Phytochemical Characterization and Chemotherapeutic Potential of Cinnamomum verum Extracts on the Multiplication of Protozoan Parasites In Vitro and In Vivo

is a commonly used herbal plant that has several documented properties against various diseases. The existing study evaluated the inhibitory effect of acetonic extract of (AECV) and ethyl acetate extract of (EAECV) against piroplasm parasites in vitro and in vivo. The drug-exposure viability assay w...

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Veröffentlicht in:Molecules (Basel, Switzerland) Switzerland), 2020-02, Vol.25 (4), p.996
Hauptverfasser: Batiha, Gaber El-Saber, Beshbishy, Amany Magdy, Guswanto, Azirwan, Nugraha, Arifin, Munkhjargal, Tserendorj, M Abdel-Daim, Mohamed, Mosqueda, Juan, Igarashi, Ikuo
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Sprache:eng
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Zusammenfassung:is a commonly used herbal plant that has several documented properties against various diseases. The existing study evaluated the inhibitory effect of acetonic extract of (AECV) and ethyl acetate extract of (EAECV) against piroplasm parasites in vitro and in vivo. The drug-exposure viability assay was tested on Madin-Darby bovine kidney (MDBK), mouse embryonic fibroblast (NIH/3T3) and human foreskin fibroblast (HFF) cells. Qualitative phytochemical estimation revealed that AECV and EAECV containing multiple bioactive constituents namely alkaloids, tannins, saponins, terpenoids and remarkable amounts of polyphenols and flavonoids. AECV and EAECV inhibited , , , , and multiplication at half-maximal inhibitory concentrations (IC ) of 23.1 ± 1.4, 56.6 ± 9.1, 33.4 ± 2.1, 40.3 ± 7.5, 18.8 ± 1.6 µg/mL, and 40.1 ± 8.5, 55.6 ± 1.1, 45.7 ± 1.9, 50.2 ± 6.2, and 61.5 ± 5.2 µg/mL, respectively. In the cytotoxicity assay, AECV and EAECV affected the viability of MDBK, NIH/3T3 and HFF cells with half-maximum effective concentrations (EC ) of 440 ± 10.6, 816 ± 12.7 and 914 ± 12.2 µg/mL and 376 ± 11.2, 610 ± 7.7 and 790 ± 12.4 µg/mL, respectively. The in vivo experiment showed that AECV and EAECV were effective against in mice at 150 mg/kg. These results showed that extracts are potential antipiroplasm drugs after further studies in some clinical cases.
ISSN:1420-3049
1420-3049
DOI:10.3390/molecules25040996