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Identification of novel cyanoacrylate monomers for use in nanoparticle drug delivery systems prepared by miniemulsion polymerisation – A multistep screening approach

Poly (alkyl cyanoacrylate) (PACA) polymeric nanoparticles (NPs) are promising drug carriers in drug delivery. However, the selection of commercially available alkyl cyanoacrylate (ACA) monomers is limited, because most monomers were designed for use in medical and industrial glues and later repurpos...

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Autores principales: Hyldbakk, Astrid, Mørch, Yrr, Snipstad, Sofie, Åslund, Andreas K.O., Klinkenberg, Geir, Nakstad, Vu To, Wågbø, Ane-Marit, Schmid, Ruth, Molesworth, Peter P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9310130/
https://www.ncbi.nlm.nih.gov/pubmed/35898812
http://dx.doi.org/10.1016/j.ijpx.2022.100124
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author Hyldbakk, Astrid
Mørch, Yrr
Snipstad, Sofie
Åslund, Andreas K.O.
Klinkenberg, Geir
Nakstad, Vu To
Wågbø, Ane-Marit
Schmid, Ruth
Molesworth, Peter P.
author_facet Hyldbakk, Astrid
Mørch, Yrr
Snipstad, Sofie
Åslund, Andreas K.O.
Klinkenberg, Geir
Nakstad, Vu To
Wågbø, Ane-Marit
Schmid, Ruth
Molesworth, Peter P.
author_sort Hyldbakk, Astrid
collection PubMed
description Poly (alkyl cyanoacrylate) (PACA) polymeric nanoparticles (NPs) are promising drug carriers in drug delivery. However, the selection of commercially available alkyl cyanoacrylate (ACA) monomers is limited, because most monomers were designed for use in medical and industrial glues and later repurposed for drug encapsulation. This study therefore aimed to seek out novel ACA materials for use in NP systems using a toxicity led screening approach. A multistep strategy, including cytotoxicity screening of alcohols as degradation products of PACA (44 alcohols), NPs (14 polymers), and a final in vivo study (2 polymers) gave poly (2-ethylhexyl cyanoacrylate) PEHCA as a promising novel PACA candidate. For the first time, this work presents cytotoxicity data on several novel ACAs, PEHCA in vivo toxicity data, and miniemulsion polymerisation-based encapsulation of the cabazitaxel and NR688 in novel PACA candidates. Furthermore, several of the ACA candidates were compatible with a wider selection of lipophilic active pharmaceutical ingredients (APIs) versus commercially available controls. Combined, this work demonstrates the potential benefits of expanding the array of available ACA materials in drug delivery. Novel ACAs have the potential to encapsulate a wider range of APIs in miniemulsion polymerisation processes and may also broaden PACA applicability in other fields.
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spelling pubmed-93101302022-07-26 Identification of novel cyanoacrylate monomers for use in nanoparticle drug delivery systems prepared by miniemulsion polymerisation – A multistep screening approach Hyldbakk, Astrid Mørch, Yrr Snipstad, Sofie Åslund, Andreas K.O. Klinkenberg, Geir Nakstad, Vu To Wågbø, Ane-Marit Schmid, Ruth Molesworth, Peter P. Int J Pharm X Research Paper Poly (alkyl cyanoacrylate) (PACA) polymeric nanoparticles (NPs) are promising drug carriers in drug delivery. However, the selection of commercially available alkyl cyanoacrylate (ACA) monomers is limited, because most monomers were designed for use in medical and industrial glues and later repurposed for drug encapsulation. This study therefore aimed to seek out novel ACA materials for use in NP systems using a toxicity led screening approach. A multistep strategy, including cytotoxicity screening of alcohols as degradation products of PACA (44 alcohols), NPs (14 polymers), and a final in vivo study (2 polymers) gave poly (2-ethylhexyl cyanoacrylate) PEHCA as a promising novel PACA candidate. For the first time, this work presents cytotoxicity data on several novel ACAs, PEHCA in vivo toxicity data, and miniemulsion polymerisation-based encapsulation of the cabazitaxel and NR688 in novel PACA candidates. Furthermore, several of the ACA candidates were compatible with a wider selection of lipophilic active pharmaceutical ingredients (APIs) versus commercially available controls. Combined, this work demonstrates the potential benefits of expanding the array of available ACA materials in drug delivery. Novel ACAs have the potential to encapsulate a wider range of APIs in miniemulsion polymerisation processes and may also broaden PACA applicability in other fields. Elsevier 2022-07-20 /pmc/articles/PMC9310130/ /pubmed/35898812 http://dx.doi.org/10.1016/j.ijpx.2022.100124 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Paper
Hyldbakk, Astrid
Mørch, Yrr
Snipstad, Sofie
Åslund, Andreas K.O.
Klinkenberg, Geir
Nakstad, Vu To
Wågbø, Ane-Marit
Schmid, Ruth
Molesworth, Peter P.
Identification of novel cyanoacrylate monomers for use in nanoparticle drug delivery systems prepared by miniemulsion polymerisation – A multistep screening approach
title Identification of novel cyanoacrylate monomers for use in nanoparticle drug delivery systems prepared by miniemulsion polymerisation – A multistep screening approach
title_full Identification of novel cyanoacrylate monomers for use in nanoparticle drug delivery systems prepared by miniemulsion polymerisation – A multistep screening approach
title_fullStr Identification of novel cyanoacrylate monomers for use in nanoparticle drug delivery systems prepared by miniemulsion polymerisation – A multistep screening approach
title_full_unstemmed Identification of novel cyanoacrylate monomers for use in nanoparticle drug delivery systems prepared by miniemulsion polymerisation – A multistep screening approach
title_short Identification of novel cyanoacrylate monomers for use in nanoparticle drug delivery systems prepared by miniemulsion polymerisation – A multistep screening approach
title_sort identification of novel cyanoacrylate monomers for use in nanoparticle drug delivery systems prepared by miniemulsion polymerisation – a multistep screening approach
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9310130/
https://www.ncbi.nlm.nih.gov/pubmed/35898812
http://dx.doi.org/10.1016/j.ijpx.2022.100124
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