Preparation and characterizations of a novel deoxycholic acid-O-carboxymethylated chitosan-folic acid conjugates and self-aggregates

被引:105
作者
Wang, Feihu [1 ]
Zhang, Dianrui [1 ]
Duan, Cunxian [1 ]
Jia, Lejiao [1 ]
Feng, Feifei [1 ]
Liu, Yue [1 ]
Wang, Yancai [1 ]
Hao, Leilei [1 ]
Zhang, Qiang [2 ]
机构
[1] Shandong Univ, Coll Pharm, Dept Pharmaceut, Jinan 250012, Peoples R China
[2] Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Beijing 100083, Peoples R China
关键词
O-carboxymethylated chitosan; Deoxycholic acid; Folic acid; Self-aggregates; BLOCK-COPOLYMER MICELLES; ASSEMBLED NANOPARTICLES; IN-VITRO; PHYSICOCHEMICAL CHARACTERISTICS; POLYMER MICELLES; DELIVERY SYSTEM; DRUG-DELIVERY; BILE-ACIDS; BEARING; WATER;
D O I
10.1016/j.carbpol.2011.01.017
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
O-carboxymethylated chitosan (OCMC) was firstly hydrophobically modified with various deoxycholic acid (DOCA) to obtain a novel kind of amphiphilic polymer, and then covalently bound with folic acid (FA) to develop a new potential cancer-targeted drug delivery system. Structural characterizations of the conjugates were investigated using FTIR, H-1 NMR and XRD. The physicochemical properties of self-aggregates in aqueous media were studied by H-1 NMR, zetasizer, zeta potential, fluorescence spectroscopy, and transmission electron microscopy (TEM). The mean diameter of self-aggregates in PBS solution (pH 7.4) decreased with the degree of substitution (DS) of DOCA increasing. Zeta potential of self-aggregates exhibited near -20 mV in PBS solution (pH 7.4), indicating these nanoparticles were covered with negatively charged OCMC shells. The critical aggregation concentrations (cac) of the conjugates were dependent on the DS of DOCA and were significantly lower than those of low molecular weight surfactants. TEM images demonstrated that the shape of self-aggregates was spherical. Crown Copyright (C) 2011 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1192 / 1200
页数:9
相关论文
共 63 条
[1]   SELF-AGGREGATES OF HYDROPHOBIZED POLYSACCHARIDES IN WATER - FORMATION AND CHARACTERISTICS OF NANOPARTICLES [J].
AKIYOSHI, K ;
DEGUCHI, S ;
MORIGUCHI, N ;
YAMAGUCHI, S ;
SUNAMOTO, J .
MACROMOLECULES, 1993, 26 (12) :3062-3068
[2]   Controlled association of amphiphilic polymers in water:: Thermosensitive nanoparticles formed by self-assembly of hydrophobically modified pullulans and poly(N-isopropylacrylamides) [J].
Akiyoshi, K ;
Kang, EC ;
Kurumada, S ;
Sunamoto, J ;
Principi, T ;
Winnik, FM .
MACROMOLECULES, 2000, 33 (09) :3244-3249
[3]   PYRENE FLUORESCENCE STUDY OF CHITOSAN SELF-ASSOCIATION IN AQUEOUS-SOLUTION [J].
AMIJI, MM .
CARBOHYDRATE POLYMERS, 1995, 26 (03) :211-213
[4]   Synthesis and characterization of chitosan-g-poly(ethylene glycol)-folate as a non-viral carrier for tumor-targeted gene delivery [J].
Chan, Peggy ;
Kurisawa, Motoichi ;
Chung, Joo Eun ;
Yang, Yi-Yan .
BIOMATERIALS, 2007, 28 (03) :540-549
[5]   Effect of the degree of deacetylation and the substitution of carboxymethyl chitosan on its aggregation behavior [J].
Chen, LY ;
Du, YM ;
Tian, ZG ;
Sun, LP .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 2005, 43 (03) :296-305
[6]   Chemical characteristics of O-carboxymethyl chitosans related to the preparation conditions [J].
Chen, XG ;
Park, HJ .
CARBOHYDRATE POLYMERS, 2003, 53 (04) :355-359
[7]   Bile acids in drug discovery [J].
Enhsen, A ;
Kramer, W ;
Wess, G .
DRUG DISCOVERY TODAY, 1998, 3 (09) :409-418
[8]   Preparation and physicochemical characteristics of self-assembled nanoparticles of deoxycholic acid modified-carboxymethyl curdlan conjugates [J].
Gao, Fu-Ping ;
Zhang, Hui-Zhu ;
Liu, Ling-Rong ;
Wang, Yin-Song ;
Jiang, Qian ;
Yang, Xin-Du ;
Zhang, Qi-Qing .
CARBOHYDRATE POLYMERS, 2008, 71 (04) :606-613
[9]   BIODEGRADABLE LONG-CIRCULATING POLYMERIC NANOSPHERES [J].
GREF, R ;
MINAMITAKE, Y ;
PERACCHIA, MT ;
TRUBETSKOY, V ;
TORCHILIN, V ;
LANGER, R .
SCIENCE, 1994, 263 (5153) :1600-1603
[10]   9-NC-loaded folate-conjugated polymer micelles as tumor targeted drug delivery system: Preparation and evaluation in vitro [J].
Han, Xue ;
Liu, Jing ;
Liu, Min ;
Xie, Cao ;
Zhan, Changyou ;
Gu, Bing ;
Liu, Yu. ;
Feng, Linglin ;
Lu, WeiYue .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2009, 372 (1-2) :125-131