邻苯二甲酸酯血管胶纳米颗粒微针:抗逆转录病毒治疗的长效透皮给药系统

IF 4.9 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Thaisa Cardoso de Oliveira , Antônia Carla de Jesus Oliveira , Salete Reis , Sofia Costa Lima , Luíse Lopes Chaves , Monica Felts de La Roca Soares , José Lamartine Soares-Sobrinho
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引用次数: 0

摘要

微针(MN)作为一种可替代的透皮给药系统(TDDS)已经引起了人们的关注,因为它们易于给药和无痛,并且可以结合游离药物或纳米颗粒来调节药物释放。本研究旨在利用含锰邻苯二甲酸酯血管胶(PAG)纳米颗粒(NP)开发抗逆转录病毒药物奈韦拉平(NVP)的TDDS。以纳米悬浮液(NPns)或冻干纳米颗粒(NPfd)的形式制备负载nvp的NP,并将其掺入壳聚糖(CS)和聚乙烯吡罗烷酮(PVP)水凝胶中制备MN (M-NPns和M-NPfd)。采用硅氧烷微模塑法制备MN。选取的M-NPns和M-NPfd通过扫描电镜(SEM)、Franz扩散细胞对猪耳皮肤的渗透实验和含有0.1%罗丹明的MN的组织学研究进行了表征。72 h后,M-NPns和M-NPfd均表现出明显的药物渗透,组织学分析表明MN促进皮肤微穿孔。将NP掺入CS: PVP-MN后,得到了合适的力学性能和NVP缓慢、渐进的释放。本研究强调了含有PAG NP的MN作为一种创新的长效TDDS的潜力,通过将MN和NP技术相结合,可以提高患者的依从性并减少给药频率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Phthalate angico gum nanoparticles-based microneedles: a long-acting transdermal delivery system for antiretroviral therapy

Phthalate angico gum nanoparticles-based microneedles: a long-acting transdermal delivery system for antiretroviral therapy
Microneedles (MN) have gained attention as an alternative transdermal drug delivery system (TDDS) due to their ease of administration and painlessness, and the possibility of incorporating free drugs or nanoparticles to modulate drug release. This study aimed to develop TDDS for the antiretroviral drug nevirapine (NVP), using MN-containing phthalate angico gum (PAG) nanoparticles (NP). NVP-loaded NP were prepared as nanosuspensions (NPns) or lyophilized nanoparticles (NPfd) and incorporated into chitosan (CS) and polyvinylpyrrolidone (PVP) hydrogels to produce MN (M-NPns and M-NPfd). The MN were fabricated using a micro-molding method with a siloxane mold. The selected M-NPns and M-NPfd were characterized by scanning electron microscopy (SEM), permeation assays using Franz diffusion cells with porcine ear skin, and histological studies using MN containing 0.1 % rhodamine. Both M-NPns and M-NPfd showed significant drug permeation after 72 h, and histological assays demonstrated that MN promoted skin micropiercing. The incorporation of NP into CS: PVP-MN resulted in suitable mechanical properties and slow, progressive release of NVP. This study highlights the potential of MN containing PAG NP as an innovative long-acting TDDS for NVP delivery, by combining the technology of MN and NP, which may improve patient adherence and reduce the frequency of administration.
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来源期刊
CiteScore
8.00
自引率
8.00%
发文量
879
审稿时长
94 days
期刊介绍: The Journal of Drug Delivery Science and Technology is an international journal devoted to drug delivery and pharmaceutical technology. The journal covers all innovative aspects of all pharmaceutical dosage forms and the most advanced research on controlled release, bioavailability and drug absorption, nanomedicines, gene delivery, tissue engineering, etc. Hot topics, related to manufacturing processes and quality control, are also welcomed.
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