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  • Background: Hyaluronan (HYA) is a high molecular weight glucosaminoglycan with a great perspective for medical applications. Because HYA is widespread in the body, it is difficult to determine the fate of exogenously administered HYA. Methods: In this study, HYA of different molecular weights (0.1-1 MDa) was labelled with Tc-99m, and the distribution profiles were determined after administrating the HYA to rats. Results: After the intravenous administration of Tc-99m-HYA, a rapid decrease in the radioactivity of blood samples was observed, presumably because of Tc-99m-HYA uptake by the liver; only minimal signs of liver radioactivity washout were detected. After the oral administration of Tc-99m-HYA, no significant absorption to the central compartment was found. A preliminary study using C-14-HYA exhibited a different distribution profile than Tc-99m-HYA because of the different administered dose and the fate of the degradation products. Even with C-14-HYA, only traces of radioactivity were absorbed after oral administration. Conclusion: This paper provides quantitative information regarding the distribution parameters of radiolabelled HYA in preclinical experiments.
  • Background: Hyaluronan (HYA) is a high molecular weight glucosaminoglycan with a great perspective for medical applications. Because HYA is widespread in the body, it is difficult to determine the fate of exogenously administered HYA. Methods: In this study, HYA of different molecular weights (0.1-1 MDa) was labelled with Tc-99m, and the distribution profiles were determined after administrating the HYA to rats. Results: After the intravenous administration of Tc-99m-HYA, a rapid decrease in the radioactivity of blood samples was observed, presumably because of Tc-99m-HYA uptake by the liver; only minimal signs of liver radioactivity washout were detected. After the oral administration of Tc-99m-HYA, no significant absorption to the central compartment was found. A preliminary study using C-14-HYA exhibited a different distribution profile than Tc-99m-HYA because of the different administered dose and the fate of the degradation products. Even with C-14-HYA, only traces of radioactivity were absorbed after oral administration. Conclusion: This paper provides quantitative information regarding the distribution parameters of radiolabelled HYA in preclinical experiments. (en)
Title
  • Preclinical pharmacokinetics of radiolabelled hyaluronan
  • Preclinical pharmacokinetics of radiolabelled hyaluronan (en)
skos:prefLabel
  • Preclinical pharmacokinetics of radiolabelled hyaluronan
  • Preclinical pharmacokinetics of radiolabelled hyaluronan (en)
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  • RIV/00216208:11160/12:10124217!RIV13-MSM-11160___
http://linked.open...avai/predkladatel
http://linked.open...avai/riv/aktivita
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  • I
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  • 2
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  • 160958
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  • RIV/00216208:11160/12:10124217
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  • pharmacokinetics; biodistribution; radiolabelling; Tc-99m; C-14; hyaluronan (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • PL - Polská republika
http://linked.open...ontrolniKodProRIV
  • [74E56B1939FF]
http://linked.open...i/riv/nazevZdroje
  • Pharmacological Reports
http://linked.open...in/vavai/riv/obor
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http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 64
http://linked.open...iv/tvurceVysledku
  • Lázníček, Milan
  • Lázníčková, Alice
  • Čožíková, Dagmar
  • Velebny, Vladimir
http://linked.open...ain/vavai/riv/wos
  • 000305546700023
issn
  • 1734-1140
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  • 11160
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