4.7 Article

Formulation of acyclovir (core)-dexpanthenol (sheath) nanofibrous patches for the treatment of herpes labialis

Journal

INTERNATIONAL JOURNAL OF PHARMACEUTICS
Volume 611, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.ijpharm.2021.121354

Keywords

Electrospun nanofiber; Coaxial electrospinning; Nanofibrous patches; Treatment of herpes labialis; Morphological-and solid-state characterization; In vitro antiviral study; 131751496); Hydroxypropyl-beta-cyclodextrin (PubChem

Funding

  1. New National Excellence Program of the Ministry for Innovation and Technology [UNKP-20-4-I-SE-27, UNKP-20-3-IISE-35]

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By formulating core-shell type nanofibrous scaffolds loaded with dexpanthenol and acyclovir, this project explored a new direction for treating herpes labialis. The electrospun fibers showed promising results in terms of morphology, physicochemical properties, and antiviral activity, releasing acyclovir and dexpanthenol within 20 minutes and demonstrating better antiviral activity compared to leading commercial creams.
Topically applied antiviral creams and patches are the commercially available options for the treatment of herpes labialis. The nanofibrous patches could be a new direction in the formulation. The project aimed to formulate core-shell type nanofibrous scaffolds loaded with dexpanthenol (shell) and acyclovir (core). To achieve the fast dissolution of the antiviral agent, hydroxypropyl-beta-cyclodextrin was used as a complexation agent. The further aim was to study the prepared electrospun scaffolds' morphological- and physicochemical properties and antiviral activity. The fibrous samples were prepared by electrospinning using polyvinylpyrrolidone (PVP) as a shell, hypromellose (HPMC), and poly(ethylene oxide)(PEO) composite or poly(vinyl alcohol) (PVA) as a core polymer. The morphology of the prepared sample was studied by scanning electron microscopy (SEM), transmission electron microscopy (TEM), and Raman spectroscopy. The SEM photos showed that fibrous structures were obtained. In the case of the PVA/PVP composition, the desired structure was obtained. While when HPMC-PEO was used as a core, the core-shell structure could not be observed. The Raman measurements revealed the mixed fibre structure of this sample. All of the fibrous samples released about 100% of acyclovir and also the dexpanthenol within 20 min. Coaxially electrospun fibres of different compositions were successfully prepared with various structural homogeneities, furthermore, a better antiviral activity could be achieved compared to the commercially available Zovirax cream.

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