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1.
Trop Med Int Health ; 26(4): 469-477, 2021 04.
Artículo en Inglés | MEDLINE | ID: mdl-33423364

RESUMEN

OBJECTIVES: To evaluate the entomological efficacy and the residual activity of indoor residual spraying with Fludora® Fusion 562.5 WP-SB, a combination formulation containing clothianidin, a neonicotinoid and deltamethrin, a pyrethroid, against the main rural malaria vector, Anopheles culicifacies s.l., in India in a small-scale trial. METHODS: In three study villages, suitable households were randomly allocated to five treatments: Fludora® Fusion 562.5 WP-SB (target dose 225 mg active ingredient AI/m2 ); clothianidin 70 WG (target dose 200 mg AI/m2 ); K-Othrine 250 WG (deltamethrin, target dose 25 mg AI/m2 ); Ficam VC 80 WP-SB (bendiocarb, target dose 400 mg AI/m2 ) and unsprayed control. Insecticides were sprayed by hand compression sprayers with control flow valves and 8002E nozzles. Post-spray cone bioassays were done on insecticide-treated walls using a colonised, deltamethrin-resistant strain of An. culicifacies. Mosquitoes were collected from treated rooms by different methods. The insecticide content on filter papers collected from the sprayed walls was determined by chemical assay to assess the spray quality. RESULTS: The ratios of applied to target doses of insecticides were within 0.84 to 1.4, showing a good spray quality. The cone bioassays revealed residual action lasting 7 months for all insecticides without significant differences in mortality between different surfaces treated nor between the four treatment arms (P > 0.05). Considering all entomological parameters such as indoor resting density, excito-repellency, blood-feeding inhibition and delayed mortality, the overall efficacy of Fludora® Fusion WG-SB was equal or better compared with other insecticides. CONCLUSIONS: Fludora® Fusion showed overall equal or better efficacy than deltamethrin and bendiocarb alone against a pyrethroid-resistant malaria vector population and can be considered as an alternative product for management of pyrethroid resistance in malaria vectors.


Asunto(s)
Anopheles/efectos de los fármacos , Culicidae/efectos de los fármacos , Composición Familiar , Insecticidas/farmacología , Malaria , Control de Mosquitos/métodos , Mosquitos Vectores/efectos de los fármacos , Animales , Bioensayo , Guanidinas/farmacología , Humanos , Resistencia a los Insecticidas , Malaria/prevención & control , Malaria/transmisión , Neonicotinoides/farmacología , Nitrilos/farmacología , Piretrinas/farmacología , Tiazoles/farmacología
2.
Phys Fluids (1994) ; 33(11): 115129, 2021 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-35002200

RESUMEN

The primary objective of this work is to investigate the mixing of droplets/aerosols, which originates from the sneezing/coughing (of possibly COVID-19 patient) with the ambient atmosphere. Effectively, we are studying the growth/decay of droplets/aerosols in the presence of inhomogeneous mixing, which focuses on the phenomena of entrainment of the (relatively) dry ambient air. We have varied the initial standard deviation, mean radius of the droplets/aerosols size distribution, and humidity of the ambient atmosphere to understand their effects on the final size spectra of droplets. Furthermore, a rigorous error analysis is carried out to understand the relative importance of these effects on the final spectra of droplets/aerosols. We find that these are vital parameters to determine the final spectra of droplets, which govern the broadening of the size spectra. Typically, broadening the size spectra of droplets/aerosols increases the probability of the virus-laden droplets/aerosols and thus could affect the transmission of infection in the ambient atmosphere.

3.
Bioorg Med Chem ; 10(10): 3187-96, 2002 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-12150864

RESUMEN

A series of acyclic deoxy carbohydrate derivatives from easily available carbohydrate enals 1, 2, 3 or 5 were prepared involving the Baylis-Hillman reaction. These newly formed carbohydrate based Baylis-Hillman adducts and their amino derivatives were evaluated for their antimycobacterial activity against Mycobacterium tuberculosis H(37)R(v). Among the compounds evaluated for their antimycobacterial activity, compound (10) showed the desired activity in the range of 3.125 microg/mL.


Asunto(s)
Antituberculosos/síntesis química , Desoxiazúcares/síntesis química , Acrilonitrilo/química , Amino Azúcares/síntesis química , Amino Azúcares/farmacología , Antibacterianos/síntesis química , Antibacterianos/farmacología , Antituberculosos/farmacología , Butanonas/química , Desoxiazúcares/farmacología , Mycobacterium tuberculosis/efectos de los fármacos , Relación Estructura-Actividad
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