ABSTRACT
Medicinal plants have been used to treat various illnesses for decades. The present study supports thephysicochemical, phytochemical, and gas chromatography–mass spectrometry (GC–MS) analysis of themethanolic extract of Pouteria campechiana leaves and fruits, in order to propose that the bona fide plantmaterial is suitably for traditional use. The physicochemical evaluations and fluorescence analysis weredetermined according to standard protocols. The phytochemical constituents were carried out by bothqualitative and quantitative methods. The GC–MS analysis was carried out to identify the compounds present.The physicochemical parameters revealed that the total ash content of P. campechiana leaves is more than thefruit. The water-soluble ash value of P. campechiana leaves is less than the acid-soluble ash value of the leaf,but the water-soluble ash value of P. campechiana fruit is greater than the acid-soluble ash value of the fruit.The water-extractive value of P. campechiana leaves and fruit is better when compared to the alcohol-extractivevalue. Moisture content, swelling index, and foaming index were found to be greater in the leaves than the fruit.Preliminary phytochemical screening showed the presence of various phytoconstituents. Quantitative analysisrevealed that the leaf extract consists of high phenolic compounds followed by total flavonoids and total tanninthan the fruit extract. The total alkaloid was found to be higher in the fruit extract than the leaf extract. Energydispersive X-ray spectrometer analysis of the leaves showed the presence of elements such as N, O, Cl, K, Ca,and C and fruits showed the presence of N, O, K, and C. The GC–MS analysis of P. campechiana leaf and fruitreveals the presence of 9 and 12 compounds, respectively. The results of the present study provide apparentinformation of the plant and also serve as an analytical tool for appropriate identification. Hence, this plantexhibits rich phytopharmaceutical importance.
ABSTRACT
Objective: To test the mosquitocidal potential of leaf extracts of Pouteria campechiana prepared with different solvents and elucidate the structure of an isolated mosquitocidal compound. Methods: The leaf extracts of Pouteria campechiana prepared with three solvents (petroleum benzene, ethyl acetate and acetone) and potential bioactive fractions were tested against various stages of Aedes aegypti and Culex quinquefasciatus by using the WHO protocols, and the chemical profile and its functional groups were identified by GC-MS and Fourier transmission-infrared spectroscopy (FT-IR). The structure of bioactive compound was characterized by nuclear magnetic resonance (NMR) spectral technique. Results: The preliminary phytochemical results revealed the presence of alkaloids, amino acids, flavonoids, quinones, saponins, steroids, tannins, and terpenoids in the acetone extract. A significant toxic potential was observed in the acetone extract against both Aedes aegypti and Culex quinquefasciatus mosquitoes. The acetone extract exhibits remarkable larvicidal (LC
ABSTRACT
Objective: To test the mosquitocidal potential of leaf extracts of Pouteria campechiana prepared with different solvents and elucidate the structure of an isolated mosquitocidal compound. Methods: The leaf extracts of Pouteria campechiana prepared with three solvents (petroleum benzene, ethyl acetate and acetone) and potential bioactive fractions were tested against various stages of Aedes aegypti and Culex quinquefasciatus by using the WHO protocols, and the chemical profile and its functional groups were identified by GC-MS and Fourier transmission-infrared spectroscopy (FT-IR). The structure of bioactive compound was characterized by nuclear magnetic resonance (NMR) spectral technique. Results: The preliminary phytochemical results revealed the presence of alkaloids, amino acids, flavonoids, quinones, saponins, steroids, tannins, and terpenoids in the acetone extract. A significant toxic potential was observed in the acetone extract against both Aedes aegypti and Culex quinquefasciatus mosquitoes. The acetone extract exhibits remarkable larvicidal (LC50: 12.232 μg/mL and LC90: 63.970 μg/mL), pupicidal (LC50: 18.949 μg/mL and LC,0: 167.669 μg/mL) and adulticidal (LC50: 20.689 μg/mL and LC90: 72.881 μg/mL) effects against Aedes aegypti. Furthermore, the same extract was subjected to isolation of bioactive compound by GC- MS and FT-IR analysis. GC-MS results showed the presence of 5 major compounds, and octacosane (18.440%) was detected as the predominant compound. The FT-IR result of acetone extract demonstrated the presence of various functional groups like alkanes/alkynes, ester, aromatic and amides. The NMR spectrum results of isolated compound were well matched to glycoside linked flavonoids. Based on the chromatography and spectral techniques the isolate molecule was identified as myricitrin by FT-IR and nuclear magnetic resonance spectral data. Conclusion: The isolated compound myricitrin possesses a significant toxic effect in all stages of Aedes aegypti and Culex quinquefasciatus mosquito's with lowest LC50 and LC90 values.
ABSTRACT
Aims: To evaluate preparation herbal mixed of Pouteria campechiana, Chrysophyllum cainito, Citrus limonum and Annona muricata (PCCA) on vasorelaxant and hypotensive effect on rat model and toxicological data after acute oral administration to give scientific support to the use ethnomedical and to explore their potential damaging on oral intake. Study Design: Experimental. Place and Duration of Study: Sample female and male Wistar rats. Pharmacology laboratory of Chemistry School and Department of Clinical and Epidemiological Research of Medicine School, Autonomous University of Yucatán. Between October 2014 and July 2016. Methodology: An ethanolic extract of PCCA was prepared at a ratio of 1:1:1:1 of each plant plus individual extracts were prepared. Vasorelaxant effect was assessed (3.03 to 100 μg/mL), hypotensive effect ((100, 200, 300 mg/Kg) and median lethal dose (LD50) by oral acute toxicity method (OECD 423 guide). Results: PCCA extract induced a significant vasorelaxation (medium effective concentration (EC50)=463.43 μg/mL) in a concentration-dependent manner in aorta’s endothelium-intact rings and this effect was partially endothelium-dependent. Acute oral administration of 200 and 300 mg/kg of PCCA exhibited significant decrease in systolic blood pressure in normotensive rats. PCCA did not show clinical toxicity of acute oral administration. Only 2000 mg/kg show histopathological inflammatory responses on gut and liver. Conclusion: PCCA induces a significant cardiovascular effect and was not toxic for rodents. The results support the popular use of some Mayan Medicinal plants as antihypertensive agents; however, clinical studies are necessary.