Stimulus-Responsive Degradable Polylactide-Based Block Copolymer Nanoassemblies for Controlled/Enhanced Drug Delivery

被引:76
作者
Bawa, Kamaljeet K. [1 ]
Oh, Jung Kwon [1 ]
机构
[1] Concordia Univ, Dept Chem & Biochem, Montreal, PQ H4B 1R6, Canada
关键词
polylactide; nanoassembly; stimulus-responsive degradation; amphiphilic block copolymer; OVERCOMING MULTIDRUG-RESISTANCE; TARGETED INTRACELLULAR DRUG; RING-OPENING POLYMERIZATION; CROSS-LINKED MICELLES; CANCER-THERAPY; BIOLOGICAL APPLICATIONS; THERMORESPONSIVE POLYMERS; BIODEGRADABLE COPOLYMERS; BIOREDUCIBLE MICELLES; ACCELERATED RELEASE;
D O I
10.1021/acs.molpharmaceut.7b00284
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Polylactide (PLA) is biocompatible and FDA-approved for clinical use and thus has been a choice of the materials valuable for extensive applications in biomedical fields. However, conventionally designed PLA-based amphiphilic block copolymer (AB?) nanoassemblies exhibit slow and uncontrolled release of encapsulated drugs because of the slow biodegradation of hydrophobic PLA in physiological conditions. To improve potentials for clinical use and commercialization of conventional PLA-based nanoassemblies, stimulus-responsive degradation (SRD) platform has been introduced into the design of PLA-based nanoassemblies for enhanced/controlled release of encapsulated drugs. This review summarizes recent strategies that allow for the development of PLA-based ABPs and their self assembled nanostructures exhibiting SRD-induced enhanced drug release. The review focuses on the design, synthesis, and evaluation of the nanoassemblies as intracellular drug delivery nanocarriers for cancer therapy. Further, the outlook is briefly discussed on the important aspects for the current and future development of more effective SRD PLA-based nanoassemblies toward tumor-targeting intracellular drug delivery.
引用
收藏
页码:2460 / 2474
页数:15
相关论文
共 137 条
[1]   Rapidly thiol-responsive degradable block copolymer nanocarriers with facile bioconjugation [J].
Aleksanian, Samuel ;
Khorsand, Behnoush ;
Schmidt, Rolf ;
Oh, Jung Kwon .
POLYMER CHEMISTRY, 2012, 3 (08) :2138-2147
[2]   Responsive polymers at the biology/materials science interface [J].
Alexander, Cameron ;
Shakesheff, Kevin M. .
ADVANCED MATERIALS, 2006, 18 (24) :3321-3328
[3]   Nano-engineering block copolymer aggregates for drug delivery [J].
Allen, C ;
Maysinger, D ;
Eisenberg, A .
COLLOIDS AND SURFACES B-BIOINTERFACES, 1999, 16 (1-4) :3-27
[4]   Smart drug delivery systems: from fundamentals to the clinic [J].
Alvarez-Lorenzo, Carmen ;
Concheiro, Angel .
CHEMICAL COMMUNICATIONS, 2014, 50 (58) :7743-7765
[5]   Poly(α-hydroxy acid)s and poly(α-hydroxy acid-co-α-amino acid)s derived from amino acid [J].
Basu, Arijit ;
Kunduru, Konda Reddy ;
Katzhendler, Joshua ;
Domb, Abraham J. .
ADVANCED DRUG DELIVERY REVIEWS, 2016, 107 :82-96
[6]   Acid-degradable polymers for drug delivery: a decade of innovation [J].
Binauld, Sandra ;
Stenzel, Martina H. .
CHEMICAL COMMUNICATIONS, 2013, 49 (21) :2082-2102
[7]  
Biswas D., 2017, MOL PHARM, DOI [10.1021/acs.mol-pharmaceut.6b01146., DOI 10.1021/ACS.M0L-PHARMACEUT.6B01146]
[8]   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
[9]   GRGDS-Functionalized Poly(lactide)-graft-poly(ethylene glycol) Copolymers: Combining Thiol-Ene Chemistry with Staudinger Ligation [J].
Borchmann, Dorothee E. ;
ten Brummelhuis, Niels ;
Weck, Marcus .
MACROMOLECULES, 2013, 46 (11) :4426-4431
[10]   Progress of drug-loaded polymeric micelles into clinical studies [J].
Cabral, Horacio ;
Kataoka, Kazunori .
JOURNAL OF CONTROLLED RELEASE, 2014, 190 :465-476