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Dissolving microneedle integrated with benidipine loaded ethosomes for transdermal delivery

Benidipine HCl (BEN) is a drug used for the treatment of hypertension. However, this drug suffers from low oral bioavailability. This study introduces a novel approach to address this issue by developing BEN-loaded ethosomes (BEN-E) that integrate into dissolving microneedles for transdermal deliver...

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Main Authors: AL-Japairai, Khater Ahmed Saeed, Almurisi, Samah Hamed, Nadiya, Abdul-Halim, Syed Mahmood, .
Format: Article
Language:English
English
Published: Elsevier 2024
Subjects:
RS Pharmacy and materia medica
TP Chemical technology
Online Access:http://umpir.ump.edu.my/id/eprint/42270/1/Dissolving%20microneedle%20integrated%20with%20benidipine%20loaded%20ethosomes_ABST.pdf
http://umpir.ump.edu.my/id/eprint/42270/2/Dissolving%20microneedle%20integrated%20with%20benidipine%20loaded%20ethosomes.pdf
http://umpir.ump.edu.my/id/eprint/42270/
https://doi.org/10.1016/j.surfin.2024.104903
https://doi.org/10.1016/j.surfin.2024.104903
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spelling my.ump.umpir.422702024-08-09T01:12:03Z http://umpir.ump.edu.my/id/eprint/42270/ Dissolving microneedle integrated with benidipine loaded ethosomes for transdermal delivery AL-Japairai, Khater Ahmed Saeed Almurisi, Samah Hamed Nadiya, Abdul-Halim Syed Mahmood, . RS Pharmacy and materia medica TP Chemical technology Benidipine HCl (BEN) is a drug used for the treatment of hypertension. However, this drug suffers from low oral bioavailability. This study introduces a novel approach to address this issue by developing BEN-loaded ethosomes (BEN-E) that integrate into dissolving microneedles for transdermal delivery. The BEN-E was prepared using a rotary evaporation method and optimised using the Box-Behnken design. Following that, the optimised BEN-E formulation was integrated into dissolving microneedles (DMNs). The optimised lipid vesicles selected comprised lipoid S75 (339.66 mg), ethanol (34.51 %), and sonication time (70 s) and showed a vesicle size of 149.4 ± 3.81 nm, an EE% of 88.57 ± 0.38 %, and a transdermal flux of 19.12 ± 0.19 μg/cm²/hr. On the other hand, the resulting BEN-E-DMNs exhibited sharp pyramidal microneedles, sufficient mechanical strength, good insertion capability, and fast dissolution in rat skin. In the ex vivo study, the permeation coefficient of BEN was significantly improved by BEN-E-DMNs compared with optimised BEN-E and BEN-DMNs. The pharmacokinetic studies showed that the BEN-E-DMNs had a Cmax of about 0.698 ± 0.037 μg/mL and an AUC₀₋ₜ of about 15.821 ± 0.868 μg/hr/mL. Moreover, it improved the relative bioavailability of BEN by about 1.58 times compared to the orally marketed BEN tablet and about 2.95 times compared to the BEN-DMNs. In conclusion, the ethosomes combined with dissolving microneedles have shown high potential as carriers for the transdermal delivery of BEN. Elsevier 2024-09 Article PeerReviewed pdf en http://umpir.ump.edu.my/id/eprint/42270/1/Dissolving%20microneedle%20integrated%20with%20benidipine%20loaded%20ethosomes_ABST.pdf pdf en http://umpir.ump.edu.my/id/eprint/42270/2/Dissolving%20microneedle%20integrated%20with%20benidipine%20loaded%20ethosomes.pdf AL-Japairai, Khater Ahmed Saeed and Almurisi, Samah Hamed and Nadiya, Abdul-Halim and Syed Mahmood, . (2024) Dissolving microneedle integrated with benidipine loaded ethosomes for transdermal delivery. Surfaces and Interfaces, 52 (104903). pp. 1-21. ISSN 2468-0230. (Published) https://doi.org/10.1016/j.surfin.2024.104903 https://doi.org/10.1016/j.surfin.2024.104903
institution Universiti Malaysia Pahang Al-Sultan Abdullah
building UMPSA Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaysia Pahang Al-Sultan Abdullah
content_source UMPSA Institutional Repository
url_provider http://umpir.ump.edu.my/
language English
English
topic RS Pharmacy and materia medica
TP Chemical technology
spellingShingle RS Pharmacy and materia medica
TP Chemical technology
AL-Japairai, Khater Ahmed Saeed
Almurisi, Samah Hamed
Nadiya, Abdul-Halim
Syed Mahmood, .
Dissolving microneedle integrated with benidipine loaded ethosomes for transdermal delivery
description Benidipine HCl (BEN) is a drug used for the treatment of hypertension. However, this drug suffers from low oral bioavailability. This study introduces a novel approach to address this issue by developing BEN-loaded ethosomes (BEN-E) that integrate into dissolving microneedles for transdermal delivery. The BEN-E was prepared using a rotary evaporation method and optimised using the Box-Behnken design. Following that, the optimised BEN-E formulation was integrated into dissolving microneedles (DMNs). The optimised lipid vesicles selected comprised lipoid S75 (339.66 mg), ethanol (34.51 %), and sonication time (70 s) and showed a vesicle size of 149.4 ± 3.81 nm, an EE% of 88.57 ± 0.38 %, and a transdermal flux of 19.12 ± 0.19 μg/cm²/hr. On the other hand, the resulting BEN-E-DMNs exhibited sharp pyramidal microneedles, sufficient mechanical strength, good insertion capability, and fast dissolution in rat skin. In the ex vivo study, the permeation coefficient of BEN was significantly improved by BEN-E-DMNs compared with optimised BEN-E and BEN-DMNs. The pharmacokinetic studies showed that the BEN-E-DMNs had a Cmax of about 0.698 ± 0.037 μg/mL and an AUC₀₋ₜ of about 15.821 ± 0.868 μg/hr/mL. Moreover, it improved the relative bioavailability of BEN by about 1.58 times compared to the orally marketed BEN tablet and about 2.95 times compared to the BEN-DMNs. In conclusion, the ethosomes combined with dissolving microneedles have shown high potential as carriers for the transdermal delivery of BEN.
format Article
author AL-Japairai, Khater Ahmed Saeed
Almurisi, Samah Hamed
Nadiya, Abdul-Halim
Syed Mahmood, .
author_facet AL-Japairai, Khater Ahmed Saeed
Almurisi, Samah Hamed
Nadiya, Abdul-Halim
Syed Mahmood, .
author_sort AL-Japairai, Khater Ahmed Saeed
title Dissolving microneedle integrated with benidipine loaded ethosomes for transdermal delivery
title_short Dissolving microneedle integrated with benidipine loaded ethosomes for transdermal delivery
title_full Dissolving microneedle integrated with benidipine loaded ethosomes for transdermal delivery
title_fullStr Dissolving microneedle integrated with benidipine loaded ethosomes for transdermal delivery
title_full_unstemmed Dissolving microneedle integrated with benidipine loaded ethosomes for transdermal delivery
title_sort dissolving microneedle integrated with benidipine loaded ethosomes for transdermal delivery
publisher Elsevier
publishDate 2024
url http://umpir.ump.edu.my/id/eprint/42270/1/Dissolving%20microneedle%20integrated%20with%20benidipine%20loaded%20ethosomes_ABST.pdf
http://umpir.ump.edu.my/id/eprint/42270/2/Dissolving%20microneedle%20integrated%20with%20benidipine%20loaded%20ethosomes.pdf
http://umpir.ump.edu.my/id/eprint/42270/
https://doi.org/10.1016/j.surfin.2024.104903
https://doi.org/10.1016/j.surfin.2024.104903
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score 13.235796

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