PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
February 14, 2026Advanced Materials Technologies0 citationsOpen Access

Embedding Perfusable Microchannel Networks in Photoclickable Bioresins via High‐Resolution Digital Light Processing

View Full Paper
RRRiccardo RizzoTSThibault SamponJWJackson K. Wilt

Key Points

  • The aim is to develop a cytocompatible photoresin for bioprinting functional microvascular structures.
  • Developed a photoresin based on fish gelatin and photoclick chemistry.
  • Utilized high-resolution digital light processing for 3D bioprinting.
  • Incorporated a radical scavenger to minimize blurring during printing.
  • Used a surfactant to reduce printing failures.
  • Achieved printing of microvascular channels less than 100 µm in diameter.
  • Successfully printed for over 5 hours without significant issues.
  • Demonstrated enhanced viability of printed structures due to cytocompatibility.

Abstract

ABSTRACT Light‐mediated 3D bioprinting methods hold great promise for the generation of biomimetic microvasculature networks for applications ranging from organ‐on‐chip models to vascularized tissue constructs. While printing microvascular channels (≤100 µm in diameter) within large hydrogel volumes (≥1 cm 3 ) is theoretically feasible, progress remains limited by the lack of suitable cytocompatible photoresins. Here, we report the development of an optimized photoresin based on fish gelatin and photoclick crosslinking chemistry for bioprinting perfusable, embedded microvascular networks via high‐resolution digital light processing (DLP). Specifically, our hydrogel matrix leverages the fast kinetics and negligible dark curing of thiol‐norbornene crosslinking as well as the low viscosity and thermal stability of fish gelatin. Using pulsed illumination and a biocompatible radical scavenger (DMPO), we further minimize radical diffusion‐induced blurring, enabling extended printing (>5 h). Finally, printing failures are reduced through the incorporation of a cytocompatible surfactant (Poloxamer‐188). Together, these advances open new avenues for printing perfusable biomimetic microvascular networks embedded in hydrogel matrices.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Rizzo et al. (2026) studied this question.

synapsesocial.com/papers/699011172ccff479cfe57879https://doi.org/10.1002/admt.202502466
Ask AI
Helpful
Bookmark
Share
View Full Paper

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Embedding Biomimetic Vascular Networks via Coaxial Sacrificial Writing into Functional Tissue2024 · 89 citations
  2. 2Imaging free radicals in organelles, cells, tissue, and in vivo with immuno-spin trapping2016 · 89 citations
  3. 3Microfluidics‐Enabled Multimaterial Maskless Stereolithographic Bioprinting2018 · 430 citations
  4. 4Creating perfused functional vascular channels using 3D bio-printing technology2014 · 498 citations
  5. 5Pendent_Drop: An ImageJ Plugin to Measure the Surface Tension from an Image of a Pendent Drop2016 · 198 citations