4.8 Article

Bespoke 3D-Printed Polydrug Implants Created via Microstructural Control of Oligomers

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 33, Pages 38969-38978

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c07850

Keywords

3D printing; drug release; implants; phase separation; inks

Funding

  1. Engineering and Physical Sciences Research Council [EP/N024818/1, EP/P031684/1, EP/N006615/1, EP/P029868/1]
  2. UK Research and Innovation
  3. EPSRC [EP/N006615/1, EP/P031684/1, EP/N024818/1, EP/P029868/1] Funding Source: UKRI

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This study demonstrates the use of phase separation to control drug release, achieving predictable microstructures through inkjet 3D printing. By manipulating drug location and microstructure, the release of drugs can be tailored for specific therapeutic needs, providing a new understanding of emergent material properties in 3D printing.
Controlling the microstructure of materials by means of phase separation is a versatile tool for optimizing material properties. Phase separation has been exploited to fabricate intricate microstructures in many fields including cell biology, tissue engineering, optics, and electronics. The aim of this study was to use phase separation to tailor the spatial location of drugs and thereby generate release profiles of drug payload over periods ranging from 1 week to months by exploiting different mechanisms: polymer degradation, polymer diluent dissolution, and control of microstructure. To achieve this, we used drop-on-demand inkjet three-dimensional (3D) printing. We predicted the microstructure resulting from phase separation using high-throughput screening combined with a model based on the Flory-Huggins interaction parameter and were able to show that drug release from 3D-printed objects can be predicted from observations based on single drops of mixtures. We demonstrated for the first time that inkjet 3D printing yields controllable phase separation using picoliter droplets of blended photoreactive oligomers/monomers. This new understanding gives us hierarchical compositional control, from droplet to device, allowing release to be dialled up without manipulation of device geometry. We exemplify this approach by fabricating a biodegradable, long-term, multiactive drug delivery subdermal implant (polyimplant) for combination therapy and personalized treatment of coronary heart disease. This is an important advance for implants that need to be delivered by cannula, where the shape is highly constrained and thus the usual geometrical freedoms associated with 3D printing cannot be easily exploited, which brings a hitherto unseen level of understanding to emergent material properties of 3D printing.

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