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

Vy Ha Nguyen TranMaria Dalgaard MikkelsenHai Bang TruongHieu Nhu Mai VoThinh Duc PhamHang Thi Thuy CaoThuan Thi NguyenAnne S MeyerThuy Thu Thi ThanhTran Thi Thanh Van
Published in: Marine drugs (2023)
Ulvan, a sulfated heteropolysaccharide with structural and functional properties of interest for various uses, was extracted from the green seaweed Ulva papenfussii . U. papenfussii is an unexplored Ulva species found in the South China Sea along the central coast of Vietnam. Based on dry weight, the ulvan yield was ~15% ( w / w ) and the ulvan had a sulfate content of 13.4 wt%. The compositional constitution encompassed L-Rhamnose (Rha p ), D-Xylose (Xyl p ), D-Glucuronic acid (GlcA p ), L-Iduronic acid (IdoA p ), D-Galactose (Gal p ), and D-Glucose (Glc p ) 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 p -(1→4)-α-L-Rha p 3S-(1→]n, and ("B3s") with the repeating disaccharide [→4)-α-L-IdoA p -(1→4)-α-L-Rha p 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 50 ≈ 90 µg/mL), human breast cancer cells (IC 50 ≈ 85 µg/mL), and cervical cancer cells (IC 50 ≈ 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.
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