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Inhibition of colon cancer cell growth by nanoemulsion carrying gold nanoparticles and lycopene

Lycopene (LP), an important functional compound in tomatoes, and gold nanoparticles (AN), have received considerable attention as potential candidates for cancer therapy. However, the extreme instability and poor bioavailability of LP limits its in vivo application. This study intends to develop a n...

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Autores principales: Huang, Rwei-Fen S, Wei, Yi-Jun, Inbaraj, Baskaran Stephen, Chen, Bing-Huei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4399598/
https://www.ncbi.nlm.nih.gov/pubmed/25914533
http://dx.doi.org/10.2147/IJN.S79107
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author Huang, Rwei-Fen S
Wei, Yi-Jun
Inbaraj, Baskaran Stephen
Chen, Bing-Huei
author_facet Huang, Rwei-Fen S
Wei, Yi-Jun
Inbaraj, Baskaran Stephen
Chen, Bing-Huei
author_sort Huang, Rwei-Fen S
collection PubMed
description Lycopene (LP), an important functional compound in tomatoes, and gold nanoparticles (AN), have received considerable attention as potential candidates for cancer therapy. However, the extreme instability and poor bioavailability of LP limits its in vivo application. This study intends to develop a nanoemulsion system incorporating both LP and AN, and to study the possible synergistic effects on the inhibition of the HT-29 colon cancer cell line. LP–nanogold nanoemulsion containing Tween 80 as an emulsifier was prepared, followed by characterization using transmission electron microscopy (TEM), dynamic light scattering (DLS) analysis, ultraviolet spectroscopy, and zeta potential analysis. The particle size as determined by TEM and DLS was 21.3±3.7 nm and 25.0±4.2 nm for nanoemulsion and 4.7±1.1 nm and 3.3±0.6 nm for AN, while the zeta potential of nanoemulsion and AN was −32.2±1.8 mV and −48.5±2.7 mV, respectively. Compared with the control treatment, both the combo (AN 10 ppm plus LP 12 μM) and nanoemulsion (AN 0.16 ppm plus LP 0.4 μM) treatments resulted in a five- and 15-fold rise in early apoptotic cells of HT-29, respectively. Also, the nanoemulsion significantly reduced the expressions of procaspases 8, 3, and 9, as well as PARP-1 and Bcl-2, while Bax expression was enhanced. A fivefold decline in the migration capability of HT-29 cells was observed for this nanoemulsion when compared to control, with the invasion-associated markers being significantly reversed through the upregulation of the epithelial marker E-cadherin and downregulation of Akt, nuclear factor kappa B, pro-matrix metalloproteinase (MMP)-2, and active MMP-9 expressions. The TEM images revealed that numerous nanoemulsion-filled vacuoles invaded cytosol and converged into the mitochondria, resulting in an abnormally elongated morphology with reduced cristae and matrix contents, demonstrating a possible passive targeting effect. The nanoemulsion containing vacuoles were engulfed and internalized by the nuclear membrane envelop for subsequent invasion into the nucleoli. Taken together, LP–nanogold nanoemulsion could provide synergistic effects at AN and LP doses 250 and 120 times lower than that in the combo treatment, respectively, demonstrating the potential of nanoemulsion developed in this study for a possible application in colon cancer therapy.
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spelling pubmed-43995982015-04-24 Inhibition of colon cancer cell growth by nanoemulsion carrying gold nanoparticles and lycopene Huang, Rwei-Fen S Wei, Yi-Jun Inbaraj, Baskaran Stephen Chen, Bing-Huei Int J Nanomedicine Original Research Lycopene (LP), an important functional compound in tomatoes, and gold nanoparticles (AN), have received considerable attention as potential candidates for cancer therapy. However, the extreme instability and poor bioavailability of LP limits its in vivo application. This study intends to develop a nanoemulsion system incorporating both LP and AN, and to study the possible synergistic effects on the inhibition of the HT-29 colon cancer cell line. LP–nanogold nanoemulsion containing Tween 80 as an emulsifier was prepared, followed by characterization using transmission electron microscopy (TEM), dynamic light scattering (DLS) analysis, ultraviolet spectroscopy, and zeta potential analysis. The particle size as determined by TEM and DLS was 21.3±3.7 nm and 25.0±4.2 nm for nanoemulsion and 4.7±1.1 nm and 3.3±0.6 nm for AN, while the zeta potential of nanoemulsion and AN was −32.2±1.8 mV and −48.5±2.7 mV, respectively. Compared with the control treatment, both the combo (AN 10 ppm plus LP 12 μM) and nanoemulsion (AN 0.16 ppm plus LP 0.4 μM) treatments resulted in a five- and 15-fold rise in early apoptotic cells of HT-29, respectively. Also, the nanoemulsion significantly reduced the expressions of procaspases 8, 3, and 9, as well as PARP-1 and Bcl-2, while Bax expression was enhanced. A fivefold decline in the migration capability of HT-29 cells was observed for this nanoemulsion when compared to control, with the invasion-associated markers being significantly reversed through the upregulation of the epithelial marker E-cadherin and downregulation of Akt, nuclear factor kappa B, pro-matrix metalloproteinase (MMP)-2, and active MMP-9 expressions. The TEM images revealed that numerous nanoemulsion-filled vacuoles invaded cytosol and converged into the mitochondria, resulting in an abnormally elongated morphology with reduced cristae and matrix contents, demonstrating a possible passive targeting effect. The nanoemulsion containing vacuoles were engulfed and internalized by the nuclear membrane envelop for subsequent invasion into the nucleoli. Taken together, LP–nanogold nanoemulsion could provide synergistic effects at AN and LP doses 250 and 120 times lower than that in the combo treatment, respectively, demonstrating the potential of nanoemulsion developed in this study for a possible application in colon cancer therapy. Dove Medical Press 2015-04-08 /pmc/articles/PMC4399598/ /pubmed/25914533 http://dx.doi.org/10.2147/IJN.S79107 Text en © 2015 Huang et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Huang, Rwei-Fen S
Wei, Yi-Jun
Inbaraj, Baskaran Stephen
Chen, Bing-Huei
Inhibition of colon cancer cell growth by nanoemulsion carrying gold nanoparticles and lycopene
title Inhibition of colon cancer cell growth by nanoemulsion carrying gold nanoparticles and lycopene
title_full Inhibition of colon cancer cell growth by nanoemulsion carrying gold nanoparticles and lycopene
title_fullStr Inhibition of colon cancer cell growth by nanoemulsion carrying gold nanoparticles and lycopene
title_full_unstemmed Inhibition of colon cancer cell growth by nanoemulsion carrying gold nanoparticles and lycopene
title_short Inhibition of colon cancer cell growth by nanoemulsion carrying gold nanoparticles and lycopene
title_sort inhibition of colon cancer cell growth by nanoemulsion carrying gold nanoparticles and lycopene
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4399598/
https://www.ncbi.nlm.nih.gov/pubmed/25914533
http://dx.doi.org/10.2147/IJN.S79107
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