4.7 Article

3D-Printed Enzyme-Embedded Plastics

Journal

BIOMACROMOLECULES
Volume 22, Issue 5, Pages 1999-2009

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.biomac.1c00105

Keywords

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Funding

  1. New Zealand Ministry of Business, Innovation and Employment (MBIE) in the framework of the Strategic Science Investment Fund

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A simple and environmentally friendly approach using 3D printing techniques for thermoplastic processing of rapidly degradable plastic-enzyme composites is described. The composites showed different degradation rates depending on the amount of AL loading, with AL capable of withstanding high in situ processing temperatures. Degradation rates of the composites in phosphate buffer were found to be faster compared to externally applied AL.
A simple and environmentally friendly approach toward the thermoplastic processing of rapidly degradable plastic-enzyme composites using three-dimensional (3D) printing techniques is described. Polycaprolactone/Amano lipase (PCL/AL) composite films (10 mm x 10 mm; height [h] = similar to 400 mu m) with an AL loading of 0.1, 1.0, and 5.0% were prepared via 3D printing techniques that entail direct mixing in the solid state and thermal layer-by-layer extrusion. It was found that AL can tolerate in situ processing temperatures up to 130 degrees C in the solid-state for 60 min without loss of enzymatic activity. The composites were degraded in phosphate buffer (8 mg/mL, composite to buffer) for 7 days at 37 degrees C and the resulting average percent total weight loss (WLavg %) was found to be 5.2, 92.9, and 100%, for the 0.1, 1.0, and 5.0% films, respectively. The degradation rates of PCL/AL composites were found to be faster than AL applied externally in the buffer. Thicker PCL/AL 1.0% films (10 mm x 10 mm; h = similar to 500 mu m) were also degraded over a 7 day period to examine how the weight loss occurs over time with 3.0, 18.1, 36.4, 46.4, and 70.2% weight loss for days 1, 2, 3, 4, and 7, respectively. Differential scanning calorimetry (DSC) analysis shows that the film's percent crystallinity (D-xtal%) increases over time with D-xtal% = 46.5 for day 0 and 53.1% for day 7. Scanning electron microscopy (SEM) analysis found that film erosion begins at the surface and that water can penetrate the interior via surface pores activating the enzymes embedded in the film. Controlled release experiments utilizing dye-loaded PCL/AL/dye (AL = 1.0%; dye = 0.1%) composites were degraded over a 7 day period with the bulk of the dye released by the fourth day. The PCL/AL multimaterial objects containing AL-resistant polylactic acid (PLA) were also printed and degraded to demonstrate the application of this material on more complex structures.

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