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DC Field | Value | Language |
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dc.contributor.author | Chittasupho C. | |
dc.contributor.author | Angklomklew J. | |
dc.contributor.author | Thongnopkoon T. | |
dc.contributor.author | Senavongse W. | |
dc.contributor.author | Jantrawut P. | |
dc.contributor.author | Ruksiriwanich W. | |
dc.date.accessioned | 2022-03-10T13:17:37Z | - |
dc.date.available | 2022-03-10T13:17:37Z | - |
dc.date.issued | 2021 | |
dc.identifier.issn | 20734360 | |
dc.identifier.other | 2-s2.0-85118320818 | |
dc.identifier.uri | https://ir.swu.ac.th/jspui/handle/123456789/17573 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85118320818&doi=10.3390%2fpolym13203580&partnerID=40&md5=2d077d8f4d9dacd1bb9e0cc2d84899e9 | |
dc.description.abstract | A hydrogel scaffold is a localized drug delivery system that can maintain the therapeutic level of drug concentration at the tumor site. In this study, the biopolymer hydrogel scaffold encapsulating doxorubicin was fabricated from gelatin, sodium carboxymethyl cellulose, and gelatin/sodium carboxymethyl cellulose mixture using a lyophilization technique. The effects of a crosslinker on scaffold morphology and pore size were determined using scanning electron microscopy. The encapsulation efficiency and the release profile of doxorubicin from the hydrogel scaffolds were determined using UV-Vis spectrophotometry. The anti-proliferative effect of the scaffolds against the lung cancer cell line was investigated using an MTT assay. The results showed that scaffolds made from different types of natural polymer had different pore configurations and pore sizes. All scaffolds had high encapsulation efficiency and drug-controlled release profiles. The viability and proliferation of A549 cells, treated with gelatin, gelatin/SCMC, and SCMC scaffolds containing doxorubicin significantly decreased compared with control. These hydrogel scaffolds might provide a promising approach for developing a superior localized drug delivery system to kill lung cancer cells. © 2021 by the authors. Licensee MDPI, Basel, Switzerland. | |
dc.language | en | |
dc.subject | Biological organs | |
dc.subject | Biomolecules | |
dc.subject | Biopolymers | |
dc.subject | Cell culture | |
dc.subject | Cell proliferation | |
dc.subject | Cellulose | |
dc.subject | Controlled drug delivery | |
dc.subject | Efficiency | |
dc.subject | Hydrogels | |
dc.subject | Scaffolds (biology) | |
dc.subject | Scanning electron microscopy | |
dc.subject | Sodium | |
dc.subject | Targeted drug delivery | |
dc.subject | A549 cells | |
dc.subject | Doxorubicin | |
dc.subject | Drug-delivery systems | |
dc.subject | Encapsulation efficiency | |
dc.subject | Freeze drying | |
dc.subject | Gelatin | |
dc.subject | Hydrogel scaffolds | |
dc.subject | Localised | |
dc.subject | Lung cancer cells | |
dc.subject | Sodium carboxymethyl cellulose | |
dc.subject | Pore size | |
dc.subject | Cellulose | |
dc.subject | Efficiency | |
dc.subject | Freeze Drying | |
dc.subject | Gelatin | |
dc.subject | Scanning Electron Microscopy | |
dc.subject | Sodium | |
dc.title | Biopolymer hydrogel scaffolds containing doxorubicin as a localized drug delivery system for inhibiting lung cancer cell proliferation | |
dc.type | Article | |
dc.rights.holder | Scopus | |
dc.identifier.bibliograpycitation | Polymers. Vol 13, No.20 (2021) | |
dc.identifier.doi | 10.3390/polym13203580 | |
Appears in Collections: | Scopus 1983-2021 |
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