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Physical and chemical processing for a human dura mater substitute

Object: Allogenic human fascia lata used in neurosurgery, as dura mater substitute, can be associated with a risk of viral and bacterial transmission. Chemical and physical procedures, developed to inactivate virus and bacteria, have been applied to fascia lata. The aim of this study consists in the...

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Published in:Biomaterials 2002-07, Vol.23 (14), p.2979-2988
Main Authors: Dufrane, D, Cornu, O, Delloye, C, Schneider, Y.J
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Language:English
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cited_by cdi_FETCH-LOGICAL-c392t-8d0c4279cb220b6270a33d6e104663ca1ecc17b1b0964dfb92b4b4b4175dfc693
cites cdi_FETCH-LOGICAL-c392t-8d0c4279cb220b6270a33d6e104663ca1ecc17b1b0964dfb92b4b4b4175dfc693
container_end_page 2988
container_issue 14
container_start_page 2979
container_title Biomaterials
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creator Dufrane, D
Cornu, O
Delloye, C
Schneider, Y.J
description Object: Allogenic human fascia lata used in neurosurgery, as dura mater substitute, can be associated with a risk of viral and bacterial transmission. Chemical and physical procedures, developed to inactivate virus and bacteria, have been applied to fascia lata. The aim of this study consists in the evaluation of the biological properties of this treated graft. Methods: Grafts were treated with solvent detergents, freeze-dried for conservation and gamma irradiated (25,000 Gy) for sterilization. The indirect toxicity evaluation was performed by extraction method, according to the International Standard Organization (ISO). First, the cytotoxic effect of each extracts incubated in the presence of human fibroblasts (WI38) was quantitatively assessed by measuring the cell growth, the viability (succinate dehydrogenase activity, MTT), the membrane integrity (uptake of the neutral red by viable cells, NR) as well as the release of lactate dehydrogenase in the culture medium. Second, confocal laser scanning microscopy (CLSM) was used to assess the direct contact between human primary fibroblasts and graft. CLSM was performed at days 3 and 7 after cells loading. Results: No acute cytotoxicity was observed for chemically processed allografts. Cells loaded on the graft have demonstrated a good growth and spreading. Conclusions: Human fascia lata secured against conventional and non-conventional agents is a fully biocompatible alternative to the available dural graft materials.
doi_str_mv 10.1016/S0142-9612(02)00027-3
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Chemical and physical procedures, developed to inactivate virus and bacteria, have been applied to fascia lata. The aim of this study consists in the evaluation of the biological properties of this treated graft. Methods: Grafts were treated with solvent detergents, freeze-dried for conservation and gamma irradiated (25,000 Gy) for sterilization. The indirect toxicity evaluation was performed by extraction method, according to the International Standard Organization (ISO). First, the cytotoxic effect of each extracts incubated in the presence of human fibroblasts (WI38) was quantitatively assessed by measuring the cell growth, the viability (succinate dehydrogenase activity, MTT), the membrane integrity (uptake of the neutral red by viable cells, NR) as well as the release of lactate dehydrogenase in the culture medium. Second, confocal laser scanning microscopy (CLSM) was used to assess the direct contact between human primary fibroblasts and graft. CLSM was performed at days 3 and 7 after cells loading. Results: No acute cytotoxicity was observed for chemically processed allografts. Cells loaded on the graft have demonstrated a good growth and spreading. 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Chemical and physical procedures, developed to inactivate virus and bacteria, have been applied to fascia lata. The aim of this study consists in the evaluation of the biological properties of this treated graft. Methods: Grafts were treated with solvent detergents, freeze-dried for conservation and gamma irradiated (25,000 Gy) for sterilization. The indirect toxicity evaluation was performed by extraction method, according to the International Standard Organization (ISO). First, the cytotoxic effect of each extracts incubated in the presence of human fibroblasts (WI38) was quantitatively assessed by measuring the cell growth, the viability (succinate dehydrogenase activity, MTT), the membrane integrity (uptake of the neutral red by viable cells, NR) as well as the release of lactate dehydrogenase in the culture medium. Second, confocal laser scanning microscopy (CLSM) was used to assess the direct contact between human primary fibroblasts and graft. 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source ScienceDirect Journals
subjects Biocompatible Materials - chemistry
Biocompatible Materials - metabolism
Cell Culture Techniques - methods
Cell Size
Cells, Cultured
Dura Mater
Dural substitute
Evaluation Studies as Topic
Fascia lata
Fascia Lata - chemistry
Fascia Lata - metabolism
Fascia Lata - transplantation
Fibroblasts - cytology
Fibroblasts - metabolism
Fluoresceins - metabolism
Fluorescent Dyes - metabolism
Human allograft
Humans
Processing
Sterilization - methods
Transplantation, Homologous
Transplants
title Physical and chemical processing for a human dura mater substitute
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