| Literature DB >> 35749472 |
Vedran Milosavljevic, Yazan Haddad, Miguel Angel Merlos Rodrigo, Amitava Moulick, Hana Polanska, David Hynek, Zbynek Heger, Pavel Kopel, Vojtech Adam.
Abstract
[This corrects the article DOI: 10.1371/journal.pone.0163983.].Entities:
Year: 2022 PMID: 35749472 PMCID: PMC9231690 DOI: 10.1371/journal.pone.0270734
Source DB: PubMed Journal: PLoS One ISSN: 1932-6203 Impact factor: 3.752
Fig 4Fluorescence microscopy images.
A) PC3 cells exposed to Zn-S-NVC (conjugated to fluorescent dye) at 0 min. B) PC3 cells exposed to Zn-S-NVC (conjugated to fluorescent dye) at 30 min. C) PC3 cells exposed to Zn-S-NVC (conjugated to fluorescent dye) at 60 min. D) PC3 cells exposed to Zn-S-NVC (conjugated to fluorescent dye) at 90 min. E) PNT1A cells exposed to Zn-S-NVC (conjugated to fluorescent dye) at 0 min. F) PNT1A cells exposed to Zn-S-NVC (conjugated to fluorescent dye) at 30 min. G) PNT1A cells exposed to Zn-S-NVC (conjugated to fluorescent dye) at 60 min. H) PNT1A cells exposed to Zn-S-NVC (conjugated to fluorescent dye) at 90 min. I) Haemocompatibility of Zn-S-NVC using human RBCs, showing negligible haemolytic activity in the selected concentration range of Zn-S-NVC (16–500 nM). Inserts show images after incubation and centrifugation. J) MTT analysis of the PC3 cell line. K) MTT analysis of the PNT1A cell line.