Synthesis, characterization, and development of alpha-pinene nanoemulsion as an apoptotic inducer with cytotoxicity activity on human melanoma and breast cancer

被引:1
|
作者
Ghanbariasad, Ali [1 ]
Osanloo, Mahmoud [2 ]
Hatami, Shekoufeh [3 ]
Khaksar, Sepideh [4 ]
Zarenezhad, Elham [5 ]
Ranjbar, Razie [1 ]
Alipanah, Hiva [6 ]
机构
[1] Fasa Univ Med Sci, Sch Med, Dept Med Biotechnol, Fasa, Iran
[2] Fasa Univ Med Sci, Sch Adv Technol Med, Dept Med Nanotechnol, Fasa, Iran
[3] Fasa Univ Med Sci, Student Res Comm, Fasa, Iran
[4] Alzahra Univ, Fac Biol Sci, Dept Plant Sci, Tehran, Iran
[5] Fasa Univ Med Sci, Noncommunicable Dis Res Ctr, Fasa, Iran
[6] Fasa Univ Med Sci, Sch Med, Dept Physiol, Fasa, Iran
关键词
alpha-Pinene; Nanoemulsion; Cell survival; Apoptosis; Drug delivery systems; L. ESSENTIAL OIL; NANOPARTICLES; ANTICANCER; DELIVERY; CHEMOTHERAPY; INDUCTION; CELLS; COLON;
D O I
10.1007/s11696-023-03156-w
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Alpha-pinene (AP) is known for with antioxidant, anti-inflammatory, and anticancer properties. Nanoemulsion-based formulations are widely used in drug delivery of hydrophobic molecules. This study formulated AP into nanoemulsion (APNE), and its cytotoxicity activity and therapeutic anticancer efficacy were evaluated. The successful loading of AP in the APNE was also confirmed using ATR-FTIR analysis. Moreover, the anticancer properties and apoptotic effects (BAX/BCL-2 ratio) of the AP and APNE on melanoma (A-375) and breast cancer (MCF-7) cell lines were investigated using a modified MTT assay. Results showed that APNE and AP with IC50 values of 106.19 and 264.20 mu g/mL on A-375 and 168.02 and 213.34 mu g/mL on MCF-7 cell lines showed proper anti-proliferation activity. However, APNE potency was significantly higher than AP, especially in melanoma cells. In addition, the BAX/BCL-2 ratio in treated cells increased. Drug delivery system-based nanoformulation can be a suitable candidate for delivery of AP which leads to the reducing dose and/or increasing the apoptotic effects of AP in breast and melanoma cancer cells.
引用
收藏
页码:1181 / 1191
页数:11
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