Biocompatible 3D Printed MXene Microlattices for Tissue‐Integrated Antibiotic Sensing
Anand P. Tiwari, Sreejith S. Panicker, Julia E. Huddy, Md. Saifur Rahman, Katherine R. Hixon, William J. Scheideler
Abstract
Abstract 3D continuous mesoscale architectures of nanomaterials possess the potential to revolutionize real‐time electrochemical biosensing through higher active site density and improved accessibility for cell proliferation. Herein, 3D microporous Ti 3 C 2 T X MXene biosensors are fabricated to monitor antibiotic release in tissue engineering scaffolds. The Ti 3 C 2 T X ‐coated 3D electrodes are prepared by conformal MXene deposition on 3D‐printed polymer microlattices. The Ti 3 C 2 T X MXene coating facilitates direct electron transfer, leading to the efficient detection of common antibiotics such as gentamicin and vancomycin. The 3D microporous architecture exposes greater electrochemically active MXene surface area, resulting in remarkable sensitivity for detecting gentamicin (10–1 m M ) and vancomycin (100–1 m M ), 1000 times more sensitive than control electrodes composed of 2D planar films of Ti 3 C 2 T X MXene. To characterize the suitability of 3D microporous Ti 3 C 2 T X MXene sensors for monitoring drug elution in bone tissue regeneration applications, osteoblast‐like (MG‐63) cells are seeded on the 3D MXene microlattices for 3, 5, and 7 days. Cell proliferation on the 3D microporous MXene is tracked over 7 days, demonstrating its promising biocompatibility and its clinical translation potential. Thus, 3D microporous Ti 3 C 2 T X MXene can provide a platform for mediator‐free biosensing, enabling new applications for in vivo monitoring of drug elution.