Detection of Astaxanthin at Different Regions of the Brain in Rats Treated with Astaxanthin Nanoemulsion.

J Pharm Bioallied Sci

Department of Pharmaceutical Life Sciences, Faculty of Pharmacy, Universiti Teknologi MARA, Kampus Puncak Alam, Bandar Puncak Alam, Selangor, Malaysia.

Published: May 2022

Context: Astaxanthin (Ast), a compound used widely as a dietary supplement, has high antioxidant properties but poor oral bioavailability. To benefit from its nutritional values in cognitive function, Ast was formulated into a nanoemulsion which may improve its penetration through the blood-brain barrier (BBB).

Aim: The present study aims to quantitate the Ast nanoemulsion in different regions of the brain tissue using the high-performance liquid chromatography method.

Materials And Methods: Sprague-Dawley rats were fed with Ast nanoemulsion formulation daily (40, 80, and 160 mg/kg body weight, bw) for 28 days before brain tissues were harvested, extracted, and quantified. A simple, sensitive, and reliable method using high-performance liquid chromatography with an ultraviolent detector was developed and validated to quantify Ast in the brain.

Statistical Analysis: Data were analyzed using the ToolPak Data Analysis in Excel for -test and analysis of variance single factor with Tukey analysis.

Results: The calibration curve demonstrated a linear regression with an of 0.9998 and absolute recovery ranging from 97.8% to 109.6%. The hippocampus of the 160 mg/kg bw treatment group showed a significantly higher concentration of Ast (77.9 ± 17.3 μg/g) compared to the cortex (22.3 ± 4.2 μg/g) and cerebellum (33.1 ± 5.4 μg/g). Ast was detected in the cerebellum of the 80 mg/kg bw (29.4 ± 7.8 μg/g) treatment group with the amount not being significantly different to the 160 mg/kg bw (33.1 ± 5.4 μg/g) treatment group.

Conclusions: It was evident that the Ast nanoemulsion formulated was able to cross the BBB and may provide protective benefits.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9245915PMC
http://dx.doi.org/10.4103/jpbs.jpbs_464_21DOI Listing

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