Related Experiment Video
Updated: May 25, 2025

Modeling and Simulations of Olfactory Drug Delivery with Passive and Active Controls of Nasally Inhaled Pharmaceutical Aerosols
Published on: May 20, 2016
Development of an Innovative Dual Construct for Targeted Drug Delivery in the Oral Cavity
Elena Mazzinelli1, Ilaria Favuzzi1, Marianna Messina2
1Dipartimento di Scienze Biotecnologiche di Base, Cliniche Intensivologiche e Perioperatorie, Università Cattolica del Sacro Cuore, Largo Francesco Vito 1, 00168 Rome, Italy.
This study developed a novel drug delivery system using chitosan-coated fibers and nanoparticles for oral lichen planus (OLP). The system enhances drug mucoadhesion and cellular uptake, offering a promising alternative for OLP treatment.
Area of Science:
- Biomaterials Science
- Drug Delivery Systems
- Oral Medicine
Background:
- Oral lichen planus (OLP) is a chronic autoimmune oral mucosa disease and a potentially malignant oral disorder.
- Current topical corticosteroid treatments for OLP have limitations including frequent application needs, poor retention, and side effects.
- Developing advanced drug delivery systems is crucial to overcome OLP treatment challenges.
Purpose of the Study:
- To engineer an innovative dexamethasone delivery system for oral application.
- To utilize poly(lactic acid) fibers coated with chitosan and poly(lactic-co-glycolic acid) nanoparticles for enhanced drug delivery.
- To evaluate the mucoadhesive and cellular uptake properties of the developed system.
Main Methods:
- Fabrication and characterization of chitosan-coated poly(lactic acid) fibers for mucoadhesion and cytocompatibility.
- Development and analysis of poly(lactic-co-glycolic acid) nanoparticles for size, shape, encapsulation, cellular uptake, drug release, and cytocompatibility.
- Assessment of the combined system's performance under simulated salivation conditions.
Main Results:
- Both poly(lactic acid) and poly(lactic-co-glycolic acid) polymers exhibited cytocompatibility.
- Chitosan-coated fibers demonstrated significant mucoadhesive properties.
- Nanoparticles showed efficient cellular internalization and drug release, with the combined system maintaining efficacy even with simulated salivation.
Conclusions:
- The developed chitosan-coated poly(lactic acid) fiber and poly(lactic-co-glycolic acid) nanoparticle system shows potential for improved mucoadhesive drug delivery in the oral cavity.
- This innovative system offers dual benefits of mucoadhesion and efficient cellular uptake for OLP treatment.
- Further research and optimization are necessary to enhance patient compliance and therapeutic outcomes for oral lichen planus.
More Related Videos
04:28Utilizing an Orally Dissolving Strip for Pharmacological and Toxicological Studies: A Simple and Humane Alternative to Oral Gavage for Animals
Published on: March 23, 2016
10:16Targeted Plasma Membrane Delivery of a Hydrophobic Cargo Encapsulated in a Liquid Crystal Nanoparticle Carrier
Published on: February 8, 2017
Related Concept Videos
Drug Delivery: Enteral Route
Drug Delivery: Overview
Enteral delivery involves administering drugs directly through swallowing, sublingual placement, or buccal application. Orally administered drugs predominantly navigate the...
Routes of Drug Administration: Enteral
Enteral administration involves drug administration via the mouth in two ways: orally or sublingually.
Unlike sublingually drugs, drugs that are taken orally pass through the gastrointestinal (GI) tract and get metabolized by the liver. Once metabolized, the drug is absorbed into the systemic circulation, reaching different body parts via the bloodstream. However, while passing through the stomach,...
Drug Delivery: Miscellaneous Routes
Oral inhalation and nasal sprays swiftly transfer drugs across the respiratory epithelium's mucosal layer. Inhaled glucocorticoids and bronchodilators directly target lung conditions such as asthma, while fluticasone nasal spray mitigates allergic rhinitis.
Transdermal patches transport drugs...
Factors Affecting Dissolution: Drug Permeability, Stability and Stereochemistry
Non-Oral Extravascular Drug Absorption Routes
Lipophilic drugs that are stable at salivary pH (6) and exhibit minimal binding to the oral mucosa are absorbed more...