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Chemical profile and in vivo toxicity evaluation of unripe Citrus aurantifolia essential oil.
Adokoh, Christian K; Asante, Du-Bois; Acheampong, Desmond O; Kotsuchibashi, Yohei; Armah, Francis A; Sirikyi, Ignatius H; Kimura, Keisuke; Gmakame, Edward; Abdul-Rauf, Sey.
Afiliación
  • Adokoh CK; Department of Forensic Sciences, School of Biological Sciences, University of Cape Coast, Cape Coast, Ghana.
  • Asante DB; Department of Forensic Sciences, School of Biological Sciences, University of Cape Coast, Cape Coast, Ghana.
  • Acheampong DO; School of Medical and Health Sciences, Edith Cowan University, Australia.
  • Kotsuchibashi Y; Department of Biomedical Sciences, School of Allied Health Sciences, University of Cape Coast, Cape Coast, Ghana.
  • Armah FA; Department of Materials and Life Science, Shizuoka Institute of Science and Technology, 2200-2 Toyosawa, Fukuroi, Shizuoka, 437-8555, Japan.
  • Sirikyi IH; Department of Biomedical Sciences, School of Allied Health Sciences, University of Cape Coast, Cape Coast, Ghana.
  • Kimura K; Directorate of University Health Service, University of Cape Coast, Cape Coast, Ghana.
  • Gmakame E; Department of Materials and Life Science, Shizuoka Institute of Science and Technology, 2200-2 Toyosawa, Fukuroi, Shizuoka, 437-8555, Japan.
  • Abdul-Rauf S; Department of Biomedical Sciences, School of Allied Health Sciences, University of Cape Coast, Cape Coast, Ghana.
Toxicol Rep ; 6: 692-702, 2019.
Article en En | MEDLINE | ID: mdl-31372347
ABSTRACT
Citrus aurantifolia (Christm.) Swingle (syn. C. MEDICA var. ACIDA Brandis) (family Rutaceae) essential oil is one of the cheapest oils found in local markets. Although, it is generally accepted as non-toxic to vital organs and cells, majority of people are cynical about it usage. Herein, the present study reports the chemical composition and in vivo oral toxicity study of unripe C. aurantifolia essential oil found in Ghana. The toxicity of C. aurantifolia essential oil extract was investigated via oral administration using two

methods:

The acute toxicity single dose study (SDS) and the repeated dose method. The oil exhibited no acute toxicity but in the sub-chronic studies, the effects was dose and time-dependent. Chemical profile investigation of the oil showed 9 constituent of phytochemicals (Germacrene isomers (61.2%), Pineen (14%), Linalool dimmer (2.9%), Bornane (11%), Citral (2.9%), Anethole (1.5%), Anisole (1.1%), Safrole (0.3%) and Demitol (0.6%)). Histopathological studies revealed conditions such as necrosis, edema and inflammatory reaction in the liver, spleen and kidneys. Marginal upsurge of biochemical parameters above normal and elevated levels of lymphocytes (35.20-46.40 g/dL) demonstrated mild toxicity among the 100 mg/kg and 500 mg/kg dose groups at the sub-chronic stage. Low levels of hemoglobin (13.60 to 12.70 g/dL), MCV (34.20-24.0 fL), MCH (40.20-36.40 g/dL) along with high levels of liver enzymes confirmed the mild toxicity of the oil at sub-chronic stage. These results demonstrate that, despite consideration of lime essential oil as safe, it can have mild hematotoxic, nephrotoxic and hepatotoxic effects.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Toxicol Rep Año: 2019 Tipo del documento: Article País de afiliación: Ghana

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Toxicol Rep Año: 2019 Tipo del documento: Article País de afiliación: Ghana