The interaction of 5, 10, 15, 20-tetrakis [4- (2, 3, 4, 6-tetra-O-acetyl-β-D-galactopyranosyl) phenyl] porphine with biopolymers. (March 2019)

• Record Type: Journal Article
• Authors: Lebedeva, Natalya Sh; Yurina, Elena S.; Guseinov, Sabir S.; Gubarev, Yury A.; Syrbu, Sergey A.
• Is Part Of: Dyes and pigments. Volume 162(2019)
• Page Start: 266
• Page End: 271
• Publication Date: 2019-03
• Subjects: Dyes and dyeing -- Periodicals; Pigments -- Periodicals; 667.2
• DOI: 10.1016/j.dyepig.2018.10.034
• Languages: English
• ISSNs: 0143-7208

Abstract

Abstract: Glycosized porphyrins are promising compounds for using in PDT, since they combine the ability to act as a photosensitizer, and their saccharide residues provide an increased tumorotropicity of this compound in the affected cells. In this work, the modified 5, 10, 15, 20-tetrakis [4-(2, 3, 4, 6-tetra-O-acetyl-β-D-galactopyranosyl) phenyl] porphine (HOGalPor) synthesis procedure providing an increased yield of the desired product is described. The affinity of natural biopolymers with reference to synthesized porphyrin has been studied. It was found that synthesized porphyrin is associated in aqueous media. There were proposed some mixed solvents and water-solvent concentration ratios were established to ensure the monomerization of porphyrin and the preservation of the native conformation of biopolymers (BSA and DNA). The affinity constants of BSA and DNA were determined with reference to the synthesized porphyrin, as well as localization of porphyrin in biopolymers was established. As part of the protein complex, porphyrin fluoresces very intensively, and this feature makes it possible to use BSA as a transport system for HOGalPor, and HOGalPor itself can act as a fluorescent marker. The interaction of HOGalPor with the intercalation complex of DNA-EtBr leads to the destruction of the latter, while porphyrin does not intercalate in DNA, but forms external complexes with a change in the zeta potential of the surface. Highlights: The modified 5, 10, 15, 20-tetrakis [4-(2, 3, 4, 6-tetra-O-acetyl-β-D-galactopyranosyl) phenyl] porphine synthesis procedure providing an increased yield of the desired product is described The affinity of DNA and protein to was studied The porphyrin localization was established A possibility of using albumin as a transport system for glycosidic substituted porphyrin was detected