Potential of hydrogel-forming and dissolving microneedles for use in paediatric populations

Ester Caffarel-Salvador1, Tuan-Mazlelaa Tuan-Mahmood1, James C McElnay1

  • 1School of Pharmacy, Queen's University Belfast, 97 Lisburn Road, Belfast BT9 7BL, UK.

Insights

Microneedles (MN) offer a painless alternative for paediatric drug delivery, enhancing skin permeability for caffeine and lidocaine hydrochloride. This innovative approach shows high acceptance among children, the public, and paediatricians.

Area of Science:

  • Pharmaceutical Sciences
  • Biomaterials Engineering
  • Paediatric Medicine

Background:

  • Paediatric drug delivery faces challenges with oral (swallowing, palatability) and parenteral (needle phobia) routes.
  • Microneedles (MN) offer a transdermal alternative by creating painless, transient aqueous conduits in the stratum corneum.
  • Investigating novel MN formulations for improved paediatric drug administration is crucial.

Purpose of the Study:

  • To fabricate and evaluate polymeric dissolving and hydrogel-forming microneedles (MN) for paediatric drug delivery.
  • To assess the in vitro and in vivo efficacy of MN for delivering caffeine and lidocaine hydrochloride.
  • To gauge the acceptance and perception of MN technology among paediatric patients, the public, and healthcare professionals.

Main Methods:

  • Fabrication of polymeric dissolving MN and hydrogel-forming MN loaded with caffeine and lidocaine hydrochloride.
  • In vitro skin permeation studies to quantify drug delivery enhancement.
  • In vivo studies in rats to assess plasma drug concentrations after MN application.
  • Surveys and interviews with schoolchildren, the general public, and paediatricians to assess acceptance and concerns.

Main Results:

  • Polymeric MN significantly enhanced the skin permeability of model drugs in vitro and in vivo.
  • Hydrogel-forming MN increased caffeine delivery by 6.1-fold, and dissolving MN increased lidocaine HCl delivery by 3.3-fold in vitro.
  • In vivo, MN application resulted in a caffeine plasma concentration of 23.87 μg/mL in rats at 24 hours.
  • High acceptance rates were reported: 93.6% of the public and 85.9% of paediatricians viewed MN positively.

Conclusions:

  • Polymeric microneedles are effective in enhancing transdermal drug delivery for paediatric applications.
  • Both dissolving and hydrogel-forming MN show promise for delivering caffeine and lidocaine hydrochloride.
  • Microneedle technology demonstrates strong potential for paediatric use, with significant public and professional endorsement.

Related Concept Videos