Zhao Zongmin, Tanner Eden E L, Kim Jayoung, Ibsen Kelly, Gao Yongsheng, Mitragotri Samir
John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, Massachusetts 02138, United States.
Wyss Institute for Biologically Inspired Engineering at Harvard University, Boston, Massachusetts 02115, United States.
ACS Biomater Sci Eng. 2021 Jun 14;7(6):2783-2790. doi: 10.1021/acsbiomaterials.1c00322. Epub 2021 May 13.
Skin is one of the most immunologically active organs of the body due to the presence of diverse immune cells and its active involvement in the innate and adaptive immunity. Because of its unique location and immunological role, skin offers an excellent site for the introduction of immunomodulators to synergize with the active immune microenviroment for the desired outcome. However, delivery of immunomodulators to the skin remains a significant challenge due to the skin's barrier properties. Here, we report an ionic liquid (IL)-based strategy to formulate and deliver immunomodulators to the skin. Using imiquimod (IMQ) and triamcinolone acetonide (TCA) as the respective model immunoactive and immunosuppressive drugs, we demonstrated that ILs significantly enhanced the solubility of immunomodulators. In addition, ILs enabled the formulation of the immunomodulators into stable, topically applicable forms. Our skin penetration studies revealed that the IL formulations outperformed respective commercial topical comparators and delivered significantly more immunomodulators to deep skin layers. The lead IMQ formulation exhibited >10-fold better efficacy in delivering IMQ to the deep skin layers as compared to the commercial 5% IMQ cream. Lead TCA formulations achieved a dose level in deep skin layers that is comparable to that by clinically used intralesional injections. Our data collectively suggest that the IL-based strategy can be a simple and effective platform for delivery of immunomodulators to the skin.
由于存在多种免疫细胞且积极参与固有免疫和适应性免疫,皮肤是人体免疫活性最高的器官之一。因其独特的位置和免疫作用,皮肤为引入免疫调节剂提供了一个绝佳场所,使其能与活跃的免疫微环境协同作用以达到预期效果。然而,由于皮肤的屏障特性,将免疫调节剂递送至皮肤仍然是一项重大挑战。在此,我们报告一种基于离子液体(IL)的策略,用于制备免疫调节剂并将其递送至皮肤。使用咪喹莫特(IMQ)和曲安奈德(TCA)分别作为免疫活性和免疫抑制药物的模型,我们证明离子液体显著提高了免疫调节剂的溶解度。此外,离子液体能够将免疫调节剂制成稳定的、可局部应用的剂型。我们的皮肤渗透研究表明,基于离子液体的制剂优于各自的市售局部对照品,并能将更多的免疫调节剂递送至皮肤深层。与市售5%咪喹莫特乳膏相比,领先的咪喹莫特制剂在将咪喹莫特递送至皮肤深层方面表现出超过10倍的疗效。领先的曲安奈德制剂在皮肤深层达到的剂量水平与临床使用的皮损内注射相当。我们的数据共同表明,基于离子液体的策略可以成为将免疫调节剂递送至皮肤的一个简单有效的平台。