Tumor microenvironment-induced structure changing drug/gene delivery system for overcoming delivery -associated challenges

被引:67
作者
Zhang, Min [1 ]
Guo, Xinli [1 ]
Wang, Mingfu [1 ,2 ]
Liu, Kehai [1 ]
机构
[1] Shanghai Ocean Univ, Coll Food Sci & Technol, Hucheng Ring Rd, Shanghai 201306, Peoples R China
[2] Univ Hong Kong, Sch Biol Sci, Pokfulam Rd, Hong Kong 999077, Peoples R China
关键词
TARGETED INTRACELLULAR DRUG; ONE-POT SYNTHESIS; MULTIDRUG-RESISTANCE; SIRNA DELIVERY; CO-DELIVERY; IN-VIVO; POLYMERIC MICELLES; HYALURONIC-ACID; CATHEPSIN-B; RESPONSIVE NANOPARTICLES;
D O I
10.1016/j.jconrel.2020.04.026
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nano-drug/gene delivery systems (DDS) are powerful weapons for the targeted delivery of various therapeutic molecules in treatment of tumors. Nano systems are being extensively investigated for drug and gene delivery applications because of their exceptional ability to protect the payload from degradation in vivo, prolong circulation of the nanoparticles (NPs), realize controlled release of the contents, reduce side effects, and enhance targeted delivery among others. However, the specific properties required for a DDS vary at different phase of the complex delivery process, and these requirements are often conflicting, including the surface charge, particle size, and stability of DDS, which severely reduces the efficiency of the drug/gene delivery. Therefore, researchers have attempted to fabricate structure, size, or charge changeable DDS by introducing various tumor microenvironment (TME) stimuli-responsive elements into the DDS to meet the varying requirements at different phases of the delivery process, thus improving drug/gene delivery efficiency. This paper summarizes the most recent developments in TME stimuli-responsive DDS and addresses the aforementioned challenges. © 2020 Elsevier B.V.
引用
收藏
页码:203 / 224
页数:22
相关论文
共 166 条
[1]   Hypoxia Responsive Drug Delivery Systems in Tumor Therapy [J].
Alimoradi, Houman ;
Matikonda, Siddharth S. ;
Gamble, Allan B. ;
Giles, Gregory I. ;
Greish, Khaled .
CURRENT PHARMACEUTICAL DESIGN, 2016, 22 (19) :2808-2820
[2]   A dendritic β-galactosidase-responsive folate-monomethylauristatin E conjugate [J].
Alsarraf, Jerome ;
Peraudeau, Elodie ;
Poinot, Pauline ;
Tranoy-Opalinski, Isabelle ;
Clarhaut, Jonathan ;
Renoux, Brigitte ;
Papot, Sebastien .
CHEMICAL COMMUNICATIONS, 2015, 51 (87) :15792-15795
[3]  
[Anonymous], [No title captured]
[4]   Phospholipase A2-susceptible liposomes of anticancer double lipid-prodrugs [J].
Arouri, Ahmad ;
Mouritsen, Ole G. .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2012, 45 (04) :408-420
[5]   Enzymatic reduction of disulfide bonds in lysosomes: Characterization of a Gamma-interferon-inducible lysosomal thiol reductase (GILT) [J].
Arunachalam, B ;
Phan, UT ;
Geuze, HJ ;
Cresswell, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (02) :745-750
[6]   Protease-Sensitive, Polymer-Caged Liposomes: A Method for Making Highly Targeted Liposomes Using Triggered Release [J].
Basel, Matthew T. ;
Shrestha, Tej B. ;
Troyer, Deryl L. ;
Bossmann, Stefan H. .
ACS NANO, 2011, 5 (03) :2162-2175
[7]   Selenoglutathione: Efficient oxidative protein folding by a diselenide [J].
Beld, Joris ;
Woycechowsky, Kenneth J. ;
Hilvert, Donald .
BIOCHEMISTRY, 2007, 46 (18) :5382-5390
[8]   Cathepsin B promotes colorectal tumorigenesis, cell invasion, and metastasis [J].
Bian, Benjamin ;
Mongrain, Sebastien ;
Cagnol, Sebastien ;
Langlois, Marie-Josee ;
Boulanger, Jim ;
Bernatchez, Gerald ;
Carrier, Julie C. ;
Boudreau, Francois ;
Rivard, Nathalie .
MOLECULAR CARCINOGENESIS, 2016, 55 (05) :671-687
[9]   Synthesis and Characterization of a Biodegradable ABC Triblock Terpolymer as Co-Delivery Carrier of Doxorubicin and DNA [J].
Bian, Jiao ;
Hao, Ying ;
He, Jinlin ;
Zhang, Wenling ;
Zhang, Mingzu ;
Ni, Peihong .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2014, 52 (21) :3005-3016
[10]   Development of a nanoprecipitation method intended for the entrapment of hydrophilic drugs into nanoparticles [J].
Bilati, U ;
Allémann, E ;
Doelker, E .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2005, 24 (01) :67-75