ZIF-8纳米纤维与丝素/聚己内酯纳米纤维构筑的双重协同包封体系对姜黄素的递送和释放促进伤口愈合。

IF 6 2区 医学 Q2 MATERIALS SCIENCE, BIOMATERIALS
Mahbubur Rahman , Mohashin Kabir , Hailei Liu , Li Zhang , Shaojuan Chen , Shaohua Wu
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引用次数: 0

摘要

利用静电纺丝技术开发和设计具有仿生结构和多功能性能的新型纳米纤维敷料引起了伤口治疗学科的极大兴趣。本研究首先将姜黄素(Cur)掺入到沸石咪唑酸骨架-8 (ZIF-8)中,得到Cur@ZIF-8纳米颗粒,该纳米颗粒具有均匀、一致、近似的菱形十二面体结构,平均直径为~190 nm。然后将Cur@ZIF-8负载到丝素(SF)/聚己内酯(PCL)复合纳米纤维中,通过静电纺丝策略获得NFD。SF/PCL、SF/PCL/ZIF-8和SF/PCL/Cur作为对照组。所有四种不同的NFDs都表现出均匀的无珠状结构。其中,SF/PCL/Cur@ZIF-8 NFD具有优异的力学性能、较高的孔隙率(83.8±3.7%)和吸水率(292.4±9.5%)。重要的是,SF/PCL/Cur@ZIF-8 NFD显示出可控的Cur释放曲线,符合Krosmeyer-Peppas模型。体外细胞实验表明,SF/PCL/Cur@ZIF-8 NFD能明显促进人真皮成纤维细胞(HDFs)的增殖和粘附。此外,SF/PCL/Cur@ZIF-8 NDF对大肠杆菌和金黄色葡萄球菌的抑制率分别为83.2±1.7%和80.2±4.7%。在体内,SF/PCL/Cur@ZIF-8 NFD不仅显著减少小鼠肝出血模型的出血量,而且通过促进胶原生长和再上皮化,明显加速伤口愈合(~ 99%)。本研究表明,由金属有机框架(MOF)合成和静电纺丝合成的SF/PCL/Cur@ZIF-8 NFD在伤口治疗和皮肤组织工程方面具有重要的应用前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Curcumin delivery and release by using a dual cooperative encapsulation system constructed with ZIF-8 MOFs and silk fibroin/polycaprolactone nanofibers for accelerated wound healing
The development and design of novel nanofibrous dressings (NFDs) with biomimetic structure and multifunctional properties through electrospinning technique have aroused significant interest in the disciplines of wound treatment. In this study, curcumin (Cur) was firstly incorporated into zeolitic imidazolate framework-8 (ZIF-8), to generate Cur@ZIF-8 nanoparticles, which displayed a homogeneous, consistent, and nearly similar rhombic dodecahedral structure with the mean diameter of ~190 nm. Then the Cur@ZIF-8 was loaded into the silk fibroin (SF)/polycaprolactone (PCL) hybrid nanofibers to obtain a NFD through an electrospinning strategy. The other three different NFDs, i.e., SF/PCL, SF/PCL/ZIF-8, and SF/PCL/Cur, were fabricated as control groups. All the four different NFDs were found to exhibit uniform and bead-free morphology. Among them, the SF/PCL/Cur@ZIF-8 NFD exhibited superior mechanical properties, high porosity (83.8 ± 3.7 %), and water uptake (292.4 ± 9.5 %). Importantly, the SF/PCL/Cur@ZIF-8 NFD showed a controlled Cur release profile, fitting the Krosmeyer-Peppas model. The in vitro cell experiments indicated that the SF/PCL/Cur@ZIF-8 NFD obviously improved the proliferation and adhesion of human dermal fibroblasts (HDFs). Moreover, the SF/PCL/Cur@ZIF-8 NDF also exhibited great antibacterial activity, with the inhibition rate of 83.2 ± 1.7 % and 80.2 ± 4.7 % against E. coli and S. aureus, correspondingly. In vivo, the SF/PCL/Cur@ZIF-8 NFD not only significantly reduced the bleeding amount in a mouse liver hemorrhage model, but also obviously accelerated the wound healing (~99 %) by augmenting the collagen growth and re-epithelialization. The present study revealed that the SF/PCL/Cur@ZIF-8 NFD generated by a combination of metal-organic framework (MOF) synthesis and electrospinning showed significant promise for applications in wound treatment and skin tissue engineering.
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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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