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3D-Printed Microarray Patches for Transdermal Applications.
Rajesh, Netra U; Coates, Ian; Driskill, Madison M; Dulay, Maria T; Hsiao, Kaiwen; Ilyin, Dan; Jacobson, Gunilla B; Kwak, Jean Won; Lawrence, Micah; Perry, Jillian; Shea, Cooper O; Tian, Shaomin; DeSimone, Joseph M.
Afiliação
  • Rajesh NU; Department of Bioengineering, Stanford University, Stanford, California94305, United States.
  • Coates I; Department of Chemical Engineering, Stanford University, Stanford, California94305, United States.
  • Driskill MM; Department of Chemical Engineering, Stanford University, Stanford, California94305, United States.
  • Dulay MT; Department of Radiology, Stanford University, Stanford, California94305, United States.
  • Hsiao K; Department of Chemical Engineering, Stanford University, Stanford, California94305, United States.
  • Ilyin D; Department of Mechanical Engineering, Stanford University, Stanford, California94305, United States.
  • Jacobson GB; Department of Radiology, Stanford University, Stanford, California94305, United States.
  • Kwak JW; Department of Radiology, Stanford University, Stanford, California94305, United States.
  • Lawrence M; Department of Bioengineering, Stanford University, Stanford, California94305, United States.
  • Perry J; Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina27599, United States.
  • Shea CO; Department of Mechanical Engineering, Stanford University, Stanford, California94305, United States.
  • Tian S; Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina27599, United States.
  • DeSimone JM; Department of Chemical Engineering, Stanford University, Stanford, California94305, United States.
JACS Au ; 2(11): 2426-2445, 2022 Nov 28.
Article em En | MEDLINE | ID: mdl-36465529
The intradermal (ID) space has been actively explored as a means for drug delivery and diagnostics that is minimally invasive. Microneedles or microneedle patches or microarray patches (MAPs) are comprised of a series of micrometer-sized projections that can painlessly puncture the skin and access the epidermal/dermal layer. MAPs have failed to reach their full potential because many of these platforms rely on dated lithographic manufacturing processes or molding processes that are not easily scalable and hinder innovative designs of MAP geometries that can be achieved. The DeSimone Laboratory has recently developed a high-resolution continuous liquid interface production (CLIP) 3D printing technology. This 3D printer uses light and oxygen to enable a continuous, noncontact polymerization dead zone at the build surface, allowing for rapid production of MAPs with precise and tunable geometries. Using this tool, we are now able to produce new classes of lattice MAPs (L-MAPs) and dynamic MAPs (D-MAPs) that can deliver both solid state and liquid cargos and are also capable of sampling interstitial fluid. Herein, we will explore how additive manufacturing can revolutionize MAP development and open new doors for minimally invasive drug delivery and diagnostic platforms.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: JACS Au Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: JACS Au Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos