Preparation and characterization of intelligent core-shell nanoparticles based on poly(D,L-lactide)-g-poly(N-isopropyl-acrylamide-co-methacrylic acid)

被引:141
作者
Lo, CL [1 ]
Lin, KM [1 ]
Hsiue, GH [1 ]
机构
[1] Natl Tsing Hua Univ, Dept Chem Engn, Hsinchu 300, Taiwan
关键词
intelligent nanoparticle; graft copolymer; structural changes; intracellular drug delivery; 5-fluorouracil;
D O I
10.1016/j.jconrel.2005.03.004
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
New thermo-responsive, pH-responsive, and biodegradable nanoparticles comprised of poly(D,L-lactide)-graft-poly(N-isopropyl acrylamide-co-methacrylic acid) (PLA-g-P(NIPAm-co-MAA)) were developed by grafting biodegradable poly(D,L-lactide) onto N-isopropyl acrylamide and methacrylic acid. A core-shell type nano-structure was formed with a hydrophilic outer shell and a hydrophobic inner core, which exhibited a phase transition temperature above 37 degrees C suitable for biomedical application. Upon heating above the phase transition temperature, PLA-g-P(NIPAm-co-MAA) nanoparticle showed a polarity increase of pyrene in either buffer solution or intra-hepato-carcinoma cells as determined by. fluorescence measurement, indicating that the structure of nanoparticles caused leakages from outer shell copolymers aggregation and collapsed. The drug loading level of 5-fluorouracil (5-FU) encapsulated in the PLA-g-P(NIPAm-co-MAA) nanoparticles can be as high as 20%. The release of 5-FU from nanoparticles was strongly controlled by the pH in the aqueous solution. Based on these results, PLA-g-P(NIPAm-co-MAA) nanoparticles can be used as a drug carrier for intracellular delivery of anti-cancer drug. (c) 2005 Elsevier B.V All rights reserved.
引用
收藏
页码:477 / 488
页数:12
相关论文
共 31 条
[11]   Enzymatic biodegradation of poly(ethylene oxide-b-ε-caprolactone) diblock copolymer and its potential biomedical applications [J].
Gan, ZH ;
Jim, TF ;
Li, M ;
Yuer, Z ;
Wang, SG ;
Wu, C .
MACROMOLECULES, 1999, 32 (03) :590-594
[12]  
HOFFMAN A S, 1986, Journal of Controlled Release, V4, P213
[13]  
ICHIHARA T, 1989, CANCER RES, V49, P4357
[14]   An AB block copolymer of oligo(methyl methacrylate) and poly(acrylic acid) for micellar delivery of hydrophobic drugs [J].
Inoue, T ;
Chen, GH ;
Nakamae, K ;
Hoffman, AS .
JOURNAL OF CONTROLLED RELEASE, 1998, 51 (2-3) :221-229
[15]   A new antisense oligonucleotide delivery system based on self-assembled ODN-PEG hybrid conjugate micelles [J].
Jeong, JH ;
Kim, SW ;
Park, TG .
JOURNAL OF CONTROLLED RELEASE, 2003, 93 (02) :183-191
[16]  
KALYANASUNDARAM K, 1997, J AM CHEM SOC, V99, P22039
[17]   Characterisation of thermally controlled chain association in aqueous solutions of poly(N-isopropyl acrylamide)-g-poly(ethylene oxide) dynamic light scattering [J].
Kjoniksen, AL ;
Nyström, B ;
Tenhu, H .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 2003, 228 (1-3) :75-83
[18]   PHYSICAL ENTRAPMENT OF ADRIAMYCIN IN AB BLOCK-COPOLYMER MICELLES [J].
KWON, GS ;
NAITO, M ;
YOKOYAMA, M ;
OKANO, T ;
SAKURAI, Y ;
KATAOKA, K .
PHARMACEUTICAL RESEARCH, 1995, 12 (02) :192-195
[19]   Macromolecular systems for chemotherapy and magnetic resonance imaging [J].
Matthews, SE ;
Pouton, CW ;
Threadgill, MD .
ADVANCED DRUG DELIVERY REVIEWS, 1996, 18 (02) :219-267
[20]   A NOVEL RECOVERY-SYSTEM FOR CULTURED-CELLS USING PLASMA-TREATED POLYSTYRENE DISHES GRAFTED WITH POLY(N-ISOPROPYLACRYLAMIDE) [J].
OKANO, T ;
YAMADA, N ;
SAKAI, H ;
SAKURAI, Y .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1993, 27 (10) :1243-1251