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Published on: February 13, 2016
Alginate-konjac glucomannan-chitosan beads as controlled release matrix
1Enzyme Technology Laboratory, Chemical Engineering Research Center, Tianjin University, Tianjin 300072, PR China.
Konjac glucomannan (KGM) enhances drug payload and controlled release in alginate-chitosan beads. These beads show improved protein retention in neutral conditions but increased leakage in acidic environments, highlighting KGM
Area of Science:
- Biomaterials Science
- Polymer Chemistry
- Drug Delivery Systems
Background:
- Controlled release systems are crucial for effective drug delivery.
- Alginate and chitosan are widely used biopolymers for bead formulation.
- Incorporating novel polysaccharides can improve bead properties.
Purpose of the Study:
- To develop and characterize controlled release beads using alginate (ALG), konjac glucomannan (KGM), and chitosan (CHI).
- To evaluate the effect of KGM on drug payload and release kinetics.
- To investigate the influence of KGM on bead structure and swelling properties.
Main Methods:
- Preparation of ALG-KGM-CHI beads using model proteins (bovine serum albumin, insulin).
- Infrared spectroscopy and scanning electron microscopy for structural analysis.
- In vitro drug release studies at different pH conditions (acidic and neutral).
- Water of hydration studies to assess swelling behavior.
Main Results:
- KGM incorporation increased drug payload and extended protein release from 1 hour (ALG-CHI) to 3 hours (ALG-KGM-CHI) at pH 7.4.
- ALG-KGM-CHI beads exhibited increased protein leakage in 0.1 N HCl.
- Swelling behavior differed in acidic (higher for ALG-KGM-CHI) versus alkaline (higher for ALG-CHI) solutions.
- Gelling ion concentration significantly impacted release rate and gel structure.
Conclusions:
- Konjac glucomannan improves the drug-loading capacity and controlled release performance of alginate-chitosan beads.
- The inclusion of KGM influences bead swelling and structural integrity, affecting protein diffusion.
- ALG-KGM-CHI beads show potential for pH-responsive drug delivery, with enhanced retention in neutral environments but susceptibility to leakage in acidic conditions.
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