A Novel Class of Compounds with Cutaneous Wound Healing Properties

被引:40
作者
Zhou, Zhiguo [1 ]
Joslin, Steve [1 ]
Dellinger, Anthony [1 ]
Ehrich, Marion [3 ]
Brooks, Brad [1 ]
Ren, Qing [2 ]
Rodeck, Ulrich [2 ]
Lenk, Robert [1 ]
Kepley, Christopher L. [1 ]
机构
[1] Luna Innovat Inc, Nanoworks Div, Danville, VA 24541 USA
[2] Thomas Jefferson Univ, Philadelphia, PA 19107 USA
[3] Virginia Tech, Virginia Maryland Reg Coll Vet Med, Blacksburg, VA 24061 USA
关键词
Wound Healing; Fullerenes; Nanotechnology; Skin; Antioxidant; FULLERENE NANOMATERIALS INHIBIT; MAST-CELLS; OXIDATIVE STRESS;
D O I
10.1166/jbn.2010.1157
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Impaired wound healing is a major complication underlying several disease processes (such as diabetes). Efficient wound healing is hampered by a wide variety of processes including hypoxia (oxygen deprivation), inflammation, infection, and oxidative stress through the generation of harmful reactive oxygen species (ROS). The inherent complexity of the healing wound has resulted in limited efficacy of most therapies that target single parameters involved in the slow healing processes. Fullerenes are carbon nanospheres previously shown to exhibit a wide range of biological activities. Given that these molecules have been shown to be potent anti-inflammatories and antioxidants we hypothesized that fullerenes could aid in wound healing based on these properties. We designed and synthesized a panel of fullerene derivatives and investigated their ability to accelerate wound healing using a modified scratch assay, an ex vivo human skin model, and a mouse model of skin irritation. Several derivatives supported cell migration, induced wound closure in human skin explants, and greatly accelerated the rate at which wound healing occurred in vivo. Therefore, fullerene derivatives represent a potential new class of wound healing therapies that may aid in wound healing treatment.
引用
收藏
页码:605 / 611
页数:7
相关论文
共 31 条
[1]   The diabetic foot [J].
Andersen, Charles A. ;
Roukis, Thomas S. .
SURGICAL CLINICS OF NORTH AMERICA, 2007, 87 (05) :1149-+
[2]   Mast cells and their mediators in cutaneous wound healing active participants or innocent bystanders? [J].
Artuc, M ;
Hermes, B ;
Steckelings, UM ;
Grützkau, A ;
Henz, BM .
EXPERIMENTAL DERMATOLOGY, 1999, 8 (01) :1-16
[3]  
AUFDEM KU, 2006, J INVEST DERMATOL, V1, P106
[4]   NORMAL KERATINIZATION IN A SPONTANEOUSLY IMMORTALIZED ANEUPLOID HUMAN KERATINOCYTE CELL-LINE [J].
BOUKAMP, P ;
PETRUSSEVSKA, RT ;
BREITKREUTZ, D ;
HORNUNG, J ;
MARKHAM, A ;
FUSENIG, NE .
JOURNAL OF CELL BIOLOGY, 1988, 106 (03) :761-771
[5]   Fullerene nanomaterials inhibit phorbol myristate acetate-induced inflammation [J].
Dellinger, Anthony ;
Zhou, Zhiguo ;
Lenk, Robert ;
MacFarland, Darren ;
Kepley, Christopher L. .
EXPERIMENTAL DERMATOLOGY, 2009, 18 (12) :1079-1081
[6]   Wound healing: An overview of acute, fibrotic and delayed healing [J].
Diegelmann, RF ;
Evans, MC .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2004, 9 :283-289
[7]   Mast cells modulate the inflammatory but not the proliferative response in healing wounds [J].
Egozi, EI ;
Ferreira, AM ;
Burns, AL ;
Gamelli, RL ;
DiPietro, LA .
WOUND REPAIR AND REGENERATION, 2003, 11 (01) :46-54
[8]   GROWTH AND DIFFERENTIATION CHARACTERISTICS OF TRANSFORMED KERATINOCYTES FROM MOUSE AND HUMAN-SKIN INVITRO AND INVIVO [J].
FUSENIG, NE ;
BREITKREUTZ, D ;
DZARLIEVA, RT ;
BOUKAMP, P ;
BOHNERT, A ;
TILGEN, W .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1983, 81 (01) :S168-S175
[9]   The mast cell stabilizer ketotifen prevents development of excessive skin wound contraction and fibrosis in red Duroc pigs [J].
Gallant-Behm, Corrie L. ;
Hildebrand, Kevin A. ;
Hart, David A. .
WOUND REPAIR AND REGENERATION, 2008, 16 (02) :226-233
[10]   Cutaneous wound healing [J].
Gibran, Nicole S. ;
Boyce, Steven ;
Greenhalgh, David G. .
JOURNAL OF BURN CARE & RESEARCH, 2007, 28 (04) :577-579