Nano Lab, Advanced Technology Laboratory, Tufts University, 200 Boston Avenue, Medford, MA, 02155, USA.
Department of Electrical and Computer Engineering, Tufts University, 161 College Ave, Medford, MA, 02155, USA.
Sci Rep. 2022 Feb 3;12(1):1853. doi: 10.1038/s41598-022-05912-6.
Microneedles offer a convenient transdermal delivery route with potential for long term sustained release of drugs. However current microneedle technologies may not have the mechanical properties for reliable and stable penetration (e.g. hydrogel microneedles). Moreover, it is also challenging to realize microneedle arrays with large size and high flexibility. There is also an inherent upper limit to the amount and kind of drugs that can be loaded in the microneedles. In this paper, we present a new class of polymeric porous microneedles made from biocompatible and photo-curable resin that address these challenges. The microneedles are unique in their ability to load solid drug formulation in concentrated form. We demonstrate the loading and release of solid formulation of anesthetic and non-steroidal anti-inflammatory drugs, namely Lidocaine and Ibuprofen. Paper also demonstrates realization of large area (6 × 20 cm) flexible and stretchable microneedle patches capable of drug delivery on any body part. Penetration studies were performed in an ex vivo porcine model supplemented through rigorous compression tests to ensure the robustness and rigidity of the microneedles. Detailed release profiles of the microneedle patches were shown in an in vitro skin model. Results show promise for large area transdermal delivery of solid drug formulations using these porous microneedles.
微针提供了一种方便的经皮给药途径,具有药物长期持续释放的潜力。然而,目前的微针技术可能不具备可靠和稳定穿透的机械性能(例如水凝胶微针)。此外,实现具有大尺寸和高柔韧性的微针阵列也具有挑战性。微针中可装载的药物的数量和种类也存在固有上限。在本文中,我们提出了一类由生物相容性和光固化树脂制成的新型聚合物多孔微针,以应对这些挑战。这些微针的独特之处在于能够以浓缩形式装载固体药物制剂。我们展示了麻醉剂和非甾体抗炎药(即利多卡因和布洛芬)的固体制剂的加载和释放。本文还展示了能够在任何身体部位进行药物输送的大面积(6×20 厘米)柔性和可拉伸微针贴片的实现,该贴片能够在任何身体部位进行药物输送。在补充了严格的压缩测试的离体猪模型中进行了穿透研究,以确保微针的坚固性和刚性。在体外皮肤模型中显示了微针贴片的详细释放曲线。结果表明,这些多孔微针有望用于大面积的固体药物制剂的经皮给药。