Authors:F. M. Momen, M. M. Abdelkader and S. F. Fahim
The chemical composition of essential oil extracted from leaves of the medicinal plant Mentha longifolia (L.) Huds growing in Egypt, were determined through Gas Chromatography/Mass Spectrometry ( GC/MS). The analyses revealed that the major component of M. longifolia was Monterpene ketone (piperitone oxide). Mentha longifolia was potent for the pest Tetranychus urticae Koch with a significant increase in repellency. In addition, it exhibited strong oviposition deterrence to the pest based on a 99.4% reduction of the total number of eggs on leaf discs treated with the oil. The LC50 values of M. longifolia against eggs, nymphs and females of T. urticae by fumigant application, were 2.95, 3.47, 3.74 μL / L, while the LC90 values were 8.99, 9.41, 11.01 μL/ L, respectively.
The toxicity of M. longifolia oil by fumigant application to females and eggs of 3 predatory phytoseiid mites was tested. Neoseiulus californicus (McGregor) is extremely insusceptible to M. longifolia oil than the pest T. urticae and both phytoseiid mites, Neoseiuls barkeri (Hughes) and Typhlodromips swirskii (Athias Henriot) under laboratory conditions. When both stages of tested predatory mites, exposed to fumigant of LC50 and LC90 μL/L values reported on T. urticae, female’s mortality of N. californicus was lesser than that reported on N. barkeri and T. swirskii.
These show that the fumigant toxicity of M. longifolia oil has the highest lethal activity to the pest T. urticae and the least to the predatory mite N. californicus. Results indicated that the mode of delivery of the essential oil was largely a result of action in the vapor phase via respiratory system. Data was suggested that M. longifolia oil have the potential agent to be used in the maintainable management of T. urticae combined with N. californicus.
Authors:Omer A. Basudan, Perwez Alam, Nasir A. Siddiqui, Mohamed F. Alajmi, Adnan J. Alrehaily, Saleh I. Alqasoumi, Maged S. Abdel-Kader, Prawez Alam and Abd El Raheim M. Donia
A simple and sensitive high-performance thin-layer chromatographic (HPTLC) method was developed for the evaluation of biomarker β-amyrin in the leaves of fve different species of genus Ficus (Ficus carica, Ficus nitida, Ficus ingens, Ficus palmata, and Ficus vasta) grown in the Kingdom of Saudi Arabia. Chromatography was performed on glass-backed silica gel 60 F254 HPTLC plates with solvents toluene–methanol (9:1, v/v) as the mobile phase. After development, the HPTLC plate was derivatized with p-anisalde-hydereagent to give well-resolved and compact spot of β-amyrin. Scanning and quantifcation were done at 550 nm. The system was found to give compact spot for β-amyrin at RF = 0.58. The linear regression analysis data for the calibration plots showed good linear relationship with r2 = 0.998 with respect to area in the concentration range of 100–900 ng. The regression equation for β-amyrin standard was found to be Y = 5.835X + 87. The precisions (n = 6) for β-amyrin were found to be 1.64–1.77% and 1.68–1.84%, respectively, for intra-day and inter-day batches, and the recovery values were found to be 97.6–98.3%. β-Amyrin was found to be present in three species, i.e., F. carica (0.29%, w/w), F. nitida (0. 5 4% w/w), and F. p almata (0.31%, w/w), while it was absent in F. vasta and F. ingens. The statistical analysis proves that the developed method for the quantifcation of β-amyrin is reproducible; hence, it can beemployed for the determination of β-amyrin in plasma and other biological fuids as well as in fnished products avai lable in the market.