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Low-temperature solvent-based 3D printing of PLGA: a parametric printability study.
Emad Naseri1, Haley Butler1, Wyatt MacNevin1
1Faculty of Sustainable Design Engineering, University of Prince Edward Island, Charlottetown, Canada.
Drug Development and Industrial Pharmacy
|January 15, 2020
Summary
This study introduces a low-temperature 3D printing method for poly-lactic-co-glycolic acid (PLGA) constructs. Optimal parameters ensure high shape fidelity for potential drug-eluting implants.
Area of Science:
- Biomaterials Engineering
- Polymer Science
- Additive Manufacturing
Background:
- Poly-lactic-co-glycolic acid (PLGA) is a widely used biodegradable polymer in biomedical applications.
- Fabrication of complex PLGA structures with high fidelity is crucial for advanced medical devices.
- Existing 3D printing methods may have limitations in processing PLGA at low temperatures.
Purpose of the Study:
- To introduce and characterize a novel low-temperature 3D printing technique for PLGA constructs.
- To investigate the parametric effects on the printability of PLGA using methyl ethyl ketone (MEK) solvent.
- To establish optimal conditions for fabricating high-fidelity PLGA scaffolds for potential drug delivery applications.
Main Methods:
- Parametric study of 3D printing parameters for PLGA/MEK solutions.
- Investigation of PLGA concentration, lactic to glycolic ratio, and molecular weight effects.
- Utilized Proton Nuclear Magnetic Resonance (¹H-NMR) spectroscopy for solvent removal verification.
Main Results:
- High shape fidelity 3D printing of PLGA requires concentrations >80% w/v, lactic:glycolic ratio >75%, molecular weight >100 kDa, and nozzle diameter <0.96 mm.
- A vacuum drying process effectively removed residual MEK solvent.
- ¹H-NMR confirmed complete solvent removal from the fabricated PLGA constructs.
Conclusions:
- A novel low-temperature 3D printing method is established for PLGA fabrication.
- Identified critical parameters for achieving high-fidelity PLGA constructs via 3D printing.
- The developed technique and optimized parameters support the creation of PLGA scaffolds for drug-eluting implants.

