Design of a pH sensitive alginate-guar gum hydrogel crosslinked with glutaraldehyde was done for the controlled delivery of protein drugs. Alginate is a non-toxic polysaccharide with favorable pH sensitive properties for intestinal delivery of protein drugs. Drug leaching during hydrogel preparation and rapid dissolution of alginate at higher pH are major limitations, as it results in very low entrapment efficiency and burst release of entrapped protein drug, once it enters the intestine. To overcome these limitations, another natural polysaccharide, guargum was included in the alginate matrix along with a cross linking agent to ensure maximum encapsulation efficiency and controlled drug release. The crosslinked alginate-guar gum matrix is novel and the drug loading process used in the study was mild and performed in aqueous environment. The release profiles of a model protein drug (BSA) from test hydrogels were studied under simulated gastric and intestinal media. The beads having an alginate to guar gum percentage combination of 3:1 showed desirable characters like better encapsulation efficiency and bead forming properties in the preliminary studies. The glutaraldehyde concentration giving maximum (100%) encapsulation efficiency and the most appropriate swelling characteristics was found to be 0.5% (w/v). Freeze-dried samples showed swelling ratios most suitable for drug release in simulated intestinal media ( approximately 8.5). Protein release from test hydrogels was minimal at pH 1.2 ( approximately 20%), and it was found to be significantly higher ( approximately 90%) at pH 7.4. Presence of guar gum and glutaraldehyde crosslinking increases entrapment efficiency and prevents the rapid dissolution of alginate in higher pH of the intestine, ensuring a controlled release of the entrapped drug.
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http://dx.doi.org/10.1016/j.ijpharm.2006.11.009 | DOI Listing |
Int J Biol Macromol
October 2024
School of Textile and Material Engineering, Dalian Polytechnic University, Dalian 116034, China; Liaoning Engineering Technology Research Center of Function Fiber and Its Composites, Dalian Polytechnic University, Dalian 116034, China.
Carbohydr Polym
April 2024
School of Chemistry, University of the Punjab, Lahore 54590, Pakistan.
Due to the expansion of industrial activities, the concentration of dyes in water has been increasing. The dire need to remove these pollutants from water has been heavily discussed. This study focuses on the reproducible and sustainable solution for wastewater treatment and dye annihilation challenges.
View Article and Find Full Text PDFJ Colloid Interface Sci
May 2024
School of Materials Science and Engineering, Chongqing Jiaotong University, Chongqing 400074, PR China.
Hydrogels, recognized for their biocompatibility, are extensively employed in the realm of wearable devices. Nevertheless, their application is often constrained by their low mechanical robustness, rendering them susceptible to damage during operation. The restoration of their load-bearing and sensory functionalities post-damage represents a captivating yet underexplored domain.
View Article and Find Full Text PDFFood Chem
March 2024
School of Food Science and Nutrition, University of Leeds, Leeds LS2 9JT, United Kingdom.
The poor biological, mechanical and water-resistance properties of sodium alginate/guar gum film (SG) limit its application in food preservation. To overcome this disadvantage, we added β-Cyclodextrin/persimmon pectin-stabilized baobab seed oil Pickering emulsion (BOPE) to enhance the mechanical and water resistance properties of SG film, and added green synthesized silver nanoparticles (AgNPS) and Lycium ruthenicum extract (LA) to improve the biological properties of the film. The properties of BOPE was optimized using Box-Behnken design (BBD).
View Article and Find Full Text PDFInt J Biol Macromol
February 2023
College of Textile and Materials Engineering, Dalian Polytechnic University, Dalian, Liaoning 116034, PR China. Electronic address:
Biomass-based aerogel fibers have attracted increasing attention due to their renewable nature. However, their disadvantages, such as low mechanical strength, poor long-range order, and easy combustion, are still significant challenges. Herein, a directed freezing-assisted forced stretching strategy is developed to fabricate sheath-core structured Ca-alginate/polyvinyl alcohol (Ca-A/PVA) aerogel fibers with Long-range-ordered pores.
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