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A head-to-head comparison of polymer interaction with mucin from porcine stomach and bovine submaxillary glands.
Stie, Mai Bay; Cunha, Cristiana; Huang, Zheng; Kirkensgaard, Jacob Judas Kain; Tuelung, Pernille Sønderby; Wan, Feng; Nielsen, Hanne Mørck; Foderà, Vito; Rønholt, Stine.
Afiliação
  • Stie MB; Department of Pharmacy, University of Copenhagen, Universitetsparken 2, 2100, Copenhagen, Denmark. mai.bay.stie@sund.ku.dk.
  • Cunha C; Center for Biopharmaceuticals and Biobarriers in Drug Delivery (BioDelivery), University of Copenhagen, Universitetsparken 2, 2100, Copenhagen, Denmark. mai.bay.stie@sund.ku.dk.
  • Huang Z; Department of Pharmacy, University of Copenhagen, Universitetsparken 2, 2100, Copenhagen, Denmark.
  • Kirkensgaard JJK; Center for Biopharmaceuticals and Biobarriers in Drug Delivery (BioDelivery), University of Copenhagen, Universitetsparken 2, 2100, Copenhagen, Denmark.
  • Tuelung PS; Department of Pharmacy, University of Copenhagen, Universitetsparken 2, 2100, Copenhagen, Denmark.
  • Wan F; Center for Biopharmaceuticals and Biobarriers in Drug Delivery (BioDelivery), University of Copenhagen, Universitetsparken 2, 2100, Copenhagen, Denmark.
  • Nielsen HM; Department of Food Science, Rolighedsvej 26, 1958, Frederiksberg, Denmark.
  • Foderà V; Niels Bohr Institute, Universitetsparken 5, 2100, Copenhagen, Denmark.
  • Rønholt S; Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Universitetsparken 2, 2100, Copenhagen, Denmark.
Sci Rep ; 14(1): 21350, 2024 09 12.
Article em En | MEDLINE | ID: mdl-39266622
ABSTRACT
Native mucus is heterogeneous, displays high inter-individual variation and is prone to changes during harvesting and storage. To overcome the lack of reproducibility and availability of native mucus, commercially available purified mucins, porcine gastric mucin (PGM) and mucin from bovine submaxillary gland (BSM), have been widely used. However, the question is to which extent the choice of mucin matters in studies of their interaction with polymers as their composition, structure and hence physicochemical properties differ. Accordingly, the interactions between PGM or BSM with two widely used polymers in drug delivery, polyethylene oxide and chitosan, was studied with orthogonal

methods:

turbidity, dynamic light scattering, and quartz crystal microbalance with dissipation monitoring. Polymer binding and adsorption to the two commercially available and purified mucins, PGM and BSM, is different depending on the mucin type. PEO, known to interact weakly with mucin, only displayed limited interaction with both mucins as confirmed by all employed methods. In contrast, chitosan was able to bind to both PGM and BSM. Interestingly, the results suggest that chitosan interacts with BSM to a greater extent than with PGM indicating that the choice of mucin, PGM or BSM, can affect the outcome of studies of mucin interactions with polymers.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Glândula Submandibular / Quitosana / Mucinas Gástricas / Mucinas Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Glândula Submandibular / Quitosana / Mucinas Gástricas / Mucinas Idioma: En Ano de publicação: 2024 Tipo de documento: Article