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INJECTHEAL – Fertigung

Development of a self-healing injectable hydrogel based on pectin and gelatin for the treatment of deep chronic wounds

INJECTHEAL Logo

INJECTHEAL (Horizon Europe Forschungsprojekt)

Italy (EU CORE Consulting srl · Project Coordination/Contact)New on Amplifa

2025Project start (01.05.2025)
12Consortium partners
8European countries
2025–2028Project duration

About the Project

INJECTHEAL is a research project under Horizon Europe and not a manufacturing company. The consortium of 12 partners from 8 European countries (including Italy, Austria, Germany, Ireland, Spain, Switzerland, and the United Kingdom) is developing a multifunctional, self-healing injectable hydrogel intended to treat deep, cavity-rich chronic wounds and support tissue regeneration. The hydrogel is based on functionalized pectin and gelatin and serves both as an active-ingredient carrier and as a biomimetic matrix. It integrates antibacterial (e.g., octenidine), anti-inflammatory, and pro-angiogenic agents (e.g., Ac2-26 peptide and siRNAs). Poly(ε-Lysine) dendrimers enable the tuning of the degree of crosslinking as well as functional groups for cell adhesion, while immuno-protected polymeric microcapsules enable controlled, targeted drug release. The project includes GLP-compliant preclinical validation, industrial scale-up, regulatory consulting, and the preparation of first clinical trials. EU CORE Consulting srl in Italy is responsible for dissemination, communication, the Data Management Plan, and the Exploitation Plan.

Site
Italy (EU CORE Consulting srl
Processes
Development of a self-healing injectable hydrogel for chronic wounds, Therapeutic release (antibacterial, anti-inflammatory, pro-angiogenic), Preclinical validation, Industrial scale-up, Dissemination and communication, Data Management Plan and Exploitation Plan
Materials
Functionalized pectin and gelatin, Poly(ε-Lysine) dendrimers, Polymeric microcapsules
Certificates
GLP preclinical testing, ISO standards (in-vitro cell tests)
Industries
Medical Technology, Wound Care, Tissue Engineering, Biotechnology
  1. 01

    Synthesis and characterization of Poly(ε-Lysine) dendrimers

  2. 02

    Integration of the dendrimers into pectin/gelatin hydrogels

  3. 03

    Functionalization with antimicrobial, anti-inflammatory and

  4. 04

    Controlled drug release via polymeric microcapsules

  5. 05

    Preclinical in-vitro and ex-vivo validation

  6. 06

    Scale-up, business strategy and exploitation

Materials and Processes

OPec/Gel-CDH

Functionalized pectin and gelatin

Basis of the self-healing hydrogel, which serves as an active-ingredient carrier and biomimetic matrix.

PεK

Poly(ε-Lysine) dendrimers

Control the degree of crosslinking, porosity, and degradation kinetics of the hydrogel and carry bioligands for cell adhesion and angiogenesis.

MC

Polymeric microcapsules

Immuno-protected vesicles protect sensitive active ingredients from enzymatic degradation and enable controlled, targeted release.

Sites

Italy

IT

Project Coordination/Contact (EU CORE Consulting srl)

Components

Treatment of deep chronic wounds
Treatment of deep chronic woundsInjectable hydrogel · Wound care
Poly(ε-Lysine) dendrimer
Poly(ε-Lysine) dendrimerCrosslinking/functionalization · Tissue engineering
Bioligand dendrimer
Bioligand dendrimerCell adhesion/angiogenesis · Tissue engineering
Microcapsule system
Microcapsule systemControlled drug release · Biotechnology

Inside the production

INJECTHEAL project overview
INJECTHEAL project overview
Chronic wound care – topic context
Chronic wound care – topic context
1st Dissemination Event at the University of Brighton
1st Dissemination Event at the University of Brighton

Industries

Medical TechnologyWound CareTissue EngineeringBiotechnology

Additional services

Development of a self-healing injectable hydrogel for chronic woundsTherapeutic release (antibacterial, anti-inflammatory, pro-angiogenic)Preclinical validationIndustrial scale-upDissemination and communicationData Management Plan and Exploitation Plan

Reference customers

University of Brighton (CRMD)Lindsay Leg Club Foundation (partner in the context of the Dissemination Event)

Preclinical Validation

Preclinical safety and efficacy testing is carried out according to GLP with progressive complexity – from ISO-standardized 2D cell tests and antimicrobial assays to 3D skin models, human wound exudates, and in-vivo animal models.

EvidenceConsortium
GLP preclinical testing
ISO standards (in-vitro cell tests)

Project Timeline

  1. 2025

    Project start of work packages WP1–WP6 on 01.05.2025; Horizon Europe consortium of 12 partners from 8 countries.

  2. 2026

    17.06.2026: 1st Dissemination Event at the University of Brighton (CRMD) as part of the TCES Conference; 18.–19.06.2026: 2nd consortium meeting in Brighton.

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