Influence of Concentration on Release and Permeation Process of Model Peptide Substance-Corticotropin-From Semisolid Formulations

The transdermal route of administration of drug substances allows clinicians to obtain a therapeutic effect bypassing the gastrointestinal tract, where the active substance could be inactivated. The hormonal substance used in the study-corticotropin (ACTH)-shows systemic effects. Therefore, the stud...

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Main Authors: Wioletta Siemiradzka, Barbara Dolińska, Florian Ryszka
Format: Article
Language:English
Published: MDPI AG 2020-06-01
Series:Molecules
Subjects:
Online Access:https://www.mdpi.com/1420-3049/25/12/2767
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author Wioletta Siemiradzka
Barbara Dolińska
Florian Ryszka
author_facet Wioletta Siemiradzka
Barbara Dolińska
Florian Ryszka
author_sort Wioletta Siemiradzka
collection DOAJ
description The transdermal route of administration of drug substances allows clinicians to obtain a therapeutic effect bypassing the gastrointestinal tract, where the active substance could be inactivated. The hormonal substance used in the study-corticotropin (ACTH)-shows systemic effects. Therefore, the study of the effect of the type of ointment base and drug concentration on the release rate and also permeation rate in in vivo simulated conditions may be a valuable source of information for clinical trials to effectively optimize corticotropin treatment. This goal was achieved by preparation ointment formulation selecting the appropriate ointment base and determining the effect of ACTH concentration on the release and permeation studies of the ACTH. Semi-solid preparations containing ACTH were prepared using Unguator CITO <i>e/s</i>. The release study of ACTH was tested using a modified USP apparatus 2 with Enhancer cells. The permeation study was conducted with vertical Franz cells. Rheograms of hydrogels were made with the use of a universal rotational rheometer. The dependence of the amount of released and permeated hormone on the ointment concentration was found. Based on the test of ACTH release from semi-solid formulations and evaluation of rheological parameters, it was found that glycerol ointment is the most favourable base for ACTH. The ACTH release and permeation process depends on both viscosity and ACTH concentration. The higher the hormone concentration, the higher the amount of released ACTH but it reduces the amount of ACTH penetrating through porcine skin.
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spelling doaj.art-67d5d04dc5b94333bf15ebd6e92a63722023-11-20T03:54:38ZengMDPI AGMolecules1420-30492020-06-012512276710.3390/molecules25122767Influence of Concentration on Release and Permeation Process of Model Peptide Substance-Corticotropin-From Semisolid FormulationsWioletta Siemiradzka0Barbara Dolińska1Florian Ryszka2Department of Pharmaceutical Technology, Medical University of Silesia in Katowice, School of Pharmacy with the Division of Laboratory Medicine, 41-200 Sosnowiec, PolandDepartment of Pharmaceutical Technology, Medical University of Silesia in Katowice, School of Pharmacy with the Division of Laboratory Medicine, 41-200 Sosnowiec, Poland“Biochefa” Pharmaceutical Research and Production Plant, 41-200 Sosnowiec, PolandThe transdermal route of administration of drug substances allows clinicians to obtain a therapeutic effect bypassing the gastrointestinal tract, where the active substance could be inactivated. The hormonal substance used in the study-corticotropin (ACTH)-shows systemic effects. Therefore, the study of the effect of the type of ointment base and drug concentration on the release rate and also permeation rate in in vivo simulated conditions may be a valuable source of information for clinical trials to effectively optimize corticotropin treatment. This goal was achieved by preparation ointment formulation selecting the appropriate ointment base and determining the effect of ACTH concentration on the release and permeation studies of the ACTH. Semi-solid preparations containing ACTH were prepared using Unguator CITO <i>e/s</i>. The release study of ACTH was tested using a modified USP apparatus 2 with Enhancer cells. The permeation study was conducted with vertical Franz cells. Rheograms of hydrogels were made with the use of a universal rotational rheometer. The dependence of the amount of released and permeated hormone on the ointment concentration was found. Based on the test of ACTH release from semi-solid formulations and evaluation of rheological parameters, it was found that glycerol ointment is the most favourable base for ACTH. The ACTH release and permeation process depends on both viscosity and ACTH concentration. The higher the hormone concentration, the higher the amount of released ACTH but it reduces the amount of ACTH penetrating through porcine skin.https://www.mdpi.com/1420-3049/25/12/2767ACTHointmentshydrogel basereleasepermeationrheology
spellingShingle Wioletta Siemiradzka
Barbara Dolińska
Florian Ryszka
Influence of Concentration on Release and Permeation Process of Model Peptide Substance-Corticotropin-From Semisolid Formulations
Molecules
ACTH
ointments
hydrogel base
release
permeation
rheology
title Influence of Concentration on Release and Permeation Process of Model Peptide Substance-Corticotropin-From Semisolid Formulations
title_full Influence of Concentration on Release and Permeation Process of Model Peptide Substance-Corticotropin-From Semisolid Formulations
title_fullStr Influence of Concentration on Release and Permeation Process of Model Peptide Substance-Corticotropin-From Semisolid Formulations
title_full_unstemmed Influence of Concentration on Release and Permeation Process of Model Peptide Substance-Corticotropin-From Semisolid Formulations
title_short Influence of Concentration on Release and Permeation Process of Model Peptide Substance-Corticotropin-From Semisolid Formulations
title_sort influence of concentration on release and permeation process of model peptide substance corticotropin from semisolid formulations
topic ACTH
ointments
hydrogel base
release
permeation
rheology
url https://www.mdpi.com/1420-3049/25/12/2767
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AT barbaradolinska influenceofconcentrationonreleaseandpermeationprocessofmodelpeptidesubstancecorticotropinfromsemisolidformulations
AT florianryszka influenceofconcentrationonreleaseandpermeationprocessofmodelpeptidesubstancecorticotropinfromsemisolidformulations