Development and evaluation of RADA-PDGF2 self-assembling peptide hydrogel for enhanced skin wound healing

被引:1
|
作者
Deptula, M. [1 ]
Sawicka, J. [2 ]
Sass, P. [3 ]
Sosnowski, P. [3 ]
Karpowicz, P. [4 ]
Zawrzykraj, M. [5 ]
Wardowska, A. [1 ,6 ]
Tyminska, A. [1 ]
Dzierzynska, M. [2 ]
Pietralik-Molinska, Z. [7 ]
Peplinska, B. [8 ]
Zielinski, J. [9 ]
Kondej, K. [10 ]
Kozak, M. [7 ]
Sachadyn, P. [3 ]
Rodziewicz-Motowidlo, S. [2 ]
Pikula, M. [1 ]
机构
[1] Med Univ Gdansk, Div Embryol, Lab Tissue Engn & Regenerat Med, Gdansk, Poland
[2] Univ Gdansk, Fac Chem, Dept Biomed Chem, Gdansk, Poland
[3] Gdansk Univ Technol, Fac Chem, Lab Regenerat Biotechnol, Gdansk, Poland
[4] Univ Gdansk, Fac Chem, Dept Organ Chem, Gdansk, Poland
[5] Med Univ Gdansk, Div Clin Anat, Gdansk, Poland
[6] Med Univ Gdansk, Fac Med, Dept Physiopathol, Gdansk, Poland
[7] Adam Mickiewicz Univ, Dept Biomed Phys, Fac Phys, Poznan, Poland
[8] Adam Mickiewicz Univ, NanoBiomed Ctr, Poznan, Poland
[9] Med Univ Gdansk, Dept Surg Oncol, Gdansk, Poland
[10] Med Univ Gdansk, Dept Plast Surg, Gdansk, Poland
关键词
hydrogels; wound healing; skin; RADA16-I; PDGF; peptides; croSEM; MIGRATION; SCAFFOLDS; PROLIFERATION;
D O I
10.3389/fphar.2023.1293647
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Wound healing complications affect numerous patients each year, creating significant economic and medical challenges. Currently, available methods are not fully effective in the treatment of chronic or complicated wounds; thus, new methods are constantly sought. Our previous studies showed that a peptide designated as PDGF2 derived from PDGF-BB could be a promising drug candidate for wound treatment and that RADA16-I can serve as a release system for bioactive peptides in wound healing. Based on that, in this work, we designed a new self-assembling hydrogel RADA-PDGF2, connecting both peptides by a sequence specific for neutrophil elastase, and evaluated its activity in wound healing.Methods: The physicochemical properties of the designed scaffold were analyzed using transmission electron microscopy, atomic force microscopy, cryoSEM microscopies, and circular dichroism spectroscopy. The enzymatic cleavage was performed using human neutrophil elastase and monitored using high-performance liquid chromatography and MS spectroscopic techniques. The aforementioned techniques (HPLC and MS) were also used to assess the stability of the peptide in water and human plasma. The biological activity was analyzed on human skin cells using a colorimetric XTT test, collagen synthesis evaluation, and a migration assay. The biocompatibility was analyzed with LDH cytotoxicity assay and flow cytometric analysis of activation of immune cells. Finally, RADA-PDGF2 activity in wound healing was checked in a mouse dorsal skin injury model.Results: The analysis showed that RADA-PDGF2 can self-assemble, form a hydrogel, and release a bioactive sequence when incubated with human elastase. It shows pro-proliferative and pro-migratory properties and accelerates wound closure in the mouse model compared to RADA16-I. In addition, it is not cytotoxic to human cells and does not show immunogenicity. RADA-PDGF2 seems to be a promising drug candidate for wound management.
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页数:17
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