Functionalization of almond gum through covalent and non-covalent interactions for biomedical applications.

IF 7.7 1区 化学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY International Journal of Biological Macromolecules Pub Date : 2025-03-01 Epub Date: 2024-12-30 DOI:10.1016/j.ijbiomac.2024.139364
Vikrant Sharma, Priyanka Sharma, Baljit Singh
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Abstract

The versatile properties of carbohydrate polymers make them a relevant, promising precursor to design innovative materials for use in biomedical applications. Recent research mainly focuses on the development of the polysaccharide based functional materials. Hydrogel derived materials are a source of great motivation for the development of drug delivery (DD) carriers with inherent therapeutic potential. Herein, almond gum-based hydrogels were synthesized for the delivery of the anticancer drug methotrexate after impregnation to improve the DD profile. Hydrogels were characterized by FESEM, EDS, AFM, 13C NMR, FTIR, TGA, DSC, XRD, mechanical strength & biomedical assay. The optimized network hydrogel exhibited a mesh size of 19.764 mm and a cross-linking density of 5.002 × 10-5 mol/cm3 of the hydrogels. Morphological features revealed irregular, uneven internal morphology of hydrogels in FE-SEM. The inclusion of sulphated and amide polymers in hydrogels was found in elemental composition (C = 60.72 %, O = 29.79 %, N = 6.63 % and S = 2.86 %) of hydrogels inferred from EDS. Spectroscopic characterization by FT-IR and 13C NMR confirmed the inclusion of PVP and PVSA through grafting reaction. The crosslinked product formed was found thermally stable and amorphous in nature through TGA and XRD analysis. The sustained release was found through supramolecular interactions and release complied a non-Fickian mechanism for drug diffusion (n = 0.73) and the release profile was best described by the Hixson-Crowell kinetic model in colonic pH. The hydrogels were mucoadhesive in nature and required 144 ± 10.54 mN force for the separation of hydrogels from the mucosal surface during the adhesion test. Hydrogel illustrated antioxidant activity (32.68 ± 0.83 μg GAE) during their radical scavenging test by FC reagent assay. Drug encapsulated hydrogels demonstrated antimicrobial efficacy against microbes. The results of physico-chemical and biomedical properties of hydrogels suggested their suitability for biomedical uses.

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通过共价和非共价相互作用功能化杏仁胶在生物医学上的应用。
碳水化合物聚合物的多用途特性使它们成为设计用于生物医学应用的创新材料的相关的、有前途的前体。近年来的研究主要集中在多糖基功能材料的开发上。水凝胶衍生材料是开发具有内在治疗潜力的药物递送(DD)载体的巨大动力。本研究合成了杏仁胶基水凝胶,用于浸渍后的抗癌药物甲氨蝶呤的递送,以改善DD谱。采用FESEM、EDS、AFM、13C NMR、FTIR、TGA、DSC、XRD、机械强度和生物医学分析等手段对水凝胶进行表征。优化后的网状水凝胶网目尺寸为19.764 mm,交联密度为5.002 × 10-5 mol/cm3。FE-SEM显示水凝胶内部形态不规则、不均匀。硫酸化的包容和酰胺聚合物水凝胶被发现在元素组成(C = 60.72  %,O  % = 29.79,6.63 N =  %和S = 2.86 %)EDS的水凝胶推断。通过FT-IR和13C NMR的光谱表征,证实了PVP和PVSA是通过接枝反应加入的。通过热重分析和x射线衍射分析发现,形成的交联产物热稳定,性质为无定形。通过超分子相互作用发现其缓释,符合非菲克式药物扩散机制(n = 0.73),结肠ph下的Hixson-Crowell动力学模型最能描述其释放曲线。在黏附试验中,水凝胶具有黏附性,需要144 ± 10.54 mN的力才能将水凝胶从粘膜表面分离。FC试剂法测定水凝胶的抗氧化活性(32.68 ± 0.83 μg GAE)。药物包封水凝胶对微生物具有抗菌作用。对水凝胶的理化性质和生物医学性质进行了研究,结果表明水凝胶具有一定的生物医学应用价值。
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来源期刊
International Journal of Biological Macromolecules
International Journal of Biological Macromolecules 生物-生化与分子生物学
CiteScore
13.70
自引率
9.80%
发文量
2728
审稿时长
64 days
期刊介绍: The International Journal of Biological Macromolecules is a well-established international journal dedicated to research on the chemical and biological aspects of natural macromolecules. Focusing on proteins, macromolecular carbohydrates, glycoproteins, proteoglycans, lignins, biological poly-acids, and nucleic acids, the journal presents the latest findings in molecular structure, properties, biological activities, interactions, modifications, and functional properties. Papers must offer new and novel insights, encompassing related model systems, structural conformational studies, theoretical developments, and analytical techniques. Each paper is required to primarily focus on at least one named biological macromolecule, reflected in the title, abstract, and text.
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