Polymeric Microneedles Enhance Transdermal Delivery of Therapeutics

This research presents the efficacy of polymeric microneedles in improving the transdermal permeation of methotrexate across human skin. These microneedles were fabricated from PLGA Expansorb<sup>®</sup> 50-2A and 50-8A and subjected to comprehensive characterization via scanning electro...

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Main Authors: Hiep X. Nguyen (Author), Thomas Kipping (Author), Ajay K. Banga (Author)
Format: Book
Published: MDPI AG, 2024-06-01T00:00:00Z.
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001 doaj_1c9300f9fcd84c67a9d9d02f1e8d5aca
042 |a dc 
100 1 0 |a Hiep X. Nguyen  |e author 
700 1 0 |a Thomas Kipping  |e author 
700 1 0 |a Ajay K. Banga  |e author 
245 0 0 |a Polymeric Microneedles Enhance Transdermal Delivery of Therapeutics 
260 |b MDPI AG,   |c 2024-06-01T00:00:00Z. 
500 |a 10.3390/pharmaceutics16070845 
500 |a 1999-4923 
520 |a This research presents the efficacy of polymeric microneedles in improving the transdermal permeation of methotrexate across human skin. These microneedles were fabricated from PLGA Expansorb<sup>®</sup> 50-2A and 50-8A and subjected to comprehensive characterization via scanning electron microscopy, Fourier-transform infrared spectroscopy, and mechanical analysis. We developed and assessed a methotrexate hydrogel for physicochemical and rheological properties. Dye binding, histological examinations, and assessments of skin integrity demonstrated the effective microporation of the skin by PLGA microneedles. We measured the dimensions of microchannels in the skin using scanning electron microscopy, pore uniformity analysis, and confocal microscopy. The skin permeation and disposition of methotrexate were researched in vitro. PLGA 50-8A microneedles appeared significantly longer, sharper, and more mechanically uniform than PLGA 50-2A needles. PLGA 50-8A needles generated substantially more microchannels, as well as deeper, larger, and more uniform channels in the skin than PLGA 50-2A needles. Microneedle insertion substantially reduced skin electrical resistance, accompanied by an elevation in transepidermal water loss values. PLGA 50-8A microneedle treatment provided a significantly higher cumulative delivery, flux, diffusion coefficient, permeability coefficient, and predicted steady-state plasma concentration; however, there was a shorter lag time than for PLGA 50-2A needles, base-treated, and untreated groups (<i>p</i> < 0.05). Conclusively, skin microporation using polymeric microneedles significantly improved the transdermal delivery of methotrexate. 
546 |a EN 
690 |a fabrication 
690 |a characterization 
690 |a polymeric microneedles 
690 |a microchannels 
690 |a methotrexate 
690 |a transdermal delivery 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceutics, Vol 16, Iss 7, p 845 (2024) 
787 0 |n https://www.mdpi.com/1999-4923/16/7/845 
787 0 |n https://doaj.org/toc/1999-4923 
856 4 1 |u https://doaj.org/article/1c9300f9fcd84c67a9d9d02f1e8d5aca  |z Connect to this object online.