Pickering Emulsion of Oleoresin from Dipterocarpus alatus Roxb. ex G. Don and Its Antiproliferation in Colon (HCT116) and Liver (HepG2) Cancer Cells

Author:

Pocasap Piman1,Tamprasit Kawintra23,Rungsri Thanyathanya4,Kaimuangpak Karnchanok2,Srisongkram Tarapong35ORCID,Katekaew Somporn6ORCID,Kamwilaisak Khanita7,Puthongking Ploenthip5ORCID,Weerapreeyakul Natthida35ORCID

Affiliation:

1. Department of Pharmacology, Faculty of Medicine, Khon Kaen University, Khon Kaen 40002, Thailand

2. Graduate School in the Program of Research and Development in Pharmaceuticals, Faculty of Pharmaceutical Sciences, Khon Kaen University, Khon Kaen 40002, Thailand

3. Research Institute for Human High Performance and Health Promotion, Khon Kaen University, Khon Kaen 40002, Thailand

4. Faculty of Pharmaceutical Sciences in the Program of Doctor of Pharmacy, Khon Kaen University, Khon Kaen 40002, Thailand

5. Division of Pharmaceutical Chemistry, Faculty of Pharmaceutical Sciences, Khon Kaen University, Khon Kaen 40002, Thailand

6. Department of Biochemistry, Faculty of Sciences, Khon Kaen University, Khon Kaen 40002, Thailand

7. Department of Chemical Engineering, Faculty of Engineering, Khon Kaen University, Khon Kaen 40002, Thailand

Abstract

Oleoresin of Dipterocarpus alatus Roxb. ex G. Don (DA) has been traditionally used for local medicinal applications. Several in vitro studies have indicated its pharmacological potential. However, the low water solubility hinders its use and development for pharmaceutical purposes. The study aimed to (1) formulate oil-in-water (o/w) Pickering emulsions of DA oleoresin and (2) demonstrate its activities in cancer cells. The Pickering emulsions were formulated using biocompatible carboxylated cellulose nanocrystal (cCNC) as an emulsifier. The optimized emulsion comprised 3% (F1) and 4% (v/v) (F2) of oleoresin in 1% cCNC and 0.1 M NaCl, which possessed homogeneity and physical stability compared with other formulations with uniform droplet size and low viscosity. The constituent analysis indicated the presence of the biomarker dipterocarpol in both F1 and F2. The pharmacological effects of the two emulsions were demonstrated in vitro against two cancer cell lines, HepG2 and HCT116. Both F1 and F2 suppressed cancer cell viability. The treated cells underwent apoptosis, as demonstrated by distinct nuclear morphological changes in DAPI-stained cells and Annexin V/PI-stained cells detected by flow cytometry. Our study highlights the prospect of Pickering emulsions for oleoresin, emphasizing enhanced stability and potential pharmacological advantages.

Funder

Fundamental Fund of Khon Kaen University

Publisher

MDPI AG

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