frutescens. The cytotoxicity assay was performed using OVCAR-8 (ovarian adenocarcinoma), NCI-H358M (bronchoalveolar lung carcinoma) and PC-3M (metastatic prostate carcinoma) human tumour cell lines, all obtained selleck chemical from the National Cancer Institute, Bethesda, MD. Cells were grown in RPMI-1640 medium supplemented with 10% foetal bovine serum, 2 mM glutamine, 100 μg/ml streptomycin and 100 U/ml penicillin. Cells were maintained at 37 °C in a 5% CO2 atmosphere. Sarcoma 180 tumour cells, which had been maintained in the peritoneal cavity of Swiss mice, were obtained from the Laboratory of Experimental Oncology at the Federal University of Ceará, Brazil. A total of 40 Swiss

mice (males, 25–30 g), obtained from the central animal house at the Federal University of Sergipe, Brazil, were used. Animals were housed in cages with free access

to food and water. All animals were kept under a 12:12 h light–dark cycle (lights on at 6:00 a.m.). Animals were treated according to the ethical principles for animal Afatinib price experimentation of SBCAL (Brazilian Association of Laboratory Animal Science), Brazil. The Animal Studies Committee at the Federal University of Sergipe approved the experimental protocol (number 08/2012). X. frutescens leaves were collected in July 2011 at “Mata do Junco” in the Municipality of Capela, Sergipe State, Brazil, coordinates: S 10° 57′ 52″ W 37° 04′ 65″. The species was identified by Dr. Ana Paula do Nascimento Prata. Voucher specimen number 22178 was deposited at the Herbarium of the Federal University of Sergipe, Brazil. The leaves were obtained from plants that were flowering and in

fructification. X. frutescens leaves (200 g) were dried in an oven with circulating air at 40 °C for 24 h and submitted to hydrodistillation for 4 h using a Clevenger-type apparatus (Amitel, São Paulo, Brazil). The essential oil was dried over anhydrous sodium sulfate and the percentage content (v/w) was calculated on the basis of the dry weight of plant material. The essential oils were stored in a freezer until analysis. Hydrodistillation Mannose-binding protein-associated serine protease was performed in triplicate. GC analyses were carried out using a Shimadzu GC-17A fitted with a flame ionisation detector (FID) and an electronic integrator (Shimadzu, Kyoto, Japan). Separation of the compounds was achieved using a ZB-5MS fused capillary column (30 m × 0.25 mm × 0.25 μm film thickness; Phenomenex, Torrance, CA). Helium was the carrier gas at 1.0 ml/min flow rate. The column temperature program was: 40 °C for 4 min, a rate of 4 °C/min to 240 °C, then a rate of 10 °C/min to 280 °C, and then 280 °C for 2 min. The injector and detector temperatures were 250 °C and 280 °C, respectively. Samples (10 mg/ml in CH2Cl2) were injected with a 1:50 split ratio. The injection volume was 0.5 μl. Retention indices were generated with a standard solution of n-alkanes (C8–C20). Peak areas and retention times were measured by an electronic integrator.