Cyclodextrin-based nanoparticles encapsulating α-mangostin and their drug release behavior: potential carriers of α-mangostin for cancer therapy

• Published in: Polymer journal Vol. 52; no. 4; pp. 457 - 466
• Main Authors: Doan, Van T. H., Lee, Ji Ha, Takahashi, Rintaro, Nguyen, Phuong T. M., Nguyen, Van Anh T., Pham, Huong T. T., Fujii, Shota, Sakurai, Kazuo
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 01-04-2020; Nature Publishing Group
• Subjects: 631/45; 631/67; Anticancer properties; Antioxidants; Bioavailability; Biocompatibility; Biodegradability; Biomaterials; Bioorganic Chemistry; Chemistry; Chemistry and Materials Science; Chemistry/Food Science; Cyclodextrins; Drug carriers; Drug delivery systems; Encapsulation; Epichlorohydrin; Fractionation; Nanoparticles; Original Article; Photon correlation spectroscopy; Polymer Sciences; Scattering; Surfaces and Interfaces; Thin Films; Toxicity
• ISSN: 0032-3896; 1349-0540
• DOI: 10.1038/s41428-019-0296-y

α-Mangostin (MGS), an anti-cancer compound, is a xanthone derivative and is extracted from the pericarps of mangosteen. MGS exhibits a variety of bioactivities, such as antioxidant, cytotoxic, anti-inflammatory, and antibacterial effects, as well as anticancer activity. However, MGS has not been approved for clinical use because of its poor bioavailability. There have been many efforts to solve this problem by use of drug carriers. Cyclodextrins (CDs) are well known as nontoxic and biodegradable drug carriers and can encapsulate MGS. In this study, we prepared CD-based nanoparticles (CDNPs) by a polyaddition reaction using epichlorohydrin and characterized them by dynamic light scattering and static light scattering coupled with fractionation. The encapsulation of MGS into CDNPs was examined, and we found that the loading ratio of MGS for CDNPs is much higher than that for CDs themselves. The cytotoxicity of the CDNP/MGS complex was examined, indicating the potential of CDNP as a carrier of MGS.
In this study, we synthesized and characterized cyclodextrin-based nanoparticles (CDNPs) by polyaddition reactions using epichlorohydrin and three different type of CDs (α-, β-, and γ-CD). We found that cyclodextrin tended to cover surface of our nanoparticles; while epichlorohydrin network enlarged when weight ratio of epichlorohydrin/cyclodextrin increased. Our CDNPs demonstrated a very high loading ratio against α-mangostin (MGS), and getting close to 1:1 ratio.