Impact insertion of transfer-molded microneedle for localized and minimally invasive ocular drug delivery

J Control Release. 2015 Jul 10:209:272-9. doi: 10.1016/j.jconrel.2015.04.041. Epub 2015 Apr 30.

Abstract

It has been challenging for microneedles to deliver drugs effectively to thin tissues with little background support such as the cornea. Herein, we designed a microneedle pen system, a single microneedle with a spring-loaded microneedle applicator to provide impact insertion. To firmly attach solid microneedles with 140 μm in height at the end of macro-scale applicators, a transfer molding process was employed. The fabricated microneedle pens were then applied to mouse corneas. The microneedle pens successfully delivered rhodamine dye deep enough to reach the stromal layer of the cornea with small entry only about 1000 μm(2). When compared with syringes or 30 G needle tips, microneedle pens could achieve more localized and minimally invasive delivery without any chances of perforation. To investigate the efficacy of microneedle pens as a way of drug delivery, sunitinib malate proven to inhibit in vitro angiogenesis, was delivered to suture-induced angiogenesis model. When compared with delivery by a 30 G needle tip dipped with sunitinib malate, only delivery by microneedle pens could effectively inhibit corneal neovascularization in vivo. Microneedle pens could effectively deliver drugs to thin tissues without impairing merits of using microneedles: localized and minimally invasive delivery.

Keywords: Angiogenesis; Drug delivery; Impact insertion; Microneedle; Mouse cornea; Transfer molding.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Ophthalmic
  • Animals
  • Corneal Neovascularization / drug therapy*
  • Drug Delivery Systems*
  • Human Umbilical Vein Endothelial Cells / drug effects
  • Human Umbilical Vein Endothelial Cells / physiology
  • Indoles / administration & dosage*
  • Indoles / therapeutic use
  • Mice, Inbred C57BL
  • Microinjections
  • Needles*
  • Neovascularization, Physiologic / drug effects
  • Pyrroles / administration & dosage*
  • Pyrroles / therapeutic use
  • Sunitinib
  • Vascular Endothelial Growth Factor A / pharmacology

Substances

  • Indoles
  • Pyrroles
  • Vascular Endothelial Growth Factor A
  • Sunitinib