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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.
Abstract:
Development of formulations and drug delivery strategies for paediatric use is challenging, partially due to the age ranges within this population, resulting in varying requirements to achieve optimised patient outcomes. Although the oral route of drug delivery remains the preferred option, there are problematic issues, such as difficulty swallowing and palatability of medicines specific to this population. The parenteral route is not well accepted by children due to needle-related fear and pain. Accordingly, a plethora of alternative routes of drug administration have been investigated. Microneedles (MN) breach the stratum corneum (SC), the outermost layer of skin, increasing the number of drug substances amenable to transdermal delivery. This strategy involves the use of micron-sized needles to painlessly, and without drawing blood, create transient aqueous conduits in the SC. In this study, polymeric dissolving MN and hydrogel-forming MN were fabricated incorporating two model drugs commonly used in paediatric patients (caffeine and lidocaine hydrochloride). The potential efficacy of these MN for paediatric dosing was investigated via in vitro and in vivo studies. Views pertaining to MN technology were sought amongst school children in Northern Ireland, members of the UK general public and UK-based paediatricians, to determine perceived benefits, acceptance, barriers and concerns for adoption of this technology. In this study, polymeric MN were shown to substantially enhance skin permeability of the model therapeutic molecules in vitro and in vivo. In particular, hydrogel-forming MN led to a 6.1-fold increase in caffeine delivery whilst lidocaine HCl delivery was increased by 3.3-fold using dissolving MN in vitro. Application of caffeine-loaded MN led to a caffeine plasma concentration of 23.87 μg/mL in rats at 24 h. This research also highlighted a strong consensus regarding MN technology amongst schoolchildren, paediatricians and the general public, regarding potential use of MN in the paediatric population. Overall, 93.6% of general public respondents and 85.9% of paediatricians regarded the use of MN as a positive approach.
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