Electrically and Ultrasonically Enhanced Transdermal Delivery of Methotrexate

In this study, we used sonophoresis and iontophoresis to enhance the in vitro delivery of methotrexate through human cadaver skin. Iontophoresis was applied for 60 min at a 0.4 mA/sq·cm current density, while low-frequency sonophoresis was applied at a 20 kHz frequency (2 min application,...

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Main Authors: Hiep X. Nguyen, Ajay K. Banga
Format: Article
Language:English
Published: MDPI AG 2018-08-01
Series:Pharmaceutics
Subjects:
Online Access:http://www.mdpi.com/1999-4923/10/3/117
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spelling doaj-d5e30b30a36945e98207642d5e6c45262020-11-24T21:34:42ZengMDPI AGPharmaceutics1999-49232018-08-0110311710.3390/pharmaceutics10030117pharmaceutics10030117Electrically and Ultrasonically Enhanced Transdermal Delivery of MethotrexateHiep X. Nguyen0Ajay K. Banga1Department of Pharmaceutical Sciences, College of Pharmacy, Mercer University, Atlanta, GA 30341, USADepartment of Pharmaceutical Sciences, College of Pharmacy, Mercer University, Atlanta, GA 30341, USAIn this study, we used sonophoresis and iontophoresis to enhance the in vitro delivery of methotrexate through human cadaver skin. Iontophoresis was applied for 60 min at a 0.4 mA/sq·cm current density, while low-frequency sonophoresis was applied at a 20 kHz frequency (2 min application, and 6.9 W/sq·cm intensity). The treated skin was characterized by dye binding, transepidermal water loss, skin electrical resistance, and skin temperature measurement. Both sonophoresis and iontophoresis resulted in a significant reduction in skin electrical resistance as well as a marked increase in transepidermal water loss value (p < 0.05). Furthermore, the ultrasonic waves resulted in a significant increase in skin temperature (p < 0.05). In permeation studies, the use of iontophoresis led to a significantly higher drug permeability than the untreated group (n = 4, p < 0.05). The skin became markedly more permeable to methotrexate after the treatment by sonophoresis than by iontophoresis (p < 0.01). A synergistic effect for the combined application of sonophoresis and iontophoresis was also observed. Drug distribution in the skin layers revealed a significantly higher level of methotrexate in the sonicated skin than that in iontophoresis and untreated groups. Iontophoresis and low-frequency sonophoresis were found to enhance the transdermal and intradermal delivery of methotrexate in vitro.http://www.mdpi.com/1999-4923/10/3/117iontophoresissonophoresischaracterizationmethotrexatetransdermal delivery
collection DOAJ
language English
format Article
sources DOAJ
author Hiep X. Nguyen
Ajay K. Banga
spellingShingle Hiep X. Nguyen
Ajay K. Banga
Electrically and Ultrasonically Enhanced Transdermal Delivery of Methotrexate
Pharmaceutics
iontophoresis
sonophoresis
characterization
methotrexate
transdermal delivery
author_facet Hiep X. Nguyen
Ajay K. Banga
author_sort Hiep X. Nguyen
title Electrically and Ultrasonically Enhanced Transdermal Delivery of Methotrexate
title_short Electrically and Ultrasonically Enhanced Transdermal Delivery of Methotrexate
title_full Electrically and Ultrasonically Enhanced Transdermal Delivery of Methotrexate
title_fullStr Electrically and Ultrasonically Enhanced Transdermal Delivery of Methotrexate
title_full_unstemmed Electrically and Ultrasonically Enhanced Transdermal Delivery of Methotrexate
title_sort electrically and ultrasonically enhanced transdermal delivery of methotrexate
publisher MDPI AG
series Pharmaceutics
issn 1999-4923
publishDate 2018-08-01
description In this study, we used sonophoresis and iontophoresis to enhance the in vitro delivery of methotrexate through human cadaver skin. Iontophoresis was applied for 60 min at a 0.4 mA/sq·cm current density, while low-frequency sonophoresis was applied at a 20 kHz frequency (2 min application, and 6.9 W/sq·cm intensity). The treated skin was characterized by dye binding, transepidermal water loss, skin electrical resistance, and skin temperature measurement. Both sonophoresis and iontophoresis resulted in a significant reduction in skin electrical resistance as well as a marked increase in transepidermal water loss value (p < 0.05). Furthermore, the ultrasonic waves resulted in a significant increase in skin temperature (p < 0.05). In permeation studies, the use of iontophoresis led to a significantly higher drug permeability than the untreated group (n = 4, p < 0.05). The skin became markedly more permeable to methotrexate after the treatment by sonophoresis than by iontophoresis (p < 0.01). A synergistic effect for the combined application of sonophoresis and iontophoresis was also observed. Drug distribution in the skin layers revealed a significantly higher level of methotrexate in the sonicated skin than that in iontophoresis and untreated groups. Iontophoresis and low-frequency sonophoresis were found to enhance the transdermal and intradermal delivery of methotrexate in vitro.
topic iontophoresis
sonophoresis
characterization
methotrexate
transdermal delivery
url http://www.mdpi.com/1999-4923/10/3/117
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