Nicotine–magnesium aluminum silicate microparticle surface modified with chitosan for mucosal delivery
Creators
- 1. Faculty of Pharmaceutical Sciences, Khon Kaen University, Khon Kaen 40002 (Thailand)
- 2. Department of Pharmacy, Faculty of Health and Medical Sciences, University of Copenhagen, DK-2100 Copenhagen (Denmark)
- 3. School of Pharmacy, University of Otago, Dunedin 9054 (New Zealand)
- 4. Department of Manufacturing Pharmacy, Faculty of Pharmacy, Mahidol University, Bangkok 10400 (Thailand)
Description
Magnesium aluminum silicate (MAS), a negatively charged clay, and nicotine (NCT), a basic drug, can interact electrostatically to form microparticles. Chitosan (CS) was used for the surface modification of the microparticles, and a lyophilization method was used to preserve the original particle morphology. The microparticles were characterized in terms of their physicochemical properties, NCT content, mucoadhesive properties, and release and permeation across porcine esophageal mucosa. The results showed that the microparticles formed via electrostatic interaction between MAS and protonated NCT had an irregular shape and that their NCT content increased with increasing NCT ratios in the microparticle preparation solution. High molecular weight CS (800 kDa) adsorbed to the microparticle surface and induced a positive surface charge. CS molecules intercalated into the MAS silicate layers and decreased the crystallinity of the microparticles, leading to an increase in the release rate and diffusion coefficient of NCT from the microparticles. Moreover, the microparticle surface modified with CS was found to have higher NCT permeation fluxes and mucoadhesive properties, which indicated the significant role of CS for NCT mucosal delivery. However, the enhancement of NCT permeation and of mucoadhesive properties depended on the molecular weight and concentration of CS. These findings suggest that NCT-MAS microparticle surface modified with CS represents a promising mucosal delivery system for NCT. Highlights: ► Nicotine–magnesium aluminum silicate microparticles were prepared using electrostatic interaction. ► Lyophilization was used for drying and maintaining an original morphology of the microparticles. ► Chitosan (CS) was used for surface modification of the microparticles at acidic pH. ► Surface modification using CS caused an increase in release and permeation of nicotine. ► Microparticle surface-modified with CS presented better mucoadhesive properties
Availability note (English)
Available from http://dx.doi.org/10.1016/j.msec.2012.12.086Additional details
Identifiers
- DOI
- 10.1016/j.msec.2012.12.086;
- PII
- S0928-4931(12)00655-8;
Publishing Information
- Journal Title
- Materials Science and Engineering. C, Biomimetic Materials, Sensors and Systems
- Journal Volume
- 33
- Journal Issue
- 3
- Journal Page Range
- p. 1727-1736
- ISSN
- 0928-4931
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 45111617
- Subject category
- S36: MATERIALS SCIENCE;
- Descriptors DEI
- ALUMINIUM SILICATES; AMINO ACIDS; CLATHRATES; CLAYS; DRYING; ESOPHAGUS; LAYERS; LYOPHILIZATION; MAGNESIUM; MOLECULAR WEIGHT; MORPHOLOGY; MUCOUS MEMBRANES; NICOTINE; OLIGOSACCHARIDES; PARTICLES; SURFACES
- Descriptors DEC
- ALKALINE EARTH METALS; ALKALOIDS; ALUMINIUM COMPOUNDS; AMINES; AUTONOMIC NERVOUS SYSTEM AGENTS; AZINES; AZOLES; BODY; CARBOHYDRATES; CARBOXYLIC ACIDS; DIGESTIVE SYSTEM; DRUGS; ELEMENTS; HETEROCYCLIC COMPOUNDS; MEMBRANES; METALS; MINERALS; ORGANIC ACIDS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; ORGANS; OXYGEN COMPOUNDS; PARASYMPATHOLYTICS; PARASYMPATHOMIMETICS; PYRIDINES; PYRROLES; PYRROLIDINES; SACCHARIDES; SILICATE MINERALS; SILICATES; SILICON COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.