In situ photo-crosslinkable hyaluronic acid-based hydrogel emb e dde d with GHK peptide nanofibers for bioactive wound healing

被引:9
|
作者
Lee, Seohui [1 ]
Lee, Sang Min [1 ]
Lee, Sang Hyun [1 ]
Choi, Woong-Ku [1 ]
Park, Sung -Jun [2 ]
Kim, Do Yeon [1 ]
Oh, Sae Woong [1 ]
Oh, Jieun [1 ]
Cho, Jae Youl [1 ]
Lee, Jongsung [1 ]
Chien, Pham Ngoc [3 ]
Nam, Sun Young [3 ]
Heo, Chan Yeong [3 ,4 ]
Lee, Yoon-Sik [2 ]
Kwak, Eun-A [5 ]
Chung, Woo -Jae [1 ,5 ,6 ]
机构
[1] Sungkyunkwan Univ, Dept Software, 2066 Seobu Ro, Suwon 16419, Gyeonggi Do, South Korea
[2] Seoul Natl Univ, Sch Chem & Biol Engn, Seoul 08826, South Korea
[3] Seoul Natl Univ, Bundang Hosp, Dept Plast & Reconstruct Surg, Seongnam, South Korea
[4] Seoul Natl Univ, Coll Med, Dept Med Device Dev, Seoul, South Korea
[5] Sungkyunkwan Univ, Inst Biomol Control, 2066 Seobu Ro, Suwon 16419, Gyeonggi Do, South Korea
[6] Sungkyunkwan Univ, Ctr Biol, Suwon 16419, South Korea
基金
新加坡国家研究基金会;
关键词
Hyaluronic acid; Photo-crosslinking; Hydrogel; Wound healing; Amphiphilic GHK peptide; Self -assembled peptide nanofiber; Copper peptide; COPPER COMPLEX GLYCYL-L-HISTIDYL-L-LYSINE-CU2+; SELF-ASSEMBLING PEPTIDES; GROWTH-FACTOR; TRIPEPTIDE; STRATEGIES; ALGINATE; DESIGN; RELEASE; LYSINE; STIMULATION;
D O I
10.1016/j.actbio.2023.10.011
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
A versatile hydrogel was developed for enhancing bioactive wound healing by introducing the amphiphilic GHK peptide (GHK-C16) into a photo-crosslinkable tyramine-modified hyaluronic acid (HA-Ty). GHK-C16 self-assembled into GHK nanofibers (GHK NF) in HA-Ty solution, which underwent in situ gelation after the wound area was filled with precursor solution. Blue light irradiation (460-490 nm), with riboflavin phosphate as a photoinitiator, was used to trigger crosslinking, which enhanced the stability of the highly degradable hyaluronic acid and enabled sustained release of the nanostructured GHK derivatives. The hydrogels provided a microenvironment that promoted the proliferation of dermal fibroblasts and the activation of cytokines, leading to reduced inflammation and increased collagen expression during wound healing. The complexation of Cu 2 + into GHK nanofibers resulted in superior wound healing capabilities compared with non-lipidated GHK peptide with a comparable level of growth factor (EGF). Additionally, nanostructured Cu-GHK improved angiogenesis through vascular endothelial growth factor (VEGF) activation, which exerted a synergistic therapeutic effect. Furthermore, in vivo wound healing experiments revealed that the Cu-GHK NF/HA-Ty hydrogel accelerated wound healing through densely packed remodeled collagen in the dermis and promoting the growth of denser fibroblasts. HA-Ty hydrogels incorporating GHK NF also possessed improved mechanical properties and a faster wound healing rate, making them suitable for advanced bioactive wound healing applications.
引用
收藏
页码:159 / 174
页数:16
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