Injectable amino-modified poly-L-lactic acid microspheres/hyaluronic acid-based hydrogel composites for soft tissue fillers

IF 6 2区 医学 Q2 MATERIALS SCIENCE, BIOMATERIALS
Chen Shen , Xingyu Zhou , Junhui Jiang , Junbo Dang , Tong Lin , Ruibo Hu , Tianhao Zhao , Dahui Sun , Mei Zhang
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引用次数: 0

Abstract

Soft tissue fillers have received much attention for the treatment of skin aging and the restoration of missing or excised soft volumes. However, the development of fillers with both safety and applicability remains a challenge. This study presented a synergistic composite filler comprising aldehyde-modified hyaluronic acid (OHA), hydrazide-modified hyaluronic acid (NHA), amino-modified poly-L-lactic acid microspheres (NPLLA), and antioxidant copper peptide. The hydrogel formed in situ via Schiff base reaction exhibited excellent mechanical properties and immediate filling effect. The amino-modified PLLA microspheres were less likely to agglomerate, avoiding the occurrence of adverse reactions and further enhancing the mechanical properties of the filler. The timed-release platform provided protection for copper peptide stability, scavenged reactive oxygen species during the fibrotic encapsulation phase, and synergistically promoted collagen deposition. In a nude mice skin aging model, hydrogels stimulated collagen production through the TGF-β/Smad signaling pathway with good long-term filler efficacy. Therefore, NPLLA microspheres/hyaluronic acid-based composite hydrogels exhibit great potential as injectable soft tissue fillers.

Abstract Image

可注射氨基修饰聚l -乳酸微球/透明质酸基水凝胶复合材料用于软组织填充
软组织填充物在治疗皮肤老化和修复缺失或切除的软组织方面受到了广泛的关注。然而,开发既安全又适用的填料仍然是一个挑战。本研究提出了一种由醛修饰透明质酸(OHA)、酰肼修饰透明质酸(NHA)、氨基修饰聚l -乳酸微球(NPLLA)和抗氧化铜肽组成的协同复合填料。通过席夫碱反应原位生成的水凝胶具有优异的力学性能和即时填充效果。氨基修饰的聚乳酸微球不易团聚,避免了不良反应的发生,进一步提高了填料的力学性能。该缓释平台保护了铜肽的稳定性,清除了纤维化包封阶段的活性氧,并协同促进胶原沉积。在裸鼠皮肤衰老模型中,水凝胶通过TGF-β/Smad信号通路刺激胶原生成,具有良好的长期填充作用。因此,NPLLA微球/透明质酸基复合水凝胶作为可注射的软组织填充物具有很大的潜力。
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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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