Thermostatically Controlled Orbital Shaker Incubator (37.0 °C)
Maintains physiological temperature and gentle agitation (50 RPM) simulating in-vivo fluid flow.
Quantify the hydrolytic degradation rate constant k_d and mass loss kinetics of a poly(lactic-co-glycolic acid) / PEG hydrogel tissue engineering scaffold in PBS at 37.0 °C. Explore interactive physiological instrumentation simulation, biomechanics, and biomedical engineering telemetry.
Ready to sample with Time t = 6.0 days.
Adjust Time t, then execute biomedical trial.
Biomedical engineering telemetry and physiological states are evaluated rigorously using 64-bit IEEE 754 precision. Residuals reflect ordinary least-squares regression across successive observations. Continuous data structures support high-fidelity biological and physiological modeling.
The linear zero-order degradation model applies to the initial mass loss phase (first 14 days); late-stage fragmentation exhibits non-linear mass loss. Evaluated on cylindrical 3D porous PLGA-PEG composite hydrogel scaffolds (porosity 85%, diameter 8.0 mm, height 4.0 mm, initial dry mass 50.0 mg) incubated in 10 mL PBS (pH 7.4) at 37 °C under gentle shaking. Linear hydrolytic degradation rate k_d = 3.2000 %/day across days 2 to 12.
Maintains physiological temperature and gentle agitation (50 RPM) simulating in-vivo fluid flow.
Determines scaffold dry mass before and after degradation incubation intervals.
Sublimates all absorbed water to measure true residual polymer dry mass without collapsing pores.
Monitors acidic lactic and glycolic acid by-product accumulation in the PBS incubation medium.
Rinses soluble buffer salts from degraded scaffolds prior to freeze drying.
Prevents ambient moisture reabsorption during post-lyophilization mass determination.
Quantify the hydrolytic degradation rate constant k_d and mass loss kinetics of a poly(lactic-co-glycolic acid) / PEG hydrogel tissue engineering scaffold in PBS at 37.0 °C. Standardized parameter settings: 2.0, 4.0, 6.0, 8.0, 10.0, 12.0 days.
Fabricate porous PLGA-PEG scaffolds via solvent casting/particulate leaching, lyophilize for 24 hours, and record initial dry mass W_0 (~50.00 mg) on analytical balance.
Prepare 10 mL sterile phosphate buffered saline (PBS, pH 7.40) aliquots in sealed centrifuge tubes and pre-warm to 37.0 °C in orbital incubator.
Submerge individual scaffolds into PBS tubes and incubate at 37.0 °C with continuous orbital shaking at 50 RPM.
At incubation intervals of 2, 4, 6, 8, 10, and 12 days, harvest duplicate scaffold specimens and record media pH to detect acidic buildup.
Gently rinse harvested scaffolds three times in deionized water to remove crystallized buffer salts, freeze at -80 °C, and lyophilize for 48 hours to complete dryness.
Weigh residual dry mass W_t, calculate residual percentage M_res = (W_t / W_0) · 100%, plot M_res versus time t, and evaluate degradation rate k_d.
Points are your recorded observations. The solid regression line validates Hydrogel Scaffold Degradation mathematical scaling.
| # | Incubation Time t (days) | Residual Dry Mass Percentage M_res (%) | Incubation time t (days) | Residual dry mass M_res (%) | Remove |
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