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基于离液剂的免疫贴片用于经皮传递抗原。

Ionic Liquid-Based Immunization Patch for the Transdermal Delivery of Antigens.

机构信息

Department of Applied Chemistry, Graduate School of Engineering, Kyushu University, 744 Motooka, Nishi-Ku, Fukuoka 819-0395, Japan.

Advanced Transdermal Drug Delivery System Center, Kyushu University, 744 Motooka, Nishi-Ku, Fukuoka 819-0395, Japan.

出版信息

Molecules. 2024 Jun 24;29(13):2995. doi: 10.3390/molecules29132995.

Abstract

Herein, we report a transdermal patch prepared using an ionic liquid-based solid in oil (IL-S/O) nanodispersion and a pressure-sensitive adhesive (PSA) to deliver the macromolecular antigenic protein, ovalbumin (OVA). The IL-S/O nanodispersion and a PSA were first mixed at an equal weight ratio, then coated onto a release liner, and covered with a support film. To evaluate the effect of the PSA, three types of PSAs, DURO-TAK 87-4098, DURO-TAK 87-4287, and DURO-TAK 87-235A, were used to obtain the corresponding IL-S/O patches SP-4098, SP-4287, and SP-235A, respectively. The prepared IL-S/O patches were characterized for surface morphology, viscoelasticity, and moisture content. In vitro skin penetration and in vivo immunization studies of the IL-S/O patches were performed using Yucatan micropig skin and the C57BL/6NJc1 mice model, respectively. The SP-4098 and SP-4287 delivered 5.49-fold and 5.47-fold higher amounts of drug compared with the aqueous formulation. Although both patches delivered a similar amount of drug, SP-4287 was not detached fully from the release liner after 30 days, indicating low stability. Mice immunized with the OVA-containing SP-4098 produced a 10-fold increase in anti-OVA IgG compared with those treated with an aqueous formulation. These findings suggested that the IL-S/O patch may be a good platform for the transdermal delivery of antigen molecules.

摘要

在此,我们报告了一种使用基于离子液体的固-油纳米分散体和压敏胶(PSA)制备的透皮贴剂,以递送大分子抗原蛋白卵清蛋白(OVA)。首先将 IL-S/O 纳米分散体和 PSA 以相等的重量比混合,然后涂覆在释放衬垫上,并覆盖支撑膜。为了评估 PSA 的效果,使用了三种 PSA,即 DURO-TAK 87-4098、DURO-TAK 87-4287 和 DURO-TAK 87-235A,分别获得相应的 IL-S/O 贴片 SP-4098、SP-4287 和 SP-235A。对制备的 IL-S/O 贴片进行了表面形貌、粘弹性和水分含量的表征。分别使用 Yucatan 微型猪皮肤和 C57BL/6NJc1 小鼠模型进行了 IL-S/O 贴片的体外皮肤渗透和体内免疫研究。SP-4098 和 SP-4287 的药物递送量分别比水性制剂高 5.49 倍和 5.47 倍。尽管两种贴片的药物递送量相似,但 SP-4287 在 30 天后并未完全从释放衬垫上脱落,表明稳定性较低。含有 OVA 的 SP-4098 免疫的小鼠产生的抗 OVA IgG 是水性制剂处理组的 10 倍。这些发现表明,IL-S/O 贴片可能是抗原分子透皮递送的良好平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3237/11243093/304f0f143870/molecules-29-02995-g001.jpg

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