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Compritol-Based Nanostrucutured Lipid Carriers (NLCs) for Augmentation of Zolmitriptan Bioavailability via the Transdermal Route: In Vitro Optimization, Ex Vivo Permeation, In Vivo Pharmacokinetic Study

Migraine is a severe neurovascular disease manifested mainly as unilateral throbbing headaches. Triptans are agonists for serotonin receptors. Zolmitriptan (ZMP) is a biopharmaceutics classification system (BCS) class III medication with an absolute oral bioavailability of less than 40%. As a result...

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Autores principales: Hassan, Doaa H., Shohdy, Joseph N., El-Setouhy, Doaa Ahmed, El-Nabarawi, Mohamed, Naguib, Marianne J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9315618/
https://www.ncbi.nlm.nih.gov/pubmed/35890379
http://dx.doi.org/10.3390/pharmaceutics14071484
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author Hassan, Doaa H.
Shohdy, Joseph N.
El-Setouhy, Doaa Ahmed
El-Nabarawi, Mohamed
Naguib, Marianne J.
author_facet Hassan, Doaa H.
Shohdy, Joseph N.
El-Setouhy, Doaa Ahmed
El-Nabarawi, Mohamed
Naguib, Marianne J.
author_sort Hassan, Doaa H.
collection PubMed
description Migraine is a severe neurovascular disease manifested mainly as unilateral throbbing headaches. Triptans are agonists for serotonin receptors. Zolmitriptan (ZMP) is a biopharmaceutics classification system (BCS) class III medication with an absolute oral bioavailability of less than 40%. As a result, our research intended to increase ZMP bioavailability by developing transdermal nanostructured lipid carriers (NLCs). NLCs were prepared utilizing a combination of hot melt emulsification and high-speed stirring in a 3(2) full factorial design. The studied variables were liquid lipid type (X(1)) and surfactant type (X(2)). The developed NLCs were evaluated in terms of particle size (Y(1), nm), polydispersity index (Y(2), PDI), zeta potential (Y(3), mV), entrapment efficacy (Y(4), %) and amount released after 6 h (Q6h, Y(5), %). At 1% Mygliol as liquid lipid component and 1% Span 20 as surfactant, the optimized formula (NLC9) showed a minimum particle size (138 ± 7.07 nm), minimum polydispersity index (0.39 ± 0.001), acceptable zeta potential (−22.1 ± 0.80), maximum entrapment efficiency (73 ± 0.10%) and maximum amount released after 6 h (83.22 ± 0.10%). The optimized formula was then incorporated into gel preparation (HPMC) to improve the system stability and ease of application. Then, the pharmacokinetic study was conducted on rabbits in a cross-over design. The calculated parameters showed a higher area under the curve (AUC(0–24,) AUC(0–∞) (ng·h/mL)) of the developed ZMP-NLCs loaded gel, with a 1.76-fold increase in bioavailability in comparison to the orally administered marketed product (Zomig(®)). A histopathological examination revealed the safety of the developed nanoparticles. The declared results highlight the potential of utilizing the proposed NLCs for the transdermal delivery of ZMP to improve the drug bioavailability.
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spelling pubmed-93156182022-07-27 Compritol-Based Nanostrucutured Lipid Carriers (NLCs) for Augmentation of Zolmitriptan Bioavailability via the Transdermal Route: In Vitro Optimization, Ex Vivo Permeation, In Vivo Pharmacokinetic Study Hassan, Doaa H. Shohdy, Joseph N. El-Setouhy, Doaa Ahmed El-Nabarawi, Mohamed Naguib, Marianne J. Pharmaceutics Article Migraine is a severe neurovascular disease manifested mainly as unilateral throbbing headaches. Triptans are agonists for serotonin receptors. Zolmitriptan (ZMP) is a biopharmaceutics classification system (BCS) class III medication with an absolute oral bioavailability of less than 40%. As a result, our research intended to increase ZMP bioavailability by developing transdermal nanostructured lipid carriers (NLCs). NLCs were prepared utilizing a combination of hot melt emulsification and high-speed stirring in a 3(2) full factorial design. The studied variables were liquid lipid type (X(1)) and surfactant type (X(2)). The developed NLCs were evaluated in terms of particle size (Y(1), nm), polydispersity index (Y(2), PDI), zeta potential (Y(3), mV), entrapment efficacy (Y(4), %) and amount released after 6 h (Q6h, Y(5), %). At 1% Mygliol as liquid lipid component and 1% Span 20 as surfactant, the optimized formula (NLC9) showed a minimum particle size (138 ± 7.07 nm), minimum polydispersity index (0.39 ± 0.001), acceptable zeta potential (−22.1 ± 0.80), maximum entrapment efficiency (73 ± 0.10%) and maximum amount released after 6 h (83.22 ± 0.10%). The optimized formula was then incorporated into gel preparation (HPMC) to improve the system stability and ease of application. Then, the pharmacokinetic study was conducted on rabbits in a cross-over design. The calculated parameters showed a higher area under the curve (AUC(0–24,) AUC(0–∞) (ng·h/mL)) of the developed ZMP-NLCs loaded gel, with a 1.76-fold increase in bioavailability in comparison to the orally administered marketed product (Zomig(®)). A histopathological examination revealed the safety of the developed nanoparticles. The declared results highlight the potential of utilizing the proposed NLCs for the transdermal delivery of ZMP to improve the drug bioavailability. MDPI 2022-07-18 /pmc/articles/PMC9315618/ /pubmed/35890379 http://dx.doi.org/10.3390/pharmaceutics14071484 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hassan, Doaa H.
Shohdy, Joseph N.
El-Setouhy, Doaa Ahmed
El-Nabarawi, Mohamed
Naguib, Marianne J.
Compritol-Based Nanostrucutured Lipid Carriers (NLCs) for Augmentation of Zolmitriptan Bioavailability via the Transdermal Route: In Vitro Optimization, Ex Vivo Permeation, In Vivo Pharmacokinetic Study
title Compritol-Based Nanostrucutured Lipid Carriers (NLCs) for Augmentation of Zolmitriptan Bioavailability via the Transdermal Route: In Vitro Optimization, Ex Vivo Permeation, In Vivo Pharmacokinetic Study
title_full Compritol-Based Nanostrucutured Lipid Carriers (NLCs) for Augmentation of Zolmitriptan Bioavailability via the Transdermal Route: In Vitro Optimization, Ex Vivo Permeation, In Vivo Pharmacokinetic Study
title_fullStr Compritol-Based Nanostrucutured Lipid Carriers (NLCs) for Augmentation of Zolmitriptan Bioavailability via the Transdermal Route: In Vitro Optimization, Ex Vivo Permeation, In Vivo Pharmacokinetic Study
title_full_unstemmed Compritol-Based Nanostrucutured Lipid Carriers (NLCs) for Augmentation of Zolmitriptan Bioavailability via the Transdermal Route: In Vitro Optimization, Ex Vivo Permeation, In Vivo Pharmacokinetic Study
title_short Compritol-Based Nanostrucutured Lipid Carriers (NLCs) for Augmentation of Zolmitriptan Bioavailability via the Transdermal Route: In Vitro Optimization, Ex Vivo Permeation, In Vivo Pharmacokinetic Study
title_sort compritol-based nanostrucutured lipid carriers (nlcs) for augmentation of zolmitriptan bioavailability via the transdermal route: in vitro optimization, ex vivo permeation, in vivo pharmacokinetic study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9315618/
https://www.ncbi.nlm.nih.gov/pubmed/35890379
http://dx.doi.org/10.3390/pharmaceutics14071484
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