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Solvent-Free Synthesis of Multifunctional Block Copolymer and Formation of DNA and Drug Nanocarriers
The synthesis of well-defined multifunctional polymers is of great importance for the development of complex materials for biomedical applications. In the current work, novel and multi-amino-functional diblock copolymer for potential gene and drug delivery applications was successfully synthesized....
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10675335/ https://www.ncbi.nlm.nih.gov/pubmed/37999289 http://dx.doi.org/10.3390/nano13222936 |
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author | Kalinova, Radostina Mladenova, Kirilka Petrova, Svetla Doumanov, Jordan Dimitrov, Ivaylo |
author_facet | Kalinova, Radostina Mladenova, Kirilka Petrova, Svetla Doumanov, Jordan Dimitrov, Ivaylo |
author_sort | Kalinova, Radostina |
collection | PubMed |
description | The synthesis of well-defined multifunctional polymers is of great importance for the development of complex materials for biomedical applications. In the current work, novel and multi-amino-functional diblock copolymer for potential gene and drug delivery applications was successfully synthesized. A highly efficient one-step and quantitative modification of an alkyne-functional polycarbonate-based precursor was performed, yielding double hydrophilic block copolymer with densely grafted primary amine side groups. The obtained positively charged block copolymer co-associated with DNA, forming stable and biocompatible nanosized polyplexes. Furthermore, polyion complex (PIC) micelles with tunable surface charge and decorated with cell targeting moieties were obtained as a result of direct mixing in aqueous media of the multi-amino-functional block copolymer and a previously synthesized oppositely charged block copolymer bearing disaccharide end-group. The obtained well-defined nanosized PIC–micelles were loaded with the hydrophobic drug curcumin. Both types of nanoaggregates (polyplexes and PIC–micelles) were physico-chemically characterized. Moreover, initial in vitro evaluations were performed to assess the nanocarriers’ potential for biomedical applications. |
format | Online Article Text |
id | pubmed-10675335 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-106753352023-11-13 Solvent-Free Synthesis of Multifunctional Block Copolymer and Formation of DNA and Drug Nanocarriers Kalinova, Radostina Mladenova, Kirilka Petrova, Svetla Doumanov, Jordan Dimitrov, Ivaylo Nanomaterials (Basel) Article The synthesis of well-defined multifunctional polymers is of great importance for the development of complex materials for biomedical applications. In the current work, novel and multi-amino-functional diblock copolymer for potential gene and drug delivery applications was successfully synthesized. A highly efficient one-step and quantitative modification of an alkyne-functional polycarbonate-based precursor was performed, yielding double hydrophilic block copolymer with densely grafted primary amine side groups. The obtained positively charged block copolymer co-associated with DNA, forming stable and biocompatible nanosized polyplexes. Furthermore, polyion complex (PIC) micelles with tunable surface charge and decorated with cell targeting moieties were obtained as a result of direct mixing in aqueous media of the multi-amino-functional block copolymer and a previously synthesized oppositely charged block copolymer bearing disaccharide end-group. The obtained well-defined nanosized PIC–micelles were loaded with the hydrophobic drug curcumin. Both types of nanoaggregates (polyplexes and PIC–micelles) were physico-chemically characterized. Moreover, initial in vitro evaluations were performed to assess the nanocarriers’ potential for biomedical applications. MDPI 2023-11-13 /pmc/articles/PMC10675335/ /pubmed/37999289 http://dx.doi.org/10.3390/nano13222936 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kalinova, Radostina Mladenova, Kirilka Petrova, Svetla Doumanov, Jordan Dimitrov, Ivaylo Solvent-Free Synthesis of Multifunctional Block Copolymer and Formation of DNA and Drug Nanocarriers |
title | Solvent-Free Synthesis of Multifunctional Block Copolymer and Formation of DNA and Drug Nanocarriers |
title_full | Solvent-Free Synthesis of Multifunctional Block Copolymer and Formation of DNA and Drug Nanocarriers |
title_fullStr | Solvent-Free Synthesis of Multifunctional Block Copolymer and Formation of DNA and Drug Nanocarriers |
title_full_unstemmed | Solvent-Free Synthesis of Multifunctional Block Copolymer and Formation of DNA and Drug Nanocarriers |
title_short | Solvent-Free Synthesis of Multifunctional Block Copolymer and Formation of DNA and Drug Nanocarriers |
title_sort | solvent-free synthesis of multifunctional block copolymer and formation of dna and drug nanocarriers |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10675335/ https://www.ncbi.nlm.nih.gov/pubmed/37999289 http://dx.doi.org/10.3390/nano13222936 |
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