Surface modification of silicone breast implants by binding the antifibrotic drug halofuginone reduces capsular fibrosis
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Surface modification of silicone breast implants by binding the antifibrotic drug halofuginone reduces capsular fibrosis. / Zeplin, Philip H; Larena-Avellaneda, Axel; Schmidt, Karsten.
In: PLAST RECONSTR SURG, Vol. 126, No. 1, 07.2010, p. 266-274.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
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TY - JOUR
T1 - Surface modification of silicone breast implants by binding the antifibrotic drug halofuginone reduces capsular fibrosis
AU - Zeplin, Philip H
AU - Larena-Avellaneda, Axel
AU - Schmidt, Karsten
PY - 2010/7
Y1 - 2010/7
N2 - BACKGROUND: Capsular fibrosis is one of the most severe complications that can occur in connection with silicone breast implants. Should this case arise, a periprosthetic deposition of fibroid tissue may evolve. Transforming growth factor (TGF)-beta is one of the most important mediators in relation to such processes.METHODS: The chinazolinone derivative halofuginone is a type I collagen synthesis inhibitor that interferes with the TGF-beta signaling pathway. The work at hand examines the local antifibrotic effectiveness of halofuginone lactate, which has been biotechnologically bound to the silicone implant's surface. The experiments in relation to this were conducted in vivo on two groups of seven Sprague-Dawley rats. Group I received untreated silicone implants, and group II received halofuginone-coated silicone implants.RESULTS: Submusculary embedded halofuginone-coated silicone implants have shown no systemic side effects. The histologic and immunohistologic examinations of the periprostatic capsules revealed a significant decrease of CD68 histiocytes, TGF-beta, fibroblasts, collagen type I and type III, and capsular thickness after a 3-month period.CONCLUSION: The results confirmed a decrease in foreign body responses to halofuginone surface-modified silicone implants and mark their potential for obtaining a lessened capsular fibrosis by way of a local antifibrotic effect.
AB - BACKGROUND: Capsular fibrosis is one of the most severe complications that can occur in connection with silicone breast implants. Should this case arise, a periprosthetic deposition of fibroid tissue may evolve. Transforming growth factor (TGF)-beta is one of the most important mediators in relation to such processes.METHODS: The chinazolinone derivative halofuginone is a type I collagen synthesis inhibitor that interferes with the TGF-beta signaling pathway. The work at hand examines the local antifibrotic effectiveness of halofuginone lactate, which has been biotechnologically bound to the silicone implant's surface. The experiments in relation to this were conducted in vivo on two groups of seven Sprague-Dawley rats. Group I received untreated silicone implants, and group II received halofuginone-coated silicone implants.RESULTS: Submusculary embedded halofuginone-coated silicone implants have shown no systemic side effects. The histologic and immunohistologic examinations of the periprostatic capsules revealed a significant decrease of CD68 histiocytes, TGF-beta, fibroblasts, collagen type I and type III, and capsular thickness after a 3-month period.CONCLUSION: The results confirmed a decrease in foreign body responses to halofuginone surface-modified silicone implants and mark their potential for obtaining a lessened capsular fibrosis by way of a local antifibrotic effect.
KW - Animals
KW - Breast Implants
KW - Coated Materials, Biocompatible
KW - Collagen Type I/antagonists & inhibitors
KW - Disease Models, Animal
KW - Female
KW - Fibrosis/pathology
KW - Foreign-Body Reaction/pathology
KW - Mammary Glands, Animal/metabolism
KW - Piperidines/administration & dosage
KW - Protein Synthesis Inhibitors/administration & dosage
KW - Quinazolinones/administration & dosage
KW - Rats
KW - Rats, Sprague-Dawley
KW - Silicon
KW - Treatment Outcome
U2 - 10.1097/PRS.0b013e3181dbc313
DO - 10.1097/PRS.0b013e3181dbc313
M3 - SCORING: Journal article
C2 - 20595874
VL - 126
SP - 266
EP - 274
JO - PLAST RECONSTR SURG
JF - PLAST RECONSTR SURG
SN - 0032-1052
IS - 1
ER -