Engineering Gelation Kinetics in Living Silk Hydrogels by Differential Dynamic Microscopy Microrheology and Machine Learning.
Rhett L MartineauAlexandra V BaylesChia-Suei HungKristofer G ReyesMatthew E HelgesonManeesh K GuptaPublished in: Advanced biology (2021)
Microbes embedded in hydrogels comprise one form of living material. Discovering formulations that balance potentially competing for mechanical and biological properties in living hydrogels-for example, gel time of the hydrogel formulation and viability of the embedded organisms-can be challenging. In this study, a pipeline is developed to automate the characterization of the gel time of hydrogel formulations. Using this pipeline, living materials comprised of enzymatically crosslinked silk and embedded E. coli-formulated from within a 4D parameter space-are engineered to gel within a pre-selected timeframe. Gelation time is estimated using a novel adaptation of microrheology analysis using differential dynamic microscopy (DDM). In order to expedite the discovery of gelation regime boundaries, Bayesian machine learning models are deployed with optimal decision-making under uncertainty. The rate of learning is observed to vary between artificial intelligence (AI)-assisted planning and human planning, with the fastest rate occurring during AI-assisted planning following a round of human planning. For a subset of formulations gelling within a targeted timeframe of 5-15 min, fluorophore production within the embedded cells is substantially similar across treatments, evidencing that gel time can be tuned independent of other material properties-at least over a finite range-while maintaining biological activity.
Keyphrases
- artificial intelligence
- hyaluronic acid
- wound healing
- machine learning
- drug delivery
- tissue engineering
- big data
- endothelial cells
- deep learning
- high throughput
- decision making
- induced pluripotent stem cells
- single molecule
- high resolution
- optical coherence tomography
- escherichia coli
- drug release
- high speed
- small molecule
- label free
- cell cycle arrest
- fluorescent probe