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CD44-Targeted Lipid Polymer Hybrid Nanoparticles Enhance Anti-Breast Cancer Effect of Cordyceps militaris Extracts

This study aimed to improve the anticancer effect of Cordyceps militaris herbal extract (CME) on breast cancer cells with hyaluronic acid (HYA) surface-decorated lipid polymer hybrid nanoparticles (LPNPs) and evaluate the applicability of a synthesized poly(glycerol adipate) (PGA) polymer for LPNP p...

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Autores principales: Suksiriworapong, Jiraphong, Pongprasert, Nutthachai, Bunsupa, Somnuk, Taresco, Vincenzo, Crucitti, Valentina Cuzzucoli, Janurai, Thitapa, Phruttiwanichakun, Pornpoj, Sakchaisri, Krisada, Wongrakpanich, Amaraporn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10302493/
https://www.ncbi.nlm.nih.gov/pubmed/37376218
http://dx.doi.org/10.3390/pharmaceutics15061771
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author Suksiriworapong, Jiraphong
Pongprasert, Nutthachai
Bunsupa, Somnuk
Taresco, Vincenzo
Crucitti, Valentina Cuzzucoli
Janurai, Thitapa
Phruttiwanichakun, Pornpoj
Sakchaisri, Krisada
Wongrakpanich, Amaraporn
author_facet Suksiriworapong, Jiraphong
Pongprasert, Nutthachai
Bunsupa, Somnuk
Taresco, Vincenzo
Crucitti, Valentina Cuzzucoli
Janurai, Thitapa
Phruttiwanichakun, Pornpoj
Sakchaisri, Krisada
Wongrakpanich, Amaraporn
author_sort Suksiriworapong, Jiraphong
collection PubMed
description This study aimed to improve the anticancer effect of Cordyceps militaris herbal extract (CME) on breast cancer cells with hyaluronic acid (HYA) surface-decorated lipid polymer hybrid nanoparticles (LPNPs) and evaluate the applicability of a synthesized poly(glycerol adipate) (PGA) polymer for LPNP preparation. Firstly, cholesterol- and vitamin E-grafted PGA polymers (PGA-CH and PGA-VE, respectively) were fabricated, with and without maleimide-ended polyethylene glycol. Subsequently, CME, which contained an active cordycepin equaling 9.89% of its weight, was encapsulated in the LPNPs. The results revealed that the synthesized polymers could be used to prepare CME-loaded LPNPs. The LPNP formulations containing Mal-PEG were decorated with cysteine-grafted HYA via thiol-maleimide reactions. The HYA-decorated PGA-based LPNPs substantially enhanced the anticancer effect of CME against MDA-MB-231 and MCF-7 breast cancer cells by enhancing cellular uptake through CD44 receptor-mediated endocytosis. This study demonstrated the successful targeted delivery of CME to the CD44 receptors of tumor cells by HYA-conjugated PGA-based LPNPs and the new application of synthesized PGA-CH- and PGA-VE-based polymers in LPNP preparation. The developed LPNPs showed promising potential for the targeted delivery of herbal extracts for cancer treatment and clear potential for translation in in vivo experiments.
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spelling pubmed-103024932023-06-29 CD44-Targeted Lipid Polymer Hybrid Nanoparticles Enhance Anti-Breast Cancer Effect of Cordyceps militaris Extracts Suksiriworapong, Jiraphong Pongprasert, Nutthachai Bunsupa, Somnuk Taresco, Vincenzo Crucitti, Valentina Cuzzucoli Janurai, Thitapa Phruttiwanichakun, Pornpoj Sakchaisri, Krisada Wongrakpanich, Amaraporn Pharmaceutics Article This study aimed to improve the anticancer effect of Cordyceps militaris herbal extract (CME) on breast cancer cells with hyaluronic acid (HYA) surface-decorated lipid polymer hybrid nanoparticles (LPNPs) and evaluate the applicability of a synthesized poly(glycerol adipate) (PGA) polymer for LPNP preparation. Firstly, cholesterol- and vitamin E-grafted PGA polymers (PGA-CH and PGA-VE, respectively) were fabricated, with and without maleimide-ended polyethylene glycol. Subsequently, CME, which contained an active cordycepin equaling 9.89% of its weight, was encapsulated in the LPNPs. The results revealed that the synthesized polymers could be used to prepare CME-loaded LPNPs. The LPNP formulations containing Mal-PEG were decorated with cysteine-grafted HYA via thiol-maleimide reactions. The HYA-decorated PGA-based LPNPs substantially enhanced the anticancer effect of CME against MDA-MB-231 and MCF-7 breast cancer cells by enhancing cellular uptake through CD44 receptor-mediated endocytosis. This study demonstrated the successful targeted delivery of CME to the CD44 receptors of tumor cells by HYA-conjugated PGA-based LPNPs and the new application of synthesized PGA-CH- and PGA-VE-based polymers in LPNP preparation. The developed LPNPs showed promising potential for the targeted delivery of herbal extracts for cancer treatment and clear potential for translation in in vivo experiments. MDPI 2023-06-20 /pmc/articles/PMC10302493/ /pubmed/37376218 http://dx.doi.org/10.3390/pharmaceutics15061771 Text en © 2023 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
Suksiriworapong, Jiraphong
Pongprasert, Nutthachai
Bunsupa, Somnuk
Taresco, Vincenzo
Crucitti, Valentina Cuzzucoli
Janurai, Thitapa
Phruttiwanichakun, Pornpoj
Sakchaisri, Krisada
Wongrakpanich, Amaraporn
CD44-Targeted Lipid Polymer Hybrid Nanoparticles Enhance Anti-Breast Cancer Effect of Cordyceps militaris Extracts
title CD44-Targeted Lipid Polymer Hybrid Nanoparticles Enhance Anti-Breast Cancer Effect of Cordyceps militaris Extracts
title_full CD44-Targeted Lipid Polymer Hybrid Nanoparticles Enhance Anti-Breast Cancer Effect of Cordyceps militaris Extracts
title_fullStr CD44-Targeted Lipid Polymer Hybrid Nanoparticles Enhance Anti-Breast Cancer Effect of Cordyceps militaris Extracts
title_full_unstemmed CD44-Targeted Lipid Polymer Hybrid Nanoparticles Enhance Anti-Breast Cancer Effect of Cordyceps militaris Extracts
title_short CD44-Targeted Lipid Polymer Hybrid Nanoparticles Enhance Anti-Breast Cancer Effect of Cordyceps militaris Extracts
title_sort cd44-targeted lipid polymer hybrid nanoparticles enhance anti-breast cancer effect of cordyceps militaris extracts
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10302493/
https://www.ncbi.nlm.nih.gov/pubmed/37376218
http://dx.doi.org/10.3390/pharmaceutics15061771
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