Formulation and Characterization of Electrospun Nanofibers for Melatonin Ocular Delivery.

Pharmaceutics

University Pharmacy Department of Pharmacy Administration, Semmelweis University, Högyes Endre utca 7-9, H-1092 Budapest, Hungary.

Published: April 2023

AI Article Synopsis

  • * Researchers used electrospinning to create poly (vinyl alcohol) (PVA) and poly (lactic acid) (PLA) nanofibers with varying MEL concentrations, combining analysis techniques like scanning electron microscopy for evaluation.
  • * Results showed that PVA nanofibers released MEL quickly, while PLA offered a slower, controlled release; adding Tween 80 altered the swelling properties, indicating these nanofiber membranes could be a better alternative to traditional liquid formulations for eye treatment.

Article Abstract

The poor ocular bioavailability of melatonin (MEL) limits the therapeutic action the molecule could exert in the treatment of ocular diseases. To date, no study has explored the use of nanofiber-based inserts to prolong ocular surface contact time and improve MEL delivery. Here, the electrospinning technique was proposed to prepare poly (vinyl alcohol) (PVA) and poly (lactic acid) (PLA) nanofiber inserts. Both nanofibers were produced with different concentrations of MEL and with or without the addition of Tween 80. Nanofibers morphology was evaluated by scanning electron microscopy. Thermal and spectroscopic analyses were performed to characterize the state of MEL in the scaffolds. MEL release profiles were observed under simulated physiological conditions (pH 7.4, 37 °C). The swelling behavior was evaluated by a gravimetric method. The results confirmed that submicron-sized nanofibrous structures were obtained with MEL in the amorphous state. Different MEL release rates were achieved depending on the nature of the polymer. Fast (20 min) and complete release was observed for the PVA-based samples, unlike the PLA polymer, which provided slow and controlled MEL release. The addition of Tween 80 affected the swelling properties of the fibrous structures. Overall, the results suggest that membranes could be an attractive vehicle as a potential alternative to liquid formulations for ocular administration of MEL.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10143234PMC
http://dx.doi.org/10.3390/pharmaceutics15041296DOI Listing

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