Masri Syafira, Fauzi Faraheda Amilia Mohd, Hasnizam Sarah Batrisyia, Azhari Aizzaty Sulha, Lim Juliana Edora Amin, Hao Looi Qi, Maarof Manira, Motta Antonella, Fauzi Mh Busra
Centre for Tissue Engineering Centre and Regenerative Medicine, Faculty of Medicine, Universiti Kebangsaan Malaysia, Cheras, Kuala Lumpur 56000, Malaysia.
My Cytohealth Sdn. Bhd., Kuala Lumpur 56000, Malaysia.
Pharmaceuticals (Basel). 2022 Oct 27;15(11):1328. doi: 10.3390/ph15111328.
Three-dimensional (3D) in vitro skin models are frequently employed in cosmetic and pharmaceutical research to minimize the demand for animal testing. Hence, three-dimensional (3D) bioprinting was introduced to fabricate layer-by-layer bioink made up of cells and improve the ability to develop a rapid manufacturing process, while maintaining bio-mechanical scaffolds and microstructural properties. Briefly, gelatin-polyvinyl alcohol (GPVA) was mixed with 1.5 × 10 and 3.0 × 10 human dermal fibroblast (HDF) cell density, together with 0.1% genipin (GNP), as a crosslinking agent, using 3D-bioprinting. Then, it was cultured under submerged and air-lifting conditions. The gross appearance of the hydrogel's surface and cross-section were captured and evaluated. The biocompatibility testing of HDFs and cell-bioink interaction towards the GPVA was analyzed by using live/dead assay, cell migration activity, cell proliferation assay, cell morphology (SEM) and protein expression via immunocytochemistry. The crosslinked hydrogels significantly demonstrated optimum average pore size (100-199 μm). The GPVA crosslinked with GNP (GPVA_GNP) hydrogels with 3.0 × 10 HDFs was proven to be outstanding, compared to the other hydrogels, in biocompatibility testing to promote cellular interaction. Moreover, GPVA-GNP hydrogels, encapsulated with 3.0 × 10 HDFs under submerged cultivation, had a better outcome than air-lifting with an excellent surface cell viability rate of 96 ± 0.02%, demonstrated by 91.3 ± 4.1% positively expressed Ki67 marker at day 14 that represented active proliferative cells, an average of 503.3 ± 15.2 μm for migration distance, and maintained the HDFs' phenotypic profiles with the presence of collagen type I expression. It also presented with an absence of alpha-smooth muscle actin positive staining. In conclusion, 3.0 × 10 of hybrid GPVA hydrogel crosslinked with GNP, produced by submerged cultivation, was proven to have the excellent biocompatibility properties required to be a potential bioinks for the rapid manufacturing of 3D in vitro of a single dermal layer for future use in cosmetic, pharmaceutic and toxicologic applications.
三维(3D)体外皮肤模型常用于化妆品和药物研究,以尽量减少动物试验的需求。因此,引入了三维(3D)生物打印技术来制造由细胞组成的逐层生物墨水,并提高快速制造工艺的能力,同时保持生物力学支架和微观结构特性。简而言之,使用3D生物打印技术将明胶 - 聚乙烯醇(GPVA)与1.5×10和3.0×10的人真皮成纤维细胞(HDF)细胞密度混合,并加入0.1%京尼平(GNP)作为交联剂。然后,在浸没和空气提升条件下进行培养。捕获并评估水凝胶表面和横截面的总体外观。通过活/死检测、细胞迁移活性、细胞增殖检测、细胞形态(扫描电子显微镜)和免疫细胞化学的蛋白质表达来分析HDFs的生物相容性测试以及细胞 - 生物墨水与GPVA的相互作用。交联水凝胶显著显示出最佳平均孔径(100 - 199μm)。与其他水凝胶相比,含有3.0×10 HDFs的与GNP交联的GPVA(GPVA_GNP)水凝胶在促进细胞相互作用的生物相容性测试中表现出色。此外,在浸没培养下封装有3.0×10 HDFs的GPVA - GNP水凝胶比空气提升培养效果更好,表面细胞活力率高达96±0.02%,在第14天有91.3±4.1%的Ki67标记呈阳性表达,代表活跃增殖细胞,迁移距离平均为503.3±15.2μm,并在存在I型胶原蛋白表达的情况下保持HDFs的表型特征。同时,它也没有α - 平滑肌肌动蛋白阳性染色。总之,通过浸没培养产生的与GNP交联的3.0×10混合GPVA水凝胶被证明具有优异的生物相容性特性,有望成为用于快速制造单一层真皮3D体外模型的潜在生物墨水,以供未来在化妆品、制药和毒理学应用中使用。