Coiled-Coil Protein Hydrogels Engineered with Minimized Fiber Diameters for Sustained Release of Doxorubicin in Triple-Negative Breast Cancer.
Dustin BrittonJakub LegockiDeven PaulOlga KatsaraOrlando AristizabalNeelam PandyaOrin MishkitYingxin XiaoMatias AristizabalNeha RahmanRobert SchneiderYoussef Zaim WadghiriJin Kim MontclarePublished in: ACS biomaterials science & engineering (2024)
Triple-negative breast cancer (TNBC) lacks expressed protein targets, making therapy development challenging. Hydrogels offer a promising new route in this regard by improving the chemotherapeutic efficacy through increased solubility and sustained release. Moreover, subcutaneous hydrogel administration reduces patient burden by requiring less therapy and shorter treatment times. We recently established the design principles for the supramolecular assembly of single-domain coiled-coils into hydrogels. Using a modified computational design algorithm, we designed Q8, a hydrogel with rapid assembly for faster therapeutic hydrogel preparation. Q8 encapsulates and releases doxorubicin (Dox), enabling localized sustained release via subcutaneous injection. Remarkably, a single subcutaneous injection of Dox-laden Q8 (Q8•Dox) significantly suppresses tumors within just 1 week. This work showcases the bottom-up engineering of a fully protein-based drug delivery vehicle for improved TBNC treatment via noninvasive localized therapy.
Keyphrases
- drug delivery
- cancer therapy
- hyaluronic acid
- drug release
- tissue engineering
- wound healing
- protein protein
- amino acid
- machine learning
- binding protein
- randomized controlled trial
- ultrasound guided
- stem cells
- extracellular matrix
- high resolution
- case report
- small molecule
- risk factors
- clinical trial
- combination therapy
- chemotherapy induced