Curcumin-Loaded N,O-Carboxymethyl Chitosan Nanoparticles for Cancer Drug Delivery

被引:105
作者
Anitha, A.
Maya, S.
Deepa, N.
Chennazhi, K. P.
Nair, S. V.
Jayakumar, R. [1 ]
机构
[1] Amrita Vishwa Vidyapeetham Univ, Amrita Ctr Nanosci & Mol Med, Amrita Inst Med Sci, Kochi 682041, India
关键词
N; O-Carboxymethyl chitosan; curcumin; nanoformulation; cytotoxicity; cellular uptake; cancer drug delivery; CHITIN; NANOCARRIER; TOXICITY;
D O I
10.1163/092050611X581534
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Chitosan (CS) and its carboxymethyl derivatives are smart biopolymers that are non-toxic, biocompatible and biodegradable, and, hence, suitable for various biomedical applications, such as drug delivery, gene therapy and tissue engineering. Curcumin is a major chemotherapeutic agent with antioxidant, anti-inflammatory, anti-proliferative, anticancer and antimicrobial effects. However, the potential of curcumin as a chemotherapeutic agent is limited by its hydrophobicity and poor bioavailability. In this work, we developed a nanoformulation of curcumin in a carboxymethyl chitosan (CMC) derivative, N,O-carboxymethyl chitosan (N,O-CMC). The curcumin-loaded N,O-CMC (curcumin-N,O-CMC) nanoparticles were characterized using DLS, AFM, SEM, FT-IR and XRD. DLS studies revealed nanoparticles with a mean diameter of 150 +/- 30 nm. AFM and SEM confirmed that the particles have a spherical morphology within the size range of 150 +/- 30 nm. Curcumin was entrapped with in N, O-CMC nanopartcles with an efficiency of 80%. The in vitro drug-release profile was studied at different pH (7.4 and 4.5) at 37 degrees C for different incubation periods with and without lysozyme. Cytotoxicity studies using MTT assay indicated that curcumin-N, O-CMC nanoparticles showed specific toxicity towards cancer cells and non-toxicity to normal cells. Cellular uptake of curcumin-N, O-CMC nanoparticles was analyzed by fluorescence microscopy and was reconfirmed by flow cytometry. Overall, these results indicate that like previously reported curcumin loaded O-CMC nanoparticles, N, O-CMC will also be an efficient nanocarrier for delivering curcumin to cancer cells. (C) Koninklijke Brill NV, Leiden, 2011
引用
收藏
页码:1381 / 1400
页数:20
相关论文
共 48 条
  • [1] Anand P., 2010, BIOCHEM PHARMACOL, V79, P310
  • [2] Curcumin and cancer: An "old-age" disease with an "age-old" solution
    Anand, Preetha
    Sundaram, Chitra
    Jhurani, Sonia
    Kunnumakkara, Ajaikumar B.
    Aggarwal, Bharat B.
    [J]. CANCER LETTERS, 2008, 267 (01) : 133 - 164
  • [3] Efficient water soluble O-carboxymethyl chitosan nanocarrier for the delivery of curcumin to cancer cells
    Anitha, A.
    Maya, S.
    Deepa, N.
    Chennazhi, K. P.
    Nair, S. V.
    Tamura, H.
    Jayakumar, R.
    [J]. CARBOHYDRATE POLYMERS, 2011, 83 (02) : 452 - 461
  • [4] Development of mucoadhesive thiolated chitosan nanoparticles for biomedical applications
    Anitha, A.
    Deepa, N.
    Chennazhi, K. P.
    Nair, S. V.
    Tamura, H.
    Jayakumar, R.
    [J]. CARBOHYDRATE POLYMERS, 2011, 83 (01) : 66 - 73
  • [5] Synthesis, characterization, cytotoxicity and antibacterial studies of chitosan, O-carboxymethyl and N,O-carboxymethyl chitosan nanoparticles
    Anitha, A.
    Rani, V. V. Divya
    Krishna, R.
    Sreeja, V.
    Selvamurugan, N.
    Nair, S. V.
    Tamura, H.
    Jayakumar, R.
    [J]. CARBOHYDRATE POLYMERS, 2009, 78 (04) : 672 - 677
  • [6] [Anonymous], [No title captured], Patent No. 4619995
  • [7] BHAVANISHANKAR TN, 1980, INDIAN J EXP BIOL, V18, P73
  • [8] Studies on effect of pH on cross-linking of chitosan with sodium tripolyphosphate: A technical note
    Bhumkar, Devika R.
    Pokharkar, Varsha B.
    [J]. AAPS PHARMSCITECH, 2006, 7 (02)
  • [9] Polymeric nanoparticle-encapsulated curcumin (nanocurcumin"): A novel strategy for human cancer therapy"
    Bisht S.
    Feldmann G.
    Soni S.
    Ravi R.
    Karikar C.
    Maitra A.
    Maitra A.
    [J]. Journal of Nanobiotechnology, 5 (1)
  • [10] Therapeutic nanoparticles for drug delivery in cancer
    Cho, Kwangjae
    Wang, Xu
    Nie, Shuming
    Chen, Zhuo
    Shin, Dong M.
    [J]. CLINICAL CANCER RESEARCH, 2008, 14 (05) : 1310 - 1316