Single and Multiple Stimuli-Responsive Polymer Particles for Controlled Drug Delivery

被引:35
作者
Lopez Ruiz, Aida [1 ]
Ramirez, Ann [2 ]
McEnnis, Kathleen [1 ]
机构
[1] New Jersey Inst Technol, Chem & Mat Engn Dept, Newark, NJ 07102 USA
[2] New Jersey Inst Technol, Dept Biomed Engn, Newark, NJ 07102 USA
关键词
stimuli-responsive; drug delivery; polymer particles; NEAR-INFRARED LIGHT; CROSS-LINKED MICELLES; CONTROLLED-RELEASE; SOLID TUMORS; IN-VITRO; PH; NANOPARTICLES; TEMPERATURE; COPOLYMERS; SYSTEMS;
D O I
10.3390/pharmaceutics14020421
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Polymers that can change their properties in response to an external or internal stimulus have become an interesting platform for drug delivery systems. Polymeric nanoparticles can be used to decrease the toxicity of drugs, improve the circulation of hydrophobic drugs, and increase a drug's efficacy. Furthermore, polymers that are sensitive to specific stimuli can be used to achieve controlled release of drugs into specific areas of the body. This review discusses the different stimuli that can be used for controlled drug delivery based on internal and external stimuli. Internal stimuli have been defined as events that evoke changes in different characteristics, inside the body, such as changes in pH, redox potential, and temperature. External stimuli have been defined as the use of an external source such as light and ultrasound to implement such changes. Special attention has been paid to the particular chemical structures that need to be incorporated into polymers to achieve the desired stimuli response. A current trend in this field is the incorporation of several stimuli in a single polymer to achieve higher specificity. Therefore, to access the most recent advances in stimuli-responsive polymers, the focus of this review is to combine several stimuli. The combination of different stimuli is discussed along with the chemical structures that can produce it.
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页数:22
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共 145 条
[1]   Polymer nanoparticles-preparations, applications and future insights: a concise review [J].
Adhikari, Chandan .
POLYMER-PLASTICS TECHNOLOGY AND MATERIALS, 2021, 60 (18) :1996-2024
[2]  
Alami-Milani M, 2017, ADV PHARM BULL, V7, P11, DOI 10.15171/apb.2017.003
[3]   Polymeric nanocarriers as stimuli-responsive systems for targeted tumor (cancer) therapy: Recent advances in drug delivery [J].
Alsehli, Mosa .
SAUDI PHARMACEUTICAL JOURNAL, 2020, 28 (03) :255-265
[4]  
Alvarez-Lorenzo C, 2013, RSC SMART MATER, P1, DOI 10.1039/9781849736800-00001
[5]   Polydopamine-Derivated Hierarchical Nanoplatforms for Efficient Dual-Modal Imaging-Guided Combination in Vivo Cancer Therapy [J].
Ao, Lijiao ;
Wu, Chunlei ;
Liu, Ke ;
Wang, Wei ;
Fang, Lijing ;
Huang, Liang ;
Su, Wu .
ACS APPLIED MATERIALS & INTERFACES, 2018, 10 (15) :12544-12552
[6]   Design of thermosensitive polymer-coated magnetic mesoporous silica nanocomposites with a core-shell-shell structure as a magnetic/temperature dual-responsive drug delivery vehicle [J].
Asgari, Mahsa ;
Soleymani, Meysam ;
Miri, Taghi ;
Barati, Aboulfazl .
POLYMERS FOR ADVANCED TECHNOLOGIES, 2021, 32 (10) :4101-4109
[7]   Design of environment-sensitive supramolecular assemblies for intracellular drug delivery: Polymeric micelles that are responsive to intracellular pH change [J].
Bae, Y ;
Fukushima, S ;
Harada, A ;
Kataoka, K .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (38) :4640-4643
[8]   pH and Redox Dual Responsive Nanoparticle for Nuclear Targeted Drug Delivery [J].
Bahadur, Remant K. C. ;
Thapa, Bindu ;
Xu, Peisheng .
MOLECULAR PHARMACEUTICS, 2012, 9 (09) :2719-2729
[9]   Folic Acid-Terminated Poly(2-Diethyl Amino Ethyl Methacrylate) Brush-Gated Magnetic Mesoporous Nanoparticles as a Smart Drug Delivery System [J].
Beagan, Abeer M. ;
Alghamdi, Ahlam A. ;
Lahmadi, Shatha S. ;
Halwani, Majed A. ;
Almeataq, Mohammed S. ;
Alhazaa, Abdulaziz N. ;
Alotaibi, Khalid M. ;
Alswieleh, Abdullah M. .
POLYMERS, 2021, 13 (01) :1-14
[10]   Wavelength-programmed solute release from photosensitive liposomes [J].
Bisby, RH ;
Mead, C ;
Morgan, CC .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 276 (01) :169-173