Abstract

Patients with psoriasis are dissatisfied with the standard pharmacological treatments, whether systemic or topical, with many of them showing interest in complementary and alternative medicine. Curcumin (Cur), a natural polyphenol derived from turmeric, has recently gained attention for skin-related diseases because of its proven anti-inflammatory action. However, topical treatment with Cur would be inadequate because of its hydrophobicity, instability, and low bioavailability. In addition, hyperkeratosis and lack of moisture in psoriatic skin result in low penetration that would prevent actives from permeating the stratum corneum. In this work, a polymer-based formulation of Cur for the topical treatment of psoriasis is reported. To improve the physicochemical stability of Cur, it was first encapsulated in chitosan nanoparticles. The Cur-loaded nanoparticles were incorporated in a hydrophilic, biocompatible collagen-based patch. The nanoparticle-containing porous collagen patches were then chemically cross-linked. Morphology, chemical interactions, swelling ratio, enzymatic hydrolysis, and Cur release from the patches were evaluated. All patches showed excellent swelling ratio, up to ~1500%, and after cross-linking, the pore size decreased, and their hydrolysis rates decelerated. The in vitro release of Cur was sustained with an initial burst release, reaching 55% after 24 h. Cur within the scaffolds imparted a proliferation inhibitory effect on psoriatic human keratinocytes in vitro.

Highlights

  • Topical and transdermal drug delivery systems are gaining growing attention in the field of pharmaceutical technology

  • Chitosan (CS) with high molecular weight (MW: 350,000 g/mol, deacetylation degree > 75%, and viscosity of 1 wt% solution in 1% acetic acid 800–2000 cps at 25 ◦ C), triphenyl phosphate (TPP) used as ionic cross-linking agent, poly(vinyl pyrrolidone) (PVP), and collagen type I from bovine Achilles tendon were supplied by Sigma-Aldrich, St

  • Cur release from the patches was performed as described for the Chitosan nanoparticles (CS-NPs) in Section 2.5.1, but using paddles instead of baskets, according to the UPS29 method with Apparatus 2 [59,60]. This method is recommended for simulating transdermal release in vitro

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Summary

Introduction

Topical and transdermal drug delivery systems are gaining growing attention in the field of pharmaceutical technology. The materials used to prepare drug delivery patches are predominately polymers, either natural or synthetic, and are considered to be the backbone of topical delivery systems [2]. Natural polymers and their hydrogels are used to fabricate patches because of their desirable characteristics, like hydrophilicity, biocompatibility, swelling ability, and controlled degradation rate that in turn controls the drug release rate. Their hydrophilicity helps with permeation by hydrating the skin [3]. Chitosan nanoparticles (CS-NPs) stand out in Polymers 2020, 12, 2393; doi:10.3390/polym12102393 www.mdpi.com/journal/polymers

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