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Pharmacological evaluation of membrane-moderated transdermal system of glipizide.格列吡嗪膜调控透皮系统的药理学评价
Clin Exp Pharmacol Physiol. 2006 Jan-Feb;33(1-2):17-26. doi: 10.1111/j.1440-1681.2006.04318.x.
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Transport numbers in transdermal iontophoresis.经皮离子电渗疗法中的迁移数
Biophys J. 2006 Apr 15;90(8):2822-30. doi: 10.1529/biophysj.105.074609. Epub 2006 Jan 27.
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Transdermal iontophoresis: combination strategies to improve transdermal iontophoretic drug delivery.经皮离子电渗疗法:改善经皮离子电渗药物递送的联合策略。
Eur J Pharm Biopharm. 2005 Jul;60(2):179-91. doi: 10.1016/j.ejpb.2004.12.008.
6
The effects of electrically assisted methods on transdermal delivery of nalbuphine benzoate and sebacoyl dinalbuphine ester from solutions and hydrogels.电辅助方法对苯甲酸纳布啡和癸二酰二纳布啡酯从溶液和水凝胶中经皮给药的影响。
Int J Pharm. 2005 Jun 13;297(1-2):162-71. doi: 10.1016/j.ijpharm.2005.03.015. Epub 2005 Apr 25.
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[Cardiovascular diseases. From epidemiology to prevention].[心血管疾病。从流行病学到预防]
Ugeskr Laeger. 2005 Mar 7;167(10):1170-3.
8
Transdermal delivery of naloxone: skin permeation, pharmacokinetic, irritancy and stability studies.纳洛酮的经皮给药:皮肤渗透、药代动力学、刺激性及稳定性研究
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9
Transdermal delivery of zidovudine (AZT): the effects of vehicles, enhancers, and polymer membranes on permeation across cadaver pig skin.齐多夫定(AZT)的经皮给药:载体、透皮促进剂和聚合物膜对其透过猪尸体皮肤的影响
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10
Electroosmosis in transdermal iontophoresis: implications for noninvasive and calibration-free glucose monitoring.经皮离子电渗疗法中的电渗作用:对无创及免校准葡萄糖监测的意义。
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赖诺普利在不同电流密度和药物浓度下的离子电渗渗透。

Iontophoretic permeation of lisinopril at different current densities and drug concentrations.

作者信息

Jain Ashish, Nayak Satish, Soni Vandana

机构信息

Bansal College of Pharmacy, Kokta, Anand Nagar, Bhopal-462021, India.

出版信息

Adv Pharm Bull. 2012;2(2):239-44. doi: 10.5681/apb.2012.036. Epub 2012 Aug 15.

DOI:10.5681/apb.2012.036
PMID:24312799
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3845985/
Abstract

PURPOSE

The purpose of the present work was to assess iontophoretic permeation of Lisinopril at different current densities and concentrations for development of patient-controlled active transdermal system.

METHODS

In vitro iontophoretic transdermal delivery of Lisinopril across the pigskin was investigated at three different drug concentrations and three different current densities (0.25- 0.75 mA/cm2) in the donor cell of the diffusion apparatus, using cathodal iontophoresis along with the passive controls.

RESULTS

For passive permeation, the steady state flux significantly increased with the increasing of donor drug concentration. At all concentration levels, iontophoresis considerably increased the permeation rate compared to passive controls. Iontophoretic transport of Lisinopril was to be found increase with current densities. Flux enhancement was highest at the lowest drug load and lowest at the highest drug load.

CONCLUSION

The obtained results indicate that permeation rate of Lisinopril across the pigskin can be considerably enhanced, controlled or optimized by the use of Iontophoresis technique.

摘要

目的

本研究旨在评估不同电流密度和浓度下赖诺普利的离子电渗渗透情况,以开发患者自控主动透皮系统。

方法

在扩散装置的供体池中,使用阴极离子电渗法并设置被动对照组,研究了三种不同药物浓度和三种不同电流密度(0.25 - 0.75 mA/cm²)下赖诺普利经猪皮的体外离子电渗透皮给药情况。

结果

对于被动渗透,稳态通量随供体药物浓度的增加而显著增加。在所有浓度水平下,与被动对照组相比,离子电渗法显著提高了渗透速率。赖诺普利的离子电渗转运随电流密度增加而增加。通量增强在最低药物负载时最高,在最高药物负载时最低。

结论

所得结果表明,通过使用离子电渗技术,赖诺普利经猪皮的渗透速率可得到显著提高、控制或优化。