Harnessing Microneedles for Delivery and Preservation of Natural Killer Cell-Derived Extracellular Vesicles.

IF 5.4 2区 医学 Q2 MATERIALS SCIENCE, BIOMATERIALS
S A Lim, S Chen, I Suzuki, K Lambaren, A Soleimani, N Ho, M Mousavi, E J Chung
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引用次数: 0

Abstract

Natural killer cell-derived extracellular vesicles (NK-EVs) have demonstrated anti-inflammatory properties similar to those of their parent cells. EVs have been commonly delivered via intravenous (IV) administration, which can be invasive and is not ideal for chronic treatment. Another limitation of nanotherapy is its storage requirements, as EVs are commonly stored at -80 °C to preserve EV cargo and stability. In order to address these limitations, we explored dissolvable microneedles (MNs) as a promising alternative method for the administration of EVs. MNs have been used to deliver drugs, vaccines, and biomolecules, offering a convenient, noninvasive route of administration while preserving the therapeutic efficacy of EVs for extended periods, even at room temperature. Thus, we hypothesize that MN has the potential to sustain NK-EV stability and successfully deliver NK-EVs with minimal invasion. To test our hypothesis, we first developed an optimal MN formulation composed of hyaluronic acid and trehalose, both protein-protective materials that are biocompatible and biodegradable. After preparing MNs, we evaluated their stiffness, EV release profile, and ability to puncture pig skin. Additionally, the long-term storage stability of the EVs in MNs in inflammatory models in vitro and in vivo was evaluated. The MN successfully maintained EV efficacy even after storage after six months at room temperature, reducing the pro-inflammatory cytokine IL-6 by about 70% in inflamed human fibroblast cells relative to nontreated groups. Furthermore, EV-loaded MN treatment reduced both pro-inflammatory cytokines (IL-6 and TNFα) and psoriasis markers (Ki67 and IL-17) expression in a psoriasis model of chronic inflammation by about 40% compared to nontreated groups. Herein, our MN demonstrates the potential for easy-to-administer NK-EV therapies with long-term storage capabilities that preserve the NK-EV's anti-inflammatory properties.

利用微针递送和保存自然杀伤细胞衍生的细胞外囊泡。
自然杀伤细胞衍生的细胞外囊泡(nk - ev)具有与其亲本细胞相似的抗炎特性。ev通常通过静脉(IV)给药,这可能是侵入性的,不适合慢性治疗。纳米疗法的另一个限制是其存储要求,因为电动汽车通常存储在-80°C,以保持电动汽车货物和稳定性。为了解决这些限制,我们探索了可溶解微针(MNs)作为一种有希望的ev管理替代方法。MNs已被用于递送药物、疫苗和生物分子,提供了一种方便、无创的给药途径,同时延长了ev的治疗效果,即使在室温下也是如此。因此,我们假设MN具有维持NK-EV稳定性的潜力,并以最小的侵袭成功递送NK-EV。为了验证我们的假设,我们首先开发了一种由透明质酸和海藻糖组成的最佳MN配方,这两种蛋白质保护材料都具有生物相容性和可生物降解性。在制备MNs后,我们评估了它们的硬度、EV释放曲线和刺穿猪皮肤的能力。此外,在体外和体内炎症模型中,评估了ev在MNs中的长期储存稳定性。即使在室温下保存6个月后,MN也成功地保持了EV的功效,与未处理组相比,炎症的人成纤维细胞中的促炎细胞因子IL-6减少了约70%。此外,与未治疗组相比,ev负载MN治疗使慢性炎症银屑病模型中的促炎细胞因子(IL-6和TNFα)和银屑病标志物(Ki67和IL-17)的表达降低了约40%。在此,我们的MN证明了易于管理的NK-EV疗法的潜力,具有长期储存能力,可以保留NK-EV的抗炎特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Biomaterials Science & Engineering
ACS Biomaterials Science & Engineering Materials Science-Biomaterials
CiteScore
10.30
自引率
3.40%
发文量
413
期刊介绍: ACS Biomaterials Science & Engineering is the leading journal in the field of biomaterials, serving as an international forum for publishing cutting-edge research and innovative ideas on a broad range of topics: Applications and Health – implantable tissues and devices, prosthesis, health risks, toxicology Bio-interactions and Bio-compatibility – material-biology interactions, chemical/morphological/structural communication, mechanobiology, signaling and biological responses, immuno-engineering, calcification, coatings, corrosion and degradation of biomaterials and devices, biophysical regulation of cell functions Characterization, Synthesis, and Modification – new biomaterials, bioinspired and biomimetic approaches to biomaterials, exploiting structural hierarchy and architectural control, combinatorial strategies for biomaterials discovery, genetic biomaterials design, synthetic biology, new composite systems, bionics, polymer synthesis Controlled Release and Delivery Systems – biomaterial-based drug and gene delivery, bio-responsive delivery of regulatory molecules, pharmaceutical engineering Healthcare Advances – clinical translation, regulatory issues, patient safety, emerging trends Imaging and Diagnostics – imaging agents and probes, theranostics, biosensors, monitoring Manufacturing and Technology – 3D printing, inks, organ-on-a-chip, bioreactor/perfusion systems, microdevices, BioMEMS, optics and electronics interfaces with biomaterials, systems integration Modeling and Informatics Tools – scaling methods to guide biomaterial design, predictive algorithms for structure-function, biomechanics, integrating bioinformatics with biomaterials discovery, metabolomics in the context of biomaterials Tissue Engineering and Regenerative Medicine – basic and applied studies, cell therapies, scaffolds, vascularization, bioartificial organs, transplantation and functionality, cellular agriculture
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