Your browser doesn't support javascript.
loading
3D-Printed Latticed Microneedle Array Patches for Tunable and Versatile Intradermal Delivery.
Rajesh, Netra U; Luna Hwang, Jihyun; Xu, Yue; Saccone, Max A; Hung, Andy H; Hernandez, Rosa A S; Coates, Ian A; Driskill, Madison M; Dulay, Maria T; Jacobson, Gunilla B; Tian, Shaomin; Perry, Jillian L; DeSimone, Joseph M.
Affiliation
  • Rajesh NU; Department of Radiology, Stanford University, Stanford, CA, 94305, USA.
  • Luna Hwang J; Department of Bioengineering, Stanford University, Stanford, CA, 94305, USA.
  • Xu Y; Department of Chemical Engineering, Stanford University, Stanford, CA, 94305, USA.
  • Saccone MA; Department of Radiology, Stanford University, Stanford, CA, 94305, USA.
  • Hung AH; Department of Radiology, Stanford University, Stanford, CA, 94305, USA.
  • Hernandez RAS; Department of Chemical Engineering, Stanford University, Stanford, CA, 94305, USA.
  • Coates IA; Department of Radiology, Stanford University, Stanford, CA, 94305, USA.
  • Driskill MM; Department of Chemical Engineering, Stanford University, Stanford, CA, 94305, USA.
  • Dulay MT; Department of Chemical Engineering, Stanford University, Stanford, CA, 94305, USA.
  • Jacobson GB; Department of Chemical Engineering, Stanford University, Stanford, CA, 94305, USA.
  • Tian S; Department of Radiology, Stanford University, Stanford, CA, 94305, USA.
  • Perry JL; Department of Radiology, Stanford University, Stanford, CA, 94305, USA.
  • DeSimone JM; Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USA.
Adv Mater ; : e2404606, 2024 Sep 02.
Article in En | MEDLINE | ID: mdl-39221508
ABSTRACT
Using high-resolution 3D printing, a novel class of microneedle array patches (MAPs) is introduced, called latticed MAPs (L-MAPs). Unlike most MAPs which are composed of either solid structures or hollow needles, L-MAPs incorporate tapered struts that form hollow cells capable of trapping liquid droplets. The lattice structures can also be coated with traditional viscous coating formulations, enabling both liquid- and solid-state cargo delivery, on a single patch. Here, a library of 43 L-MAP designs is generated and in-silico modeling is used to down-select optimal geometries for further characterization. Compared to traditionally molded and solid-coated MAPs, L-MAPs can load more cargo with fewer needles per patch, enhancing cargo loading and drug delivery capabilities. Further, L-MAP cargo release kinetics into the skin can be tuned based on formulation and needle geometry. In this work, the utility of L-MAPs as a platform is demonstrated for the delivery of small molecules, mRNA lipid nanoparticles, and solid-state ovalbumin protein. In addition, the production of programmable L-MAPs is demonstrated with tunable cargo release profiles, enabled by combining needle geometries on a single patch.
Key words

Full text: 1 Database: MEDLINE Language: En Journal: Adv Mater Journal subject: BIOFISICA / QUIMICA Year: 2024 Type: Article Affiliation country: United States

Full text: 1 Database: MEDLINE Language: En Journal: Adv Mater Journal subject: BIOFISICA / QUIMICA Year: 2024 Type: Article Affiliation country: United States