Epidermal and dermal integration into sphere-templated porous poly(2-hydroxyethyl methacrylate) implants in mice.
Epidermal and dermal integration into sphere-templated porous poly(2-hydroxyethyl methacrylate) implants in mice.
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DOI:
10.1002/jbm.a.32798
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发表时间:
2010-09-15
影响因子:
4.9
通讯作者:
Fleckman, P.
中科院分区:
文献类型:
--
作者:
Fukano, Y.;Usui, M. L.;Underwood, R. A.;Isenhath, S.;Marshall, A. J.;Hauch, K. D.;Ratner, B. D.;Olerud, J. E.;Fleckman, P.
Percutaneous medical devices remain susceptible to infection and failure. We hypothesize that healing of the skin into the percutaneous device will provide a seal preventing bacterial attachment, biofilm formation, and subsequent device failure. Porous poly(2-hydroxyethyl methacrylate) [poly(HEMA)] with sphere-templated pores (40μm) and interconnecting throats (16μm) were implanted in normal C57BL/6 mice for 7, 14 and 28 days. Poly(HEMA) was either untreated, keeping the surface non-adhesive for cells and proteins, or modified with carbonyldiimidazole (CDI) or CDI reacted with laminin 332 to enhance adhesion. No clinical signs of infection were observed. Epidermal and dermal response within the poly(HEMA) pores was evaluated using light and transmission electron microscopy. Cells (keratinocytes, fibroblasts, endothelial cells, inflammatory cells) and basement membrane proteins (laminin 332, β4 integrin, type VII collagen) could be demonstrated within the poly(HEMA) pores of all implants. Blood vessels and dermal collagen bundles were evident in all of the 14 and 28 day implants. Fibrous capsule formation and permigration were not observed. Sphere-templated polymers with 40μm pores demonstrate an ability to recapitulate key elements of both the dermal and the epidermal layers of skin. Our morphological findings indicate that the implant model can be used to study the effects of biomaterial pore size, pore interconnect (throat) size, and surface treatments on cutaneous biointegration. Further, this model may be used for bacterial challenge studies.
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影响因子:
2.9
作者:
Fukano, Yuko;Knowles, Negar G.;Olerud, John E.
通讯作者:
Olerud, John E.
DOI:
10.1002/jbm.1253
发表时间:
2002-02-01
期刊:
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH
影响因子:
--
作者:
Kidd, KR;Nagle, RB;Williams, SK
通讯作者:
Williams, SK
影响因子:
11.8
作者:
Crnich, CJ;Maki, DG
通讯作者:
Maki, DG
DOI:
10.1083/jcb.9.2.409
发表时间:
1961-02
期刊:
The Journal of biophysical and biochemical cytology
影响因子:
--
作者:
LUFT JH
通讯作者:
LUFT JH
影响因子:
2.8
作者:
Chin, Curtis D.;Khanna, Krishn;Sia, Samuel K.
通讯作者:
Sia, Samuel K.