نویسندگان | Bahareh Azimi,Claudio Ricci,Teresa Macchi,Cemre Günday,Sara Munafò,Federico Pratesi,Veronika Tempesti,Caterina Cristallini,Luca Bruschini,Andrea Lazzeri,Serena Danti,Nazende Günday-Türeli |
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نشریه | Polymers |
شماره صفحات | 3494-3512 |
شماره سریال | 15 |
شماره مجلد | 17 |
نوع مقاله | Full Paper |
تاریخ انتشار | 2023 |
نوع نشریه | چاپی |
کشور محل چاپ | سوئیس |
نمایه نشریه | ISI،JCR،Scopus |
چکیده مقاله
The delivery of drugs through the skin barrier at a predetermined rate is the aim of transdermal drug delivery systems (TDDSs). However, so far, TDDS has not fully attained its potential as an alternative to hypodermic injections and oral delivery. In this study, we presented a proof of concept of a dual drug-loaded patch made of nanoparticles (NPs) and ultrafine fibers fabricated by using one equipment, i.e., the electrospinning apparatus. Such NP/fiber systems can be useful to release drugs locally through the skin and the tympanic membrane. Briefly, dexamethasone (DEX)-loaded poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBHV) fiber meshes were decorated with rhodamine (RHO)-loaded poly(lactic-co-glycolic acid) (PLGA) NPs, with RHO representing as a second drug model. By properly tuning the working parameters of electrospinning, DEX-loaded PHBHV fibers (i.e., by electrospinning mode) and RHO-loaded PLGA NPs (i.e., by electrospray mode) were successfully prepared and straightforwardly assembled to form a TDDS patch, which was characterized via Fourier transform infrared spectroscopy and dynamometry. The patch was then tested in vitro using human dermal fibroblasts (HDFs). The incorporation of DEX significantly reduced the fiber mesh stiffness. In vitro tests showed that HDFs were viable for 8 days in contact with drug-loaded samples, and significant signs of cytotoxicity were not highlighted. Finally, thanks to a beaded structure of the fibers, a controlled release of DEX from the electrospun patch was obtained over 4 weeks, which may accomplish the therapeutic objective of a local, sustained and prolonged anti-inflammatory action of a TDDS, as is requested in chronic inflammatory conditions, and other pathological conditions, such as in sudden sensorineural hearing loss treatment.
tags: fibers; nanoparticles; poly(hydroxybutyrate-co-hydroxyvalerate) (PHBHV); poly(lactic-glycolic acid) (PLGA); controlled drug release; dexamethasone; rhodamine; human dermal fibroblasts; eardrum; bio-based