Curcumin-loaded poly(ε-caprolactone) nanofibres: Diabetic wound dressing with anti-oxidant and anti-inflammatory properties

被引:362
作者
Merrell, Jonathan G. [2 ]
McLaughlin, Shaun W. [3 ]
Tie, Lu [6 ]
Laurencin, Cato T. [4 ]
Chen, Alex F. [5 ]
Nair, Lakshmi S. [1 ,4 ]
机构
[1] Univ Connecticut, Ctr Hlth, New England Musculoskeletal Inst, Dept Orthopaed Surg,Dept Chem Mat & Biomol Engn, Farmington, CT 06030 USA
[2] Univ Virginia, Dept Biomed Engn, Charlottesville, VA USA
[3] Univ Virginia, Dept Orthopaed Surg, Charlottesville, VA USA
[4] Univ Connecticut, Dept Chem Mat & Biomol Engn, Storrs, CT USA
[5] Michigan State Univ, Neurosci Program, E Lansing, MI 48824 USA
[6] Peking Univ, Hlth Sci Ctr, Dept Pharmacol, Beijing 100871, Peoples R China
基金
美国国家卫生研究院;
关键词
anti-inflammatory; anti-oxidant; diabetic wound healing; electrospinning; nanofibres; CHEMOPREVENTIVE AGENT CURCUMIN; CAPACITY; INHIBITION; IMPROVES; DAMAGE;
D O I
10.1111/j.1440-1681.2009.05216.x
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
P>Curcumin is a naturally occurring poly-phenolic compound with a broad range of favourable biological functions, including anti-cancer, anti-oxidant and anti-inflammatory activities. The low bioavailability and in vivo stability of curcumin require the development of suitable carrier vehicles to deliver the molecule in a sustained manner at therapeutic levels. In the present study, we investigated the feasibility and potential of poly(caprolactone) (PCL) nanofibres as a delivery vehicle for curcumin for wound healing applications. By optimizing the electrospinning parameters, bead-free curcumin-loaded PCL nanofibres were developed. The fibres showed sustained release of curcumin for 72 h and could be made to deliver a dose much lower than the reported cytotoxic concentration while remaining bioactive. Human foreskin fibroblast cells (HFF-1) showed more than 70% viability on curcumin-loaded nanofibres. The anti-oxidant activity of curcumin-loaded nanofibres was demonstrated using an oxygen radical absorbance capacity (ORAC) assay and by the ability of the fibres to maintain the viability of HFF-1 cells under conditions of oxidative stress. The curcumin-loaded nanofibres also reduced inflammatory induction, as evidenced by low levels of interleukin-6 release from mouse monocyte-macrophages seeded onto the fibres following stimulation by Escherichia coli-derived lipopolysaccharide. The in vivo wound healing capability of the curcumin loaded PCL nanofibres was demonstrated by an increased rate of wound closure in a streptozotocin-induced diabetic mice model. These results demonstrate that the curcumin-loaded PCL nanofibre matrix is bioactive and has potential as a wound dressing with anti-oxidant and anti-inflammatory properties.
引用
收藏
页码:1149 / 1156
页数:8
相关论文
共 37 条
[1]
Curcumin inhibition of inflammatory cytokine production by human peripheral blood monocytes and alveolar macrophages [J].
Abe, Y ;
Hashimoto, S ;
Horie, T .
PHARMACOLOGICAL RESEARCH, 1999, 39 (01) :41-47
[2]
PHARMACOLOGY OF CURCUMA-LONGA [J].
AMMON, HPT ;
WAHL, MA .
PLANTA MEDICA, 1991, 57 (01) :1-7
[3]
Determination of acidity constants of curcumin in aqueous solution and apparent rate constant of its decomposition [J].
Bernabé-Pineda, M ;
Ramírez-Silva, MT ;
Romero-Romo, M ;
Gonzádlez-Vergara, E ;
Rojas-Hernández, A .
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 2004, 60 (05) :1091-1097
[4]
Polymeric nanoparticle-encapsulated curcumin (nanocurcumin"): A novel strategy for human cancer therapy" [J].
Bisht S. ;
Feldmann G. ;
Soni S. ;
Ravi R. ;
Karikar C. ;
Maitra A. ;
Maitra A. .
Journal of Nanobiotechnology, 5 (1)
[5]
Cao GH, 1999, METHOD ENZYMOL, V299, P50
[6]
INHIBITION OF TUMOR-NECROSIS-FACTOR BY CURCUMIN, A PHYTOCHEMICAL [J].
CHAN, MMY .
BIOCHEMICAL PHARMACOLOGY, 1995, 49 (11) :1551-1556
[7]
Cheng AL, 2001, ANTICANCER RES, V21, P2895
[8]
Cho JW, 2007, INT J MOL MED, V19, P469
[9]
Supplementation with a pine bark extract rich in polyphenols increases plasma antioxidant capacity and alters the plasma lipoprotein profile [J].
Devaraj, S ;
Vega-López, S ;
Kaul, N ;
Schönlau, F ;
Rohdewald, P ;
Jialal, I .
LIPIDS, 2002, 37 (10) :931-934
[10]
Chemopreventive and therapeutic effects of curcumin [J].
Duvoix, A ;
Blasius, R ;
Delhalle, S ;
Schnekenburger, M ;
Morceau, F ;
Henry, E ;
Dicato, M ;
Diederich, M .
CANCER LETTERS, 2005, 223 (02) :181-190