
Radl, S. V. ;
Manhart, J. ;
Ayalur-Karunakaran, S. ;
Griesser, T. ;
Moser, A. ;
Ganser, C. ;
Teichert, C. ;
Kern, W. ;
Schloegl, S. .
SOFT MATTER, 2018, 14 (13) :2547-2559
[22]   Stimuli-responsive self-assembly of nanoparticles [J].
Grzelczak, Marek ;
Liz-Marzan, Luis M. ;
Klajn, Rafal .
CHEMICAL SOCIETY REVIEWS, 2019, 48 (05) :1342-1361
[23]   Stimuli-Responsive Theragrippers for Chemomechanical Controlled Release [J].
Malachowski, Kate ;
Breger, Joyce ;
Kwag, Hye Rin ;
Wang, Martha O. ;
Fisher, John P. ;
Selaru, Florin M. ;
Gracias, David H. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2014, 53 (31) :8045-8049
[24]   Stimuli-Responsive Shapeshifting Mesoporous Silica Nanoparticles [J].
Sun, Yao ;
Sai, Hiroaki ;
Spoth, Katherine A. ;
Tan, Kwan Wee ;
Werner-Zwanziger, Ulrike ;
Zwanziger, Josef ;
Gruner, Sol M. ;
Kourkoutis, Lena F. ;
Wiesner, Ulrich .
NANO LETTERS, 2016, 16 (01) :651-655
[25]   Stimuli-Responsive Nanocomposite Hydrogels for Oral Diseases [J].
Conte, Raffaele ;
Valentino, Anna ;
Romano, Silvia ;
Margarucci, Sabrina ;
Petillo, Orsolina ;
Calarco, Anna .
GELS, 2024, 10 (07)
[26]   Stimuli-responsive hydrogels for intratumoral drug delivery [J].
Marques, Ana C. ;
Costa, Paulo J. ;
Velho, Sergia ;
Amaral, Maria H. .
DRUG DISCOVERY TODAY, 2021, 26 (10) :2397-2405
[27]   Supramolecular copolymers with stimuli-responsive sequence control [J].
Albertazzi, Lorenzo ;
van der Veeken, Nick ;
Baker, Matthew B. ;
Palmans, Anja R. A. ;
Meijer, E. W. .
CHEMICAL COMMUNICATIONS, 2015, 51 (90) :16166-16168
[28]   Bioinspired Actuators Based on Stimuli-Responsive Polymers [J].
Cui, Huanqing ;
Zhao, Qilong ;
Wang, Yunlong ;
Du, Xuemin .
CHEMISTRY-AN ASIAN JOURNAL, 2019, 14 (14) :2369-2387
[29]   Microfluidic synthesis of stimuli-responsive hydrogel particles [J].
Zhao, Danshan ;
Qian, Lu ;
Yang, Qiaoyi ;
Li, Xiang ;
Ye, Chao ;
Shi, Tianqiong ;
Wang, Yuetong .
APPLIED MATERIALS TODAY, 2025, 42
[30]   Stimuli-Responsive Polymer Actuator for Soft Robotics [J].
Kim, Seewoo ;
Lee, Sang-Nam ;
Melvin, Ambrose Ashwin ;
Choi, Jeong-Woo .
POLYMERS, 2024, 16 (18)