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中国精品科技期刊2020
周睿,吴江萍,姜娜娜,等. 绿茶末多糖的理化特性及其体外抗氧化和抗糖尿病活性[J]. 食品工业科技,2026,47(2):1−9. doi: 10.13386/j.issn1002-0306.2025020215.
引用本文: 周睿,吴江萍,姜娜娜,等. 绿茶末多糖的理化特性及其体外抗氧化和抗糖尿病活性[J]. 食品工业科技,2026,47(2):1−9. doi: 10.13386/j.issn1002-0306.2025020215.
ZHOU Rui, WU Jiangping, JIANG Nana, et al. Physicochemical Properties and In Vitro Antioxidant and Antidiabetic Activities of Green Tea Dust Polysaccharide[J]. Science and Technology of Food Industry, 2026, 47(2): 1−9. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2025020215.
Citation: ZHOU Rui, WU Jiangping, JIANG Nana, et al. Physicochemical Properties and In Vitro Antioxidant and Antidiabetic Activities of Green Tea Dust Polysaccharide[J]. Science and Technology of Food Industry, 2026, 47(2): 1−9. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2025020215.

绿茶末多糖的理化特性及其体外抗氧化和抗糖尿病活性

Physicochemical Properties and In Vitro Antioxidant and Antidiabetic Activities of Green Tea Dust Polysaccharide

  • 摘要: 为探究绿茶末多糖的理化性质及其体外抗氧化和抗糖尿病活性,以绿茶末为实验材料通过水提醇沉法提取绿茶末多糖,对其化学组成、流变学特性、热稳定性、微观结构等理化性质进行表征,并通过铁离子还原能力、DPPH自由基清除能力和亚铁离子螯合能力以及糖基化与α-葡萄糖苷酶抑制能力评价其体外抗氧化和抗糖尿病活性。结果表明,绿茶末多糖的得率以及总糖、糖醛酸、蛋白质和总酚含量分别为6.50%、44.73%、22.58%、2.92%和4.35%,主要含有3种不同分子质量分布的多糖组分,其中含量最大的组分其相对分子质量为88.88 kDa,单糖组成主要包括葡萄糖、阿拉伯糖、半乳糖、鼠李糖、半乳糖醛酸、甘露糖、葡萄糖醛酸和木糖,其摩尔质量比分别为31.59:27.11:22.73:8.26:6.29:1.91:1.24:0.87。绿茶末多糖呈现无定形片状结构,具有多糖的特征吸收基团和良好的热稳定性,其多糖溶液为剪切稀化型假塑性非牛顿流体并呈现弱凝胶型黏弹性特征行为。绿茶末多糖对DPPH自由基清除能力、铁离子还原能力(FRAP)和亚铁离子螯合能力(FIC)的半抑制浓度(IC50)分别为90.85、473.37和1159.68 mg/L,对α-葡萄糖苷酶抑制作用的IC50值为0.42 mg/mL,其活性相当于阿卡波糖的2.21倍。1 mg/mL的绿茶末多糖对晚期糖基化终产物抑制率为56.55%,约为氨基胍抑制能力的63%。本研究可为绿茶末资源综合利用及其多糖在天然抗氧化剂和抗糖尿病或功能食品开发或药物中的潜在应用提供理论依据。

     

    Abstract: In this study, we investigated the physicochemical properties and in vitro antioxidant and antidiabetic activities of a green tea dust polysaccharide (GTDP). GTDP was extracted from green tea dust using hot water extraction followed by alcohol precipitation. Its physicochemical characteristics, including chemical composition, rheological properties, thermal stability, and microstructure, were analyzed. The in vitro antioxidant and antidiabetic activities of GTDP were evaluated using ferric reducing antioxidant power (FRAP), 1,1-diphenyl-2-picrylhydrazyl (DPPH) free radical scavenging ability, ferrous ion chelating ability (FIC), and glycosylation and α-glucosidase inhibition assays. The results showed that the GTDP yield was 6.50%, with sugar, uronic acid, protein, and total phenolic contents of 44.73%, 22.58%, 2.92%, and 4.35%, respectively. GTDP contained three polysaccharide fractions with different molecular weights, of which the major component had a relative molecular weight of 88.88 kDa. Monosaccharide composition analysis revealed that GTDP was composed of glucose, arabinose, galactose, rhamnose, galacturonic acid, mannose, glucuronic acid, and xylose in a molar ratio of 31.59:27.11:22.73:8.26:6.29:1.91:1.24:0.87. GTDP exhibited an irregular flake-like structure, characteristic polysaccharide absorption bands, and good thermal stability. Its solution demonstrated shear-thinning, pseudoplastic, non-Newtonian fluid behavior with weak gel-like viscoelasticity. The semi-inhibitory concentration (IC50) values of GTDP in the DPPH, FRAP, and FIC assays were 90.85, 473.37, and 1,159.68 mg/L, respectively. Moreover, the IC50 value of GTDP against α-glucosidase was 0.42 mg/mL, showing an inhibitory activity approximately 2.21 times higher than that of acarbose. The inhibition rate of GTDP on advanced glycation end products (AGEs) was 56.55% at 1 mg/mL, which was approximately 63% higher than that of aminoguanidine. These findings provide a theoretical basis for the comprehensive utilization of green tea dust and highlight the potential of GTDP as a natural antioxidant and antidiabetic agent for functional food and pharmaceutical applications.

     

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