2024
Sulfation of furcellaran and its effect on hemocompatibility in vitro
ŠTĚPÁNKOVÁ, Kateřina; Kadir OZALTIN; Radka GOREJOVÁ; Hana DOUDOVÁ; Eva BERGEROVÁ et al.Základní údaje
Originální název
Sulfation of furcellaran and its effect on hemocompatibility in vitro
Autoři
ŠTĚPÁNKOVÁ, Kateřina; Kadir OZALTIN; Radka GOREJOVÁ; Hana DOUDOVÁ; Eva BERGEROVÁ; Iveta MASKALOVÁ; Monika STUPAVSKÁ; Pavel SŤAHEL; David TRUNEC; Jana PELKOVÁ; Miran MOZETIČ a Marián LEHOCKÝ
Vydání
International Journal of Biological Macromolecules, Amsterdam, Elsevier Science BV, 2024, 0141-8130
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10608 Biochemistry and molecular biology
Stát vydavatele
Nizozemské království
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 8.500
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14310/24:00135341
Organizační jednotka
Přírodovědecká fakulta
UT WoS
EID Scopus
Klíčová slova anglicky
Anticoagulant; Furcellaran; Hemocompatibility; Platelet adhesion; Seaweed polysaccharide; Sulfation
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 29. 1. 2024 10:11, Mgr. Marie Novosadová Šípková, DiS.
Anotace
V originále
In this study, furcellaran (FUR) obtained from Furcellaria lumbricalis was firstly employed for sulfation via various methods, including SO3-pyridine (SO3∙Py) complex in different aprotic solvents, chlorosulfonic acid and sulfuric acid with a "coupling" reagent N,N'-Dicyclohexylcarbodiimide. Structural characterization through FT-IR, GPC, XPS and elemental analyses confirmed the successful synthesis of 6-O-sulfated FUR derivates characterized by varying degrees of sulfation (DS) ranging from 0.15 to 0.91 and molecular weight (Mw) spanning from12.5kDa to 2.7kDa. In vitro clotting assays, partial thromboplastin time (aPTT), thrombin time (TT), and prothrombin time (PT) underscored the essential role of sulfate esters in conferring anticoagulant activity whereas FUR prepared via chlorosulfonic acid with DS of 0.91 reached 311.4s in aPPT showing almost 4-fold higher anticoagulant activity than native FUR at the concentration 2mg/mL. MTT test showed all tested samples decreased cell viability in a dose dependent manner while all of them are non-cytotoxic up to the concentration of 0.1mg/mL. Furthermore, sulfated derivates deposited onto polyethylene terephthalate surface presented substantial decrease in platelet adhesion, as well as absence of the most activated platelet stages. These findings support the pivotal role of O-6 FUR sulfates in enhancing hemocompatibility and provide valuable insights for a comparative assessment of effective sulfating approaches.