Optimization of fabrication parameters to produce chitosan-tripolyphosphate nanoparticles for delivery of tea catechins

被引:312
作者
Hu, Bing [1 ,2 ]
Pan, Chenliang [1 ]
Sun, Yi [1 ]
Hou, Zhiyun [3 ]
Ye, Hong [1 ]
Hu, Bing [1 ,2 ]
Zeng, Xiaoxiong [1 ]
机构
[1] Nanjing Agr Univ, Coll Food Sci & Technol, Nanjing 210095, Peoples R China
[2] Nanjing Agr Univ, Electron Microscopy Lab, Nanjing 210095, Peoples R China
[3] Malvern Instruments China, Shanghai 200233, Peoples R China
关键词
chitosan; chitosan-tripolyphosphate nanoparticles; controlled release; encapsulation; nanoparticle surface charge; nanoparticle size; tea catechins;
D O I
10.1021/jf801111c
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
This work investigated the polyanion-initiated gelation process in fabricating chitosan-tripolyphosphate (CS-TPP) nanoparticles intended to be used as carriers for delivering tea catechins. The results demonstrated that the particle size and surface charge of CS-TPP nanoparticles could be controlled by fabrication conditions. For preparation of CS-TPP nanoparticles loaded with tea catechins, the effects of modulating conditions including contact time between CS and tea catechins, CS molecular mass, CS concentration, CS-TPP mass ratio, initial pH value of CS solution, and concentration of tea catechins on encapsulation efficiency and the release profile of tea catechins in vitro were examined systematically. The study found that the encapsulation efficiency of tea catechins in CS-TPP nanoparticles ranged from 24 to 53%. In addition, FT-IR analysis showed that the covalent bonding and hydrogen bonding between tea catechins and CS occurred during the formation of CS-TPP nanoparticles loaded with tea catechins. Furthermore, studies on the release profile of tea catechins in vitro demonstrated that the controlled release of tea catechins using CS-TPP nanoparticles was achievable.
引用
收藏
页码:7451 / 7458
页数:8
相关论文
共 31 条
[1]   Recent advances on chitosan-based micro- and nanoparticles in drug delivery [J].
Agnihotri, SA ;
Mallikarjuna, NN ;
Aminabhavi, TM .
JOURNAL OF CONTROLLED RELEASE, 2004, 100 (01) :5-28
[2]   In vivo comparison of the bioavailability of (+)-catechin, (-)-epicatechin and their mixture in orally administered rats [J].
Baba, S ;
Osakabe, N ;
Natsume, M ;
Muto, Y ;
Takizawa, T ;
Terao, J .
JOURNAL OF NUTRITION, 2001, 131 (11) :2885-2891
[3]   Preparation, characterization and biodistribution of ultrafine chitosan nanoparticles [J].
Banerjee, T ;
Mitra, S ;
Singh, AK ;
Sharma, RK ;
Maitra, A .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2002, 243 (1-2) :93-105
[4]  
Bei Z, 2008, CHINESE J ANAL CHEM, V36, P494
[5]   Chitosan nanoparticles for oral drug and gene delivery [J].
Bowman, Katherine ;
Leong, Kam W. .
INTERNATIONAL JOURNAL OF NANOMEDICINE, 2006, 1 (02) :117-128
[6]   Contribution of presystemic hepatic extraction to the low oral bioavailability of green tea catechins in rats [J].
Cai, Y ;
Anavy, ND ;
Chow, HHS .
DRUG METABOLISM AND DISPOSITION, 2002, 30 (11) :1246-1249
[7]  
Calvo P, 1997, J APPL POLYM SCI, V63, P125, DOI 10.1002/(SICI)1097-4628(19970103)63:1<125::AID-APP13>3.0.CO
[8]  
2-4
[9]   Bioavailability of dietary doses of 3H-labelled tea antioxidants (+)-catechin and (-)-epicatechin in rat [J].
Catterall, F ;
King, LJ ;
Clifford, MN ;
Ioannides, C .
XENOBIOTICA, 2003, 33 (07) :743-753
[10]   Degradation of methylcellulose during ultra-high pressure homogenisation [J].
Floury, J ;
Desrumaux, A ;
Axelos, MAV ;
Legrand, J .
FOOD HYDROCOLLOIDS, 2002, 16 (01) :47-53