Self-cross-linked starch/chitosan hydrogel as a biocompatible vehicle for controlled release of drug

被引:29
|
作者
Sarmah, Dimpee [1 ]
Rather, Muzamil Ahmad [2 ]
Sarkar, Anupama [2 ]
Mandal, Manabendra [2 ]
Sankaranarayanan, Kamatchi [3 ]
Karak, Niranjan [1 ]
机构
[1] Tezpur Univ, Dept Chem Sci, Adv Polymer & Nanomat Lab, Tezpur 784028, Assam, India
[2] Tezpur Univ, Dept Mol Biol & Biotechnol, Tezpur 784028, Assam, India
[3] Inst Adv Study Sci & Technol, Biophys Life Sci Div, Gauhati 781035, Assam, India
关键词
Oxidized starch; Schiff base; Controlled release; Antibacterial; pH sensitive; Diffusion; CHITOSAN-BASED HYDROGEL; XANTHAN GUM; RHEOLOGICAL BEHAVIOR; DELIVERY; LINKING; SUPERABSORBENT; CIPROFLOXACIN; ENCAPSULATION; ADSORBENT; OXIDATION;
D O I
10.1016/j.ijbiomac.2023.124206
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A facile one-pot approach was adopted to prepare a polysaccharide-based hydrogel of oxidized starch (OS)-chitosan. The synthetic monomer-free, eco-friendly hydrogel was prepared in an aqueous solution and employed for controlled drug release application. The starch was first oxidized under mild conditions to prepare its bial-dehydic derivative. Subsequently, the amino group-containing a modified polysaccharide, "chitosan" was introduced on the backbone of OS via a dynamic Schiff-base reaction. The bio-based hydrogel was obtained via a one-pot in-situ reaction, where functionalized starch acts as a macro-cross-linker that contributes structural stability and integrity to the hydrogel. The introduction of chitosan contributes to stimuli-responsive properties and thus pH-sensitive swelling behavior was obtained. The hydrogel showed its potential as a pH-dependent controlled drug release system and a maximum of 29 h sustained release period was observed for ampicillin sodium salt drug. In vitro studies confirmed that the prepared drug-loaded hydrogels showed excellent anti-bacterial ability. Most importantly, the hydrogel could find potential use in the biomedical field due to its facile reaction conditions, biocompatibility along with controlled releasing ability of the encapsulated drug.
引用
收藏
页数:17
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