2.6. In vitro degradation

CX Cancan Xu
YH Yihui Huang
JW Jinglei Wu
LT Liping Tang
YH Yi Hong
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The hydrolytic and reductive degradation of polymer films and scaffolds were measured in PBS and GSH/PBS solutions, respectively. For hydrolysis, the weighed sample (W0) was immersed in 10 mL PBS at 37 °C. For reductive degradation, the weighed sample (W0) was placed in 10 mL GSH/PBS solution (10 mM) at 37°C. For controlled degradation, the samples (W0) were first immersed in PBS at 37°C for 2 wk, and then immersed into 10 mM GSH/PBS solution at 37°C for another 2 wk. At a predetermined time point, the sample was rinsed 3 times with deionized water, dried in a freeze-dryer for 3 d, and then weighed (W1). The mass remaining was calculated as W1/W0 × 100%. Three samples were used for each polymer at each time point. The IVs were measured for the remained polymer films after degradation in GSH solution for 7 d and 14 d using a viscometer as described above. The mechanical properties of the films after GSH treatment (n=3) were measured as described above. The scaffold morphologies after degradation were observed under an SEM.

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