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Extraction of Fucoidan from Turbinaria decurrens and the Synthesis of Fucoidan-Coated AgNPs for Anticoagulant Application

[Image: see text] Brown seaweeds usually contain alginate as a major polymer. The second major sulfated polymer in brown seaweeds is fucoidan, which has huge potential in medicinal applications. In this study, the photosynthetic pigments from Turbinaria decurrens were first extracted using chlorofor...

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Autores principales: Shanthi, Nagarajan, Arumugam, Ponnan, Murugan, Marudhamuthu, Sudhakar, Muthiyal Prabakaran, Arunkumar, Kulanthaiyesu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8613821/
https://www.ncbi.nlm.nih.gov/pubmed/34841142
http://dx.doi.org/10.1021/acsomega.1c03776
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author Shanthi, Nagarajan
Arumugam, Ponnan
Murugan, Marudhamuthu
Sudhakar, Muthiyal Prabakaran
Arunkumar, Kulanthaiyesu
author_facet Shanthi, Nagarajan
Arumugam, Ponnan
Murugan, Marudhamuthu
Sudhakar, Muthiyal Prabakaran
Arunkumar, Kulanthaiyesu
author_sort Shanthi, Nagarajan
collection PubMed
description [Image: see text] Brown seaweeds usually contain alginate as a major polymer. The second major sulfated polymer in brown seaweeds is fucoidan, which has huge potential in medicinal applications. In this study, the photosynthetic pigments from Turbinaria decurrens were first extracted using chloroform/methanol in the ratio of 1:1 (v/v), followed by fucoidan extraction with yields of 5.58% (crude) and 1.28% (purified fucoidan) from the dry weight of seaweed, whereas alginate was extracted with a yield of 14.7% DW of seaweed. The isolated fucoidan possessing anticoagulation property was identified and characterized as (1–3)-α-l-fucopyranosyl residues with sulfate groups primarily at the C(4) position and to a lesser extent at the C(2) position, whereas in the case of galactose, at the C(3) and C(6) positions. The AgNPs synthesized using isolated fucoidan exhibit strong anticoagulant activity and possess a good antibacterial property against Gram-negative clinical bacteria. Functional groups such as O–H, C–H, and S=O associated with sugar residues in sulfated fucoidan are involved in the synthesis of the nanoparticles with a spherical shape, size ranging from 10 to 60 nm, and showing polydispersity. From this study, we conclude that fucoidan-coated anionic AgNPs synthesized from T. decurrens have tremendous potential in drug development.
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spelling pubmed-86138212021-11-26 Extraction of Fucoidan from Turbinaria decurrens and the Synthesis of Fucoidan-Coated AgNPs for Anticoagulant Application Shanthi, Nagarajan Arumugam, Ponnan Murugan, Marudhamuthu Sudhakar, Muthiyal Prabakaran Arunkumar, Kulanthaiyesu ACS Omega [Image: see text] Brown seaweeds usually contain alginate as a major polymer. The second major sulfated polymer in brown seaweeds is fucoidan, which has huge potential in medicinal applications. In this study, the photosynthetic pigments from Turbinaria decurrens were first extracted using chloroform/methanol in the ratio of 1:1 (v/v), followed by fucoidan extraction with yields of 5.58% (crude) and 1.28% (purified fucoidan) from the dry weight of seaweed, whereas alginate was extracted with a yield of 14.7% DW of seaweed. The isolated fucoidan possessing anticoagulation property was identified and characterized as (1–3)-α-l-fucopyranosyl residues with sulfate groups primarily at the C(4) position and to a lesser extent at the C(2) position, whereas in the case of galactose, at the C(3) and C(6) positions. The AgNPs synthesized using isolated fucoidan exhibit strong anticoagulant activity and possess a good antibacterial property against Gram-negative clinical bacteria. Functional groups such as O–H, C–H, and S=O associated with sugar residues in sulfated fucoidan are involved in the synthesis of the nanoparticles with a spherical shape, size ranging from 10 to 60 nm, and showing polydispersity. From this study, we conclude that fucoidan-coated anionic AgNPs synthesized from T. decurrens have tremendous potential in drug development. American Chemical Society 2021-11-09 /pmc/articles/PMC8613821/ /pubmed/34841142 http://dx.doi.org/10.1021/acsomega.1c03776 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Shanthi, Nagarajan
Arumugam, Ponnan
Murugan, Marudhamuthu
Sudhakar, Muthiyal Prabakaran
Arunkumar, Kulanthaiyesu
Extraction of Fucoidan from Turbinaria decurrens and the Synthesis of Fucoidan-Coated AgNPs for Anticoagulant Application
title Extraction of Fucoidan from Turbinaria decurrens and the Synthesis of Fucoidan-Coated AgNPs for Anticoagulant Application
title_full Extraction of Fucoidan from Turbinaria decurrens and the Synthesis of Fucoidan-Coated AgNPs for Anticoagulant Application
title_fullStr Extraction of Fucoidan from Turbinaria decurrens and the Synthesis of Fucoidan-Coated AgNPs for Anticoagulant Application
title_full_unstemmed Extraction of Fucoidan from Turbinaria decurrens and the Synthesis of Fucoidan-Coated AgNPs for Anticoagulant Application
title_short Extraction of Fucoidan from Turbinaria decurrens and the Synthesis of Fucoidan-Coated AgNPs for Anticoagulant Application
title_sort extraction of fucoidan from turbinaria decurrens and the synthesis of fucoidan-coated agnps for anticoagulant application
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8613821/
https://www.ncbi.nlm.nih.gov/pubmed/34841142
http://dx.doi.org/10.1021/acsomega.1c03776
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