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Exploring the enzymatic degradation of poly(glycerol adipate).
Swainson, Sadie M E; Taresco, Vincenzo; Pearce, Amanda K; Clapp, Lucie H; Ager, Barry; McAllister, Mark; Bosquillon, Cynthia; Garnett, Martin C.
Afiliación
  • Swainson SME; School of Pharmacy, University of Nottingham, Nottingham NG7 2RD, United Kingdom.
  • Taresco V; School of Pharmacy, University of Nottingham, Nottingham NG7 2RD, United Kingdom.
  • Pearce AK; School of Pharmacy, University of Nottingham, Nottingham NG7 2RD, United Kingdom.
  • Clapp LH; Department of Medicine, University College London, London WC1E 6JF, United Kingdom.
  • Ager B; Drug Product Design, Pfizer Ltd, Sandwich CT13 9ND, United Kingdom.
  • McAllister M; Drug Product Design, Pfizer Ltd, Sandwich CT13 9ND, United Kingdom.
  • Bosquillon C; School of Pharmacy, University of Nottingham, Nottingham NG7 2RD, United Kingdom.
  • Garnett MC; School of Pharmacy, University of Nottingham, Nottingham NG7 2RD, United Kingdom. Electronic address: martin.garnett@nottingham.ac.uk.
Eur J Pharm Biopharm ; 142: 377-386, 2019 Sep.
Article en En | MEDLINE | ID: mdl-31319123
Poly(glycerol adipate) (PGA) is a biodegradable, biocompatible, polymer with a great deal of potential in the field of drug delivery. Active drug molecules can be conjugated to the polymer backbone or encapsulated in self-assembled nanoparticles for targeted and systemic delivery. Here, a range of techniques have been used to characterise the enzymatic degradation of PGA extensively for the first time and to provide an indication of the way the polymer will behave and release drug payloads in vivo. Dynamic Light Scattering was used to monitor change in nanoparticle size, indicative of degradation. The release of a fluorescent dye, coupled to PGA, upon incubation with enzymes was measured over a 96 h period as a model of drug release from polymer drug conjugates. The changes to the chemical structure and molecular weight of PGA following enzyme exposure were characterised using FTIR, NMR and GPC. These techniques provided evidence of the biodegradability of PGA, its susceptibility to degradation by a range of enzymes commonly found in the human body and the polymer's potential as a drug delivery platform.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polímeros / Adipatos / Plásticos Biodegradables / Glicerol Límite: Humans Idioma: En Revista: Eur J Pharm Biopharm Asunto de la revista: FARMACIA / FARMACOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polímeros / Adipatos / Plásticos Biodegradables / Glicerol Límite: Humans Idioma: En Revista: Eur J Pharm Biopharm Asunto de la revista: FARMACIA / FARMACOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido
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