Characterisation, in-vitro and in-vivo evaluation of valproic acid-loaded nanoemulsion for improved brain bioavailability

OBJECTIVE: This study was aimed to investigate the potential of formulated valproic acid-encapsulated nanoemulsion (VANE) to improve the brain bioavailability of valproic acid (VPA). METHODS: Valproic acid-encapsulated nanoemulsions were formulated and physically characterised (osmolarity, viscosity...

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Main Authors: Tan, Suk Fei, Kirby, Brian P., Stanslas, Johnson, Basri, Hamidon
Format: Article
Language:English
Published: John Wiley & Sons 2017
Online Access:http://psasir.upm.edu.my/id/eprint/61082/
http://psasir.upm.edu.my/id/eprint/61082/1/Characterisation%2C%20in-vitro%20and%20in-vivo%20evaluation%20of%20valproic%20acid-loaded%20nanoemulsion%20for%20improved%20brain%20bioavailability.pdf
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author Tan, Suk Fei
Kirby, Brian P.
Stanslas, Johnson
Basri, Hamidon
author_facet Tan, Suk Fei
Kirby, Brian P.
Stanslas, Johnson
Basri, Hamidon
author_sort Tan, Suk Fei
building UPM Institutional Repository
collection Online Access
description OBJECTIVE: This study was aimed to investigate the potential of formulated valproic acid-encapsulated nanoemulsion (VANE) to improve the brain bioavailability of valproic acid (VPA). METHODS: Valproic acid-encapsulated nanoemulsions were formulated and physically characterised (osmolarity, viscosity, drug content, drug encapsulation efficiency). Further investigations were also conducted to estimate the drug release, cytotoxic profile, in-vitro blood-brain barrier (BBB) permeability, pharmacokinetic parameter and the concentration of VPA and VANE in blood and brain. KEY FINDINGS: Physical characterisation confirmed that VANE was suitable for parenteral administration. Formulating VPA into nanoemulsion significantly reduced the cytotoxicity of VPA. In-vitro drug permeation suggested that VANEs crossed the BBB as freely as VPA. Pharmacokinetic parameters of VANE-treated rats in plasma and brain showed F3 VANE had a remarkable improvement in AUC, prolongation of half-life and reduction in clearance compared to VPA. Given the same extent of in-vitro BBB permeation of VPA and VANE, the higher bioavailability of VANE in brain was believed to have due to higher concentration of VANE in blood. The brain bioavailability of VPA was improved by prolonging the half-life of VPA by encapsulating it within the nanoemulsion-T80. CONCLUSIONS: Nanoemulsion containing VPA has alleviated the cytotoxic effect of VPA and improved the plasma and brain bioavailability for parenteral delivery of VPA.
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spelling upm-610822019-05-06T08:10:37Z http://psasir.upm.edu.my/id/eprint/61082/ Characterisation, in-vitro and in-vivo evaluation of valproic acid-loaded nanoemulsion for improved brain bioavailability Tan, Suk Fei Kirby, Brian P. Stanslas, Johnson Basri, Hamidon OBJECTIVE: This study was aimed to investigate the potential of formulated valproic acid-encapsulated nanoemulsion (VANE) to improve the brain bioavailability of valproic acid (VPA). METHODS: Valproic acid-encapsulated nanoemulsions were formulated and physically characterised (osmolarity, viscosity, drug content, drug encapsulation efficiency). Further investigations were also conducted to estimate the drug release, cytotoxic profile, in-vitro blood-brain barrier (BBB) permeability, pharmacokinetic parameter and the concentration of VPA and VANE in blood and brain. KEY FINDINGS: Physical characterisation confirmed that VANE was suitable for parenteral administration. Formulating VPA into nanoemulsion significantly reduced the cytotoxicity of VPA. In-vitro drug permeation suggested that VANEs crossed the BBB as freely as VPA. Pharmacokinetic parameters of VANE-treated rats in plasma and brain showed F3 VANE had a remarkable improvement in AUC, prolongation of half-life and reduction in clearance compared to VPA. Given the same extent of in-vitro BBB permeation of VPA and VANE, the higher bioavailability of VANE in brain was believed to have due to higher concentration of VANE in blood. The brain bioavailability of VPA was improved by prolonging the half-life of VPA by encapsulating it within the nanoemulsion-T80. CONCLUSIONS: Nanoemulsion containing VPA has alleviated the cytotoxic effect of VPA and improved the plasma and brain bioavailability for parenteral delivery of VPA. John Wiley & Sons 2017 Article PeerReviewed text en http://psasir.upm.edu.my/id/eprint/61082/1/Characterisation%2C%20in-vitro%20and%20in-vivo%20evaluation%20of%20valproic%20acid-loaded%20nanoemulsion%20for%20improved%20brain%20bioavailability.pdf Tan, Suk Fei and Kirby, Brian P. and Stanslas, Johnson and Basri, Hamidon (2017) Characterisation, in-vitro and in-vivo evaluation of valproic acid-loaded nanoemulsion for improved brain bioavailability. Journal of Pharmacy and Pharmacology, 69 (11). 1447 - 1457. ISSN 0022-3573; ESSN: 2042-7158 https://onlinelibrary.wiley.com/doi/full/10.1111/jphp.12800 10.1111/jphp.12800
spellingShingle Tan, Suk Fei
Kirby, Brian P.
Stanslas, Johnson
Basri, Hamidon
Characterisation, in-vitro and in-vivo evaluation of valproic acid-loaded nanoemulsion for improved brain bioavailability
title Characterisation, in-vitro and in-vivo evaluation of valproic acid-loaded nanoemulsion for improved brain bioavailability
title_full Characterisation, in-vitro and in-vivo evaluation of valproic acid-loaded nanoemulsion for improved brain bioavailability
title_fullStr Characterisation, in-vitro and in-vivo evaluation of valproic acid-loaded nanoemulsion for improved brain bioavailability
title_full_unstemmed Characterisation, in-vitro and in-vivo evaluation of valproic acid-loaded nanoemulsion for improved brain bioavailability
title_short Characterisation, in-vitro and in-vivo evaluation of valproic acid-loaded nanoemulsion for improved brain bioavailability
title_sort characterisation, in-vitro and in-vivo evaluation of valproic acid-loaded nanoemulsion for improved brain bioavailability
url http://psasir.upm.edu.my/id/eprint/61082/
http://psasir.upm.edu.my/id/eprint/61082/
http://psasir.upm.edu.my/id/eprint/61082/
http://psasir.upm.edu.my/id/eprint/61082/1/Characterisation%2C%20in-vitro%20and%20in-vivo%20evaluation%20of%20valproic%20acid-loaded%20nanoemulsion%20for%20improved%20brain%20bioavailability.pdf