Novel Core–Shell Polyamine Phosphate Nanoparticles Self-Assembled from PEGylated Poly(allylamine hydrochloride) with Low Toxicity and Increased In Vivo Circulation Time
- Autores
- Andreozzi, Patrizia; Simó, Cristina; Moretti, Paolo; Martinez Porcel, Joaquin; Lüdtke, Tanja Ursula; Ramirez, Maria de Los Angeles; Tamberi, Lorenza; Marradi, Marco; Amenitsch, Heinz; Llop, Jordi; Ortore, Maria Grazia; Moya, Sergio Enrique
- Año de publicación
- 2021
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- An approach for reducing toxicity and enhancing therapeutic potential of supramolecular polyamine phosphate nanoparticles (PANs) through PEGylation of polyamines before their assembly into nanoparticles is presented here. It is shown that the number of polyethylene glycol (PEG) chains for polyamine largely influence physico-chemical properties of PANs and their biological endpoints. Poly(allylamine hydrochloride) (PAH) are functionalized through carbodiimide chemistry with three ratios of PEG molecules per PAH chain: 0.1, 1, and 10. PEGylated PAH is then assembled into PANs by exposing the polymer to phosphate buffer solution. PANs decrease size and surface charge with increasing PEG ratios as evidenced by dynamic light scattering and zeta potential measurements, with the ten PEG/PAH ratio PANs having practically zero charge. Small angle X-ray scattering (SAXS) proves that PEG chains form a shell around a polyamine core, which is responsible for the screening of positive charges. MTT experiments show that the screening of amine groups decreases nanoparticle toxicity, with the lowest toxicity for the 10 PEG/PAH ratio. Fluorescence correlation spectroscopy (FCS) proves less interaction with proteins for PEGylated PANs. Positron emission tomography (PET) imaging of 18F labelled PANs shows longer circulation time in healthy mice for PEGylated PANs than non-PEGylated ones.
Fil: Andreozzi, Patrizia. Basque Research and Technology Alliance; España. Università degli Studi di Firenze; Italia
Fil: Simó, Cristina. Basque Research and Technology Alliance; España
Fil: Moretti, Paolo. Università Politecnica delle Marche; Italia
Fil: Martinez Porcel, Joaquin. Basque Research and Technology Alliance; España
Fil: Lüdtke, Tanja Ursula. Basque Research and Technology Alliance; España
Fil: Ramirez, Maria de Los Angeles. Basque Research and Technology Alliance; España. Universidad Nacional de San Martin. Instituto de Nanosistemas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Tamberi, Lorenza. Basque Research and Technology Alliance; España
Fil: Marradi, Marco. Università degli Studi di Firenze; Italia
Fil: Amenitsch, Heinz. Graz University Of Technology.; Austria
Fil: Llop, Jordi. Basque Research and Technology Alliance; España. Centro de Investigación Biomédica En Red de Enfermedades Respiratorias; España
Fil: Ortore, Maria Grazia. Università Politecnica Delle Marche; Italia
Fil: Moya, Sergio Enrique. Basque Research and Technology Alliance; España - Materia
-
BIOLOGICAL FATE
POLYAMINE PHOSPHATE NANOPARTICLES
POLYETHYLENE GLYCOL
SELF ASSEMBLY
SMALL ANGLE X-RAY SCATTERING - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/166058
Ver los metadatos del registro completo
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Novel Core–Shell Polyamine Phosphate Nanoparticles Self-Assembled from PEGylated Poly(allylamine hydrochloride) with Low Toxicity and Increased In Vivo Circulation TimeAndreozzi, PatriziaSimó, CristinaMoretti, PaoloMartinez Porcel, JoaquinLüdtke, Tanja UrsulaRamirez, Maria de Los AngelesTamberi, LorenzaMarradi, MarcoAmenitsch, HeinzLlop, JordiOrtore, Maria GraziaMoya, Sergio EnriqueBIOLOGICAL FATEPOLYAMINE PHOSPHATE NANOPARTICLESPOLYETHYLENE GLYCOLSELF ASSEMBLYSMALL ANGLE X-RAY SCATTERINGhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1An approach for reducing toxicity and enhancing therapeutic potential of supramolecular polyamine phosphate nanoparticles (PANs) through PEGylation of polyamines before their assembly into nanoparticles is presented here. It is shown that the number of polyethylene glycol (PEG) chains for polyamine largely influence physico-chemical properties of PANs and their biological endpoints. Poly(allylamine hydrochloride) (PAH) are functionalized through carbodiimide chemistry with three ratios of PEG molecules per PAH chain: 0.1, 1, and 10. PEGylated PAH is then assembled into PANs by exposing the polymer to phosphate buffer solution. PANs decrease size and surface charge with increasing PEG ratios as evidenced by dynamic light scattering and zeta potential measurements, with the ten PEG/PAH ratio PANs having practically zero charge. Small angle X-ray scattering (SAXS) proves that PEG chains form a shell around a polyamine core, which is responsible for the screening of positive charges. MTT experiments show that the screening of amine groups decreases nanoparticle toxicity, with the lowest toxicity for the 10 PEG/PAH ratio. Fluorescence correlation spectroscopy (FCS) proves less interaction with proteins for PEGylated PANs. Positron emission tomography (PET) imaging of 18F labelled PANs shows longer circulation time in healthy mice for PEGylated PANs than non-PEGylated ones.Fil: Andreozzi, Patrizia. Basque Research and Technology Alliance; España. Università degli Studi di Firenze; ItaliaFil: Simó, Cristina. Basque Research and Technology Alliance; EspañaFil: Moretti, Paolo. Università Politecnica delle Marche; ItaliaFil: Martinez Porcel, Joaquin. Basque Research and Technology Alliance; EspañaFil: Lüdtke, Tanja Ursula. Basque Research and Technology Alliance; EspañaFil: Ramirez, Maria de Los Angeles. Basque Research and Technology Alliance; España. Universidad Nacional de San Martin. Instituto de Nanosistemas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Tamberi, Lorenza. Basque Research and Technology Alliance; EspañaFil: Marradi, Marco. Università degli Studi di Firenze; ItaliaFil: Amenitsch, Heinz. Graz University Of Technology.; AustriaFil: Llop, Jordi. Basque Research and Technology Alliance; España. Centro de Investigación Biomédica En Red de Enfermedades Respiratorias; EspañaFil: Ortore, Maria Grazia. Università Politecnica Delle Marche; ItaliaFil: Moya, Sergio Enrique. Basque Research and Technology Alliance; EspañaWiley VCH Verlag2021-09-02info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/166058Andreozzi, Patrizia; Simó, Cristina; Moretti, Paolo; Martinez Porcel, Joaquin; Lüdtke, Tanja Ursula; et al.; Novel Core–Shell Polyamine Phosphate Nanoparticles Self-Assembled from PEGylated Poly(allylamine hydrochloride) with Low Toxicity and Increased In Vivo Circulation Time; Wiley VCH Verlag; Small; 17; 35; 2-9-2021; 1-101613-68101613-6829CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/10.1002/smll.202102211info:eu-repo/semantics/altIdentifier/doi/10.1002/smll.202102211info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-11-05T10:19:47Zoai:ri.conicet.gov.ar:11336/166058instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-11-05 10:19:48.236CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
Novel Core–Shell Polyamine Phosphate Nanoparticles Self-Assembled from PEGylated Poly(allylamine hydrochloride) with Low Toxicity and Increased In Vivo Circulation Time |
| title |
Novel Core–Shell Polyamine Phosphate Nanoparticles Self-Assembled from PEGylated Poly(allylamine hydrochloride) with Low Toxicity and Increased In Vivo Circulation Time |
| spellingShingle |
Novel Core–Shell Polyamine Phosphate Nanoparticles Self-Assembled from PEGylated Poly(allylamine hydrochloride) with Low Toxicity and Increased In Vivo Circulation Time Andreozzi, Patrizia BIOLOGICAL FATE POLYAMINE PHOSPHATE NANOPARTICLES POLYETHYLENE GLYCOL SELF ASSEMBLY SMALL ANGLE X-RAY SCATTERING |
| title_short |
Novel Core–Shell Polyamine Phosphate Nanoparticles Self-Assembled from PEGylated Poly(allylamine hydrochloride) with Low Toxicity and Increased In Vivo Circulation Time |
| title_full |
Novel Core–Shell Polyamine Phosphate Nanoparticles Self-Assembled from PEGylated Poly(allylamine hydrochloride) with Low Toxicity and Increased In Vivo Circulation Time |
| title_fullStr |
Novel Core–Shell Polyamine Phosphate Nanoparticles Self-Assembled from PEGylated Poly(allylamine hydrochloride) with Low Toxicity and Increased In Vivo Circulation Time |
| title_full_unstemmed |
Novel Core–Shell Polyamine Phosphate Nanoparticles Self-Assembled from PEGylated Poly(allylamine hydrochloride) with Low Toxicity and Increased In Vivo Circulation Time |
| title_sort |
Novel Core–Shell Polyamine Phosphate Nanoparticles Self-Assembled from PEGylated Poly(allylamine hydrochloride) with Low Toxicity and Increased In Vivo Circulation Time |
| dc.creator.none.fl_str_mv |
Andreozzi, Patrizia Simó, Cristina Moretti, Paolo Martinez Porcel, Joaquin Lüdtke, Tanja Ursula Ramirez, Maria de Los Angeles Tamberi, Lorenza Marradi, Marco Amenitsch, Heinz Llop, Jordi Ortore, Maria Grazia Moya, Sergio Enrique |
| author |
Andreozzi, Patrizia |
| author_facet |
Andreozzi, Patrizia Simó, Cristina Moretti, Paolo Martinez Porcel, Joaquin Lüdtke, Tanja Ursula Ramirez, Maria de Los Angeles Tamberi, Lorenza Marradi, Marco Amenitsch, Heinz Llop, Jordi Ortore, Maria Grazia Moya, Sergio Enrique |
| author_role |
author |
| author2 |
Simó, Cristina Moretti, Paolo Martinez Porcel, Joaquin Lüdtke, Tanja Ursula Ramirez, Maria de Los Angeles Tamberi, Lorenza Marradi, Marco Amenitsch, Heinz Llop, Jordi Ortore, Maria Grazia Moya, Sergio Enrique |
| author2_role |
author author author author author author author author author author author |
| dc.subject.none.fl_str_mv |
BIOLOGICAL FATE POLYAMINE PHOSPHATE NANOPARTICLES POLYETHYLENE GLYCOL SELF ASSEMBLY SMALL ANGLE X-RAY SCATTERING |
| topic |
BIOLOGICAL FATE POLYAMINE PHOSPHATE NANOPARTICLES POLYETHYLENE GLYCOL SELF ASSEMBLY SMALL ANGLE X-RAY SCATTERING |
| purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
| dc.description.none.fl_txt_mv |
An approach for reducing toxicity and enhancing therapeutic potential of supramolecular polyamine phosphate nanoparticles (PANs) through PEGylation of polyamines before their assembly into nanoparticles is presented here. It is shown that the number of polyethylene glycol (PEG) chains for polyamine largely influence physico-chemical properties of PANs and their biological endpoints. Poly(allylamine hydrochloride) (PAH) are functionalized through carbodiimide chemistry with three ratios of PEG molecules per PAH chain: 0.1, 1, and 10. PEGylated PAH is then assembled into PANs by exposing the polymer to phosphate buffer solution. PANs decrease size and surface charge with increasing PEG ratios as evidenced by dynamic light scattering and zeta potential measurements, with the ten PEG/PAH ratio PANs having practically zero charge. Small angle X-ray scattering (SAXS) proves that PEG chains form a shell around a polyamine core, which is responsible for the screening of positive charges. MTT experiments show that the screening of amine groups decreases nanoparticle toxicity, with the lowest toxicity for the 10 PEG/PAH ratio. Fluorescence correlation spectroscopy (FCS) proves less interaction with proteins for PEGylated PANs. Positron emission tomography (PET) imaging of 18F labelled PANs shows longer circulation time in healthy mice for PEGylated PANs than non-PEGylated ones. Fil: Andreozzi, Patrizia. Basque Research and Technology Alliance; España. Università degli Studi di Firenze; Italia Fil: Simó, Cristina. Basque Research and Technology Alliance; España Fil: Moretti, Paolo. Università Politecnica delle Marche; Italia Fil: Martinez Porcel, Joaquin. Basque Research and Technology Alliance; España Fil: Lüdtke, Tanja Ursula. Basque Research and Technology Alliance; España Fil: Ramirez, Maria de Los Angeles. Basque Research and Technology Alliance; España. Universidad Nacional de San Martin. Instituto de Nanosistemas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Tamberi, Lorenza. Basque Research and Technology Alliance; España Fil: Marradi, Marco. Università degli Studi di Firenze; Italia Fil: Amenitsch, Heinz. Graz University Of Technology.; Austria Fil: Llop, Jordi. Basque Research and Technology Alliance; España. Centro de Investigación Biomédica En Red de Enfermedades Respiratorias; España Fil: Ortore, Maria Grazia. Università Politecnica Delle Marche; Italia Fil: Moya, Sergio Enrique. Basque Research and Technology Alliance; España |
| description |
An approach for reducing toxicity and enhancing therapeutic potential of supramolecular polyamine phosphate nanoparticles (PANs) through PEGylation of polyamines before their assembly into nanoparticles is presented here. It is shown that the number of polyethylene glycol (PEG) chains for polyamine largely influence physico-chemical properties of PANs and their biological endpoints. Poly(allylamine hydrochloride) (PAH) are functionalized through carbodiimide chemistry with three ratios of PEG molecules per PAH chain: 0.1, 1, and 10. PEGylated PAH is then assembled into PANs by exposing the polymer to phosphate buffer solution. PANs decrease size and surface charge with increasing PEG ratios as evidenced by dynamic light scattering and zeta potential measurements, with the ten PEG/PAH ratio PANs having practically zero charge. Small angle X-ray scattering (SAXS) proves that PEG chains form a shell around a polyamine core, which is responsible for the screening of positive charges. MTT experiments show that the screening of amine groups decreases nanoparticle toxicity, with the lowest toxicity for the 10 PEG/PAH ratio. Fluorescence correlation spectroscopy (FCS) proves less interaction with proteins for PEGylated PANs. Positron emission tomography (PET) imaging of 18F labelled PANs shows longer circulation time in healthy mice for PEGylated PANs than non-PEGylated ones. |
| publishDate |
2021 |
| dc.date.none.fl_str_mv |
2021-09-02 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
| format |
article |
| status_str |
publishedVersion |
| dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/166058 Andreozzi, Patrizia; Simó, Cristina; Moretti, Paolo; Martinez Porcel, Joaquin; Lüdtke, Tanja Ursula; et al.; Novel Core–Shell Polyamine Phosphate Nanoparticles Self-Assembled from PEGylated Poly(allylamine hydrochloride) with Low Toxicity and Increased In Vivo Circulation Time; Wiley VCH Verlag; Small; 17; 35; 2-9-2021; 1-10 1613-6810 1613-6829 CONICET Digital CONICET |
| url |
http://hdl.handle.net/11336/166058 |
| identifier_str_mv |
Andreozzi, Patrizia; Simó, Cristina; Moretti, Paolo; Martinez Porcel, Joaquin; Lüdtke, Tanja Ursula; et al.; Novel Core–Shell Polyamine Phosphate Nanoparticles Self-Assembled from PEGylated Poly(allylamine hydrochloride) with Low Toxicity and Increased In Vivo Circulation Time; Wiley VCH Verlag; Small; 17; 35; 2-9-2021; 1-10 1613-6810 1613-6829 CONICET Digital CONICET |
| dc.language.none.fl_str_mv |
eng |
| language |
eng |
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info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/10.1002/smll.202102211 info:eu-repo/semantics/altIdentifier/doi/10.1002/smll.202102211 |
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info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
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openAccess |
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https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
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application/pdf application/pdf |
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Wiley VCH Verlag |
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Wiley VCH Verlag |
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reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
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Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
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dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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