Acute and Subchronic Toxicological Study of the Cocktail Extract from Curcuma xanthorrhiza Roxb, Phyllanthus niruri L. and Morinda citrifolia L.

Author:

Rosidah Idah1ORCID,Renggani Tiya Novlita1ORCID,Firdausi Nisrina1,Ningsih Sri1ORCID,Yunianto Prasetyawan1ORCID,Permatasari Devi1,Pongtuluran Olivia Bunga2,Bahua Hismiaty3ORCID,Efendi Julham1,Kusumastuti Siska Andrina1ORCID,Nuralih 1ORCID,El Muttaqien Sjaikhurrizal4,Nizar 5ORCID,Kusumaningrum Susi1ORCID,Agustini Kurnia1ORCID

Affiliation:

1. Research Center for Pharmaceutical Ingredients and Traditional Medicine, National Research and Innovation Agency (BRIN), Bogor, Indonesia

2. Research Center for Agroindustry, National Research and Innovation Agency (BRIN), Bogor, Indonesia

3. Research Center for Sustainable Production System and Life Cycle Assessment, National Research and Innovation Agency (BRIN), Tangerang Selatan, Indonesia

4. Research Center for Vaccine and Drugs, National Research and Innovation Agency (BRIN), Bogor, Indonesia

5. Directorate of Utilization of Research and Innovation by Industry, National Research and Innovation Agency (BRIN), Jakarta, Indonesia

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.

Funder

Center for Pharmaceuticals and Medical of Technology

Publisher

Hindawi Limited

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