Sodium alginate-f-GO composite hydrogels for tissue regeneration and antitumor applications

Biopolymer-based composite hydrogels have attracted tremendous attention for tissue regeneration and antitumor applications. Since sodium alginate is a biopolymer, they offer excellent therapeutic options with long-term drug release and low side effects. To prepare multifunctional composite hydrogel...

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Main Authors: Aslam Khan, Muhammad Umar, Abd. Razak, Saiful Izwan, Haider, Sajjad, Abdul Mannan, Hafiz, Hussain, Javed, Hasan, Anarwul
Format: Article
Language:English
Published: Elsevier B.V. 2022
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Online Access:http://eprints.utm.my/id/eprint/100948/1/SaifulIzwanAbdRazak2022_SodiumAlginatefGOCompositeHydrogel.pdf
http://eprints.utm.my/id/eprint/100948/
http://dx.doi.org/10.1016/j.ijbiomac.2022.03.091
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spelling my.utm.1009482023-05-18T04:58:04Z http://eprints.utm.my/id/eprint/100948/ Sodium alginate-f-GO composite hydrogels for tissue regeneration and antitumor applications Aslam Khan, Muhammad Umar Abd. Razak, Saiful Izwan Haider, Sajjad Abdul Mannan, Hafiz Hussain, Javed Hasan, Anarwul Q Science (General) Biopolymer-based composite hydrogels have attracted tremendous attention for tissue regeneration and antitumor applications. Since sodium alginate is a biopolymer, they offer excellent therapeutic options with long-term drug release and low side effects. To prepare multifunctional composite hydrogels with anticancer and tissue regeneration capabilities, sodium alginate (SA) and graphene oxide (GO) were covalently linked and crosslinked with tetraethyl orthosilicate (TEOS) by the solvothermal method. The structural and morphological results show that the hydrogels exhibit the desired functionality and porosity. The swelling of hydrogels in an aqueous and PBS medium was investigated. SGT-4 had the highest swelling in both aqueous and PBS media. Swelling and biodegradation of the hydrogel were inversely related. The drug release of SGT-4 was determined in different pH media (pH 6.4, 7.4, and 8.4) and the kinetics of drug release was determined according to the Higuchi model (R2 = 0.93587). Antibacterial activities were evaluated against severe infectious agents. Uppsala (U87) and osteoblast (MC3T3-E1) cell lines were used to determine the anticancer and biocompatibility of the composite hydrogels, respectively. These results suggest that the composite hydrogels could be used as potential biomaterials for tissue regeneration and antitumor applications. Elsevier B.V. 2022 Article PeerReviewed application/pdf en http://eprints.utm.my/id/eprint/100948/1/SaifulIzwanAbdRazak2022_SodiumAlginatefGOCompositeHydrogel.pdf Aslam Khan, Muhammad Umar and Abd. Razak, Saiful Izwan and Haider, Sajjad and Abdul Mannan, Hafiz and Hussain, Javed and Hasan, Anarwul (2022) Sodium alginate-f-GO composite hydrogels for tissue regeneration and antitumor applications. International Journal of Biological Macromolecules, 208 (-). pp. 475-485. ISSN 0141-8130 http://dx.doi.org/10.1016/j.ijbiomac.2022.03.091 DOI: 10.1016/j.ijbiomac.2022.03.091
institution Universiti Teknologi Malaysia
building UTM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Teknologi Malaysia
content_source UTM Institutional Repository
url_provider http://eprints.utm.my/
language English
topic Q Science (General)
spellingShingle Q Science (General)
Aslam Khan, Muhammad Umar
Abd. Razak, Saiful Izwan
Haider, Sajjad
Abdul Mannan, Hafiz
Hussain, Javed
Hasan, Anarwul
Sodium alginate-f-GO composite hydrogels for tissue regeneration and antitumor applications
description Biopolymer-based composite hydrogels have attracted tremendous attention for tissue regeneration and antitumor applications. Since sodium alginate is a biopolymer, they offer excellent therapeutic options with long-term drug release and low side effects. To prepare multifunctional composite hydrogels with anticancer and tissue regeneration capabilities, sodium alginate (SA) and graphene oxide (GO) were covalently linked and crosslinked with tetraethyl orthosilicate (TEOS) by the solvothermal method. The structural and morphological results show that the hydrogels exhibit the desired functionality and porosity. The swelling of hydrogels in an aqueous and PBS medium was investigated. SGT-4 had the highest swelling in both aqueous and PBS media. Swelling and biodegradation of the hydrogel were inversely related. The drug release of SGT-4 was determined in different pH media (pH 6.4, 7.4, and 8.4) and the kinetics of drug release was determined according to the Higuchi model (R2 = 0.93587). Antibacterial activities were evaluated against severe infectious agents. Uppsala (U87) and osteoblast (MC3T3-E1) cell lines were used to determine the anticancer and biocompatibility of the composite hydrogels, respectively. These results suggest that the composite hydrogels could be used as potential biomaterials for tissue regeneration and antitumor applications.
format Article
author Aslam Khan, Muhammad Umar
Abd. Razak, Saiful Izwan
Haider, Sajjad
Abdul Mannan, Hafiz
Hussain, Javed
Hasan, Anarwul
author_facet Aslam Khan, Muhammad Umar
Abd. Razak, Saiful Izwan
Haider, Sajjad
Abdul Mannan, Hafiz
Hussain, Javed
Hasan, Anarwul
author_sort Aslam Khan, Muhammad Umar
title Sodium alginate-f-GO composite hydrogels for tissue regeneration and antitumor applications
title_short Sodium alginate-f-GO composite hydrogels for tissue regeneration and antitumor applications
title_full Sodium alginate-f-GO composite hydrogels for tissue regeneration and antitumor applications
title_fullStr Sodium alginate-f-GO composite hydrogels for tissue regeneration and antitumor applications
title_full_unstemmed Sodium alginate-f-GO composite hydrogels for tissue regeneration and antitumor applications
title_sort sodium alginate-f-go composite hydrogels for tissue regeneration and antitumor applications
publisher Elsevier B.V.
publishDate 2022
url http://eprints.utm.my/id/eprint/100948/1/SaifulIzwanAbdRazak2022_SodiumAlginatefGOCompositeHydrogel.pdf
http://eprints.utm.my/id/eprint/100948/
http://dx.doi.org/10.1016/j.ijbiomac.2022.03.091
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