Su Tong, Tang Zequn, Hu Jiayi, Zhu Yuyu, Shen Teng
Department of Pharmaceutics, School of Pharmacy, Fudan University, Shanghai, People's Republic of China.
Key Laboratory of Smart Drug Delivery, Ministry of Education, Shanghai, 201203, People's Republic of China.
Drug Deliv Transl Res. 2024 Nov;14(11):3112-3127. doi: 10.1007/s13346-024-01531-y. Epub 2024 Mar 2.
Microneedle patch (MNP) has become a hot research topic in the field of transdermal drug delivery due to its ability to overcome the stratum corneum barrier. Among the various types of microneedles, dissolving microneedles represent one of the most promising transdermal delivery methods. However, the most used method for preparing dissolving microneedles, namely microfabrication, suffers from issues such as long drying time, susceptibility to humidity, and large batch-to-batch variability, which limit the development of dissolving microneedles. In this study, we report for the first time a method for preparing dissolving microneedles using freeze-drying technology. We screened substrates suitable for freeze-dried microneedle patch (FD-MNP) and used coating technology to enhance the mechanical strength of FD-MNP, allowing them to meet the requirements for skin penetration. We successfully prepared FD-MNP using hyaluronic acid as the substrate and insulin as the model drug. Scanning electron microscopy revealed that the microneedles had a porous structure. After coating, the mechanical strength of the microneedles was 0.61 N/Needle, and skin penetration rate was 97%, with a penetration depth of 215 μm. The tips of the FD-MNP dissolved completely within approximately 60 s after skin penetration, which is much faster than conventional MNP (180 s). In vitro transdermal experiments showed that the FD-MNP shortened the lag time for transdermal delivery of rhodamine 123 and insulin compared to conventional MNP, indicating a faster transdermal delivery rate. Pharmacological experiments showed that the FD-MNP lowered mouse blood glucose levels more effectively than conventional MNP, with a relative pharmacological availability of 96.59 ± 2.84%, higher than that of conventional MNP (84.34 ± 3.87%), P = 0.0095. After storage under 40℃ for two months, the insulin content within the FD-MNP remained high at 95.27 ± 4.46%, which was much higher than that of conventional MNP (58.73 ± 3.71%), P < 0.0001. In conclusion, freeze-drying technology is a highly valuable method for preparing dissolving microneedles with potential applications in transdermal drug delivery.
微针贴片(MNP)因其能够克服角质层屏障而成为透皮给药领域的一个热门研究课题。在各种类型的微针中,溶解微针是最有前景的透皮给药方法之一。然而,制备溶解微针最常用的方法,即微制造,存在干燥时间长、易受潮以及批次间差异大等问题,这些问题限制了溶解微针的发展。在本研究中,我们首次报道了一种使用冷冻干燥技术制备溶解微针的方法。我们筛选了适合冷冻干燥微针贴片(FD-MNP)的基质,并使用涂层技术提高FD-MNP的机械强度,使其能够满足皮肤穿透的要求。我们成功地以透明质酸为基质、胰岛素为模型药物制备了FD-MNP。扫描电子显微镜显示微针具有多孔结构。涂层后,微针的机械强度为0.61 N/针,皮肤穿透率为97%,穿透深度为215μm。FD-MNP的尖端在皮肤穿透后约60秒内完全溶解,这比传统MNP(180秒)快得多。体外透皮实验表明,与传统MNP相比,FD-MNP缩短了罗丹明123和胰岛素透皮给药的滞后时间,表明透皮给药速率更快。药理实验表明,FD-MNP比传统MNP更有效地降低小鼠血糖水平,相对药理利用率为96.59±2.84%,高于传统MNP(84.34±3.87%),P = 0.0095。在40℃下储存两个月后,FD-MNP内的胰岛素含量仍高达95.27±4.46%,远高于传统MNP(58.73±3.71%),P < 0.0001。总之,冷冻干燥技术是一种极具价值的制备溶解微针的方法,在透皮给药方面具有潜在应用。