New N- and C-modified RGD-hemorphins as potential biomedical application on Ti-surface materials: synthesis, characterization and antinociceptive activity

被引:3
|
作者
Georgieva, Stela [1 ]
Todorov, Petar [2 ]
Nikolov, Spas [1 ]
Dzhambazova, Elena [4 ]
Peneva, Petia [2 ]
Assenov, Borislav [3 ,4 ]
Pechlivanova, Daniela [3 ,4 ]
机构
[1] Univ Chem Technol & Met, Dept Analyt Chem, Sofia 1756, Bulgaria
[2] Univ Chem Technol & Met, Dept Organ Chem, Sofia 1756, Bulgaria
[3] Bulgarian Acad Sci, Inst Neurobiol, Sofia 1113, Bulgaria
[4] Sofia Univ, Med Fac, St Kliment Ohridski, Sofia 1407, Bulgaria
关键词
Peptide; RGD; Hemorphins; Ti materials; Electrochemistry; Antinociceptive activity; ARG-GLY-ASP; AT(4) RECEPTOR; ANGIOTENSIN-IV; CELL-ADHESION; HEMOGLOBIN; LVV-HEMORPHIN-7; LIGANDS; PEPTIDE; AMINOPEPTIDASE; VV-HEMORPHIN-7;
D O I
10.1007/s11030-022-10428-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This manuscript presented the synthesis and characterization of two new N- and C-modified analogues of VV-hemorphin-7 containing RGD (Arg-Gly-Asp) residues as potential nociceptive agents and bioactive materials. It has been shown that the addition of one or two RGD sequences to natural VV-hemorphin-7 increases its effect on acute nociception, but the reduction of the inflammatory phase depends on the concentration of the peptide. The structure-property relationship of the new peptide derivatives was highlighted by electrochemical and FT-IR methods of analysis. Because of the proven bone-structural bonds of hydroxyapatite, the simultaneous deposition of peptide/hydroxyapatite on the surface of a titanium surface was investigated. The deposition was performed in a medium of gelatin solution containing dissolved amounts of peptide and hydroxyapatite using ultrasound. SEM-EDS analyzes confirmed the presence of a layer of the studied system.
引用
收藏
页码:263 / 280
页数:18
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  • [1] New N- and C-modified RGD-hemorphins as potential biomedical application on Ti-surface materials: synthesis, characterization and antinociceptive activity
    Stela Georgieva
    Petar Todorov
    Spas Nikolov
    Elena Dzhambazova
    Petia Peneva
    Borislav Assenov
    Daniela Pechlivanova
    Molecular Diversity, 2023, 27 : 263 - 280