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Metabolic fate of poly-(lactic-co-glycolic acid)-based curcumin nanoparticles following oral administration.

作者信息

Harigae Takahiro, Nakagawa Kiyotaka, Miyazawa Taiki, Inoue Nao, Kimura Fumiko, Ikeda Ikuo, Miyazawa Teruo

机构信息

Food and Biodynamic Chemistry Laboratory, Graduate School of Agricultural Science, Tohoku University, Sendai, Japan.

Vascular Biology Laboratory, Jean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA, USA.

出版信息

Int J Nanomedicine. 2016 Jun 28;11:3009-22. doi: 10.2147/IJN.S107442. eCollection 2016.


DOI:10.2147/IJN.S107442
PMID:27418823
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4935090/
Abstract

PURPOSE: Curcumin (CUR), the main polyphenol in turmeric, is poorly absorbed and rapidly metabolized following oral administration, which severely curtails its bioavailability. Poly-(lactic-co-glycolic acid)-based CUR nanoparticles (CUR-NP) have recently been suggested to improve CUR bioavailability, but this has not been fully verified. Specifically, no data are available about curcumin glucuronide (CURG), the major metabolite of CUR found in the plasma following oral administration of CUR-NP. Herein, we investigated the absorption and metabolism of CUR-NP and evaluated whether CUR-NP improves CUR bioavailability. METHODS: Following oral administration of CUR-NP in rats, we analyzed the plasma and organ distribution of CUR and its metabolites using high-performance liquid chromatography-tandem mass spectrometry. To elucidate the mechanism of increased intestinal absorption of CUR-NP, we prepared mixed micelles comprised of phosphatidylcholine and bile salts and examined the micellar solubility of CUR-NP. Additionally, we investigated the cellular incorporation of the resultant micelles into differentiated Caco-2 human intestinal cells. RESULTS: Following in vivo administration of CUR-NP, CUR was effectively absorbed and present mainly as CURG in the plasma which contained significant amounts of the metabolite compared with other organs. Thus, CUR-NP increased intestinal absorption of CUR rather than decreasing metabolic degradation and conversion to other metabolites. In vitro, CUR encapsulated in CUR-NP was solubilized in mixed micelles; however, whether the micelles contained CUR or CUR-NP had little influence on cellular uptake efficiency. Therefore, we suggest that the high solubilization capacity of CUR-NP in mixed micelles, rather than cellular uptake efficiency, explains the high intestinal absorption of CUR-NP in vivo. CONCLUSION: These findings provide a better understanding of the bioavailability of CUR and CUR-NP following oral administration. To improve the bioavailability of CUR, future studies should focus on enhancing the resistance to metabolic degradation and conversion of CUR to other metabolites, which may lead to novel discoveries regarding food function and disease prevention.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fd/4935090/606b4e7a7fe2/ijn-11-3009Fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fd/4935090/d66bb6a6acb4/ijn-11-3009Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fd/4935090/7feacfa401ff/ijn-11-3009Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fd/4935090/e442070b7e60/ijn-11-3009Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fd/4935090/801ea853c96d/ijn-11-3009Fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fd/4935090/37a696d22826/ijn-11-3009Fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fd/4935090/c87d8186c94b/ijn-11-3009Fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fd/4935090/8c2598d1c78a/ijn-11-3009Fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fd/4935090/95c4b32b5601/ijn-11-3009Fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fd/4935090/606b4e7a7fe2/ijn-11-3009Fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fd/4935090/d66bb6a6acb4/ijn-11-3009Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fd/4935090/7feacfa401ff/ijn-11-3009Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fd/4935090/e442070b7e60/ijn-11-3009Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fd/4935090/801ea853c96d/ijn-11-3009Fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fd/4935090/37a696d22826/ijn-11-3009Fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fd/4935090/c87d8186c94b/ijn-11-3009Fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fd/4935090/8c2598d1c78a/ijn-11-3009Fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fd/4935090/95c4b32b5601/ijn-11-3009Fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fd/4935090/606b4e7a7fe2/ijn-11-3009Fig9.jpg

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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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本文引用的文献

[1]
Synthesis and Evaluation of the Anti-Oxidant Capacity of Curcumin Glucuronides, the Major Curcumin Metabolites.

Antioxidants (Basel). 2015-12-2

[2]
Distribution of β-carotene-encapsulated polysorbate 80-coated poly(D, L-lactide-co-glycolide) nanoparticles in rodent tissues following intravenous administration.

Int J Nanomedicine. 2015-11-27

[3]
Curcumin, inflammation, and chronic diseases: how are they linked?

Molecules. 2015-5-20

[4]
Optimised nano-formulation on the bioavailability of hydrophobic polyphenol, curcumin, in freely-moving rats.

Food Chem. 2011-1-25

[5]
Enhanced bioavailability and intestinal uptake of Gemcitabine HCl loaded PLGA nanoparticles after oral delivery.

Eur J Pharm Sci. 2014-8-18

[6]
Differential cellular uptake and metabolism of curcuminoids in monocytes/macrophages: regulatory effects on lipid accumulation.

Br J Nutr. 2014-7-14

[7]
Recent developments in delivery, bioavailability, absorption and metabolism of curcumin: the golden pigment from golden spice.

Cancer Res Treat. 2014-1

[8]
Comparison of the effects of curcumin and curcumin glucuronide in human hepatocellular carcinoma HepG2 cells.

Food Chem. 2013-11-13

[9]
Study on interaction of bile salts with curcumin and curcumin embedded in dipalmitoyl-sn-glycero-3-phosphocholine liposome.

Colloids Surf B Biointerfaces. 2013-5-4

[10]
Development of a validated UPLC-qTOF-MS Method for the determination of curcuminoids and their pharmacokinetic study in mice.

Daru. 2013-1-29

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