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首页> 外文期刊>European journal of pharmaceutics and biopharmaceutics: official journal of Arbeitsgemeinschaft fuer Pharmazeutische Verfahrenstechnik e.V >Novel strategy for immunomodulation: Dissolving microneedle array encapsulating thymopentin fabricated by modified two-step molding technology
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Novel strategy for immunomodulation: Dissolving microneedle array encapsulating thymopentin fabricated by modified two-step molding technology

机译:免疫调节的新策略:溶解通过改进的两步成型技术制造的粒化胸腺蛋白的溶解微针阵列

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Graphical abstract Display Omitted Highlights ? TP5-DMNA was developed using a two-step molding technology for immunomodulation. ? BSA was used as co-material to fabricate TP5-DMNA for higher mechanical strength. ? The TP5-DMNA had equivalent immunomodulation efficiency to intravenous injection. ? The TP5-DMNA can be self-administrated with minimal pain and good compliance. 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.
机译:图形抽象显示省略了亮点?使用两步模制技术开发TP5-DMNA用于免疫调节。还BSA用作共材料以制造TP5-DMNA,以获得更高的机械强度。还TP5-DMNA对静脉内注射有等同的免疫调节效率。还TP5-DMNA可以自我管理,疼痛最小,良好的顺应性。摘要胸腺蛋白(TP5)通常用于治疗自身免疫疾病,具有短的血浆半衰期(30s)和长治疗期(7天至6个月)。它通常由注射器注射给药,导致患者依从性受损。溶解微针阵列(DMNA)提供了一种用于生物大分子的透皮递送的优异方法,因为它可以通过角质层无痛渗透,并在溶解皮肤后产生最小的生物危害废物。尽管近期DMNA进展作为透皮药物递送的新方法,但机械强度不足的问题仍有待解决。在该研究中,使用改进的两步模制技术唯一地开发TP5负载DMNA(TP5-DMNA)。通过使用牛血清白蛋白(BSA)作为制造针的共材料来提供更高的机械强度。所获得的TP5-DMNA含有BSA的BSA显示出更好的皮肤渗透和更高的药物负载效率,而不是没有BSA。体内药效学研究表明,在改善CD4 + / CD8 +比,SOD活性和MDA值至基础水平方面,TP5-DMNA对免疫调节对静脉内注射TP5的比较作用。在给药部位观察到才能观察到温和的刺激。这些结果表明,利用BSA的新型TP5-DMNA提供了TP5方便和安全的透皮递送的替代方法,这是未来临床应用的有希望的给药策略。

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