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可溶解双层安全微针透皮递药系统:一种用于治疗类风湿关节炎的生物舒适型新尝试。

Flexible two-layer dissolving and safing microneedle transdermal of neurotoxin: A biocomfortable attempt to treat Rheumatoid Arthritis.

机构信息

College of Pharmaceutical Science, Zhejiang Chinese Medical University, Hangzhou 310053, China.

Libraries of Zhejiang, Chinese Medical University, Zhejiang Chinese Medical University, Hangzhou 310053, China.

出版信息

Int J Pharm. 2019 May 30;563:91-100. doi: 10.1016/j.ijpharm.2019.03.033. Epub 2019 Mar 16.

Abstract

This study is directed towards the gentle transdermal delivery of Neurotoxin (NT) and study of the treatment of Rheumatoid Arthritis (RA) in rats by NT loaded dissolving Microneedles (DMNs-NT). The DMNs-NT fabrication involved a two-step centrifugation method. The quadrangular pyramid shape needles had great mechanical strength. The upper part of the needle contained 15.4 ± 0.5 μg of drug per patch. Blank DMNs showed favorable biocompatibility and low toxicity on the chondrocyte cells. Both NT and DMNs-NT displayed anti-inflammatory capabilities ex-vitro. The results of ex-vitro evaluation of DMNs the skin penetration depth of DMNs-NT rats was higher than 70 μm and the cumulative penetration of NT in DMNs could reach 95.8% in 4 h, whereas, the NT solution could barely penetrate the skin, thereby proving the favorable facilitation of NT transdermal delivery. The needle structure dissolved completely after 10 min in vivo and the channel on the Stratum Corneum (SC) was closed after 6 h. There was no significant adverse reaction on the skin after 15 days of administration. The pharmacodynamic study showed that DMNs-NT significantly reduced the toe swelling of RA rats and reduced the levels of TNF-α and IL-1β in serum to alleviate the injury of the ankle joints. DMNs-NT held favorable stability in 3 months. All these results established that DMNs-NT could penetrate the skin of rats in a biocompatible manner, and have a strong therapeutic effect on rat RA by transdermal delivery.

摘要

本研究旨在通过负载神经毒素(NT)的溶解微针(DMNs-NT)实现 NT 的经皮递药,并探讨其在大鼠类风湿关节炎(RA)治疗中的应用。DMNs-NT 的制备涉及两步离心法。四棱锥形针具有很强的机械强度。针的上部每贴含有 15.4±0.5μg 的药物。空白 DMNs 显示出良好的生物相容性和对软骨细胞的低毒性。NT 和 DMNs-NT 均显示出体外抗炎能力。DMNs 的体外评价结果表明,DMNs-NT 对皮肤的穿透深度大于 70μm,在 4h 内 DMNs 中 NT 的累积渗透量可达 95.8%,而 NT 溶液几乎无法穿透皮肤,从而证明了有利于 NT 经皮递药。在体内,针结构在 10min 内完全溶解,角质层(SC)上的通道在 6h 后关闭。给药 15 天后皮肤无明显不良反应。药效学研究表明,DMNs-NT 可显著减轻 RA 大鼠的足肿胀,降低血清中 TNF-α和 IL-1β的水平,从而减轻踝关节损伤。DMNs-NT 在 3 个月内保持良好的稳定性。所有这些结果都表明,DMNs-NT 可以以生物相容的方式穿透大鼠皮肤,并通过经皮递药对大鼠 RA 具有很强的治疗作用。

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