| Title: |
Waste Citrus limon Leaves as Source of Essential Oil Rich in Limonene and Citral: Chemical Characterization, Antimicrobial and Antioxidant Properties, and Effects on Cancer Cell Viability |
| Authors: |
Petretto, Giacomo Luigi; Vacca, Giuseppe; Addis, Roberta; Pintore, Giorgio; Nieddu, Mariella; Piras, Franca; Sogos, Valeria; Fancello, Francesco; Zara, Severino; Rosa, Antonella |
| Contributors: |
Petretto, Giacomo Luigi; Vacca, Giuseppe; Addis, Roberta; Pintore, Giorgio; Nieddu, Mariella; Piras, Franca; Sogos, Valeria; Fancello, Francesco; Zara, Severino; Rosa, Antonella |
| Publication Year: |
2023 |
| Collection: |
Università degli Studi di Cagliari: UNICA IRIS |
| Subject Terms: |
Citrus limon; Discarded leave; Leaf essential oil; Bioactivity; Cytotoxicity |
| Description: |
This study investigated chemical composition, cytotoxicity in normal and cancer cells, and antimicrobial and antioxidant activity of the essential oil (EO) isolated by hydrodistillation from the discarded leaves of lemon (Citrus limon) plants cultivated in Sardinia (Italy). The volatile chemical composition of lemon leaf EO (LLEO) was analyzed with gas chromatography-mass spectrometry combined with flame ionization detection (GC/MS and GC/FID). The most abundant component of LLEO was limonene (260.7 mg/mL), followed by geranial (102.6 mg/mL) and neral (88.3 mg/mL). The antimicrobial activity of LLEO was tested using eight bacterial strains and two types of yeasts by a microdilution broth test. Candida albicans showed the greatest susceptibility (MIC = 0.625 μL/mL) and Listeria monocytogenes and Staphylococcus aureus were inhibited at low LLEO concentration (MIC values from 2.5 to 5 μL/mL). The C. limon leaf EO displayed radical scavenging ability (IC50 value of 10.24 mg/mL) in the 2,2-diphenyl-1-picryl-hydrazylhydrate (DPPH) assay. Furthermore, the LLEO impact on cell viability was explored by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay in cancer HeLa cells, A375 melanoma cell line, normal fibroblasts (3T3 cells), and keratinocytes (HaCaT cells). LLEO, at 24 h of incubation, significantly reduced viability from 25 μM in Hela cells (33% reduction) and A375 cells (27%), greatly affecting cell morphology, whereas this effect was found from 50 μM on 3T3 fibroblasts and keratinocytes. LLEO’s pro-oxidant effect was also established in HeLa cells by 2′,7′-dichlorodihydrofluorescein diacetate assay. |
| Document Type: |
article in journal/newspaper |
| Language: |
English |
| Relation: |
info:eu-repo/semantics/altIdentifier/wos/WOS:001013855000001; volume:12; issue:6; numberofpages:21; journal:ANTIOXIDANTS; https://hdl.handle.net/11584/364304 |
| DOI: |
10.3390/antiox12061238 |
| Availability: |
https://hdl.handle.net/11584/364304; https://doi.org/10.3390/antiox12061238; https://www.mdpi.com/2076-3921/12/6/1238 |
| Rights: |
info:eu-repo/semantics/openAccess |
| Accession Number: |
edsbas.4F5695BF |
| Database: |
BASE |