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Sweet corn phytoglycogen dendrimers as a lyoprotectant for dry-state protein storage.
Park, Junha; Liu, Renjie; Kim, Alexander S; Cyr, Noah N; Boehlein, Susan K; Resende, Marcio F R; Savin, Daniel A; Bailey, Laura S; Sumerlin, Brent S; Hudalla, Gregory A.
Afiliação
  • Park J; J. Crayton Pruitt Family Department of Biomedical Engineering, Wertheim College of Engineering, University of Florida, Gainesville, Florida, USA.
  • Liu R; J. Crayton Pruitt Family Department of Biomedical Engineering, Wertheim College of Engineering, University of Florida, Gainesville, Florida, USA.
  • Kim AS; Department of Chemistry, University of Florida, Gainesville, Florida, USA.
  • Cyr NN; Polymer Chemical Characterization Lab, Department of Chemistry, University of Florida, Gainesville, Florida, USA.
  • Boehlein SK; Horticultural Sciences Department, University of Florida, Gainesville, Florida, USA.
  • Resende MFR; Horticultural Sciences Department, University of Florida, Gainesville, Florida, USA.
  • Savin DA; Department of Chemistry, University of Florida, Gainesville, Florida, USA.
  • Bailey LS; Polymer Chemical Characterization Lab, Department of Chemistry, University of Florida, Gainesville, Florida, USA.
  • Sumerlin BS; Polymer Chemical Characterization Lab, Department of Chemistry, University of Florida, Gainesville, Florida, USA.
  • Hudalla GA; Department of Chemistry, University of Florida, Gainesville, Florida, USA.
J Biomed Mater Res A ; 2024 Jun 10.
Article em En | MEDLINE | ID: mdl-38856491
ABSTRACT
Protein biotherapeutics typically require expensive cold-chain storage to maintain their fold and function. Packaging proteins in the dry state via lyophilization can reduce these cold-chain requirements. However, formulating proteins for lyophilization often requires extensive optimization of excipients that both maintain the protein folded state during freezing and drying (i.e., "cryoprotection" and "lyoprotection"), and form a cake to carry the dehydrated protein. Here we show that sweet corn phytoglycogens, which are glucose dendrimers, can act as both a protein lyoprotectant and a cake-forming agent. Phytoglycogen (PG) dendrimers from 16 different maize sources (PG1-16) were extracted via ethanol precipitation. PG size was generally consistent at ~70-100 nm for all variants, whereas the colloidal stability in water, protein contaminant level, and maximum density of cytocompatibility varied for PG1-16. 10 mg/mL PG1, 2, 9, 13, 15, and 16 maintained the activity of various proteins, including green fluorescent protein, lysozyme, ß-galactosidase, and horseradish peroxidase, over a broad range of concentrations, through multiple rounds of lyophilization. PG13 was identified as the lead excipient candidate as it demonstrated narrow dispersity, colloidal stability in phosphate-buffered saline, low protein contaminants, and cytocompatibility up to 10 mg/mL in NIH3T3 cell cultures. All dry protein-PG13 mixtures had a cake-like appearance and all frozen protein-PG13 mixtures had a Tg' of ~ -26°C. The lyoprotection and cake-forming properties of PG13 were density-dependent, requiring a minimum density of 5 mg/mL for maximum activity. Collectively these data establish PG dendrimers as a new class of excipient to formulate proteins in the dry state.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article