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Injectable Biodegradable Silica Depot: Two Months of Sustained Release of the Blood Glucose Lowering Peptide, Pramlintide.
Tyagi, Puneet; Koskinen, Mika; Mikkola, Jari; Sarkhel, Sanjay; Leino, Lasse; Seth, Asha; Madalli, Shimona; Will, Sarah; Howard, Victor G; Brant, Helen; Corkill, Dominic.
Afiliación
  • Tyagi P; Dosage Form Design and Development, BioPharmaceuticals R&D, AstraZeneca, Gaithersburg, MD 20874, USA.
  • Koskinen M; DelSiTech Ltd., PharmaCity, Itäinen Pitkäkatu 4 B, 20520 Turku, Finland.
  • Mikkola J; DelSiTech Ltd., PharmaCity, Itäinen Pitkäkatu 4 B, 20520 Turku, Finland.
  • Sarkhel S; DelSiTech Ltd., PharmaCity, Itäinen Pitkäkatu 4 B, 20520 Turku, Finland.
  • Leino L; DelSiTech Ltd., PharmaCity, Itäinen Pitkäkatu 4 B, 20520 Turku, Finland.
  • Seth A; Renal BioScience, Early CVRM, BioPharmaceuticals R&D, AstraZeneca, Cambridge CB21 6GP, UK.
  • Madalli S; Renal BioScience, Early CVRM, BioPharmaceuticals R&D, AstraZeneca, Cambridge CB21 6GP, UK.
  • Will S; Metabolism BioScience, Early CVRM, BioPharmaceuticals R&D, AstraZeneca, Gaithersburg, MD 20878, USA.
  • Howard VG; Metabolism BioScience, Early CVRM, BioPharmaceuticals R&D, AstraZeneca, Gaithersburg, MD 20878, USA.
  • Brant H; Animal Science & Technologies UK, Clinical Pharmacology & Safety Sciences, AstraZeneca, Cambridge CB21 6GP, UK.
  • Corkill D; Early R&I BioPharmaceuticals R&D, AstraZeneca, Cambridge CB21 6GP, UK.
Pharmaceutics ; 14(3)2022 Mar 02.
Article en En | MEDLINE | ID: mdl-35335929
Diabetes mellitus is a major healthcare challenge. Pramlintide, a peptide analogue of the hormone amylin, is currently used as an adjunct with insulin for patients who fail to achieve glycemic control with only insulin therapy. However, hypoglycemia is the dominant risk factor associated with such approaches and careful dosing of both drugs is needed. To mitigate this risk factor and compliance issues related to multiple dosing of different drugs, sustained delivery of Pramlintide from silica depot administered subcutaneously (SC) was investigated in a rat model. The pramlintide-silica microparticle hydrogel depot was formulated by spray drying of silica sol-gels. In vitro dissolution tests revealed an initial burst of pramlintide followed by controlled release due to the dissolution of the silica matrix. At higher dosing, pramlintide released from subcutaneously administered silica depot in rats showed a steady concentration of 500 pM in serum for 60 days. Released pramlintide retained its pharmacological activity in vivo, as evidenced by loss of weight. The biodegradable silica matrix offers a sustained release of pramlintide for at least two months in the rat model and shows potential for clinical applications.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Pharmaceutics Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Pharmaceutics Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Suiza