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Acute and Subchronic Toxicological Study of the Cocktail Extract from Curcuma xanthorrhiza Roxb, Phyllanthus niruri L. and Morinda citrifolia L.
Rosidah, Idah; Renggani, Tiya Novlita; Firdausi, Nisrina; Ningsih, Sri; Yunianto, Prasetyawan; Permatasari, Devi; Pongtuluran, Olivia Bunga; Bahua, Hismiaty; Efendi, Julham; Kusumastuti, Siska Andrina; El Muttaqien, Sjaikhurrizal; Kusumaningrum, Susi; Agustini, Kurnia.
Afiliación
  • Rosidah I; Research Center for Pharmaceutical Ingredients and Traditional Medicine, National Research and Innovation Agency (BRIN), Bogor, Indonesia.
  • Renggani TN; Research Center for Pharmaceutical Ingredients and Traditional Medicine, National Research and Innovation Agency (BRIN), Bogor, Indonesia.
  • Firdausi N; Research Center for Pharmaceutical Ingredients and Traditional Medicine, National Research and Innovation Agency (BRIN), Bogor, Indonesia.
  • Ningsih S; Research Center for Pharmaceutical Ingredients and Traditional Medicine, National Research and Innovation Agency (BRIN), Bogor, Indonesia.
  • Yunianto P; Research Center for Pharmaceutical Ingredients and Traditional Medicine, National Research and Innovation Agency (BRIN), Bogor, Indonesia.
  • Permatasari D; Research Center for Pharmaceutical Ingredients and Traditional Medicine, National Research and Innovation Agency (BRIN), Bogor, Indonesia.
  • Pongtuluran OB; Research Center for Agroindustry, National Research and Innovation Agency (BRIN), Bogor, Indonesia.
  • Bahua H; Research Center for Sustainable Production System and Life Cycle Assessment, National Research and Innovation Agency (BRIN), Tangerang Selatan, Indonesia.
  • Efendi J; Research Center for Pharmaceutical Ingredients and Traditional Medicine, National Research and Innovation Agency (BRIN), Bogor, Indonesia.
  • Kusumastuti SA; Research Center for Pharmaceutical Ingredients and Traditional Medicine, National Research and Innovation Agency (BRIN), Bogor, Indonesia.
  • Nuralih; Research Center for Pharmaceutical Ingredients and Traditional Medicine, National Research and Innovation Agency (BRIN), Bogor, Indonesia.
  • El Muttaqien S; Research Center for Vaccine and Drugs, National Research and Innovation Agency (BRIN), Bogor, Indonesia.
  • Nizar; Directorate of Utilization of Research and Innovation by Industry, National Research and Innovation Agency (BRIN), Jakarta, Indonesia.
  • Kusumaningrum S; Research Center for Pharmaceutical Ingredients and Traditional Medicine, National Research and Innovation Agency (BRIN), Bogor, Indonesia.
  • Agustini K; Research Center for Pharmaceutical Ingredients and Traditional Medicine, National Research and Innovation Agency (BRIN), Bogor, Indonesia.
J Toxicol ; 2024: 9445226, 2024.
Article en En | MEDLINE | ID: mdl-38571743
ABSTRACT
Curcuma xanthorrhiza Roxb, Phyllanthus niruri L., and Morinda citrifolia L. are Indonesian medicinal herbs used empirically as traditional therapeutics for maintaining health. The cocktail extract of these three plants (CECPM) had been developed and demonstrated immunostimulant activity in rats. This study aimed to evaluate the acute and subchronic toxicity of CECPM in vivo. The acute toxicity assay was conducted by orally administering a range dose of CECPM (313, 625, 1250, 2500, or 5000 mg/kg body weight (bw) on female mice once and then evaluating the toxic symptom every day for 14 days later. The chronic toxicity test was carried out by giving various doses of CECPM (600, 800, and 1000 mg/kg·bw) to female and male rats orally continuously for 90 consecutive days. The signs of toxicities were evaluated at the 90- and 28 days postadministration. The acute oral toxicity assays showed that there was no toxic syndrome and mortality found during the period of the experiment. The lethal dose level (LD50) of CECPM was more than 5000 g/kg, which was categorized as practically non-toxic. Meanwhile, in the sub-chronic toxicity study, some parameters tested at 90 days postadministration and after 28 days of withdrawal, such as the body weight, relative organ weight, food intake, hematological and biochemical blood parameters, and also histopathological examination of five primary tissues (heart, liver, kidney, spleen, and lung) revealed no abnormalities. There was no-observed adverse effect level (NOAEL) for the present study of CECPM 1000 mg/kg·bw of the rat. Therefore, it is concluded that the orally administered CECPM was relatively nontoxic during acute and subchronic toxicology studies.

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: J Toxicol Año: 2024 Tipo del documento: Article País de afiliación: Indonesia

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: J Toxicol Año: 2024 Tipo del documento: Article País de afiliación: Indonesia