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使用包衣微针阵列贴片系统经皮递送去氨加压素。

Transdermal delivery of desmopressin using a coated microneedle array patch system.

作者信息

Cormier Michel, Johnson Bonny, Ameri Mahmoud, Nyam Kofi, Libiran Luz, Zhang Dee Dee, Daddona Pete

机构信息

Biological Sciences Department, ALZA Corporation, 1900 Charleston Road, Mountain View, CA 94043, USA.

出版信息

J Control Release. 2004 Jul 7;97(3):503-11. doi: 10.1016/j.jconrel.2004.04.003.

Abstract

Desmopressin is a synthetic peptide hormone chiefly used for treatment of enuresis in young children. It is available in injectable, intranasal, and oral formulations. While administration by injection is poorly suited for routine use in young children, intranasal and oral administration result in low and variable bioavailability. This study therefore explored the feasibility of administering desmopressin transdermally using Macroflux technology, which uses a microneedle array to overcome the skin barrier. The tips of microneedles in 2-cm2 arrays were covered with a solid coating of various amounts of desmopressin and applied to the skin of hairless guinea pigs for 5 or 15 min. Pharmacologically relevant amounts of desmopressin were delivered after 5 min. Bioavailability was as high as 85% and showed acceptable variability (30%). Immunoreactive serum desmopressin reached peak levels after a Tmax of 60 min. Elimination kinetics for serum desmopressin was similar after transdermal and intravenous (IV) delivery, suggesting the absence of a skin depot. Only 10% of the desmopressin dose loaded onto the microneedle array was found on the skin surface after application. Additionally, the patches were well tolerated. These results suggest that transdermal delivery of desmopressin by Macroflux is a safe and efficient alternative to currently available routes of administration.

摘要

去氨加压素是一种合成肽激素,主要用于治疗幼儿遗尿症。它有注射剂、鼻内制剂和口服制剂。虽然注射给药不太适合幼儿常规使用,但鼻内和口服给药的生物利用度较低且变化不定。因此,本研究探讨了使用Macroflux技术经皮给药去氨加压素的可行性,该技术使用微针阵列来克服皮肤屏障。将2平方厘米阵列中的微针尖端覆盖有不同量去氨加压素的固体涂层,并应用于无毛豚鼠的皮肤5或15分钟。5分钟后递送了药理学相关量的去氨加压素。生物利用度高达85%,且显示出可接受的变异性(30%)。免疫反应性血清去氨加压素在60分钟的Tmax后达到峰值水平。经皮和静脉内(IV)给药后血清去氨加压素的消除动力学相似,表明不存在皮肤贮库。应用后,在皮肤表面仅发现加载到微针阵列上的去氨加压素剂量的10%。此外,贴片耐受性良好。这些结果表明,Macroflux经皮递送去氨加压素是目前可用给药途径的一种安全有效的替代方法。

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