Chitosan oligosaccharide copolymer micelles with double disulphide linkage in the backbone associated by H-bonding duplexes for targeted intracellular drug delivery

被引:29
作者
Yang, Qinglai [1 ]
He, Changyu [2 ]
Xu, Yuhong [3 ]
Liu, Bingya [1 ,2 ]
Shao, Zhifeng [4 ]
Zhu, Zhenggang [2 ]
Hou, Yongtai [5 ]
Gong, Bing [6 ,7 ]
Shen, Yu-Mei [1 ]
机构
[1] Shanghai Jiao Tong Univ, Key Lab Syst Biomed, Shanghai Ctr Syst Biomed, Shanghai 200240, Peoples R China
[2] Shanghai Jiao Tong Univ, Ruijin Hosp, Shanghai Inst Digest Surg, Dept Surg,Shanghai Key Lab Gastric Neoplasm, Shanghai 200240, Peoples R China
[3] Shanghai Jiao Tong Univ, School Pharm, Shanghai 200240, Peoples R China
[4] Shanghai Jiao Tong Univ, Sch Biomed Engn, BioID Ctr, Shanghai 200240, Peoples R China
[5] Shanghai Qisheng Co, Shanghai 201106, Peoples R China
[6] Beijing Normal Univ, Coll Chem, Beijing 100875, Peoples R China
[7] SUNY Buffalo, Dept Chem, Buffalo, NY 14260 USA
基金
美国国家科学基金会;
关键词
POLYMERIC MICELLES; BLOCK-COPOLYMER; TUMOR-CELLS; DIBLOCK COPOLYMERS; CROSS-LINKING; IN-VITRO; NANOPARTICLES; CYTOTOXICITY; EFFICIENCY; RELEASE;
D O I
10.1039/c4py01473a
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A folic acid (FA) conjugated chitosan oligosaccharide (CSO) polylactic acid (PLA) copolymer FA-CSO-PLA with double disulphide linkage in the backbone directed by H-bonding association duplex was synthesized, and its self-assembled micelles were evaluated as smart targeted drug delivery carriers. Both of the intermediates and the terminal copolymers were characterized by 1H-NMR and gel permeation chromatography (GPC). The critical micelle concentration (CMC) value is 0.045 mg mL-1 which suggests the micelles are highly stable in dilute solution. TEM and DLS further confirmed the successful formation of micelles with an average size of 61 and 100 nm, PDI of 0.209 and 0.230 for blank and DOX loaded micelles, respectively. The micelles were destructed under a reductive environment, leading to encapsulated drug release. Moreover, fluorescence microscopy demonstrated that the micelles exhibited both a passive and active targeting ability in HeLA cells due to an EPR effect and folate-mediated endocytosis. These results suggested the micelles would provide a favourable platform for constructing excellent drug delivery systems for cancer therapy.
引用
收藏
页码:1454 / 1464
页数:11
相关论文
共 77 条
[1]   Synthesis of poly(β-amino ester)s optimized for highly effective gene delivery [J].
Akinc, A ;
Anderson, DG ;
Lynn, DM ;
Langer, R .
BIOCONJUGATE CHEMISTRY, 2003, 14 (05) :979-988
[2]   Drug delivery systems: Entering the mainstream [J].
Allen, TM ;
Cullis, PR .
SCIENCE, 2004, 303 (5665) :1818-1822
[3]   Ligand-targeted therapeutics in anticancer therapy [J].
Allen, TM .
NATURE REVIEWS CANCER, 2002, 2 (10) :750-763
[4]   Influence of molecular weight on oral absorption of water soluble chitosans [J].
Chae, SY ;
Jang, MK ;
Nah, JW .
JOURNAL OF CONTROLLED RELEASE, 2005, 102 (02) :383-394
[5]  
Cheng Y., 2012, Dendrimer-Based Drug Delivery Systems: From Theory to Practice
[6]   Cancer Nanomedicine: From Drug Delivery to Imaging [J].
Chow, Edward Kai-Hua ;
Ho, Dean .
SCIENCE TRANSLATIONAL MEDICINE, 2013, 5 (216)
[7]   Thermo-responsive "hairy-rod" polypeptides for smart antitumor drug delivery [J].
Ding, Jianxun ;
Zhao, Li ;
Li, Di ;
Xiao, Chunsheng ;
Zhuang, Xiuli ;
Chen, Xuesi .
POLYMER CHEMISTRY, 2013, 4 (11) :3345-3356
[8]   Tailor-Made Dual pH-Sensitive Polymer-Doxorubicin Nanoparticles for Efficient Anticancer Drug Delivery [J].
Du, Jin-Zhi ;
Du, Xiao-Jiao ;
Mao, Cheng-Qiong ;
Wang, Jun .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2011, 133 (44) :17560-17563
[9]   Tumor cells-specific targeting delivery achieved by A54 peptide functionalized polymeric micelles [J].
Du, Yong-Zhong ;
Cai, Li-Li ;
Liu, Ping ;
You, Jian ;
Yuan, Hong ;
Hu, Fu-Qiang .
BIOMATERIALS, 2012, 33 (34) :8858-8867
[10]   Linoleic acid-grafted chitosan oligosaccharide micelles for intracellular drug delivery and reverse drug resistance of tumor cells [J].
Du, Yong-Zhong ;
Wang, Ling ;
Yuan, Hong ;
Hu, Fu-Qiang .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2011, 48 (01) :215-222