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A New Ex Vivo Model for the Evaluation of Endoscopic Submucosal Injection Material Performance
Published on: October 19, 2018
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Advancements in injection materials for submucosal lifting in endoscopic interventions
Peng-Wei Xu1, Zheng-Han Xiao1, Miao Yu1
1Department of Gastroenterology, The Second Affiliated Hospital of Harbin Medical University, Harbin 150086, Heilongjiang Province, China.
World Journal of Gastrointestinal Surgery
|December 8, 2025
Summary
Submucosal injection cushions are vital for endoscopic resections, but clinical adoption is hindered by challenges in injectability, biocompatibility, and manufacturing. Overcoming these requires coordinated efforts in research, regulation, and policy.
Area of Science:
- Gastroenterology
- Biomaterials Science
- Surgical Innovation
Background:
- Endoscopic submucosal dissection (ESD) and endoscopic mucosal resection (EMR) utilize submucosal injection cushions to create a safe operative field.
- These cushions enhance lesion separation from the muscularis propria, improving resection precision and reducing complications.
Purpose of the Study:
- To comprehensively evaluate current and emerging submucosal injection materials for gastrointestinal endoscopic procedures.
- To assess the mechanical performance, biocompatibility, and intraoperative usability of these materials.
- To identify translational hurdles and propose strategies for wider clinical adoption.
Main Methods:
- Comparative analysis of conventional and novel functionalized submucosal injection agents.
- Evaluation of material properties including mechanical performance, biocompatibility, and injectability.
- Review of manufacturing, supply chain, clinical, and reimbursement factors.
Main Results:
- Despite advancements, limitations in injectability, biocompatibility, multifunctionality, and evidence hinder widespread clinical use.
- Key barriers identified include manufacturing constraints and lack of robust clinical and reimbursement data.
- Emerging materials show promise but require further validation.
Conclusions:
- Bridging the gap between innovative submucosal injection materials and clinical practice necessitates addressing injectability, biocompatibility, and multifunctionality.
- Standardized protocols, regulatory engagement, optimized production, and clinical/economic analyses are crucial.
- Coordinated efforts across research, industry, and policy are essential for successful translation.

