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How the molecular weight affects the in vivo fate of exogenous hyaluronan delivered intravenously: A stable-isotope labelling strategy

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    SYSNO ASEP0542790
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleHow the molecular weight affects the in vivo fate of exogenous hyaluronan delivered intravenously: A stable-isotope labelling strategy
    Author(s) Simek, M. (CZ)
    Nešporová, K. (CZ)
    Kocurková, Anna (BFU-R) ORCID
    Foglova, T. (CZ)
    Ambrožová, Gabriela (BFU-R) RID
    Velebný, V. (CZ)
    Kubala, Lukáš (BFU-R) RID, ORCID
    Hermannová, M. (CZ)
    Number of authors8
    Article number117927
    Source TitleCarbohydrate Polymers. - : Elsevier - ISSN 0144-8617
    Roč. 263, JUL 1 2021 (2021)
    Number of pages10 s.
    Publication formOnline - E
    Languageeng - English
    CountryGB - United Kingdom
    Keywordschondroitin sulfate ; acid ; size ; pharmacokinetics ; biodistribution
    Subject RIVCC - Organic Chemistry
    OECD categoryOrganic chemistry
    Method of publishingLimited access
    Institutional supportBFU-R - RVO:68081707
    UT WOS000640429500006
    EID SCOPUS85103127618
    DOI10.1016/j.carbpol.2021.117927
    AnnotationThere is inconsistent information regarding the size effects of exogenously given hyaluronan on its in vivo fate. The data are often biased by the poor quality of hyaluronan and non-ideal labelling strategies used for resolving exogenous/endogenous hyaluronan, which only monitor the label and not hyaluronan itself. To overcome these drawbacks and establish the pharmacokinetics of intravenous hyaluronan in relation to its Mw, 13C-labelled HA of five Mws from 13.6?1562 kDa was prepared and administered to mice at doses 25-50 mg kg?1. The elimination efficiency increased with decreasing Mw. Low Mw hyaluronan was rapidly eliminated as small hyaluronan fragments in urine, while high Mw hyaluronan exhibited saturable kinetics and complete metabolization within 48 h. All tested Mws exhibited a similar uptake by liver cells and metabolization into activated sugars. 13Clabelling combined with LC?MS provides an excellent approach to elucidating in vivo fate and biological activities of hyaluronan.
    WorkplaceInstitute of Biophysics
    ContactJana Poláková, polakova@ibp.cz, Tel.: 541 517 244
    Year of Publishing2022
    Electronic addresshttps://reader.elsevier.com/reader/sd/pii/S0144861721003143?token=3B1E30F1EFFA8B688701DCC15BDDC999A5E187E791E15A519C7A4D380A7A798486099FF4C0AB22482C63D972D480C238&originRegion=eu-west-1&originCreation=20210528071650
Number of the records: 1  

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