Curcumin-Poly(sodium 4-styrenesulfonate) Conjugates as Potent Zika Virus Entry Inhibitors

被引:3
|
作者
Obloza, Magdalena [1 ]
Milewska, Aleksandra [2 ]
Botwina, Pawel [2 ,3 ]
Szczepanski, Artur [2 ]
Medaj, Aneta [1 ,4 ]
Bonarek, Piotr [5 ]
Szczubialka, Krzysztof [1 ]
Pyrc, Krzysztof [2 ]
Nowakowska, Maria [1 ]
机构
[1] Jagiellonian Univ, Fac Chem, PL-30087 Krakow, Poland
[2] Jagiellonian Univ, Malopolska Ctr Biotechnol, Virogenet Lab Virol, PL-30387 Krakow, Poland
[3] Jagiellonian Univ, Fac Biochem Biophys & Biotechnol, Dept Microbiol, PL-30387 Krakow, Poland
[4] Jagiellonian Univ, Doctoral Sch Exact & Nat Sci, PL-30348 Krakow, Poland
[5] Jagiellonian Univ, Fac Biochem Biophys & Biotechnol, Dept Phys Biochem, PL-30387 Krakow, Poland
关键词
Zika virus; antiviral; polymer; poly(sodium4-styrenesulfonate); curcumin; flavivirus; HUMAN SERUM-ALBUMIN; CIRCULAR-DICHROISM; OFF-PATHWAY; CURCUMIN; NANOPARTICLES; INFECTION; CYTOTOXICITY; FIBRILLATION; INFANTS;
D O I
10.1021/acsami.3c13893
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Curcumin, a natural product with recognized antiviral properties, is limited in its application largely due to its poor solubility. This study presents the synthesis of water-soluble curcumin-poly-(sodium 4-styrenesulfonate) (Cur-PSSNan) covalent conjugates. The antiflaviviral activity of conjugates was validated in vitro by using the Zika virus as a model. In the development of these water-soluble curcumin-containing derivatives, we used the macromolecules reported by us to also hamper viral infections. Mechanistic investigations indicated that the conjugates exhibited excellent stability and bioavailability. The curcumin and macromolecules in concerted action interact directly with virus particles and block their attachment to host cells, hampering the infection process.
引用
收藏
页码:5426 / 5437
页数:12
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