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Enhanced Oral Bioavailability of β-Caryophyllene in Healthy Subjects Using the VESIsorb(®) Formulation Technology, a Novel Self-Emulsifying Drug Delivery System (SEDDS)

β-Caryophyllene (BCP), a common constituent of many spice and food plants, is gaining increased attention due to recent research identifying numerous potential health benefits. Due to limited oral bioavailability observed in preclinical models, the described benefits of BCP may be maximized by using...

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Autores principales: Mödinger, Yvonne, Knaub, Katharina, Dharsono, Tanita, Wacker, Roland, Meyrat, Remo, Land, M. Hunter, Petraglia, Anthony L., Schön, Christiane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9104399/
https://www.ncbi.nlm.nih.gov/pubmed/35566210
http://dx.doi.org/10.3390/molecules27092860
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author Mödinger, Yvonne
Knaub, Katharina
Dharsono, Tanita
Wacker, Roland
Meyrat, Remo
Land, M. Hunter
Petraglia, Anthony L.
Schön, Christiane
author_facet Mödinger, Yvonne
Knaub, Katharina
Dharsono, Tanita
Wacker, Roland
Meyrat, Remo
Land, M. Hunter
Petraglia, Anthony L.
Schön, Christiane
author_sort Mödinger, Yvonne
collection PubMed
description β-Caryophyllene (BCP), a common constituent of many spice and food plants, is gaining increased attention due to recent research identifying numerous potential health benefits. Due to limited oral bioavailability observed in preclinical models, the described benefits of BCP may be maximized by using a suitable delivery system. Additionally, human pharmacokinetics (PK) remain unknown. This study evaluates the relative oral bioavailability of BCP formulated in a self-emulsifying drug delivery system (SEDDS) based on VESIsorb(®) formulation technology (BCP-SEDDS) compared to BCP neat oil. Hence, a randomized, double-blind, cross-over design, single oral dose study (100 mg BCP) in 24 healthy subjects (12 men/12 women) was performed under fasting conditions. Pharmacokinetic parameters were analyzed from individual concentration-time curves. The data show that BCP-SEDDS resulted in a 2.2/2.0-fold increase in AUC(0–12h)/AUC(0–24h) and a 3.6-fold increase in C(max) compared to BCP neat oil. Moreover, BCP was absorbed faster from BCP-SEDDS (T(max): 1.43 h) compared to BCP neat oil (T(max): 3.07 h). Gender analysis revealed that there is no significant difference between men and women for both the investigated formulations and all investigated PK endpoints. In conclusion, BCP-SEDDS offers a well-tolerated and effective oral delivery system to significantly enhance the oral bioavailability of BCP in humans.
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spelling pubmed-91043992022-05-14 Enhanced Oral Bioavailability of β-Caryophyllene in Healthy Subjects Using the VESIsorb(®) Formulation Technology, a Novel Self-Emulsifying Drug Delivery System (SEDDS) Mödinger, Yvonne Knaub, Katharina Dharsono, Tanita Wacker, Roland Meyrat, Remo Land, M. Hunter Petraglia, Anthony L. Schön, Christiane Molecules Article β-Caryophyllene (BCP), a common constituent of many spice and food plants, is gaining increased attention due to recent research identifying numerous potential health benefits. Due to limited oral bioavailability observed in preclinical models, the described benefits of BCP may be maximized by using a suitable delivery system. Additionally, human pharmacokinetics (PK) remain unknown. This study evaluates the relative oral bioavailability of BCP formulated in a self-emulsifying drug delivery system (SEDDS) based on VESIsorb(®) formulation technology (BCP-SEDDS) compared to BCP neat oil. Hence, a randomized, double-blind, cross-over design, single oral dose study (100 mg BCP) in 24 healthy subjects (12 men/12 women) was performed under fasting conditions. Pharmacokinetic parameters were analyzed from individual concentration-time curves. The data show that BCP-SEDDS resulted in a 2.2/2.0-fold increase in AUC(0–12h)/AUC(0–24h) and a 3.6-fold increase in C(max) compared to BCP neat oil. Moreover, BCP was absorbed faster from BCP-SEDDS (T(max): 1.43 h) compared to BCP neat oil (T(max): 3.07 h). Gender analysis revealed that there is no significant difference between men and women for both the investigated formulations and all investigated PK endpoints. In conclusion, BCP-SEDDS offers a well-tolerated and effective oral delivery system to significantly enhance the oral bioavailability of BCP in humans. MDPI 2022-04-30 /pmc/articles/PMC9104399/ /pubmed/35566210 http://dx.doi.org/10.3390/molecules27092860 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
Mödinger, Yvonne
Knaub, Katharina
Dharsono, Tanita
Wacker, Roland
Meyrat, Remo
Land, M. Hunter
Petraglia, Anthony L.
Schön, Christiane
Enhanced Oral Bioavailability of β-Caryophyllene in Healthy Subjects Using the VESIsorb(®) Formulation Technology, a Novel Self-Emulsifying Drug Delivery System (SEDDS)
title Enhanced Oral Bioavailability of β-Caryophyllene in Healthy Subjects Using the VESIsorb(®) Formulation Technology, a Novel Self-Emulsifying Drug Delivery System (SEDDS)
title_full Enhanced Oral Bioavailability of β-Caryophyllene in Healthy Subjects Using the VESIsorb(®) Formulation Technology, a Novel Self-Emulsifying Drug Delivery System (SEDDS)
title_fullStr Enhanced Oral Bioavailability of β-Caryophyllene in Healthy Subjects Using the VESIsorb(®) Formulation Technology, a Novel Self-Emulsifying Drug Delivery System (SEDDS)
title_full_unstemmed Enhanced Oral Bioavailability of β-Caryophyllene in Healthy Subjects Using the VESIsorb(®) Formulation Technology, a Novel Self-Emulsifying Drug Delivery System (SEDDS)
title_short Enhanced Oral Bioavailability of β-Caryophyllene in Healthy Subjects Using the VESIsorb(®) Formulation Technology, a Novel Self-Emulsifying Drug Delivery System (SEDDS)
title_sort enhanced oral bioavailability of β-caryophyllene in healthy subjects using the vesisorb(®) formulation technology, a novel self-emulsifying drug delivery system (sedds)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9104399/
https://www.ncbi.nlm.nih.gov/pubmed/35566210
http://dx.doi.org/10.3390/molecules27092860
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