TY - JOUR
T1 - Enhancing the Oral Bioavailability of Natural Astaxanthin Using Plantbased Micro- and Nano-Encapsulation Materials
T2 - Results of an in Vitro Evaluation and a Crossover Study in Humans
AU - Abuhassira-Cohen, Yarden
AU - Edelman, Ravit
AU - Abbas, Randa
AU - Kurnik, Daniel
AU - Shibela, Rand
AU - Livneya, Yoav D.
N1 - Publisher Copyright:
© 2020, Andover House, Inc.. All rights reserved.
PY - 2020
Y1 - 2020
N2 - Astaxanthin (AX) is a red xanthophyll carotenoid found mainly in algae (notably Haeniatococcus Pluvialis microalga) and marine animals. AX is a stronger antioxidant than vitamin E and 0-carotene but has very low oral bioavailability. The purpose of this study was to develop a potato protein (PP)-based delivery system for increasing oral bioavailability of lipophilic bioactives (nutraceuticals and drags), using AX as a model, and to evaluate the system in vitro and in vivo in a crossover clinical study in human volunteers. Three different formulations were prepared, encapsulating AX oleoresin (AXO) with (1) PP only, (2) PP+lecithin (LEC), and (3) PP+olive oil (00). The average particle diameters after preparation were 0.29, 0.29, and 1.76 pm, and after freeze-drying and reconstitution 0.17, 0.07, and 6.93 pm, respectively. In vitro bioaccessibility was 33,47, and 69%, respectively, versus 16% only for the raw AXO. In a randomized, double-blind, crossover study in human subjects, the PP-OO-AX formulation had a 4.8-fold higher median plasma AX area under the concentration-over time curve (AUC; P<0.001) compared to the raw AXO formulation. In conclusion, a non-allergenic, vegan, PP-based delivery system made of “all-natural ingredients” offers a great promise for increasing oral bioavailability of lipophilic bioactives such as AX, for the enrichment of food and for dietary supplements, or oral delivery of lipophilic drugs.
AB - Astaxanthin (AX) is a red xanthophyll carotenoid found mainly in algae (notably Haeniatococcus Pluvialis microalga) and marine animals. AX is a stronger antioxidant than vitamin E and 0-carotene but has very low oral bioavailability. The purpose of this study was to develop a potato protein (PP)-based delivery system for increasing oral bioavailability of lipophilic bioactives (nutraceuticals and drags), using AX as a model, and to evaluate the system in vitro and in vivo in a crossover clinical study in human volunteers. Three different formulations were prepared, encapsulating AX oleoresin (AXO) with (1) PP only, (2) PP+lecithin (LEC), and (3) PP+olive oil (00). The average particle diameters after preparation were 0.29, 0.29, and 1.76 pm, and after freeze-drying and reconstitution 0.17, 0.07, and 6.93 pm, respectively. In vitro bioaccessibility was 33,47, and 69%, respectively, versus 16% only for the raw AXO. In a randomized, double-blind, crossover study in human subjects, the PP-OO-AX formulation had a 4.8-fold higher median plasma AX area under the concentration-over time curve (AUC; P<0.001) compared to the raw AXO formulation. In conclusion, a non-allergenic, vegan, PP-based delivery system made of “all-natural ingredients” offers a great promise for increasing oral bioavailability of lipophilic bioactives such as AX, for the enrichment of food and for dietary supplements, or oral delivery of lipophilic drugs.
KW - Astaxanthin
KW - Bioavailability
KW - Encapsulation
KW - Olive oil
KW - Potato protein
UR - https://www.scopus.com/pages/publications/85117826811
U2 - 10.33218/001c.16781
DO - 10.33218/001c.16781
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AN - SCOPUS:85117826811
SN - 2639-9431
VL - 3
SP - 641
EP - 655
JO - Precision Nanomedicine
JF - Precision Nanomedicine
IS - 3
ER -