Preparation and characterization of ibuprofen-loaded poly(lactide-co-glycolide)/poly(ethylene glycol)-g-chitosan electrospun membranes

Ibuprofen-loaded composite membranes composed of poly(lactide-co-glycolide) (PLGA) and poly(ethylene glycol)-g-chitosan (PEG-g-CHN) were prepared by electrospinning. The electrospun membranes were characterized by scanning electron microscopy (SEM), differential scanning calorimetry (DSC), mechanical evaluation and contact angle measurements. Shrinkage behavior of the membrane in buffer at 37°C was also evaluated. It was found that PLGA glass transition temperature (T g) decreased with increasing PEG-g-CHN content in the composite membranes, which results in a decrease in tensile stress at break but an increase in tensile strain of the membranes. The degree of shrinkage of these composite membranes decreased from 76 to only 3% when the PEG-g-CHN content in the membranes increased from 10 to 30%. The presence of PEG-g-CHN significantly moderated the burst release rate of ibuprofen from the electrospun PLGA membranes. Moreover, ibuprofen could be conjugated to the side chains of PEG-g-CHN to prolong its release for more than two weeks. The sustained release capacity of the PLGA/PEG-g-CHN composite membranes, together with their compliant and stable mechanical properties, renders them ideal matrices for atrial fibrillation.

[1]  S. Nishimura,et al.  Chemospecific manipulations of a rigid polysaccharide: syntheses of novel chitosan derivatives with excellent solubility in common organic solvents by regioselective chemical modifications , 1991 .

[2]  Elliot L. Chaikof,et al.  Generation of Synthetic Elastin-Mimetic Small Diameter Fibers and Fiber Networks , 2000 .

[3]  F. Veronese Peptide and protein PEGylation: a review of problems and solutions. , 2001, Biomaterials.

[4]  Thomas E. Moritz,et al.  Atrial fibrillation after cardiac surgery: a major morbid event? , 1997, Annals of surgery.

[5]  M. Morimoto,et al.  Preparation and characterization of water-soluble chitin and chitosan derivatives , 1998 .

[6]  Y. Ohya,et al.  Aggregation phenomenon of PEG-grafted chitosan in aqueous solution , 1998 .

[7]  Cato T Laurencin,et al.  Electrospun nanofibrous structure: a novel scaffold for tissue engineering. , 2002, Journal of biomedical materials research.

[8]  Chih-Chang Chu,et al.  Biodegradable dextran-polylactide hydrogel networks: their swelling, morphology and the controlled release of indomethacin. , 2002, Journal of biomedical materials research.

[9]  D. Reneker,et al.  Nanometre diameter fibres of polymer, produced by electrospinning , 1996 .

[10]  You-Lo Hsieh,et al.  Ultrafine fibrous cellulose membranes from electrospinning of cellulose acetate , 2002 .

[11]  C. Booth,et al.  A DSC study of the miscibility of poly(ethylene oxide)-block-poly(DL-lactide) copolymers with poly(DL-lactide). , 1999, Biomaterials.

[12]  R. Muzzarelli,et al.  Preparation and characterization of poly(ethylene glycol)-crosslinked reacetylated chitosans , 2000 .

[13]  Kwangsok Kim,et al.  Structure and process relationship of electrospun bioabsorbable nanofiber membranes , 2002 .

[14]  Gary E. Wnek,et al.  TAILORING TISSUE ENGINEERING SCAFFOLDS USING ELECTROSTATIC PROCESSING TECHNIQUES: A STUDY OF POLY(GLYCOLIC ACID) ELECTROSPINNING , 2001 .

[15]  N. Wang,et al.  A novel biodegradable system based on gelatin nanoparticles and poly(lactic-co-glycolic acid) microspheres for protein and peptide drug delivery. , 1997, Journal of pharmaceutical sciences.

[16]  John Layman,et al.  Release of tetracycline hydrochloride from electrospun poly(ethylene-co-vinylacetate), poly(lactic acid), and a blend. , 2002, Journal of controlled release : official journal of the Controlled Release Society.

[17]  R Marks,et al.  Evaluation of biomechanical properties of human skin. , 1995, Clinics in dermatology.

[18]  K. Kurita,et al.  Comb-shaped chitosan derivatives having oligo(ethylene glycol) side chains , 1999 .

[19]  David G Simpson,et al.  Electrospinning of collagen nanofibers. , 2002, Biomacromolecules.

[20]  Karthik Nagapudi,et al.  Engineered collagen–PEO nanofibers and fabrics , 2001, Journal of biomaterials science. Polymer edition.

[21]  D. Grijpma,et al.  High molecular weight poly(l-lactide) and poly(ethylene oxide) blends: thermal characterization and physical properties , 1996 .

[22]  R. Leachman,et al.  Cardiac arrhythmias during and after heart surgery: diagnosis and management. , 1974, Progress in cardiovascular diseases.

[23]  L. Cohn,et al.  Predictors of atrial fibrillation after coronary artery surgery. Current trends and impact on hospital resources. , 1996, Circulation.

[24]  J. Vacanti,et al.  A biodegradable nanofiber scaffold by electrospinning and its potential for bone tissue engineering. , 2003, Biomaterials.

[25]  D. Cohn,et al.  Biodegradable PEO/PLA block copolymers. , 1988, Journal of biomedical materials research.

[26]  Chih-Chang Chu,et al.  Synthesis and characterization of biodegradable hydrophobic-hydrophilic hydrogel networks with a controlled swelling property , 2000 .

[27]  A. Ravve,et al.  Principles of Polymer Chemistry , 1995 .