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

Author:

Suksiriworapong Jiraphong1ORCID,Pongprasert Nutthachai2ORCID,Bunsupa Somnuk3ORCID,Taresco Vincenzo4ORCID,Crucitti Valentina Cuzzucoli5,Janurai Thitapa1,Phruttiwanichakun Pornpoj1,Sakchaisri Krisada6,Wongrakpanich Amaraporn1

Affiliation:

1. Department of Pharmacy, Faculty of Pharmacy, Mahidol University, Bangkok 10400, Thailand

2. Division of Postharvest Technology, School of Bioresources and Technology, King Mongkut’s University of Technology Thonburi, Bangkok 10150, Thailand

3. Department of Pharmacognosy, Faculty of Pharmacy, Mahidol University, Bangkok 10400, Thailand

4. School of Chemistry, University of Nottingham, Nottingham NG7 2RD, UK

5. Centre for Additive Manufacturing and Department of Chemical and Environmental Engineering, University of Nottingham, Nottingham NG7 2RD, UK

6. Department of Pharmacology, Faculty of Pharmacy, Mahidol University, Bangkok 10400, Thailand

Abstract

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.

Funder

MU-KMUTT Biomedical Engineering and Biomaterials Research Consortium through Mahidol University

University of Nottingham

Publisher

MDPI AG

Subject

Pharmaceutical Science

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