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Physicochemical Properties of A New PEGylated Polybenzofulvene Brush for Drug Encapsulation

Autor: Chiara Botta, Gianluca Giorgi, Mariano Licciardi, Antonella Caterina Boccia, Germano Giuliani, Eugenio Paccagnini, Vincenzo Razzano, Annalisa Reale, Mariangela Gentile, Marco Paolino, Filippo Samperi, Alessandro Donati, Laura Salvini, Raniero Mendichi, Daniele Piovani, Andrea Cappelli, Cristina Savoca

Publikováno v: Pharmaceutics 11 (2019): 1–22. doi:10.3390/pharmaceutics11090444
info:cnr-pdr/source/autori:Marco Paolino, Annalisa Reale, Vincenzo Razzano, Germano Giuliani, Alessandro Donati, Gianluca Giorgi, Antonella Caterina Boccia, Raniero Mendichi, Daniele Piovani, Chiara Botta, Laura Salvini Filippo Samperi, Cristina Savoca, Mariano Licciardi, Eugenio Paccagnini, Mariangela Gentile, Andrea Cappelli/titolo:Physicochemical Properties of a New PEGylated Polybenzofulvene Brush for Drug Encapsulation/doi:10.3390%2Fpharmaceutics11090444/rivista:Pharmaceutics/anno:2019/pagina_da:1/pagina_a:22/intervallo_pagine:1–22/volume:11
Pharmaceutics, Vol 11, Iss 9, p 444 (2019)
Pharmaceutics
Volume 11
Issue 9

A new polymer brush was synthesized by spontaneous polymerization of benzofulvene macromonomer 6-MOEG-9-T-BF3k bearing a nona(ethylene glycol) side chain linked to the 3-phenylindene scaffold by means of a triazole heterocycle. The polymer structure

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb08e016e445f56100bade1ac3e800fe
https://doi.org/10.3390/pharmaceutics11090444

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Synthesis and Spontaneous Polymerization of Oligo(ethylene glycol)-Conjugated Benzofulvene Macromonomers. A Polymer Brush Forming a Physical Hydrogel

Autor: Salvatore Vomero, Andrea Cappelli, Lucia Zetta, Fabio Bertini, B. Dapas, R. Farra, Antonella Caterina Boccia, Marianna Aggravi, Romano Lapasin, Simone Galeazzi, Gabriele Grassi, Maurizio Anzini, Filippo Samperi, Mario Grassi, Alessandro Donati, Germano Giuliani

Publikováno v: Macromolecules
42 (2009): 2368–2378. doi:10.1021/ma802429g
info:cnr-pdr/source/autori:A. Cappelli; S. Galeazzi; G. Giuliani; M. Anzini; M. Grassi; R. Lapasin; G. Grassi; R. Farra; B. Dapas; M. Aggravi; A. Donati; L. Zetta; A.C. Boccia; F. Bertini; F. Samperi; S. Vomero/titolo:Synthesis and spontaneous polymerization of oligo(ethylene glycol)-conjugated benzofulvene macromonomers. A polymer brush forming a physical hydrogel/doi:10.1021%2Fma802429g/rivista:Macromolecules (Print)/anno:2009/pagina_da:2368/pagina_a:2378/intervallo_pagine:2368–2378/volume:42

Two methyl end-capped oligo(ethylene glycol) esters (1a,b) of benzofulvene derivative BF1 were synthesized and induced to polymerize spontaneously by solvent removal to give poly-1a,b showing both NMR and absorption/emission spectra very similar to t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c297c766307e97befc9eb77e111bd8a3
https://doi.org/10.1021/ma802429g

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Akademický článek

Single-Component Starch-Based Hydrogels for Therapeutic Delivery.

Autor: Pulvirenti A; Istituto di Scienze e Tecnologie Chimiche (SCITEC) 'Giulio Natta', C.N.R., Via Alfonso Corti 12, 20133 Milano, Italy., Boccia AC; Istituto di Scienze e Tecnologie Chimiche (SCITEC) 'Giulio Natta', C.N.R., Via Alfonso Corti 12, 20133 Milano, Italy., Constantin C; 'Victor Babes' National Institute of Pathology, 99-101 Splaiul Independenței, 050096 Bucharest, Romania.; Colentina Clinical Hospital, 19-21, Sos Stefan Cel Mare, 020125 Bucharest, Romania., Surcel M; 'Victor Babes' National Institute of Pathology, 99-101 Splaiul Independenței, 050096 Bucharest, Romania., Munteanu A; 'Victor Babes' National Institute of Pathology, 99-101 Splaiul Independenței, 050096 Bucharest, Romania., Peteu VE; 'Victor Babes' National Institute of Pathology, 99-101 Splaiul Independenței, 050096 Bucharest, Romania.; Doctoral School, Politechnica University of Bucharest, 313 Splaiul Independenței, 060042 Bucharest, Romania., Neagu M; 'Victor Babes' National Institute of Pathology, 99-101 Splaiul Independenței, 050096 Bucharest, Romania.

Publikováno v: Molecules (Basel, Switzerland) [Molecules] 2024 Nov 20; Vol. 29 (22). Date of Electronic Publication: 2024 Nov 20.

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Akademický článek

Reactivity of a Morita-Baylis-Hillman Adduct Derivative Bearing a Triphenylamine Moiety with Lysine Models.

Autor: Venditti J; Dipartimento di Biotecnologie, Chimica e Farmacia, Università degli Studi di Siena, Via Aldo Moro 2, 53100, Siena, Italy., Saletti M; Dipartimento di Biotecnologie, Chimica e Farmacia, Università degli Studi di Siena, Via Aldo Moro 2, 53100, Siena, Italy., Paolino M; Dipartimento di Biotecnologie, Chimica e Farmacia, Università degli Studi di Siena, Via Aldo Moro 2, 53100, Siena, Italy., Contena S; Dipartimento di Biotecnologie, Chimica e Farmacia, Università degli Studi di Siena, Via Aldo Moro 2, 53100, Siena, Italy., Bonechi C; Dipartimento di Biotecnologie, Chimica e Farmacia, Università degli Studi di Siena, Via Aldo Moro 2, 53100, Siena, Italy., Giuliani G; Dipartimento di Biotecnologie, Chimica e Farmacia, Università degli Studi di Siena, Via Aldo Moro 2, 53100, Siena, Italy., Giorgi G; Dipartimento di Biotecnologie, Chimica e Farmacia, Università degli Studi di Siena, Via Aldo Moro 2, 53100, Siena, Italy., Boccia AC; Istituto di Scienze e Tecnologie Chimiche 'G. Natta' - SCITEC (CNR), Via A. Corti 12, 20133, Milano, Italy., Botta C; Istituto di Scienze e Tecnologie Chimiche 'G. Natta' - SCITEC (CNR), Via A. Corti 12, 20133, Milano, Italy., Blancafort L; Department of Chemistry, Institute of Computational Chemistry and Catalysis, University of Girona, C/ M. A. Capmany 69, 17003, Girona, Spain., Cappelli A; Dipartimento di Biotecnologie, Chimica e Farmacia, Università degli Studi di Siena, Via Aldo Moro 2, 53100, Siena, Italy.

Publikováno v: Chemistry, an Asian journal [Chem Asian J] 2024 Oct 16; Vol. 19 (20), pp. e202400617. Date of Electronic Publication: 2024 Sep 21.

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