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
[31]   Challenges and solutions for the delivery of biotech drugs - a review of drug nanocrystal technology and lipid nanoparticles [J].
Muller, RH ;
Keck, CM .
JOURNAL OF BIOTECHNOLOGY, 2004, 113 (1-3) :151-170
[32]   Targeted delivery of low molecular drugs using chitosan and its derivatives [J].
Park, Jae Hyung ;
Saravanakumar, Gurusamy ;
Kim, Kwangmeyung ;
Kwon, Ick Chan .
ADVANCED DRUG DELIVERY REVIEWS, 2010, 62 (01) :28-41
[33]   Carboxymethyl chitosan-graft-phosphatidylethanolamine:: Amphiphilic matrices for controlled drug delivery [J].
Prabaharan, M. ;
Reis, R. L. ;
Mano, J. F. .
REACTIVE & FUNCTIONAL POLYMERS, 2007, 67 (01) :43-52
[34]   TOXICITY STUDIES ON ALPINIA-GALANGA AND CURCUMA-LONGA [J].
QURESHI, S ;
SHAH, AH ;
AGEEL, AM .
PLANTA MEDICA, 1992, 58 (02) :124-127
[35]  
Rao SB, 1997, J BIOMED MATER RES, V34, P21, DOI 10.1002/(SICI)1097-4636(199701)34:1<21::AID-JBM4>3.0.CO
[36]  
2-P
[37]   Biodegradable and thermo-sensitive chitosan-g-poly(N-vinylcaprolactam) nanoparticles as a 5-fluorouracil carrier [J].
Rejinold, N. Sanoj ;
Chennazhi, K. P. ;
Nair, S. V. ;
Tamura, H. ;
Jayakumar, R. .
CARBOHYDRATE POLYMERS, 2011, 83 (02) :776-786
[38]   5-Fluorouracil loaded fibrinogen nanoparticles for cancer drug delivery applications [J].
Rejinold, N. Sanoj ;
Muthunarayanan, M. ;
Chennazhi, K. P. ;
Nair, S. V. ;
Jayakumar, R. .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2011, 48 (01) :98-105
[39]   Anti cancer effects of curcumin: cycle of life and death [J].
Sa, Gaurisankar ;
Das, Tanya .
CELL DIVISION, 2008, 3 (1)
[40]   Synthesis of novel biodegradable and self-assembling methoxy poly(ethylene glycol)-palmitate nanocarrier for curcumin delivery to cancer cells [J].
Sahu, Abhishek ;
Bora, Utpal ;
Kasoju, Naresh ;
Goswami, Pranab .
ACTA BIOMATERIALIA, 2008, 4 (06) :1752-1761