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Continuous drying of a protein-type drug using scaled-up fiber formation with HP-ß-CD matrix resulting in a directly compressible powder for tableting.
Vass, Panna; Nagy, Zsombor K; Kóczián, Rita; Fehér, Csaba; Démuth, Balázs; Szabó, Edina; Andersen, Sune K; Vigh, Tamás; Verreck, Geert; Csontos, István; Marosi, György; Hirsch, Edit.
Afiliação
  • Vass P; Department of Organic Chemistry and Technology, Budapest University of Technology and Economics (BME), H-1111, Budapest, Muegyetem rakpart 3, Hungary.
  • Nagy ZK; Department of Organic Chemistry and Technology, Budapest University of Technology and Economics (BME), H-1111, Budapest, Muegyetem rakpart 3, Hungary. Electronic address: zsknagy@oct.bme.hu.
  • Kóczián R; Department of Organic Chemistry and Technology, Budapest University of Technology and Economics (BME), H-1111, Budapest, Muegyetem rakpart 3, Hungary.
  • Fehér C; Department of Applied Biotechnology and Food Science, Budapest University of Technology and Economics (BME), H-1111, Budapest, Muegyetem rakpart 3, Hungary.
  • Démuth B; Department of Organic Chemistry and Technology, Budapest University of Technology and Economics (BME), H-1111, Budapest, Muegyetem rakpart 3, Hungary.
  • Szabó E; Department of Organic Chemistry and Technology, Budapest University of Technology and Economics (BME), H-1111, Budapest, Muegyetem rakpart 3, Hungary.
  • Andersen SK; Oral Solids Development, Janssen R&D, B-2340 Beerse, Turnhoutseweg 30, Belgium.
  • Vigh T; Oral Solids Development, Janssen R&D, B-2340 Beerse, Turnhoutseweg 30, Belgium.
  • Verreck G; Oral Solids Development, Janssen R&D, B-2340 Beerse, Turnhoutseweg 30, Belgium.
  • Csontos I; Department of Organic Chemistry and Technology, Budapest University of Technology and Economics (BME), H-1111, Budapest, Muegyetem rakpart 3, Hungary.
  • Marosi G; Department of Organic Chemistry and Technology, Budapest University of Technology and Economics (BME), H-1111, Budapest, Muegyetem rakpart 3, Hungary.
  • Hirsch E; PharmaTech Model Laboratory (PML), Center for University-Industry Cooperation (FIEK), H-1111, Budapest, Egry József utca 1, Hungary. Electronic address: edit.hirsch@gmail.com.
Eur J Pharm Sci ; 141: 105089, 2020 Jan 01.
Article em En | MEDLINE | ID: mdl-31626967
The goals of this work were to evaluate if high-speed electrospinning can be used as a gentle and continuous drying technology to produce protein-containing cyclodextrin-based fibers from an aqueous solution and to convert the produced protein-cyclodextrin fibers into a directly compressible powder. A 400 mL/h feeding rate was used during the electrospinning experiments, corresponding to a ~270 g/h production rate of the dried material. The produced fibers were collected in a cyclone. The fibers were found grindable without secondary drying, and the ground powder was mixed with tableting excipients and was successfully tableted by direct compression. The model protein-type drug (ß-galactosidase) remained stable during each of the processing steps (electrospinning, grinding, tableting) and after 6 months of storage at room temperature in the tablets. The obtained results demonstrate that high speed electrospinning can be a gentle alternative to traditional drying methods used for protein-type drugs, and that tablet formulation is achievable from the electrospun material prepared this way.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tecnologia Farmacêutica / Beta-Galactosidase / 2-Hidroxipropil-beta-Ciclodextrina Idioma: En Revista: Eur J Pharm Sci Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tecnologia Farmacêutica / Beta-Galactosidase / 2-Hidroxipropil-beta-Ciclodextrina Idioma: En Revista: Eur J Pharm Sci Ano de publicação: 2020 Tipo de documento: Article