Tissue augmentation with fibrin sealant and cultured fibroblasts: a preliminary study

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Tissue augmentation with fibrin sealant and cultured fibroblasts : a preliminary study. / Hoben, Gwendolyn; Schmidt, Volker J; Bannasch, Holger; Horch, Raymund E.

I: Aesthetic Plastic Surgery, Bind 35, Nr. 6, 12.2011, s. 1009-15.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Hoben, G, Schmidt, VJ, Bannasch, H & Horch, RE 2011, 'Tissue augmentation with fibrin sealant and cultured fibroblasts: a preliminary study', Aesthetic Plastic Surgery, bind 35, nr. 6, s. 1009-15. https://doi.org/10.1007/s00266-011-9724-x

APA

Hoben, G., Schmidt, V. J., Bannasch, H., & Horch, R. E. (2011). Tissue augmentation with fibrin sealant and cultured fibroblasts: a preliminary study. Aesthetic Plastic Surgery, 35(6), 1009-15. https://doi.org/10.1007/s00266-011-9724-x

Vancouver

Hoben G, Schmidt VJ, Bannasch H, Horch RE. Tissue augmentation with fibrin sealant and cultured fibroblasts: a preliminary study. Aesthetic Plastic Surgery. 2011 dec.;35(6):1009-15. https://doi.org/10.1007/s00266-011-9724-x

Author

Hoben, Gwendolyn ; Schmidt, Volker J ; Bannasch, Holger ; Horch, Raymund E. / Tissue augmentation with fibrin sealant and cultured fibroblasts : a preliminary study. I: Aesthetic Plastic Surgery. 2011 ; Bind 35, Nr. 6. s. 1009-15.

Bibtex

@article{f9ce0fd847644c0eb916e739a72228f9,
title = "Tissue augmentation with fibrin sealant and cultured fibroblasts: a preliminary study",
abstract = "BACKGROUND: Nonoperative subdermal tissue augmentation is one of the most frequently performed procedures in plastic surgery and dermatological practice. Many products, from biological to synthetic filler substances, are currently available. However, none has achieved ideal clinical efficacy, especially regarding volume maintenance and longevity. We examined the use of fibrin sealant as a biological and fully degradable matrix for dermal augmentation in combination with precultured human fibroblasts and hyaluronic acid gel (HYAFF).METHODS: Four implant preparations were studied: fibrin glue only (F); 1% HYAFF mixed in fibrin glue (FH); 1.8 × 10(6) cells/ml of fibrin glue (FC); and 1% HYAFF and 1.8 × 10(6) cells/ml of fibrin glue (FHC). Each mouse was given two separate subcutaneous injections of implant material. At 1, 3, and 6 weeks two mice from each group were sacrificed, such that there was an n = 4 for each implant group at each time point. The mice were grossly examined for implant retention and the implants were evaluated by means of immunohistochemistry for fibrosis, integration into surrounding tissue, presence of elastin, and blood vessel infiltration.RESULTS: Only the implants in the cell-containing groups, FC and FHC, remained after 6 weeks. Moreover, with the exception of a mild inflammatory response, no adverse affects of the cell-seeded implants were noted.CONCLUSION: Presence of fibroblasts increases implant durability. Further studies should evaluate the ideal hyaluronic acid and fibroblast concentration for long-term longevity.",
keywords = "Animals, Cells, Cultured, Cosmetic Techniques, Fibrin Tissue Adhesive, Fibroblasts, Humans, Mice, Mice, Nude, Tissue Adhesives",
author = "Gwendolyn Hoben and Schmidt, {Volker J} and Holger Bannasch and Horch, {Raymund E}",
year = "2011",
month = dec,
doi = "10.1007/s00266-011-9724-x",
language = "English",
volume = "35",
pages = "1009--15",
journal = "Aesthetic Plastic Surgery",
issn = "0364-216X",
publisher = "Springer",
number = "6",

}

RIS

TY - JOUR

T1 - Tissue augmentation with fibrin sealant and cultured fibroblasts

T2 - a preliminary study

AU - Hoben, Gwendolyn

AU - Schmidt, Volker J

AU - Bannasch, Holger

AU - Horch, Raymund E

PY - 2011/12

Y1 - 2011/12

N2 - BACKGROUND: Nonoperative subdermal tissue augmentation is one of the most frequently performed procedures in plastic surgery and dermatological practice. Many products, from biological to synthetic filler substances, are currently available. However, none has achieved ideal clinical efficacy, especially regarding volume maintenance and longevity. We examined the use of fibrin sealant as a biological and fully degradable matrix for dermal augmentation in combination with precultured human fibroblasts and hyaluronic acid gel (HYAFF).METHODS: Four implant preparations were studied: fibrin glue only (F); 1% HYAFF mixed in fibrin glue (FH); 1.8 × 10(6) cells/ml of fibrin glue (FC); and 1% HYAFF and 1.8 × 10(6) cells/ml of fibrin glue (FHC). Each mouse was given two separate subcutaneous injections of implant material. At 1, 3, and 6 weeks two mice from each group were sacrificed, such that there was an n = 4 for each implant group at each time point. The mice were grossly examined for implant retention and the implants were evaluated by means of immunohistochemistry for fibrosis, integration into surrounding tissue, presence of elastin, and blood vessel infiltration.RESULTS: Only the implants in the cell-containing groups, FC and FHC, remained after 6 weeks. Moreover, with the exception of a mild inflammatory response, no adverse affects of the cell-seeded implants were noted.CONCLUSION: Presence of fibroblasts increases implant durability. Further studies should evaluate the ideal hyaluronic acid and fibroblast concentration for long-term longevity.

AB - BACKGROUND: Nonoperative subdermal tissue augmentation is one of the most frequently performed procedures in plastic surgery and dermatological practice. Many products, from biological to synthetic filler substances, are currently available. However, none has achieved ideal clinical efficacy, especially regarding volume maintenance and longevity. We examined the use of fibrin sealant as a biological and fully degradable matrix for dermal augmentation in combination with precultured human fibroblasts and hyaluronic acid gel (HYAFF).METHODS: Four implant preparations were studied: fibrin glue only (F); 1% HYAFF mixed in fibrin glue (FH); 1.8 × 10(6) cells/ml of fibrin glue (FC); and 1% HYAFF and 1.8 × 10(6) cells/ml of fibrin glue (FHC). Each mouse was given two separate subcutaneous injections of implant material. At 1, 3, and 6 weeks two mice from each group were sacrificed, such that there was an n = 4 for each implant group at each time point. The mice were grossly examined for implant retention and the implants were evaluated by means of immunohistochemistry for fibrosis, integration into surrounding tissue, presence of elastin, and blood vessel infiltration.RESULTS: Only the implants in the cell-containing groups, FC and FHC, remained after 6 weeks. Moreover, with the exception of a mild inflammatory response, no adverse affects of the cell-seeded implants were noted.CONCLUSION: Presence of fibroblasts increases implant durability. Further studies should evaluate the ideal hyaluronic acid and fibroblast concentration for long-term longevity.

KW - Animals

KW - Cells, Cultured

KW - Cosmetic Techniques

KW - Fibrin Tissue Adhesive

KW - Fibroblasts

KW - Humans

KW - Mice

KW - Mice, Nude

KW - Tissue Adhesives

U2 - 10.1007/s00266-011-9724-x

DO - 10.1007/s00266-011-9724-x

M3 - Journal article

C2 - 21512867

VL - 35

SP - 1009

EP - 1015

JO - Aesthetic Plastic Surgery

JF - Aesthetic Plastic Surgery

SN - 0364-216X

IS - 6

ER -

ID: 329569368