2
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Analysis of 1,4 naphthoquinone in the Indonesian medical plant from extract Eleutherine palmifolia (L.) Merr by UHPLC

      , ,
      IOP Conference Series: Earth and Environmental Science
      IOP Publishing

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Medicinal plants are widely used for the preparation of various pharmaceutical forms. Eleutherine palmifolia is a typical plant in Central Borneo in Indonesian. 1,4 naphthoquinone is a bioactive compound from E. palmifolia which has potential as a medicinal ingredient, one of which is anticancer. This study aimed to determine the levels of 1.4 naphthoquinone as a marker compound for the standardization of standardized herbal medicine (OHT) formulas of E. palmifolia extract. The separation was carried out with Thermo Fisher Scientific UHPLC Ultimate 3000 RS coupled with a diode array detector, and the C18 column was employed. The UV detection was performed at 254 nm, and the run time of 0.8 minutes. The mobile phase consists of an isocratic method, 95% methanol (A) and 0.5% chloroform (B). The results showed that 1,4 naphthoquinone was eluted at 3.260 min. The response of the standard 1,4 naphthoquinone linear in the concentration range of 3.0-21.0 μg/mL with r 2 = 0.9951. The accuracy of this method, which was 99.95% with RSD value ≤ 2%. UHPLC method was developed, which has been validated and shown applies to the determination and quantification of 1,4 naphthoquinone in E. palmifolia. Analysis of 1.4 naphthoquinone levels contained in E. palmifolia 12 μg/mL was 7.79 μg/mL ± 0.01.

          Related collections

          Most cited references4

          • Record: found
          • Abstract: found
          • Article: not found

          Phase I clinical trial of oral curcumin: biomarkers of systemic activity and compliance.

          Curcumin, a polyphenolic antioxidant derived from a dietary spice, exhibits anticancer activity in rodents and in humans. Its efficacy appears to be related to induction of glutathione S-transferase enzymes, inhibition of prostaglandin E(2) (PGE(2)) production, or suppression of oxidative DNA adduct (M(1)G) formation. We designed a dose-escalation study to explore the pharmacology of curcumin in humans. Fifteen patients with advanced colorectal cancer refractory to standard chemotherapies consumed capsules compatible with curcumin doses between 0.45 and 3.6 g daily for up to 4 months. Levels of curcumin and its metabolites in plasma, urine, and feces were analyzed by high-pressure liquid chromatography and mass spectrometry. Three biomarkers of the potential activity of curcumin were translated from preclinical models and measured in patient blood leukocytes: glutathione S-transferase activity, levels of M(1)G, and PGE(2) production induced ex vivo. Dose-limiting toxicity was not observed. Curcumin and its glucuronide and sulfate metabolites were detected in plasma in the 10 nmol/L range and in urine. A daily dose of 3.6 g curcumin engendered 62% and 57% decreases in inducible PGE(2) production in blood samples taken 1 hour after dose on days 1 and 29, respectively, of treatment compared with levels observed immediately predose (P < 0.05). A daily oral dose of 3.6 g of curcumin is advocated for Phase II evaluation in the prevention or treatment of cancers outside the gastrointestinal tract. PGE(2) production in blood and target tissue may indicate biological activity. Levels of curcumin and its metabolites in the urine can be used to assess general compliance.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Synthesis of novel rhinacanthins and related anticancer naphthoquinone esters.

            Rhinacanthin-M, -N and -Q, natural products isolated from the medicinal plant Rhinacanthus nasutus, and 39 novel naphthoquinone esters have been synthesized in excellent yield by esterification of naphthoquinone-3-(propan-3'-ols) with benzoic or naphthoic acids. Almost all the naphthoquinone esters that contain a C-3 hydroxy group showed significant cytotoxicities against KB, HeLa, and HepG2 cell lines. In contrast, ester derivatives lacking the C-3 hydroxy group were inactive to the cancer cell lines. Two methyl substituents on the C-2' of propyl chain conferred more potent cytotoxicity than when there is only one or no methyl group. Naphthoate esters exhibited greater cytotoxicity than benzoate esters. Computer modeling has been done to obtain a first look at the mode of action in connection with these observations.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Identification of a new naphthalene and its derivatives from the bulb of eleutherine americana with inhibitory activity on lipopolysaccharide-induced nitric oxide production.

              A new naphthoquinone, (-)-3-[2-(acetyloxy)propyl]-2-hydroxy-8-methoxy-1,4-naphthoquinone (1) was isolated from the bulb of Eleutherine americana MERR. et HEYNE (Iridaceae) together with two known compounds, eleutherinol (6) and 1,5-dihydroxy-3-methylanthraquinone (7) which were found in this species for the first time. The other known compounds, (-)-isoeleutherin (2), (+)-eleutherin (3), (-)-hongconin (4), and (+)-dihydroeleutherinol (5) which were reported previously from this species, were also isolated in the present study. Compounds 2-6 exhibited potent inhibitory activity on nitric oxide production in RAW 264.7 lipopolysaccharide-activated mouse macrophage cells with IC(50) values of 7.7, 11.4, 19.8, 21.7, and 34.4 microM, respectively, whereas the other two compounds, 1 and 7, were inactive. The structure of compound 1 was elucidated by spectroscopic data analysis including 1D and 2D NMR experiments.
                Bookmark

                Author and article information

                Journal
                IOP Conference Series: Earth and Environmental Science
                IOP Conf. Ser.: Earth Environ. Sci.
                IOP Publishing
                1755-1307
                1755-1315
                February 01 2020
                February 01 2020
                : 456
                : 1
                : 012020
                Article
                10.1088/1755-1315/456/1/012020
                da5b215a-9cfc-44f5-9dbe-a9c487455690
                © 2020

                http://creativecommons.org/licenses/by/3.0/

                History

                Comments

                Comment on this article