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Injectable hydrogels of newly designed brush biopolymers as sustained drug-delivery vehicle for melanoma treatment

Novel biocompatible and brush copolymers have been developed for cancer treatment using its controlled drug-release potential. Polyurethane graft on linear dextrin has been synthesized to control the hydrophilic–hydrophobic balance for regulated drug delivery. The properties of the graft copolymers...

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Autores principales: Shukla, Aparna, Singh, Akhand Pratap, Maiti, Pralay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884735/
https://www.ncbi.nlm.nih.gov/pubmed/33589586
http://dx.doi.org/10.1038/s41392-020-00431-0
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author Shukla, Aparna
Singh, Akhand Pratap
Maiti, Pralay
author_facet Shukla, Aparna
Singh, Akhand Pratap
Maiti, Pralay
author_sort Shukla, Aparna
collection PubMed
description Novel biocompatible and brush copolymers have been developed for cancer treatment using its controlled drug-release potential. Polyurethane graft on linear dextrin has been synthesized to control the hydrophilic–hydrophobic balance for regulated drug delivery. The properties of the graft copolymers have been tuned through graft density. The prepared grafts are thermally stable and mechanically strong. An injectable hydrogel has been developed by embedding the drug-loaded brush copolymers in methyl cellulose to better control the release for a prolonged period, importantly by keeping the drug release at a constant rate. Cellular studies indicate the biocompatible nature of the brush copolymers whose controlled and slow release of drug exhibit significant cytotoxic effects on cancer cells. Endocytosis of drug tagged contrast agent indicates greater transport of biologically active material inside cell as observed through cellular uptake studies. In vivo studies on melanoma mice exhibit the real efficacy of the controlled drug release from the injectable hydrogel with significant melanoma suppression without any side effects as opposed to severe toxic effects observed in conventional chemotherapy. Special application method of drug-loaded hydrogel just beneath the tumor makes this system incredibly effective through confinement. Thus, brush copolymer injectable hydrogel is a promising vehicle for control release of drug for cancer treatment in future.
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spelling pubmed-78847352021-02-25 Injectable hydrogels of newly designed brush biopolymers as sustained drug-delivery vehicle for melanoma treatment Shukla, Aparna Singh, Akhand Pratap Maiti, Pralay Signal Transduct Target Ther Article Novel biocompatible and brush copolymers have been developed for cancer treatment using its controlled drug-release potential. Polyurethane graft on linear dextrin has been synthesized to control the hydrophilic–hydrophobic balance for regulated drug delivery. The properties of the graft copolymers have been tuned through graft density. The prepared grafts are thermally stable and mechanically strong. An injectable hydrogel has been developed by embedding the drug-loaded brush copolymers in methyl cellulose to better control the release for a prolonged period, importantly by keeping the drug release at a constant rate. Cellular studies indicate the biocompatible nature of the brush copolymers whose controlled and slow release of drug exhibit significant cytotoxic effects on cancer cells. Endocytosis of drug tagged contrast agent indicates greater transport of biologically active material inside cell as observed through cellular uptake studies. In vivo studies on melanoma mice exhibit the real efficacy of the controlled drug release from the injectable hydrogel with significant melanoma suppression without any side effects as opposed to severe toxic effects observed in conventional chemotherapy. Special application method of drug-loaded hydrogel just beneath the tumor makes this system incredibly effective through confinement. Thus, brush copolymer injectable hydrogel is a promising vehicle for control release of drug for cancer treatment in future. Nature Publishing Group UK 2021-02-15 /pmc/articles/PMC7884735/ /pubmed/33589586 http://dx.doi.org/10.1038/s41392-020-00431-0 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Shukla, Aparna
Singh, Akhand Pratap
Maiti, Pralay
Injectable hydrogels of newly designed brush biopolymers as sustained drug-delivery vehicle for melanoma treatment
title Injectable hydrogels of newly designed brush biopolymers as sustained drug-delivery vehicle for melanoma treatment
title_full Injectable hydrogels of newly designed brush biopolymers as sustained drug-delivery vehicle for melanoma treatment
title_fullStr Injectable hydrogels of newly designed brush biopolymers as sustained drug-delivery vehicle for melanoma treatment
title_full_unstemmed Injectable hydrogels of newly designed brush biopolymers as sustained drug-delivery vehicle for melanoma treatment
title_short Injectable hydrogels of newly designed brush biopolymers as sustained drug-delivery vehicle for melanoma treatment
title_sort injectable hydrogels of newly designed brush biopolymers as sustained drug-delivery vehicle for melanoma treatment
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884735/
https://www.ncbi.nlm.nih.gov/pubmed/33589586
http://dx.doi.org/10.1038/s41392-020-00431-0
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