Dual delivery of hydrophilic and hydrophobic drugs from chitosan/diatomaceous earth composite membranes.

J Mater Sci Mater Med

3B's Research Group - Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark- Parque de Ciência e Tecnologia, Zona Industrial da Gandra, 4805-017, Barco, Guimarães, Portugal.

Published: February 2018

AI Article Synopsis

  • Oral drug administration has significant limitations, including loss due to hepatic metabolism and challenges for patients unable to swallow.
  • Sublingual membranes made from β-chitosan and marine sediments offer a promising alternative for drug delivery, potentially improving absorption.
  • Testing showed these membranes effectively delivered both hydrophilic (gentamicin) and hydrophobic (dexamethasone) drugs, with diatomaceous earth enhancing the performance for hydrophobic drugs.

Article Abstract

Oral administration of drugs presents important limitations, which are frequently not granted the importance that they really have. For instance, hepatic metabolism means an important drug loss, while some patients have their ability to swell highly compromised (i.e. unconsciousness, cancer…). Sublingual placement of an accurate Pharmaceutical Dosage Form is an attractive alternative. This work explores the use of the β-chitosan membranes, from marine industry residues, composed with marine sediments for dual sublingual drug delivery. As proof of concept, the membranes were loaded with a hydrophilic (gentamicin) and a hydrophobic (dexamethasone) drug. The physico-chemical and morphological characterization indicated the successful incorporated of diatomaceous earth within the chitosan membranes. Drug delivery studies showed the potential of all formulations for the immediate release of hydrophilic drugs, while diatomaceous earth improved the loading and release of the hydrophobic drug. These results highlight the interest of the herein developed membranes for dual drug delivery.

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Source
http://dx.doi.org/10.1007/s10856-018-6025-9DOI Listing

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