Fluorescent Nanoparticles of Chitosan Complex for Real-Time Monitoring Drug Release

被引:38
作者
Cui, Wei [2 ]
Lu, Xuemin [2 ]
Cui, Kun [2 ]
Wu, Jun [2 ]
Wei, Yen [1 ]
Let, Qinghua [2 ]
机构
[1] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, State Key Lab Met Matrix Composites, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
DELIVERY; ENCAPSULATION; GLYCOL; LIGHT;
D O I
10.1021/la200552k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
New types of fluorescent nanoparticles (FNPs) were prepared through ionic self-assembly of anthracene derivative and chitosan for applications as drug delivery carriers with real-time monitoring of the process of drug release. Because of the presence of the hydrophilic groups, these FNPs showed excellent dispersion and stability in aqueous solution. The structure and properties of the FNPs were investigated by using means of H-1 NMR, FTIR, SEM, dynamic light scattering (DLS), and so on. The potential practical applications as drug delivery carriers for real-time detection of the drug release process were demonstrated using Nicardipine as a model drug. Upon loading the drug, the strong blue fluorescence of FNPs was quenched due to electron transfer and fluorescence resonance energy transfer (FRET). With release of drug in vitro, the fluorescence was recovered again. The relationship between the accumulative drug release of FNPs and the recovered fluorescence intensity has been established. Such FNPs may open up new perspectives for designing a new class of detection system for monitoring drug release.
引用
收藏
页码:8384 / 8390
页数:7
相关论文
共 37 条
[1]  
BAKY SH, 1985, CARDIOVASC DRUG REV, V3, P153
[2]   INTERACTION OF CALCIUM-CHANNEL ANTAGONISTS WITH CALCIUM - STRUCTURAL STUDIES ON NICARDIPINE AND ITS CA2+ COMPLEX [J].
BELCIUG, MP ;
ANANTHANARAYANAN, VS .
JOURNAL OF MEDICINAL CHEMISTRY, 1994, 37 (25) :4392-4399
[3]   Preparation, Characterization, and Oral Delivery of Insulin Loaded Carboxylated Chitosan Grafted Poly(methyl methacrylate) Nanoparticles [J].
Cui, Fuying ;
Qian, Feng ;
Zhao, Ziming ;
Yin, Lichen ;
Tang, Cui ;
Yin, Chunhua .
BIOMACROMOLECULES, 2009, 10 (05) :1253-1258
[4]   Conjugated Polymer Nanoparticles for Drug Delivery and Imaging [J].
Feng, Xuli ;
Lv, Fengting ;
Liu, Libing ;
Tang, Hongwei ;
Xing, Chengfen ;
Yang, Qiong ;
Wang, Shu .
ACS APPLIED MATERIALS & INTERFACES, 2010, 2 (08) :2429-2435
[5]   Exploiting the vitamin B12 pathway to enhance oral drug delivery via polymeric micelles [J].
Francis, MF ;
Cristea, M ;
Winnik, FM .
BIOMACROMOLECULES, 2005, 6 (05) :2462-2467
[6]   Structure of Self-Organized Multilayer Nanoparticles for Drug Delivery [J].
Gerelli, Y. ;
Barbieri, S. ;
Di Bari, M. T. ;
Deriu, A. ;
Cantu, L. ;
Brocca, P. ;
Sonvico, F. ;
Colombo, P. ;
May, R. ;
Motta, S. .
LANGMUIR, 2008, 24 (20) :11378-11384
[7]   Synthetic micelle sensitive to IR light via a two-photon process [J].
Goodwin, AP ;
Mynar, JL ;
Ma, YZ ;
Fleming, GR ;
Fréchet, JMJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (28) :9952-9953
[8]   Novel polymer micelles prepared from chitosan grafted hydrophobic palmitoyl groups for drug delivery [J].
Jiang, Gang-Biao ;
Quan, Daping ;
Liao, Kairong ;
Wang, Haihua .
MOLECULAR PHARMACEUTICS, 2006, 3 (02) :152-160
[9]   Physicochemical characterizations of self-assembled nanoparticles of glycol chitosan-deoxycholic acid conjugates [J].
Kim, K ;
Kwon, S ;
Park, JH ;
Chung, H ;
Jeong, SY ;
Kwon, IC .
BIOMACROMOLECULES, 2005, 6 (02) :1154-1158
[10]  
Kown S., 2003, LANGMUIR, V19, P10188