scholarly journals Phytochemistry and Antioxidant Activity of Irvingiagabonensis (Bush mango) Seed Sample

Author(s):  
Ezekwe Ahamefula Sunday ◽  
Nwadike Constance Nnedimma ◽  
Wokocha Gift Peter ◽  
George Boma Orlando

Phytochemistry and antioxidant activity of Irvingiagabonensis (Bush mango) seed sample were evaluated. Dried milled seeds of I.gabonensis popularly known as “ogbono” passed through phytochemical screening, Gas chromatography-mass spectrometry (GC-MS) analysis and antioxidant studies. Tannins, saponins, flavonoids, alkaloids, steroids, and reducing sugars were among the phytochemicals found present after screening. About 20 constituents were revealed by the GC-MS analysis out of which 1,3-O-Benzylidine glyceryl-2-myristate had the highest molecular weight, 2-Undecanone had the highest peak area of 45.39% whereas 3-Dibenzofuranamine had the highest retention time. Some of these constituents could have one or two applications in medicinal, food or cosmetic industries. I.gabonensis seeds showed better antioxidant activity against the control at concentrations considered in this study. Some of these constituents as well could be behind the observed antioxidant activity. This study has evaluated the phytochemistry and antioxidant activity of I.gabonensis (Bush mango) seed sample.

2021 ◽  
pp. 33-45
Author(s):  
Ezekwe Ahamefula Sunday ◽  
Nwadike Constance Nnedimma ◽  
Wokocha Gift Peter ◽  
George Boma Orlando

This study evaluated the phytochemical screening, gas chromatography-mass spectrometry (GC-MS) analysis and antioxidant activity of Curcurbitapepo L. using its leaf sample with standard methods. The sample used for the study was procured from Imo State University school farm and was properly identified. Result of phytochemical screening revealed the presence of  saponins, flavonoids, alkaloids, steroids, phlobactannins, proteins, and anthraquinnones, while the GC-MS analysis revealed a total of 78 compounds, out which Bis(2-ethylhexyl) phthalate (C24H38O4) had the highest molecular weight, 2,4,6-Octatriene, 2,6-dimethyl- (C10H16) had the highest peak area of 10.21% while Morphinan-6-ol, 4,5-epoxy-N-methyl-, (5α 6α- (C17H21NO2) had the highest retention time. The antioxidant activity of the studied sample was enhanced against the control. Some of the compounds as revealed by GC-MS analysis could be of healthcare or industrial importance.  There is need for further studies on the leaf sample to ascertain further the observations of the present study. This study has evaluated the phytochemical screening, GC-MS analysis and antioxidant activity of C.pepo L. using its leaf sample.


Author(s):  
M. Idu ◽  
M. O. Aihiokhai ◽  
C. A. Imoni ◽  
C. E. Akokigho ◽  
N. C. Olali

Background: Polyherbal plant extracts which usually comprise of two or more plant parts often contain a wide array of key phytoactive constituents relevant in attaining greater therapeutic efficacy. The active constituents derived from individual plants are insufficient to provide attractive pharmacological action when compared to a combination of multiple herbs. Objective: To conduct phytochemical screening of polyherbal aqueous leaf extracts                            (PALE) and analysis of compounds present in it by gas chromatography-mass spectrometry (GC-MS). Materials and Methods: The polyherbal extract was prepared from the combined aqueous extracts of leaves of Alchornea cordifolia, Sorghum bicolor and Pennisetum glaucum using ratio 1:1:1 w/v. Phytochemical screening was done via standard analytical methods. The identification and characterization of compounds by GC-MS analysis was performed on gas chromatography system coupled with mass spectrometry. Results: The phytochemical analysis of PALE revealed the presence of phenols, saponins, flavonoids, alkaloids and tannins in varying quantities. GC-MS analysis of the extract depicts the presence of key bioactive compounds. Thirty-two bioactive compounds were identified with various retention time and % peaks. The major compounds identified in terms of % peak area are n-Hexadecanoic acid (6.72), Hexadecanoic acid, ethyl ester (7.28), 9,12-Octadecadienoic acid (16.54) and 9-Octadecenoic acid ethyl ester (12.92). Disulfide, dimethyl (0.04), 2-Methoxy-4-vinylphenol (0.28), 1-Dodecanol (0.85), 10-Phenyldecanoic acid (0.12), 1-Hexadecanol (0.75), Methoxyacetic acid, pentadecyl ester (0.27), 9-Octadecenoic acid (Z)-, phenylmethyl ester (0.16), Hexadecanoic acid, 2-hydroxy-1-(hydroxymethyl) (1.09), were among the minor compounds identified in the extract. From the study, 9,12-Octadecadienoic acid indicated the highest peak with a retention time of 20.556 minutes and % peak area of 16.54%. Conclusion: The presence of the revealed bioactive constituents in PALE may suggest its nutraceutical, pharmacological and therapeutic relevance. Therefore, in view of the medicinal importance associated with the observed bioactive constituents, further studies on the toxicity level of  the extract is advised subsequently.


2019 ◽  
Vol 9 (4-A) ◽  
pp. 145-150
Author(s):  
S Vasanthakumar ◽  
G Dineshkumar ◽  
K Jayaseelan

Medicinal plants were used to treat diseases traditionally since ancient times. The present work aims to investigate the bioactive constituents through GC MS analysis of ethanolic leaf extracts of A.marina. Phytochemical screening confirmed the presence of Alkaloids, Flavonoids, Phenols, Reducing sugars, Saponins, Tannin, Glycoside, Triterpenoids and Carbohydrate in A.marina. The characterization of the compounds by Gas Chromatography – Mass Spectrometry (GC-MS) technique has reported the presence of thirty compounds in A.marina leaves. These compounds possess different pharmacological properties like anti-microbial, antioxidant, anti-inflammatory and hepatoprotective properties. Keywords: Avicennia marina, GC-MS, Bioactive compounds, Antibacterial activity.


Proceedings ◽  
2021 ◽  
Vol 57 (1) ◽  
pp. 101
Author(s):  
Virgil Badescu ◽  
Raluca Senin

The aim of this article was the gas chromatography–mass spectrometry (GC-MS) analysis oforganic matter from a residual liquor sample (S.C. Alum S.A., Tulcea), extracted by the solid-phasemicroextraction method (SPMA) and derivatized with N-(tert-butyldimethylsilyl)-Nmethyltrifluoroacetamide(MTBSTFA) as the silylating agent. [...]


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Priyanka Verma ◽  
Atul Bajaj ◽  
R. M. Tripathi ◽  
Sudhir K. Shukla ◽  
Suman Nagpal

Abstract Background Recent advances in the diversified anti-diabetic drugs have appeared in the startling increase in the count of poisoning cases. The epidemics of diabetes mellitus are increasing; hence, the no. of anti-diabetic drug users raised by 42.9%. The use of glimepiride raised to 24%. As the toxicity and drug cases are also escalating with increasing epidemics of diabetes mellitus, a novel gas chromatography-mass spectrometry (GC-MS) method for detecting glimepiride in biological matrices is developed. Results Liquid-liquid extraction method was employed by using 1-butanol: hexane (50:50, v/v) under an alkaline medium, and then back extraction was done via acetic acid. Distinct derivatization techniques were employed for the sample preparation for GC-MS analysis, i.e., silylation and acylation. Derivatization approaches were optimized under different parameters, i.e., reaction temperature and reaction time. N-Methyl-N-(trimethylsilyl) trifluoroacetamide [MSTFA] was found to be the best sound derivatization reagent for the GC-MS analysis of glimepiride. Total ion current (TIC) mode was selected for the monitoring of ions of trimethylsilyl (TMS) derivative of glimepiride with an m/z ratio of 256. Distinct parameters like specificity, carryover, stability, precision, and accuracy were evaluated for validating the identification method. The GC-MS method is found to be linear and illustrated within the range 500 to 2500 ng/ml with the value of R2 (coefficient of determination) at 0.9924. The stability of the extracted and derivatized glimepiride was accessed with regard to processed/extracted sample conditions and autosampler conditions, respectively. Accuracy at each concentration level was within the + 15% of the nominal concentration. Precision (%) for the interday and intraday analysis was found to be in the respectable spectrum. Conclusion Henceforth, the proposed GC-MS method can be employed for the determination of glimepiride in biological matrices.


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