PCL/Mesoglycan Devices Obtained by Supercritical Foaming and Impregnation.

Pharmaceutics

Department of Industrial Engineering, University of Salerno, Via Giovanni Paolo II, 132, 84084 Fisciano (SA), Italy.

Published: November 2019

AI Article Synopsis

  • A new one-shot process was developed to foam polycaprolactone (PCL) while simultaneously impregnating mesoglycan (MSG) using supercritical carbon dioxide, aiming to create an innovative topical device for skin lesion treatment.
  • The optimized conditions for this process included a pressure of 17 MPa, a temperature of 35 °C, and a 24-hour impregnation time, resulting in effective PCL foaming and MSG incorporation, with a demonstrated prolonged release of MSG.
  • Functional assays showed that the PCL-MSG composite actively promotes the activation of key skin cells involved in tissue regeneration, confirming its potential benefits for wound healing.

Article Abstract

In this work, a one-shot process for the simultaneous foaming of polycaprolactone (PCL) and impregnation of mesoglycan (MSG) into the porous structure was successfully attempted. Supercritical carbon dioxide plays the role of the foaming agent with respect to PCL and of the solvent with respect to MSG. The main objective is to produce an innovative topical device for application on skin lesions, promoting prolonged pro-resolving effects. The obtained device offers a protective barrier to ensure a favorable and sterilized environment for the wound healing process. The impregnation kinetics revealed that a pressure of 17 MPa, a temperature of 35 °C, and a time of impregnation of 24 h assured a proper foaming of PCL in addition to the impregnation of the maximum amount of MSG; i.e., 0.22 mg/mg. After a preliminary study conducted on PCL granules used as brought, the MSG impregnation was performed at the optimized process conditions also on a PCL film, produced by compression molding, with the final goal of producing medical patches. Comparing the dissolution profiles in phosphate buffered saline solution (PBS) of pure MSG and MSG impregnated on foamed PCL, it was demonstrated that the release of MSG was significantly prolonged up to 70 times. Next, we performed functional assays of in vitro wound healing, cell invasion, and angiogenesis to evaluate the biological effects of the PCL-derived MSG. Interestingly, we found the ability of this composite system to promote the activation of human keratinocytes, fibroblasts, and endothelial cells, as the main actors of tissue regeneration, confirming what we previously showed for the MSG alone.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6956126PMC
http://dx.doi.org/10.3390/pharmaceutics11120631DOI Listing

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