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琼胶多糖的结构表征和细胞毒性活性评价

Structural Characterization and Cytotoxic Activity Evaluation of Ulvan Polysaccharides Extracted from the Green Algae .

机构信息

NhaTrang Institute of Technology Research and Application, Vietnam Academy of Science and Technology, 02 Hung Vuong Street, Nhatrang 650000, Vietnam.

Section for Protein Chemistry and Enzyme Technology, DTU Bioengineering-Department of Biotechnology and Biomedicine, Technical University of Denmark, 2800 Kongens Lyngby, Denmark.

出版信息

Mar Drugs. 2023 Oct 25;21(11):556. doi: 10.3390/md21110556.

Abstract

Ulvan, a sulfated heteropolysaccharide with structural and functional properties of interest for various uses, was extracted from the green seaweed . is an unexplored species found in the South China Sea along the central coast of Vietnam. Based on dry weight, the ulvan yield was ~15% (/) and the ulvan had a sulfate content of 13.4 wt%. The compositional constitution encompassed L-Rhamnose (Rha), D-Xylose (Xyl), D-Glucuronic acid (GlcA), L-Iduronic acid (IdoA), D-Galactose (Gal), and D-Glucose (Glc) with a molar ratio of 1:0.19:0.35:0.52:0.05:0.11, respectively. The structure of ulvan was determined using High-Performance Liquid Chromatography (HPLC), Fourier Transform Infrared Spectroscopy (FT-IR), and Nuclear Magnetic Resonance spectroscopy (NMR) methods. The results showed that the extracted ulvan comprised a mixture of two different structural forms, namely ("A3s") with the repeating disaccharide [→4)-β-D-GlcA-(1→4)-α-L-Rha 3S-(1→]n, and ("B3s") with the repeating disaccharide [→4)-α-L-IdoA-(1→4)-α-L-Rha 3S(1→]n. The relative abundance of A3s, and B3s was 1:1.5, respectively. The potential anticarcinogenic attributes of ulvan were evaluated against a trilogy of human cancer cell lineages. Concomitantly, Quantitative Structure-Activity Relationship (QSAR) modeling was also conducted to predict potential adverse reactions stemming from pharmacological interactions. The ulvan showed significant antitumor growth activity against hepatocellular carcinoma (IC ≈ 90 µg/mL), human breast cancer cells (IC ≈ 85 µg/mL), and cervical cancer cells (IC ≈ 67 µg/mL). The QSAR models demonstrated acceptable predictive power, and seven toxicity indications confirmed the safety of ulvan, warranting its candidacy for further in vivo testing and applications as a biologically active pharmaceutical source for human disease treatment.

摘要

从南海沿越南北部中部海岸发现的一种未经探索的绿藻中提取出具有各种用途的结构和功能特性的硫酸化杂多糖岩藻聚糖。基于干重,岩藻聚糖的产率约为 15%(/),岩藻聚糖的硫酸根含量为 13.4wt%。组成结构包括 L-鼠李糖(Rha)、D-木糖(Xyl)、D-葡萄糖醛酸(GlcA)、L-古洛糖醛酸(IdoA)、D-半乳糖(Gal)和 D-葡萄糖(Glc),摩尔比分别为 1:0.19:0.35:0.52:0.05:0.11。使用高效液相色谱法(HPLC)、傅里叶变换红外光谱法(FT-IR)和核磁共振光谱法(NMR)确定了岩藻聚糖的结构。结果表明,提取的岩藻聚糖由两种不同结构形式的混合物组成,即("A3s"),其重复二糖为[→4)-β-D-GlcA-(1→4)-α-L-Rha 3S-(1→]n,和("B3s"),其重复二糖为[→4)-α-L-IdoA-(1→4)-α-L-Rha 3S-(1→]n。A3s 和 B3s 的相对丰度分别为 1:1.5。评估了岩藻聚糖对一系列人类癌细胞系的潜在抗癌特性。同时,还进行了定量构效关系(QSAR)建模,以预测源于药理相互作用的潜在不良反应。岩藻聚糖对肝癌(IC ≈ 90µg/mL)、人乳腺癌细胞(IC ≈ 85µg/mL)和宫颈癌细胞(IC ≈ 67µg/mL)的生长均有显著的抗肿瘤活性。QSAR 模型显示出可接受的预测能力,七种毒性指标证实了岩藻聚糖的安全性,这使其有资格作为生物活性药物来源进行进一步的体内测试和应用,以治疗人类疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a9/10672449/bea8d847a50d/marinedrugs-21-00556-g001.jpg

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