Cargando…

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....

Descripción completa

Detalles Bibliográficos
Autores principales: Kalinova, Radostina, Mladenova, Kirilka, Petrova, Svetla, Doumanov, Jordan, Dimitrov, Ivaylo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
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
_version_ 1785149807067660288
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
work_keys_str_mv AT kalinovaradostina solventfreesynthesisofmultifunctionalblockcopolymerandformationofdnaanddrugnanocarriers
AT mladenovakirilka solventfreesynthesisofmultifunctionalblockcopolymerandformationofdnaanddrugnanocarriers
AT petrovasvetla solventfreesynthesisofmultifunctionalblockcopolymerandformationofdnaanddrugnanocarriers
AT doumanovjordan solventfreesynthesisofmultifunctionalblockcopolymerandformationofdnaanddrugnanocarriers
AT dimitrovivaylo solventfreesynthesisofmultifunctionalblockcopolymerandformationofdnaanddrugnanocarriers