糖肽微针触发ECM过程,促进成纤维细胞活力,用于抗衰老治疗

IF 5.5 2区 医学 Q2 MATERIALS SCIENCE, BIOMATERIALS Materials Science & Engineering C-Materials for Biological Applications Pub Date : 2024-11-26 DOI:10.1016/j.bioadv.2024.214124
Wenjie Zhang , Qing Shao , Hua Zhong , Yingying Yang , Ruixue Li , Yaxian Liu , Yi Hu , Penghui Wang , Bo Chi
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引用次数: 0

摘要

由于复杂的微环境中累积的有害影响,皮肤抗衰老仍然具有挑战性。在这里,我们提出了由聚γ-谷氨酸和透明质酸组成的糖肽水凝胶(γ-PGA/HA)微针贴片作为一种潜在的解决方案。这些微针旨在有效穿透皮肤屏障,同时重塑细胞外基质,调节皮肤微环境。为配合临床需要,对微环境调节材料的功能特性进行了表征,测试了材料的吸水潴留、氧化还原平衡、炎症微环境调节能力。γ-PGA/HA具有显著的保湿、生物相容性、促进成纤维细胞活力、消耗ROS和抑制TNF-α的作用。组织学分析提供了支持微针功能功效的经验证据,从而验证了模拟自然衰老过程的模型的抗皮肤衰老潜力。因此,γ-PGA/HA具有调节皮肤微环境的潜力,在皮肤衰老治疗中具有潜在的应用前景。
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Glycopeptide microneedles triggering the ECM process to promote fibroblast viability for anti-aging treatments
Skin anti-aging remains challenging due to the cumulative detrimental effects within the intricate microenvironment. Here, we present glycopeptide hydrogel (γ-PGA/HA) microneedle patches composed of poly (γ-glutamic acid) and hyaluronic acid as a potential solution. These microneedles aim to effectively penetrate the skin barrier while remodeling extracellular matrix to regulate the skin microenvironment. To align with clinical requirements, the functional properties of microenvironment regulation materials are characterized by testing the water absorption and retention, redox balance, and inflammatory microenvironment regulation ability. The γ-PGA/HA exhibited remarkable moisturizing, biocompatibility, fibroblast viability promotion, ROS consumption, and TNF-α inhibiting effects. Histological analysis provides empirical evidence supporting the functional efficacy of the microneedle, thus validating the anti-skin-aging potential of a model that mimics natural aging processes. Therefore, γ-PGA/HA holds promise for regulating the skin microenvironment, offering potential applications in skin aging treatments.
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来源期刊
CiteScore
17.80
自引率
0.00%
发文量
501
审稿时长
27 days
期刊介绍: Biomaterials Advances, previously known as Materials Science and Engineering: C-Materials for Biological Applications (P-ISSN: 0928-4931, E-ISSN: 1873-0191). Includes topics at the interface of the biomedical sciences and materials engineering. These topics include: • Bioinspired and biomimetic materials for medical applications • Materials of biological origin for medical applications • Materials for "active" medical applications • Self-assembling and self-healing materials for medical applications • "Smart" (i.e., stimulus-response) materials for medical applications • Ceramic, metallic, polymeric, and composite materials for medical applications • Materials for in vivo sensing • Materials for in vivo imaging • Materials for delivery of pharmacologic agents and vaccines • Novel approaches for characterizing and modeling materials for medical applications Manuscripts on biological topics without a materials science component, or manuscripts on materials science without biological applications, will not be considered for publication in Materials Science and Engineering C. New submissions are first assessed for language, scope and originality (plagiarism check) and can be desk rejected before review if they need English language improvements, are out of scope or present excessive duplication with published sources. Biomaterials Advances sits within Elsevier''s biomaterials science portfolio alongside Biomaterials, Materials Today Bio and Biomaterials and Biosystems. As part of the broader Materials Today family, Biomaterials Advances offers authors rigorous peer review, rapid decisions, and high visibility. We look forward to receiving your submissions!
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