Multifunctionalised skin substitute of hybrid gelatin-polyvinyl alcohol bioinks for chronic wound: injectable vs. 3D bioprinting

被引:5
|
作者
Masri, Syafira [1 ]
Fadilah, Nur Izzah Md [1 ]
Hao, Looi Qi [1 ,2 ]
Maarof, Manira [1 ]
Tabata, Yasuhiko [3 ]
Hiraoka, Yosuke [4 ]
Fauzi, Mh Busra [1 ,2 ]
机构
[1] Univ Kebangsaan Malaysia, Fac Med, Ctr Tissue Engn & Regenerat Med, Med Ctr, 15th Floor Pre Clin Bldg,Jalan Yaacob Latif, Kuala Lumpur 56000, Malaysia
[2] My Cytohlth Sdn Bhd, Kuala Lumpur 56000, Malaysia
[3] Kyoto Univ, Inst Life & Med Sci LiMe, Dept Regenerat Sci & Engn, Lab Biomat, Kyoto 6068500, Japan
[4] R&D Ctr, Biomat Grp, Yao 5810000, Japan
关键词
3D bioprinting; Injectable; Hydrogels; Wound healing; Bioinks; Gelatin; Polyvinyl alcohol; Genipin; CROSS-LINKING; HYDROGELS; SCAFFOLD;
D O I
10.1007/s13346-023-01447-z
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
Chronic wounds are challenging to heal and increase global mortality. The effectiveness of skin graft is limited by rejection, fibrosis, and inadequate donor site. Multifunctionalised-hydrogel skin substitutes promoted higher wound healing by maintaining the moisture microenvironment and permit gas exchange/nourishment in prolong cell viability/activity. The purpose of this study was to evaluate a skin substitute using two strategies; via injectable and 3D bioprinting technique. New hydrogel formulations that composed of gelatin (GE) and polyvinyl-alcohol (PVA) were constructed using a pre-mix crosslinking approach with genipin (GNP) to generate the biodegradable and biocompatible skin substitute with reduced secondary traumatic wound. GPVA5_GNP (6% GE: 5% PVA crosslinked with GNP) was the most stable hydrogel for wound healing application with the longest enzymatic degradation and stable hydrogel for absorption of excess wound exudates. Primary human dermal fibroblasts (HDFs) migrated extensively through 3D bioprinted hydrogels with larger average pore sizes and interconnected pores than injectable hydrogels. Moreover, 3D bioprinted GPVA hydrogels were biocompatible with HDFs and demonstrated > 90% cell viability. HDFs maintained their phenotype and positively expressed collagen type-I, vinculin, short and dense F-actin, alpha-smooth muscle actin, and Ki67. Additionally, the presence of GNP demonstrated antioxidant capacity and high-ability of angiogenesis. The utilisation of the 3D bioprinting (layer-by-layer) approach did not compromise the HDFs' growth capacity and biocompatibility with selected bioinks. In conclusion, it allows the cell encapsulation sustainability in a hydrogel matrix for a longer period, in promoting tissue regeneration and accelerating healing capacity, especially for difficult or chronic wound.
引用
收藏
页码:1005 / 1027
页数:23
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