-
Je něco špatně v tomto záznamu ?
Larvicidal Activity of Essential Oils of Five Apiaceae Taxa and Some of Their Main Constituents Against Culex quinquefasciatus
R. Pavela, F. Maggi, K. Cianfaglione, M. Bruno, G. Benelli,
Jazyk angličtina Země Švýcarsko
Typ dokumentu časopisecké články
PubMed
28990348
DOI
10.1002/cbdv.201700382
Knihovny.cz E-zdroje
- MeSH
- Apiaceae chemie MeSH
- Culex účinky léků MeSH
- insekticidy chemie izolace a purifikace farmakologie MeSH
- larva účinky léků MeSH
- oleje prchavé chemie izolace a purifikace farmakologie MeSH
- vztah mezi dávkou a účinkem léčiva MeSH
- vztahy mezi strukturou a aktivitou MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
Apiaceae are aromatic herbs producing essential oils which are used on an industrial scale for various purposes. Notably, Apiaceae essential oils may replace synthetic insecticides keeping most of their efficacy and avoiding environmental pollution and human poisoning. In the present work, we explored the insecticidal potential of the essential oils from five Apiaceae taxa, namely Sison amomum, Echinophora spinosa, Heracleum sphondylium subsp. sphondylium, Heracleum sphondylium subsp. ternatum, and Trachyspemum ammi, as well as their major constituents (sabinene, p-cymene, terpinolene, myristicin, and thymol), against the filariasis vector Culex quinquefasciatus. For the purpose, the essential oils were obtained by hydrodistillation and their composition was achieved by gas chromatography/mass spectrometry (GC/MS). Their acute toxicity on third instar larvae of C. quinquefasciatus was determined. The two most active essential oils were those from T. ammi fruits and E. spinosa roots, showing LC50below 20 μl/l and LD90below 50 μl/l. These oils were dominated by the monoterpene phenol thymol and the phenylpropanoid myristicin, respectively, which showed the strongest larvicidal activity (LC50of 15.1 and 16.3 μl/l, respectively) among the pure compounds tested. These results showed that Apiaceae may be useful as source of larvicidal compounds to be used for the development of cheap, effective and eco-friendly insecticidal formulations.
Crop Research Institute Drnovska 507 161 06 Prague 6 Czech Republic
Department STEBICEF University of Palermo Viale delle Scienze Parco d'Orleans 2 90128 Palermo Italy
School of Pharmacy University of Camerino Via Sant'Agostino 1 62032 Camerino Italy
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc18010313
- 003
- CZ-PrNML
- 005
- 20201203121700.0
- 007
- ta
- 008
- 180404s2018 sz f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1002/cbdv.201700382 $2 doi
- 035 __
- $a (PubMed)28990348
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a sz
- 100 1_
- $a Pavela, Roman, $u Crop Research Institute, Drnovska 507, 161 06, Prague 6, Czech Republic. $d 1970- $7 mzk2005318033
- 245 10
- $a Larvicidal Activity of Essential Oils of Five Apiaceae Taxa and Some of Their Main Constituents Against Culex quinquefasciatus / $c R. Pavela, F. Maggi, K. Cianfaglione, M. Bruno, G. Benelli,
- 520 9_
- $a Apiaceae are aromatic herbs producing essential oils which are used on an industrial scale for various purposes. Notably, Apiaceae essential oils may replace synthetic insecticides keeping most of their efficacy and avoiding environmental pollution and human poisoning. In the present work, we explored the insecticidal potential of the essential oils from five Apiaceae taxa, namely Sison amomum, Echinophora spinosa, Heracleum sphondylium subsp. sphondylium, Heracleum sphondylium subsp. ternatum, and Trachyspemum ammi, as well as their major constituents (sabinene, p-cymene, terpinolene, myristicin, and thymol), against the filariasis vector Culex quinquefasciatus. For the purpose, the essential oils were obtained by hydrodistillation and their composition was achieved by gas chromatography/mass spectrometry (GC/MS). Their acute toxicity on third instar larvae of C. quinquefasciatus was determined. The two most active essential oils were those from T. ammi fruits and E. spinosa roots, showing LC50below 20 μl/l and LD90below 50 μl/l. These oils were dominated by the monoterpene phenol thymol and the phenylpropanoid myristicin, respectively, which showed the strongest larvicidal activity (LC50of 15.1 and 16.3 μl/l, respectively) among the pure compounds tested. These results showed that Apiaceae may be useful as source of larvicidal compounds to be used for the development of cheap, effective and eco-friendly insecticidal formulations.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a Apiaceae $x chemie $7 D019661
- 650 _2
- $a Culex $x účinky léků $7 D003465
- 650 _2
- $a vztah mezi dávkou a účinkem léčiva $7 D004305
- 650 _2
- $a insekticidy $x chemie $x izolace a purifikace $x farmakologie $7 D007306
- 650 _2
- $a larva $x účinky léků $7 D007814
- 650 _2
- $a oleje prchavé $x chemie $x izolace a purifikace $x farmakologie $7 D009822
- 650 _2
- $a vztahy mezi strukturou a aktivitou $7 D013329
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Maggi, Filippo $u School of Pharmacy, University of Camerino, Via Sant'Agostino 1, 62032, Camerino, Italy.
- 700 1_
- $a Cianfaglione, Kevin $u EA 2219 Géoarchitecture, UFR Sciences & Techniques, Université de Bretagne Occidentale, 6 Avenue Victor Le Gorgeu, 29200, Brest, France. School of Biosciences and Veterinary Medicine, University of Camerino, Via Pontoni, 5, 62032, Camerino, MC, Italy.
- 700 1_
- $a Bruno, Maurizio $u Department STEBICEF, University of Palermo, Viale delle Scienze, Parco d'Orleans II, 90128, Palermo, Italy.
- 700 1_
- $a Benelli, Giovanni $u Department of Agriculture, Food and Environment, University of Pisa, via del Borghetto 80, 56124, Pisa, Italy. The BioRobotics Institute, Scuola Superiore Sant'Anna, Viale Rinaldo Piaggio 34, 56025, Pontedera, Pisa, Italy.
- 773 0_
- $w MED00008421 $t Chemistry and biodiversity $x 1612-1880 $g Roč. 15, č. 1 (2018)
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/28990348 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20180404 $b ABA008
- 991 __
- $a 20201203121657 $b ABA008
- 999 __
- $a ok $b bmc $g 1287798 $s 1007125
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2018 $b 15 $c 1 $e 20171225 $i 1612-1880 $m Chemistry and biodiversity $n Chem Biodivers $x MED00008421
- LZP __
- $a Pubmed-20180404