Biodegradable diblock copolymeric PEG-PCL nanoparticles: Synthesis, characterization and applications as anticancer drug delivery agents

被引:66
作者
Behl, Akanksha [1 ]
Parmar, Virinder S. [2 ]
Malhotra, Shashwat [3 ]
Chhillar, Anil K. [1 ]
机构
[1] Maharshi Dayanand Univ, Ctr Biotechnol, Rohtak 124001, Haryana, India
[2] CUNY, Dept Chem & Environm Sci, Medgar Evers Coll, 1638 Bedford Ave, Brooklyn, NY 11225 USA
[3] Kirori Mal Coll, Dept Chem, Delhi 110007, India
关键词
PEG-PCL; Block copolymer; Anticancer drug; Nanoparticles; Drug delivery system; Drug release kinetics; BLOCK-COPOLYMERS; MACROMOLECULAR THERAPEUTICS; POLY(D; L-LACTIC ACID); POLY(ETHYLENE GLYCOL); OXIDE NANOPARTICLES; SOLID DISPERSION; ANTITUMOR AGENT; RELEASE; MICELLES; SYSTEM;
D O I
10.1016/j.polymer.2020.122901
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Poly (ethylene glycol) methyl ether-block-poly (epsilon-caprolactone) copolymers are useful biomedical materials owing to their amphiphilic nature, biodegradability, biocompatibility and also due to their semi-crystalline form having a low glass transition temperature. Due to their slow drug release profile, PEG-PCL copolymers are excellent candidates for sustained delivery applications over a period of time of more than a year. This unique property has provoked their relevance specially in the area of anticancer drug delivery applications in the form of various nanoaggregates like microspheres, nanogels, nanospheres, polymersomes, micelles, etc. A large variety of anticancer drugs/bioactives have been encapsulated in PEG-PCL copolymers for developing effective anticancer drug delivery systems and also for producing controlled drug release profiles. In recent times, PEG-PCL co-polymers based nanoparticles have shown tremendous advancements as anticancer drug delivery vehicles owing to their higher drug loading capacities of the hydrophobic drugs, enhanced bioavailability, keeping away from being overpowered by way of phagocytes, decreased blasted discharge, and also in increasing the scattering time of drug within the blood stream during their systemic inoculation. These nano-formulated drug delivery systems can be used for the delivery of anticancer drugs at a specific site in a targeted approach. The developed nano-formulations possess promising potential in the treatment of cancer with improved anticancer efficacy and reduced toxicity invivo. In the current review, our main focus is to highlight the development and synthesis of different types of PEG-PCL copolymers (both conventional and greener approaches) along with the physicochemical characterization techniques used primarily for the PEG-PCL co-polymeric systems. We have also summarized the uses of PEG-PCL co-polymeric nano formulations with various anticancer drugs as drug delivery platforms in the area of anticancer chemotherapy.
引用
收藏
页数:11
相关论文
共 115 条
[1]   Amphiphilic block copolymers for drug delivery [J].
Adams, ML ;
Lavasanifar, A ;
Kwon, GS .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2003, 92 (07) :1343-1355
[2]  
Aguilar ZP, 2013, NANOMATERIALS FOR MEDICAL APPLICATIONS, P1
[3]   Biodegradation and biocompatibility of PLA and PLGA microspheres [J].
Anderson, James M. ;
Shive, Matthew S. .
ADVANCED DRUG DELIVERY REVIEWS, 2012, 64 :72-82
[4]   RETRACTED: Synthesis, characterization and in vitro evaluation of magnetic nanoparticles modified with PCL-PEG-PCL for controlled delivery of 5FU (Retracted article. See vol. 50, pg. 108, 2022) [J].
Asadi, Nahideh ;
Annabi, Nasim ;
Mostafavi, Ebrahim ;
Anzabi, Maryam ;
Khalilov, Rovshan ;
Saghfi, Siamak ;
Mehrizadeh, Masoud ;
Akbarzadeh, Abolfazl .
ARTIFICIAL CELLS NANOMEDICINE AND BIOTECHNOLOGY, 2018, 46 :S938-S945
[5]   Cancer nanotechnology: The impact of passive and active targeting in the era of modern cancer biology [J].
Bertrand, Nicolas ;
Wu, Jun ;
Xu, Xiaoyang ;
Kamaly, Nazila ;
Farokhzad, Omid C. .
ADVANCED DRUG DELIVERY REVIEWS, 2014, 66 :2-25
[6]   MONOCRYL(R) SUTURE, A NEW ULTRA-PLIABLE ABSORBABLE MONOFILAMENT SUTURE [J].
BEZWADA, RS ;
JAMIOLKOWSKI, DD ;
LEE, IY ;
AGARWAL, V ;
PERSIVALE, J ;
TRENKABENTHIN, S ;
ERNETA, M ;
SURYADEVARA, J ;
YANG, A ;
LIU, S .
BIOMATERIALS, 1995, 16 (15) :1141-1148
[7]   Multistage delivery of chemotherapeutic nanoparticles for breast cancer treatment [J].
Blanco, Elvin ;
Sangai, Takafumi ;
Hsiao, Angela ;
Ferrati, Silvia ;
Bai, Litao ;
Liu, Xuewu ;
Meric-Bernstam, Funda ;
Ferrari, Mauro .
CANCER LETTERS, 2013, 334 (02) :245-252
[8]   Poly(lactide-co-glycolide) microsphere formulations of darbepoetin alfa: Spray drying is an alternative to encapsulation by spray-freeze drying [J].
Burke, PA ;
Klumb, LA ;
Herberger, JD ;
Nguyen, XCC ;
Harrell, RA ;
Zordich, M .
PHARMACEUTICAL RESEARCH, 2004, 21 (03) :500-506
[9]   POLY(ESTER-ETHER-ESTER) BLOCK-COPOLYMERS AS BIOMATERIALS [J].
CERRAI, P ;
GUERRA, GD ;
LELLI, L ;
TRICOLI, M ;
DELGUERRA, RS ;
CASCONE, MG ;
GIUSTI, P .
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 1994, 5 (01) :33-39
[10]   Targeting tumor microenvironment with PEG-based amphiphilic nanoparticles to overcome chemoresistance [J].
Chen, Shizhu ;
Yang, Keni ;
Tuguntaev, Ruslan G. ;
Mozhi, Anbu ;
Zhang, Jinchao ;
Wang, Paul C. ;
Liang, Xing-Jie .
NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE, 2016, 12 (02) :269-286