Department of Bionano Technology and Gachon BioNano Research Institute, Gachon University, Gyeonggi-do, Republic of Korea.
Department of Microbiology and Immunology, Institute for Immunology and Immunological Diseases, Graduate School of Medical Science, Brain Korea 21 Project, Yonsei University College of Medicine, Seoul, Republic of Korea.
Drug Deliv Transl Res. 2021 Aug;11(4):1390-1400. doi: 10.1007/s13346-021-00964-z. Epub 2021 Mar 23.
The oral mucosa is an effective site for vaccination. However, for oral mucosal vaccines, delivery of the right dose of vaccine is not possible due to the water-rich environment. In this study, the buccal mucosa, which is easy to access using a microneedle array in the oral cavity, was selected as the administration site. The immune responses to the use of microneedles to conventional transmucosal delivery were compared. In addition, the adjuvant effect of the addition of cholera toxin (CT) to the drug formulation was observed. Two kinds of patches were prepared: (1) Ovalbumin (OVA) was dip coated only on the tips of microneedles (C-OVA-MN) and (2) OVA was coated on the surface of a flat disk patch substrate without microneedles (C-OVA-D). The drug delivery properties of C-OVA-MN and C-OVA-D were investigated using fluorescent-labeled OVA (OVA/FITC). Each patch was administered to mice twice, 2 weeks apart, and then antibody titers were measured. A microneedle patch can deliver vaccine into the epithelium of the buccal mucosa in a short period of time compared to transmucosal delivery. A microneedle system of C-OVA-MN showed a high serum IgG titer. In addition, CT triggered CD8 and CD4 T cell-mediated immune responses. Through this study, we present the possibility of a new method of vaccination to the buccal mucosa using microneedles and CT adjuvant. Illustration of delivery of vaccine to the oral mucosal epithelium using a microneedle patch: Ovalbumin (OVA)-coated microneedle (C-OVA-MN) consists of tip, step, and coating formulation. Microneedle patch coated with OVA formulation is targeting buccal mucosa, which is easy to access in the oral cavity. OVA is delivered to the buccal epithelium precisely using a microneedle patch, and OVA is delivered by transmucosal route using a disk patch.
口腔黏膜是疫苗接种的有效部位。然而,对于口腔黏膜疫苗,由于水富环境,无法输送正确剂量的疫苗。在这项研究中,选择易于通过口腔中的微针阵列到达的颊黏膜作为给药部位。比较了使用微针进行传统经黏膜传递的免疫反应。此外,还观察了向药物制剂中添加霍乱毒素 (CT) 的佐剂作用。制备了两种贴片:(1) 卵清蛋白 (OVA) 仅涂覆在微针的尖端上(C-OVA-MN)和 (2) OVA 涂覆在无微针的平板贴片基底上(C-OVA-D)。使用荧光标记的 OVA(OVA/FITC)研究了 C-OVA-MN 和 C-OVA-D 的药物传递特性。每个贴片在 2 周的间隔内两次给药给小鼠,然后测量抗体滴度。与经黏膜传递相比,微针贴片可以在短时间内将疫苗递送到颊黏膜的上皮细胞中。C-OVA-MN 的微针系统显示出较高的血清 IgG 滴度。此外,CT 引发了 CD8 和 CD4 T 细胞介导的免疫反应。通过这项研究,我们提出了使用微针和 CT 佐剂向颊黏膜进行新的疫苗接种方法的可能性。使用微针贴片向口腔黏膜上皮递送疫苗的示意图:卵清蛋白 (OVA)-涂覆的微针(C-OVA-MN)由尖端、台阶和涂覆配方组成。涂覆有 OVA 配方的微针贴片靶向颊黏膜,在口腔中易于到达。使用微针贴片将 OVA 精确递送到颊上皮,使用圆盘贴片通过经黏膜途径递送 OVA。