EKF parameters of the diagonal terms of process noise covariance matrix and those of measurement model noise covariance matrix are tuned in the range where the estimator is stable and selected basing on the least IAE score.
The specific surface area, pore size and the interaction between CoFe2O4 nanoparticles and carbon matrix were tuned via pyrolysis temperature.
During the training and testing of LVQ1, the randomly generated weight matrix was tuned for a particular character in the data set.
So the weight matrices can be tuned automatically.
SHG and OCM were further used to show that other ECM physical properties such as porosity and pore size did not change with mTG treatment, thus verifying that matrix stiffness was tuned independently of matrix density.
With this base system, various degradable peptide crosslinks derived from ECM proteins (e.g., GPQG↓IWGQ or IPVS↓LRSG derived from collagen I) can be incorporated within the gels to allow cell-controlled matrix degradation, where the degradation rate of the matrix can be tuned by peptide selection for different applications.
DNA content and GAG deposition of chondrocytes within the matrix can be tuned by incorporation of bioactive signaling molecules such as dexamethasone, chondroitin sulphate, platelet derived growth factor (PDGF-BB) and combination of these three agents.
We show that nanostructures composed of ferrimagnetic NiFe2O4 pillars in a multiferroic BiFeO3 matrix can be tuned magnetically by altering the aspect ratio of the pillars by depositing films of varying thickness.
The porosity of the support matrix can be tuned to change the functional surface area available.
The kinetics of dosing of a compound from a PHA matrix can be tuned by altering the polymer properties, along with the use of different types of PHA with different monomer side chains.
In several recent 3D studies, matrix degradability was used to control cell spreading and morphology in 3D, suggesting that matrix degradation could be tuned to regulate local ECM remodeling events.
