Chemical Investigation and Screening of Anti-Proliferative Activity on Human Cell Lines of Pure and Nano-Formulated Lavandin Essential Oil

被引:16
|
作者
Ovidi, Elisa [1 ]
Masci, Valentina Laghezza [1 ]
Taddei, Anna Rita [2 ]
Paolicelli, Patrizia [3 ]
Petralito, Stefania [3 ]
Trilli, Jordan [3 ]
Mastrogiovanni, Fabio [1 ]
Tiezzi, Antonio [1 ]
Casadei, Maria Antonietta [3 ]
Giacomello, Pierluigi [3 ]
Garzoli, Stefania [3 ]
机构
[1] Tuscia Univ, Dept Innovat Biol Agrofood & Forestal Syst, I-01100 Viterbo, Italy
[2] Tuscia Univ, High Equipment Ctr, I-01100 Viterbo, Italy
[3] Sapienza Univ, Dept Drug Chem & Technol, I-00185 Rome, RM, Italy
关键词
lavandin essential oil; antiproliferative activity; HS-GC; MS analysis; nanoemulsion; CERVICAL-CANCER CELLS; L. ESSENTIAL OIL; ANTICANCER ACTIVITY; GOLD NANOPARTICLES; LEUKEMIA-CELLS; CYCLE ARREST; IN-VITRO; APOPTOSIS; LAVENDER; ANGUSTIFOLIA;
D O I
10.3390/ph13110352
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Lavandin essential oil (LEO), a natural sterile hybrid obtained by crossbreeding L. angustifolia x L. latifolia, is mainly composed by active components belonging to the family of terpenes endowed with relevant anti-proliferative activity, which can be enhanced by proper application of nanotechnology. In particular, this study reports the chemical characterization and the screening of the anti-proliferative activity on different human cell lines of pure and nano-formulated lavandin essential oil (EO). LEO and its formulation (NanoLEO) were analyzed by HS/GC-MS (Headspace/Gas Chromatography-Mass Spectrometry) to describe and compare their chemical volatile composition. The most abundant compounds were linalool and 1,8-cineole (LEO: 28.6%; 27.4%) (NanoLEO: 60.4%; 12.6%) followed by alpha-pinene (LEO: 9.6%; NanoLEO: 4.5%), camphor (LEO: 6.5%; NanoLEO: 7.0%) and linalyl acetate (LEO: 6.5%; NanoLEO: 3.6%). The cytotoxic effects of LEO and NanoLEO were investigated on human neuroblastoma cells (SHSY5Y), human breast adenocarcinoma cells (MCF-7), human lymphoblastic leukemia cells (CCRF CEM), human colorectal adenocarcinoma cells (Caco-2) and one normal breast epithelial cell (MCF10A) by the MTT (3-(4,5-Dimethylthiazol-2-yl)-2,5-Diphenyltetrazolium Bromide)-assay. Caco-2, MCF7 and MCF10A normal cells resulted more resistant to the treatment with LEO, while CCRF-CEM and SHSY5Y cells were more sensitive. The antiproliferative effect of LEO resulted amplified when the essential oil was supplied as nanoformulation, mainly in Caco-2 cells. Scanning and transmission electron microscopy investigations were carried out on Caco-2 cells to outline at ultrastructural level possible affections induced by LEO and NanoLEO treatments.
引用
收藏
页码:1 / 17
页数:17
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