Influence of MMP inhibitor GM6001 loading of fibre coated polypropylene meshes on wound healing

Autor: H. P. Alizai, Gabriele Böhm, Karl-Heinz Heffels, Ursula Mirastschijski, Reinhild Schnabel, Ulf P. Neumann, Jürgen Groll, Nicole Heussen, Peter Josef Ink
Přispěvatelé: Surgery, RS: FHML non-thematic output
Jazyk: angličtina
Rok vydání: 2018
Předmět:
Male
0301 basic medicine
HUMAN-SKIN
Hernia
Matrix metalloproteinase inhibitor
medicine.medical_treatment
Nanofibers
sP(EO-stat-PO)
GROIN HERNIA
Polypropylene mesh
Matrix metalloproteinase
Matrix (biology)
matrix metalloproteinase inhibitor
GM6001
Rats
Sprague-Dawley

chemistry.chemical_compound
Drug Delivery Systems
0302 clinical medicine
INGUINAL-HERNIA
Coated Materials
Biocompatible

Polylactic Acid-Polyglycolic Acid Copolymer
MYOFIBROBLAST FORMATION
GROWTH-FACTORS
Chemistry
Dipeptides
Hernia repair
Matrix Metalloproteinase 9
030220 oncology & carcinogenesis
Matrix Metalloproteinase 2
medicine.symptom
neovascularization
Myofibroblast
poly(lactic-co-glycolic acid)
nanofibre
Biomedical Engineering
Neovascularization
Physiologic

Inflammation
Matrix Metalloproteinase Inhibitors
Polypropylenes
matrix metalloproteinase-2
Biomaterials
03 medical and health sciences
matrix metalloproteinase-9
medicine
Animals
Herniorrhaphy
electrospinning
Wound Healing
ENVIRONMENT
Abdominal Wall
INFLAMMATORY RESPONSE
Surgical Mesh
MATRIX-METALLOPROTEINASE INHIBITION
COLLAGEN
030104 developmental biology
sense organs
IMPLANTATION
Wound healing
Biomedical engineering
hernia repair
Zdroj: Journal of Biomaterials Applications, 32(10), 1343-1359. SAGE Publications Ltd
ISSN: 0885-3282
DOI: 10.1177/0885328218759043
Popis: Polypropylene meshes are standard for hernia repair. Matrix metalloproteinases play a central role in inflammation. To reduce the inflammatory response and improve remodelling with an associated reduction of hernia recurrence, we modified polypropylene meshes by nanofibre coating and saturation with the broad-spectrum matrix metalloproteinase inhibitor GM6001. The aim was to modulate the inflammatory reaction, increase collagen deposition and improve mesh biointegration. Polypropylene meshes were surface-modified with star-configured NCO-sP(EO -stat-PO) and covered with electrospun nanofibres (polypropylene-nano) and GM6001 (polypropylene-nano-GM). In a hernia model, defects were reconstructed with one of the meshes. Inflammation, neovascularization, bio-integration, proliferation and apoptosis were assessed histologically, collagen content and gelatinases biochemically. Mesh surface modification resulted in higher inflammatory response compared to polypropylene. Pro-inflammatory matrix metalloproteinase-9 paralleled findings while GM6001 reduced matrix metalloproteinase-9 significantly. Significantly increased matrix metalloproteinase-2 beneficial for remodelling was noted with polypropylene-nano-meshes. Increased vascular endothelial growth factor, neo-vascularization and collagen content were measured in polypropylene-nano-meshes compared to polypropylene. GM6001 significantly reduced myofibroblasts. This effect ended after d14 due to engineering limitations with release of maximal GM6001 loading. Nanofibre-coating of polypropylene-meshes confers better tissue vascularization to the cost of increased inflammation. This phenomenon can be only partially compensated by GM6001. Future research will enable higher GM6001 uptake in nano-coated meshes and may alter mesh biointegration in a more pronounced way.
Databáze: OpenAIRE