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Fully Natural Lecithin Encapsulated Nano-Resveratrol for Anti-Cancer Therapy

INTRODUCTION: Chemotherapeutics are known to have undesirable side effects (i.e. nausea, weight loss, hair loss, weakened immune system, etc.) due to the non-specificity of the drugs. Encapsulation of these chemotherapeutics inside nanoparticles significantly improves the bioavailability and half-li...

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Autores principales: Liang, Meiyi, Guo, Mingyan, Saw, Phei Er, Yao, Yandan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9091702/
https://www.ncbi.nlm.nih.gov/pubmed/35571257
http://dx.doi.org/10.2147/IJN.S362418
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author Liang, Meiyi
Guo, Mingyan
Saw, Phei Er
Yao, Yandan
author_facet Liang, Meiyi
Guo, Mingyan
Saw, Phei Er
Yao, Yandan
author_sort Liang, Meiyi
collection PubMed
description INTRODUCTION: Chemotherapeutics are known to have undesirable side effects (i.e. nausea, weight loss, hair loss, weakened immune system, etc.) due to the non-specificity of the drugs. Encapsulation of these chemotherapeutics inside nanoparticles significantly improves the bioavailability and half-life of drugs, while increasing their tumor penetration and localization. However, most, if not all, nanoparticles in clinics or research are synthetic, with no long-term studies on the effect of these nanoparticles in vivo. Herein, we developed a synergistic resveratrol nanoparticle system by using lecithin encapsulation. Lecithin, being a fully natural phospholipid derived from soybean, possesses inherent anti-tumor activity. METHODS: Lec(RSV) was successfully prepared using the nanoprecipitation method, and characterized by particle size and zeta potential analysis, and transmission electron microscopy (TEM). The in vitro cellular uptake and cytotoxic effects of Lec(RSV) were investigated in human breast cancer cell line BT474. Finally, the in vivo tumoral uptake of Lec(RSV) was carried out in the BT474 orthotopic model. RESULTS: Lec(RSV) showed a uniform distribution of ~120 nm, with prolonged stability. Lec(RSV) showed high cellular uptake and anti-cancer properties in vitro. Time-dependent uptake in the BT474 xenograft model indicated an increased tumoral uptake and apoptosis rate at 4 hours after tail vein injection of Lec(RSV). CONCLUSION: Taken together, we successfully developed a fully natural Lec(RSV) that possesses potent anti-cancer activity in vitro, with good tumoral uptake in vivo. We hypothesize that Lec(RSV) could be a safe anti-cancer therapeutic that could be easily translated into clinical application.
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spelling pubmed-90917022022-05-12 Fully Natural Lecithin Encapsulated Nano-Resveratrol for Anti-Cancer Therapy Liang, Meiyi Guo, Mingyan Saw, Phei Er Yao, Yandan Int J Nanomedicine Original Research INTRODUCTION: Chemotherapeutics are known to have undesirable side effects (i.e. nausea, weight loss, hair loss, weakened immune system, etc.) due to the non-specificity of the drugs. Encapsulation of these chemotherapeutics inside nanoparticles significantly improves the bioavailability and half-life of drugs, while increasing their tumor penetration and localization. However, most, if not all, nanoparticles in clinics or research are synthetic, with no long-term studies on the effect of these nanoparticles in vivo. Herein, we developed a synergistic resveratrol nanoparticle system by using lecithin encapsulation. Lecithin, being a fully natural phospholipid derived from soybean, possesses inherent anti-tumor activity. METHODS: Lec(RSV) was successfully prepared using the nanoprecipitation method, and characterized by particle size and zeta potential analysis, and transmission electron microscopy (TEM). The in vitro cellular uptake and cytotoxic effects of Lec(RSV) were investigated in human breast cancer cell line BT474. Finally, the in vivo tumoral uptake of Lec(RSV) was carried out in the BT474 orthotopic model. RESULTS: Lec(RSV) showed a uniform distribution of ~120 nm, with prolonged stability. Lec(RSV) showed high cellular uptake and anti-cancer properties in vitro. Time-dependent uptake in the BT474 xenograft model indicated an increased tumoral uptake and apoptosis rate at 4 hours after tail vein injection of Lec(RSV). CONCLUSION: Taken together, we successfully developed a fully natural Lec(RSV) that possesses potent anti-cancer activity in vitro, with good tumoral uptake in vivo. We hypothesize that Lec(RSV) could be a safe anti-cancer therapeutic that could be easily translated into clinical application. Dove 2022-05-06 /pmc/articles/PMC9091702/ /pubmed/35571257 http://dx.doi.org/10.2147/IJN.S362418 Text en © 2022 Liang et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Liang, Meiyi
Guo, Mingyan
Saw, Phei Er
Yao, Yandan
Fully Natural Lecithin Encapsulated Nano-Resveratrol for Anti-Cancer Therapy
title Fully Natural Lecithin Encapsulated Nano-Resveratrol for Anti-Cancer Therapy
title_full Fully Natural Lecithin Encapsulated Nano-Resveratrol for Anti-Cancer Therapy
title_fullStr Fully Natural Lecithin Encapsulated Nano-Resveratrol for Anti-Cancer Therapy
title_full_unstemmed Fully Natural Lecithin Encapsulated Nano-Resveratrol for Anti-Cancer Therapy
title_short Fully Natural Lecithin Encapsulated Nano-Resveratrol for Anti-Cancer Therapy
title_sort fully natural lecithin encapsulated nano-resveratrol for anti-cancer therapy
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9091702/
https://www.ncbi.nlm.nih.gov/pubmed/35571257
http://dx.doi.org/10.2147/IJN.S362418
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