Thermally sensitive micelles self-assembled from poly(N-isopropylacrylamide-co-N,N-dimethylacrylamide)-b-poly(D,L-lactide-co-glycolide) for controlled delivers of paclitaxel

被引:52
作者
Liu, SQ
Tong, YW
Yang, YY
机构
[1] Inst Bioengn & Nanotechnol, Singapore 138669, Singapore
[2] Natl Univ Singapore, Dept Chem & Biomol Engn, Singapore 117576, Singapore
关键词
D O I
10.1039/b501756b
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Thermally sensitive micelles self-assembled from poly(N-isopropylacrylamide-co- N,N-dimethylacrylamide)-b-poly(D,L-lactide-co-glycolide) [P(NIPAAm-co-DMAAm)-b-PLGA] are fabricated and used as a carrier for the controlled delivery of paclitaxel. Paclitaxel is efficiently loaded into the micelles by a membrane dialysis method. The lower critical solution temperature (LCST) of the micelles is 39.0 degrees C in PBS. Encapsulation efficiency and loading level of paclitaxel are affected by the initial loading level of paclitaxel, fabrication temperature and polymer composition. The blank and paclitaxel-loaded micelles are characterized by particle size analysis (DLS), morphology (TEM and AFM) and paclitaxel distribution (NMR, DSC and WAXRD). The micelles are spherical in shape, having an average size less than 130 nm. Paclitaxel is molecularly distributed within the core of micelles. Sustained release of paclitaxel is achieved, which is much faster at a temperature above the LCST than at the normal body temperature (37 degrees C). Cytotoxicity of free paclitaxel and paclitaxel-loaded micelles against a human breast carcinoma cell line (MDA-MB-435S) is studied at different temperatures. The cytotoxicity of the paclitaxol-loaded micelles is greater as compared to free paclitaxel. Enhanced cytotoxicity is achieved by the paclitaxol-loaded micelles when the environmental temperature increases slightly above the LCST. Paclitaxel-loaded P(NIAAm-co-DMAAm)-b-PLGA micelles may provide a good formulation for cancer therapy.
引用
收藏
页码:158 / 165
页数:8
相关论文
共 26 条
  • [1] Nano-engineering block copolymer aggregates for drug delivery
    Allen, C
    Maysinger, D
    Eisenberg, A
    [J]. COLLOIDS AND SURFACES B-BIOINTERFACES, 1999, 16 (1-4) : 3 - 27
  • [2] Preparation, characterization, cytotoxicity and pharmacokinetics of liposomes containing water-soluble prodrugs of paclitaxel
    Ceruti, M
    Crosasso, P
    Brusa, P
    Arpicco, S
    Dosio, F
    Cattel, L
    [J]. JOURNAL OF CONTROLLED RELEASE, 2000, 63 (1-2) : 141 - 153
  • [3] Thermally responsive core-shell nanoparticles self-assembled from cholesteryl end-capped and grafted polyacrylamides: drug incorporation and in vitro release
    Chaw, CS
    Chooi, KW
    Liu, XM
    Tan, CW
    Wang, L
    Yang, YY
    [J]. BIOMATERIALS, 2004, 25 (18) : 4297 - 4308
  • [4] Das GS, 2001, J BIOMED MATER RES, V55, P96, DOI 10.1002/1097-4636(200104)55:1<96::AID-JBM130>3.3.CO
  • [5] 2-V
  • [6] PEG-PE/phosphatidylcholine mixed immunomicelles specifically deliver encapsulated taxol to tumor cells of different origin and promote their efficient killing
    Gao, Z
    Lukyanov, AN
    Chakilam, AR
    Torchilin, VP
    [J]. JOURNAL OF DRUG TARGETING, 2003, 11 (02) : 87 - 92
  • [7] Hydrotropic polymer micelle system for delivery of paclitaxel
    Huh, KM
    Lee, SC
    Cho, YW
    Lee, JW
    Jeong, JH
    Park, K
    [J]. JOURNAL OF CONTROLLED RELEASE, 2005, 101 (1-3) : 59 - 68
  • [8] Polymeric micelles - a new generation of colloidal drug carriers
    Jones, MC
    Leroux, JC
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 1999, 48 (02) : 101 - 111
  • [9] Block copolymer micelles for delivery of gene and related compounds
    Kakizawa, Y
    Kataoka, K
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 2002, 54 (02) : 203 - 222
  • [10] Block copolymer micelles for drug delivery: design, characterization and biological significance
    Kataoka, K
    Harada, A
    Nagasaki, Y
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 2001, 47 (01) : 113 - 131