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白喉类毒素溶解微针疫苗接种:佐剂筛选和重复分次剂量给药的效果。

Diphtheria toxoid dissolving microneedle vaccination: Adjuvant screening and effect of repeated-fractional dose administration.

机构信息

Division of BioTherapeutics, Leiden Academic Centre for Drug Research, Leiden University, the Netherlands.

Division of Drug Discovery and Safety, Leiden Academic Centre for Drug Research, Leiden University, the Netherlands.

出版信息

Int J Pharm. 2020 Apr 30;580:119182. doi: 10.1016/j.ijpharm.2020.119182. Epub 2020 Feb 28.

Abstract

In this study the effect of repeated-fractional intradermal administration of diphtheria toxoid (DT) compared to a single administration in the presence or absence of adjuvants formulated in dissolving microneedles (dMNs) was investigated. Based on an adjuvant screening with a hollow microneedle (hMN) system, poly(I:C) and gibbsite, a nanoparticulate aluminum salt, were selected for further studies: they were co-encapsulated with DT in dMNs with either a full or fractional DT-adjuvant dose. Sharp dMNs were prepared regardless the composition and were capable to penetrate the skin, dissolve within 20 min and deposit the intended antigen-adjuvant dose, which remained in the skin for at least 5 h. Dermal immunization with hMN in repeated-fractional dosing (RFrD) resulted in a higher immune response than a single-full dose (SFD) administration. Vaccination by dMNs led overall to higher responses than hMN but did not show an enhanced response after RFrD compared to a SFD administration. Co-encapsulation of the adjuvant in dMNs did not increase the immune response further. Immunization by dMNs without adjuvant gave a comparable response to subcutaneously injected DT-AlPO in a 15 times higher dose of DT, as well as subcutaneous injected DT-poly(I:C) in a similar DT dose. Summarizing, adjuvant-free dMNs showed to be a promising delivery tool for vaccination performed in SFD administration.

摘要

在这项研究中,比较了重复皮内给予白喉类毒素 (DT) 与单次皮内给予 DT 加或不加佐剂在溶解微针 (dMN) 中的效果。基于空心微针 (hMN) 系统的佐剂筛选,选择聚肌苷酸和氢氧化铝,一种纳米级铝盐,用于进一步研究:它们与 DT 共包封在 dMN 中,有全剂量或分剂量的 DT-佐剂。无论组成如何,锋利的 dMN 都可以穿透皮肤,在 20 分钟内溶解,并沉积预期的抗原-佐剂剂量,至少在皮肤中保留 5 小时。与单次全剂量 (SFD) 相比,hMN 的重复分剂量 (RFrD) 导致更高的免疫反应。与 hMN 相比,dMN 总体上导致更高的反应,但与 SFD 相比,RFrD 后没有增强的反应。佐剂共包封在 dMN 中并没有进一步增加免疫反应。无佐剂的 dMN 免疫与皮下注射 DT-AlPO 在 15 倍高剂量的 DT 以及皮下注射 DT-聚肌苷酸在类似剂量的 DT 中具有可比的反应。总之,无佐剂的 dMN 显示出作为单次皮内给药疫苗接种的有前途的递送工具。

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