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新型免疫调节策略:采用改良两步模塑技术制备的胸腺五肽微针阵列的溶解。

Novel strategy for immunomodulation: Dissolving microneedle array encapsulating thymopentin fabricated by modified two-step molding technology.

机构信息

School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China.

School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China.

出版信息

Eur J Pharm Biopharm. 2018 Jan;122:104-112. doi: 10.1016/j.ejpb.2017.10.011. Epub 2017 Oct 16.

Abstract

Thymopentin (TP5) is commonly used in the treatment for autoimmune diseases, with a short plasma half-life (30s) and a long treatment period (7 days to 6 months). It is usually administrated by syringe injection, resulting in compromised patient compliance. Dissolving microneedle array (DMNA) offers a superior approach for transdermal delivery of biological macromolecules, as it allows painless penetration through the stratum corneum and generates minimal biohazardous waste after dissolving in the skin. Despite recent advances in DMNA as a novel approach for transdermal drug delivery, problem of insufficient mechanical strength remains to be solved. In this study, TP5-loaded DMNA (TP5-DMNA) was uniquely developed using a modified two-step molding technology. The higher mechanical strength was furnished by employing bovine serum albumin (BSA) as a co-material to fabricate the needles. The obtained TP5-DMNA containing BSA displayed better skin penetration and higher drug loading efficiency than that without BSA. The in vivo pharmacodynamics study demonstrated that TP5-DMNA had comparative effect on immunomodulation to intravenous injection of TP5, in terms of ameliorating the CD4+/CD8+ ratio, SOD activity and MDA value to the basal level. Only mild irritation was observed at the site of administration. These results suggest that the novel TP5-DMNA utilizing BSA provides an alternative approach for convenient and safe transdermal delivery of TP5, which is a promising administration strategy for future clinical application.

摘要

胸腺五肽(TP5)常用于治疗自身免疫性疾病,其血浆半衰期较短(30s),治疗周期较长(7 天至 6 个月)。通常通过注射器注射给药,导致患者顺应性差。溶解微针贴片(DMNA)为生物大分子的经皮给药提供了一种优越的方法,因为它可以无痛地穿透角质层,并在溶解在皮肤后产生最小的生物危害性废物。尽管 DMNA 作为一种新型经皮药物输送方法最近取得了进展,但机械强度不足的问题仍有待解决。在这项研究中,使用改良的两步成型技术独特地开发了负载 TP5 的 DMNA(TP5-DMNA)。通过使用牛血清白蛋白(BSA)作为共材料来制造针,提供了更高的机械强度。与不含 BSA 的相比,含有 BSA 的获得的 TP5-DMNA 显示出更好的皮肤穿透性和更高的药物负载效率。体内药效学研究表明,TP5-DMNA 在免疫调节方面对静脉注射 TP5 具有可比性,能够将 CD4+/CD8+比值、SOD 活性和 MDA 值恢复到基础水平。仅在给药部位观察到轻微刺激。这些结果表明,利用 BSA 的新型 TP5-DMNA 为方便、安全的 TP5 经皮给药提供了一种替代方法,这是未来临床应用的一种有前途的给药策略。

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