Physical stimuli-responsive liposomes and polymersomes as drug delivery vehicles based on phase transitions in the membrane

被引:57
作者
Deng, Yangwei [1 ]
Ling, Jun [2 ]
Li, Min-Hui [1 ,2 ,3 ]
机构
[1] PSL Univ Paris, CNRS, Inst Rech Chim Paris, Chim ParisTech,UMR8247, 11 Rue Pierre & Marie Curie, F-75005 Paris, France
[2] Zhejiang Univ, Dept Polymer Sci & Engn, MOE Key Lab Macromol Synth & Functionalizat, Hangzhou 310027, Zhejiang, Peoples R China
[3] Beijing Univ Chem Technol, Beijing Adv Innovat Ctr Soft Matter Sci & Engn, 15 North Third Ring Rd, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
CATANIONIC SURFACTANT SOLUTIONS; AMPHIPHILIC DIBLOCK COPOLYMERS; TEMPERATURE-SENSITIVE LIPOSOME; SELF-ASSEMBLED STRUCTURES; TUMOR XENOGRAFT MODEL; BLOCK-COPOLYMERS; BIODEGRADABLE POLYMERSOMES; IN-VIVO; THERMOSENSITIVE LIPOSOMES; PHOSPHOLIPID-VESICLES;
D O I
10.1039/c8nr00923f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This paper reviews liposomes with crystalline phase and polymersomes exhibiting crystalline and thermotropic liquid crystalline phases in the membrane. Intriguing morphologies of vesicles are described, including spherical, ellipsoidal and faceted vesicles, produced by a large variety of amphiphilic molecules and polymers with nematic phase, smectic phase or crystalline phase. It is highlighted how the phase transitions and the phase grain boundaries could be used ingeniously to destabilize the vesicular structure and to achieve cargo-release under the action of external stimulation. These liposomes and polymersomes are responsive to physical stimuli, such as temperature variation, shear stress, light illumination, and magnetic and electric fields. These stimuli-responsive properties make them promising candidates as new smart drug delivery systems.
引用
收藏
页码:6781 / 6800
页数:20
相关论文
共 121 条
[1]   Advanced strategies in liposomal cancer therapy: Problems and prospects of active and tumor specific drug release [J].
Andresen, TL ;
Jensen, SS ;
Jorgensen, K .
PROGRESS IN LIPID RESEARCH, 2005, 44 (01) :68-97
[2]   Vesicles and liposomes:: A self-assembly principle beyond lipids [J].
Antonietti, M ;
Förster, S .
ADVANCED MATERIALS, 2003, 15 (16) :1323-1333
[3]   Enhancement of the phase transition permeability of DPPC liposomes by incorporation of MPPC: A new temperature-sensitive liposome for use with mild hyperthermia [J].
Anyarambhatla, GR ;
Needham, D .
JOURNAL OF LIPOSOME RESEARCH, 1999, 9 (04) :491-506
[4]   Tailored drug-release from multi-functional polymer-peptide hybrid vesicles [J].
Bacinello, Daniel ;
Garanger, Elisabeth ;
Taton, Daniel ;
Tam, Kam Chui ;
Lecommandoux, Sebastien .
EUROPEAN POLYMER JOURNAL, 2015, 62 :363-373
[5]   Self-Assembled Block Copolymer Aggregates: From Micelles to Vesicles and their Biological Applications [J].
Blanazs, Adam ;
Armes, Steven P. ;
Ryan, Anthony J. .
MACROMOLECULAR RAPID COMMUNICATIONS, 2009, 30 (4-5) :267-277
[6]   Immunological response to nitroglycerin-loaded shear-responsive liposomes in vitro and in vivo [J].
Buscema, Marzia ;
Matviykiv, Sofiya ;
Meszaros, Tamas ;
Gerganova, Gabriela ;
Weinberger, Andreas ;
Mettal, Ute ;
Mueller, Dennis ;
Neuhaus, Frederik ;
Stalder, Etienne ;
Ishikawa, Takashi ;
Urbanics, Rudolf ;
Saxer, Till ;
Pfohl, Thomas ;
Szebeni, Janos ;
Zumbuehl, Andreas ;
Mueller, Bert .
JOURNAL OF CONTROLLED RELEASE, 2017, 264 :14-23
[7]  
Celsion Corporation, AN MOD THERMODOX HAS
[8]  
ClinicalTrial. gov, TARG CHEM US FOC ULT
[9]  
ClinicalTrials. gov, STUD THERMODOX STAND
[10]  
ClinicalTrials. gov, PHAS 1 2 STUD THERMO