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Thymoquinone-Loaded Soy-Phospholipid-Based Phytosomes Exhibit Anticancer Potential against Human Lung Cancer Cells

Authors :
Nabil A. Alhakamy
Usama A. Fahmy
Adel F. Alghaith
Zuhier Awan
Faris O Arif
Mohamed A. Alfaleh
Nabil K. Alruwaili
Ahmed L. Alaofi
Shaimaa M Badr-Eldin
Osama A. A. Ahmed
Giuseppe Caruso
Source :
Pharmaceutics, Pharmaceutics, Vol 12, Iss 761, p 761 (2020), Volume 12, Issue 8
Publication Year :
2020
Publisher :
MDPI, 2020.

Abstract

Thymoquinone (TQ), a natural polyphenol, has been associated with various pharmacological responses<br />however, low bioavailability of TQ limits its clinical application. Thus, a novel phytosomal delivery system of TQ-Phospholipon&reg<br />90H complex (TQ-phytosome) was developed by refluxing combined with anti-solvent precipitation. This TQ delivery system was optimized by a three-factor, three-level Box-Behnken design. The optimized TQ-phytosome size was (45.59 &plusmn<br />1.82 nm) and the vesicle size was confirmed by transmission electron microscopy. The in vitro release pattern of the formulation indicated a biphasic release pattern, where an initial burst release was observed within 2 h, followed by a prolonged release. A remarkable increase in dose-dependent cytotoxicity was evident from the significant decrease in IC50 value of TQ-phytosomes (4.31 &plusmn<br />2.21 &micro<br />M) against the A549 cell line. The differential effect of TQ-phytosomes in cell cycle analysis was observed, where cancer cells were accumulated on G2-M and pre-G1 phases. Furthermore, increased apoptotic induction and cell necrosis of TQ-phytosomes were revealed with the annexin V staining technique via activation of caspase-3. In reactive oxygen species (ROS) analysis, TQ-phytosomes acted to significantly increase ROS generation in A549 cells. In conclusion, the sustained release profile with significantly-improved anticancer potential could be obtained with TQ by this phytosomal nanocarrier platform.

Details

Language :
English
ISSN :
19994923
Volume :
12
Issue :
8
Database :
OpenAIRE
Journal :
Pharmaceutics
Accession number :
edsair.doi.dedup.....ead3ad550fc8a525f9ff0079e92716f2