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可溶解鸟嘴状微针阵列的制备及其力学/生物学评价

Fabrication and mechanical/biological evaluations of dissolving bird-bill microneedle arrays.

作者信息

Amano Natsumi, Takaki Yuusei, Takei Harunori, Matsuo Masaaki, Hara Masaya, Tashiro Yasunori, Oniki Takahiro, Ito Takahiro, Hikima Tomohiro

机构信息

Department of Bioscience and Bioinformatics, Kyushu Institute of Technology, 680-4 Kawazu, Iizuka, Fukuoka, 820-8502, Japan.

Department of Systems Design and Informatics, Kyushu Institute of Technology, 680-4 Kawazu, Iizuka, Fukuoka, 820-8502, Japan.

出版信息

Drug Deliv Transl Res. 2025 Jul;15(7):2581-2588. doi: 10.1007/s13346-024-01757-w. Epub 2024 Dec 9.

DOI:10.1007/s13346-024-01757-w
PMID:39653959
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12137373/
Abstract

Coated microneedles (MNs) have several disadvantages, including limited drug doses, decreased skin puncture ability due to drug coating, and a risk of clogging and infection due to repeated application. We aimed to fabricate a dissolving bird-bill MN (dBB MN) with a vertical groove between two thin plate-shaped needles and needle pedestal. Moreover, we evaluated its ability to transdermally deliver a large-molecular-weight insulin into the systemic circulation. Hydrogels with various concentrations of polyvinylpyrrolidone (PVP) or sodium hyaluronate (HA) were prepared, and dBB MN arrays were fabricated by micromolding under negative pressure for potential mass production. The needle height of the dBB MN was at the maximum when the hydrogel was 25 w/w% PVP, with a viscosity of 8-9 Pa∙s. Furthermore, the buckling force of dBB MNs made from 25 w/w% PVP was 130.6 ± 51.0 mN, which increased to 195.6 ± 65.3 mN when insulin was added at 1 w/w%. The skin insertion ability of dBB MN was investigated using swain skin, with micro-holes were confirmed on the skin surface. dBB MN showed biphasic dissolution in the skin; the plate-shaped needles were immediately dissolved within 10 min, while the needle pedestal was slowly dissolved over 180 min. The blood glucose concentration in diabetic rats decreased slowly and significantly after a 3-h application of the insulin-loaded dBB MN array. Therefore, the dBB MN array demonstrated sufficient ability to puncture skin and transdermally deliver a large-molecular-weight drug into the systemic circulation. These findings suggest that the dBB MN array holds promise as a minimal invasive drug delivery platform, with potential applications in improving patient adherence and expanding access to essential therapies, particularly in resource-limited settings.

摘要

包衣微针(MNs)存在几个缺点,包括药物剂量有限、由于药物包衣导致皮肤穿刺能力下降,以及由于重复使用而存在堵塞和感染的风险。我们旨在制造一种在两个薄板状针和针座之间有垂直凹槽的可溶解鸟嘴形微针(dBB MN)。此外,我们评估了其将大分子量胰岛素经皮递送至体循环的能力。制备了具有不同浓度聚乙烯吡咯烷酮(PVP)或透明质酸钠(HA)的水凝胶,并通过负压微成型制备dBB MN阵列以实现潜在的大规模生产。当水凝胶为25 w/w% PVP且粘度为8 - 9 Pa∙s时,dBB MN的针高最大。此外,由25 w/w% PVP制成的dBB MN的屈曲力为130.6±51.0 mN,当以1 w/w%添加胰岛素时,屈曲力增加到195.6±65.3 mN。使用猪皮研究了dBB MN的皮肤插入能力,在皮肤表面确认有微孔。dBB MN在皮肤中呈现双相溶解;板状针在10分钟内立即溶解,而针座在180分钟内缓慢溶解。在应用载有胰岛素的dBB MN阵列3小时后,糖尿病大鼠的血糖浓度缓慢且显著下降。因此,dBB MN阵列表现出足够的穿刺皮肤并将大分子量药物经皮递送至体循环的能力。这些发现表明,dBB MN阵列有望成为一种微创给药平台,在改善患者依从性和扩大基本治疗的可及性方面具有潜在应用,特别是在资源有限的环境中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/017e/12137373/710eb4c7b56b/13346_2024_1757_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/017e/12137373/b70a49a3d179/13346_2024_1757_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/017e/12137373/f93a77d04e0d/13346_2024_1757_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/017e/12137373/90d87ee3d679/13346_2024_1757_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/017e/12137373/35f2e55417ce/13346_2024_1757_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/017e/12137373/22da855ffabd/13346_2024_1757_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/017e/12137373/710eb4c7b56b/13346_2024_1757_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/017e/12137373/b70a49a3d179/13346_2024_1757_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/017e/12137373/f93a77d04e0d/13346_2024_1757_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/017e/12137373/90d87ee3d679/13346_2024_1757_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/017e/12137373/35f2e55417ce/13346_2024_1757_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/017e/12137373/22da855ffabd/13346_2024_1757_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/017e/12137373/710eb4c7b56b/13346_2024_1757_Fig6_HTML.jpg

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Elucidating the Impact of Surfactants on the Performance of Dissolving Microneedle Array Patches.
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