A novel bioconjugation crosslinker using hydrazine-benzaldehyde chemistry with hydrolytically cleavable acetal/ketal linkages, enabling degradable crosslinked materials in biocompatible environments. Tailored for drug delivery and biomedical applications.
This innovative bioconjugation technology leverages hydrazine-benzaldehyde chemistry to create crosslinkers with hydrolytically cleavable acetal or ketal linkages. These crosslinkers enable the formation of degradable materials under biocompatible conditions, offering significant potential in drug delivery and other biomedical applications. By integrating acetal/ketal functionalities, the technology allows for the precise tuning of degradation rates, making it suitable for applications where controlled release or material degradation is crucial.
The current development stage is at Technology Readiness Level 4, indicating that the technology has been validated in a laboratory environment and is ready for further development and optimization in more practical settings.
Stanford University is a comprehensive private research university known for cross-disciplinary scholarship and an entrepreneurial culture. Industry engages through a long-standing research park that co-locates corporate R&D with university labs, plus corporate affiliates programs and sponsored research mechanisms. Integration with a major academic medical center enables clinical translation, while shared core facilities and prototyping spaces streamline collaboration. Research is supported by competitive federal funding from agencies such as NIH, NSF, DOE, and DARPA, alongside philanthropy and industry partnerships. A dedicated Office of Technology Licensing supports IP strategy, licensing, and startup formation.