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Modification of Poly(Glycerol Adipate) with Tocopherol and Cholesterol Modulating Nanoparticle Self-Assemblies and Cellular Responses of Triple-Negative Breast Cancer Cells to SN-38 Delivery

Suksiriworapong, Jiraphong; Achayawat, Chittin; Juangrattanakamjorn, Phutthikom; Taresco, Vincenzo; Cuzzucoli Crucitti, Valentina; Sakchaisri, Krisada; Bunsupa, Somnuk

Modification of Poly(Glycerol Adipate) with Tocopherol and Cholesterol Modulating Nanoparticle Self-Assemblies and Cellular Responses of Triple-Negative Breast Cancer Cells to SN-38 Delivery Thumbnail


Authors

Jiraphong Suksiriworapong

Chittin Achayawat

Phutthikom Juangrattanakamjorn

Krisada Sakchaisri

Somnuk Bunsupa



Contributors

Xiaowei Zeng
Editor

Abstract

This study aimed to fabricate new variations of glycerol-based polyesters by grafting poly(glycerol adipate) (PGA) with hydrophobic bioactive moieties, tocopherol (TOC), and cholesterol (CHO). Their effects on nanoparticle (NP) formation, drug release, and cellular responses in cancer and normal cells were evaluated. CHO and TOC were successfully grafted onto PGA backbones with 30% and 50% mole grafting. Increasing the percentage of mole grafting in both molecules increased the glass transition temperature and water contact angle of the final polymers but decreased the critical micelle concentration of the formulated particles. PGA-TOC NPs reduced the proliferation of MDA-MB-231 cancer cells. However, they enhanced the proliferation of primary dermal fibroblasts within a specific concentration range. PGA-CHO NPs minimally affected the growth of cancer and normal cells. Both types of NPs did not affect apoptosis or the cell cycle of cancer cells. PGA-CHO and PGA-TOC NPs were able to entrap SN-38, a hydrophobic anticancer drug, with a particle size <200 nm. PGA-CHO NPs had a higher drug loading capacity and a greater drug release than PGA-TOC NPs. However, SN-38-loaded PGA-TOC NPs showed higher toxicity than SN-38 and SN-38-loaded PGA-CHO NPs due to the combined effects of antiproliferation and higher cellular uptake. Compared with SN-38, the drug-loaded NPs more profoundly induced sub-G1 in the cell cycle analysis and apoptosis of cancer cells in a similar pattern. Therefore, PGA-CHO and PGA-TOC polymers have potential applications as delivery systems for anticancer drugs.

Citation

Suksiriworapong, J., Achayawat, C., Juangrattanakamjorn, P., Taresco, V., Cuzzucoli Crucitti, V., Sakchaisri, K., & Bunsupa, S. (2023). Modification of Poly(Glycerol Adipate) with Tocopherol and Cholesterol Modulating Nanoparticle Self-Assemblies and Cellular Responses of Triple-Negative Breast Cancer Cells to SN-38 Delivery. Pharmaceutics, 15(8), Article 2100. https://doi.org/10.3390/pharmaceutics15082100

Journal Article Type Article
Acceptance Date Aug 5, 2023
Online Publication Date Aug 8, 2023
Publication Date 2023-08
Deposit Date Aug 22, 2023
Publicly Available Date Aug 23, 2023
Journal Pharmaceutics
Electronic ISSN 1999-4923
Publisher MDPI
Peer Reviewed Peer Reviewed
Volume 15
Issue 8
Article Number 2100
DOI https://doi.org/10.3390/pharmaceutics15082100
Keywords poly(glycerol adipate); tocopherol; cholesterol; nanoparticle; SN-38; breast cancer
Public URL https://nottingham-repository.worktribe.com/output/24148891
Publisher URL https://www.mdpi.com/1999-4923/15/8/2100

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