Amine-containing core-shell nanoparticles as potential drug carriers for intracellular delivery

被引:41
作者
Feng, Min [1 ]
Li, Pei [1 ]
机构
[1] Hong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Open Lab Chirotechnol, Inst Mol Technol Drug Discovery & Synth, Kowloon, Hong Kong, Peoples R China
关键词
poly(ethyleneimine)-poly(methyl methacrylate) copolymer; core-shell nanoparticles; polymer-drug complexes; drug delivery;
D O I
10.1002/jbm.a.30882
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The present study aimed at exploring the use of amine-containing core-shell nanoparticles as potential drug carriers for intracellular delivery. Stable nanoparticles (100-200 nm in diameter) that consisted of poly (methyl methacrylate) (PMMA) cores with hydrophilic poly(ethyleneimine) (PEI) shells were synthesized and used to study their complexation with model drug, ibuprofen (IB), and release it under various electrolyte concentrations. The complexed IB/PEI-PMMA nanoparticles were characterized with FTIR, photon correlation spectroscopy, zeta-potential, and transmission electron microscopy (TEM). Results suggested that the PEI-PMMA nanoparticles could effectively complex with the IB via electrostatic interaction. The thick PEI shells (similar to 30 nm) significantly enhanced the drug loading capacity up to 23% (w/w) of the complexed nanopartricle. In vitro release of the drug from the complexed nanoparticles was sensitive to the ionic strength of the media. Study of cellular entry of fluorescently labeled IB/nanoparticle complexes using a confocal laser scanning microscopy demonstrated that the entry of the complexed nanoparticles strongly depended on the complexing ratio between IB and PEI-PMMA nanoparticles. (c) 2006 Wiley Periodicals, Inc.
引用
收藏
页码:184 / 193
页数:10
相关论文
共 23 条
[11]  
Moghimi SM, 2001, PHARMACOL REV, V53, P283
[12]   Release of adriamycin from poly(γ-benzyl-L-glutamate)/poly(ethylene oxide) nanoparticles [J].
Oh, I ;
Lee, K ;
Kwon, HY ;
Lee, YB ;
Shin, SC ;
Cho, CS ;
Kim, CK .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 181 (01) :107-115
[13]   PEGylated nanoparticles for biological and pharmaceutical applications [J].
Otsuka, H ;
Nagasaki, Y ;
Kataoka, K .
ADVANCED DRUG DELIVERY REVIEWS, 2003, 55 (03) :403-419
[14]   Biodegradable nanoparticles for drug and gene delivery to cells and tissue [J].
Panyam, J ;
Labhasetwar, V .
ADVANCED DRUG DELIVERY REVIEWS, 2003, 55 (03) :329-347
[15]   Poly(lactic acid)-poly(ethylene glycol) nanoparticles as new carriers for the delivery of plasmid DNA [J].
Perez, C ;
Sanchez, A ;
Putnam, D ;
Ting, D ;
Langer, R ;
Alonso, MJ .
JOURNAL OF CONTROLLED RELEASE, 2001, 75 (1-2) :211-224
[16]   Advanced drug delivery devices via self-assembly of amphiphilic block copolymers [J].
Rösler, A ;
Vandermeulen, GWM ;
Klok, HA .
ADVANCED DRUG DELIVERY REVIEWS, 2001, 53 (01) :95-108
[17]   Clonazepam release from core-shell type nanoparticles of poly(ε-caprolactone)/poly(ethylene glycol)/poly(ε-caprolactone) triblock copolymers [J].
Ryu, JG ;
Jeong, YI ;
Kim, IS ;
Lee, JH ;
Nah, JW ;
Kim, SH .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2000, 200 (02) :231-242
[18]   Biodegradable polymeric nanoparticles as drug delivery devices [J].
Soppimath, KS ;
Aminabhavi, TM ;
Kulkarni, AR ;
Rudzinski, WE .
JOURNAL OF CONTROLLED RELEASE, 2001, 70 (1-2) :1-20
[19]   Crystal structure of ciprofloxacin hexahydrate and its characterization [J].
Turel, I ;
Bukovec, P ;
Quiros, M .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1997, 152 (01) :59-65
[20]   Preparation and modification of N-(2-hydroxyl) propyl-3-trimethyl ammonium chitosan chloride nanoparticle as a protein carrier [J].
Xu, YM ;
Du, YM ;
Huang, RH ;
Gao, LP .
BIOMATERIALS, 2003, 24 (27) :5015-5022