Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add more filters










Database
Language
Publication year range
1.
Environ Sci Pollut Res Int ; 29(47): 71326-71337, 2022 Oct.
Article in English | MEDLINE | ID: mdl-35595904

ABSTRACT

Aedes aegypti is the main vector of yellow fever, chikungunya, Zika, and dengue worldwide and is managed by using chemical insecticides. Though effective, their indiscriminate use brings in associated problems on safety to non-target and the environment. This supports the use of plant-based essential oil (EO) formulations as they are safe to use with limited effect on non-target organisms. Quick volatility and degradation of EO are a hurdle in its use; the present study attempts to develop nanoemulsions (NE) of Trachyspermum ammi EO and its constituent thymol using Tween 80 as surfactant by ultrasonication method. The NE of EO had droplet size ranging from 65 ± 0.7 to 83 ± 0.09 nm and a poly dispersity index (PDI) value of 0.18 ± 0.003 to 0.20 ± 0.07 from 1 to 60 days of storage. The NE of thymol showed a droplet size ranging from 167 ± 1 to 230 ± 1 nm and PDI value of 0.30 ± 0.03 to 0.40 ± 0.008 from 1 to 60 days of storage. The droplet shape of both NEs appeared spherical under a transmission electron microscope (TEM). The larvicidal effect of NEs of EO and thymol was better than BEs (Bulk emulsion) of EO and thymol against Ae. aegypti. Among the NEs, thymol (LC50 34.89 ppm) had better larvicidal action than EO (LC50 46.73 ppm). Exposure to NEs of EO and thymol causes the shrinkage of the larval cuticle and inhibited the acetylcholinesterase (AChE) activity in Ae. aegypti. Our findings show the enhanced effect of NEs over BEs which facilitate its use as an alternative control measure for Ae. aegypti.


Subject(s)
Aedes , Ammi , Apiaceae , Insecticides , Oils, Volatile , Zika Virus , Acetylcholinesterase , Alkanesulfonic Acids , Animals , Emulsions/pharmacology , Insecticides/chemistry , Larva , Mosquito Vectors , Oils, Volatile/chemistry , Oils, Volatile/pharmacology , Plant Oils/pharmacology , Polysorbates/pharmacology , Surface-Active Agents/pharmacology , Thymol/pharmacology
2.
Chem Sci ; 6(11): 6334-6340, 2015 Nov 01.
Article in English | MEDLINE | ID: mdl-30090251

ABSTRACT

Templates with specific microenvironments have been long employed to facilitate specialized reactions. From enzymes to metal organic frameworks (MOFs), various systems have exerted their prowess to affect specific chemical reactions. Here we report, for the first time, the acceleration of a ring closure photo-oxidation reaction due to the specific structural constraints provided by layered materials. A stilbene derivative has been used as a prototype reactant and the di-hydrophenanthrene intermediate has been isolated and characterized en route to the complete photo-oxidation. Combining the gathered evidence, a possible mechanism for the chemical transformation has been proposed. Kinetic analysis showed that layered materials help to manipulate the rate of the electrocyclic ring closure and, in turn, accelerate the complete reaction sequence. The structural microenvironment induced by layered materials could be a unique platform to probe and stabilize a plethora of photo-oxidative reactions and intermediates.

3.
Chem Commun (Camb) ; 49(38): 3937-9, 2013 May 11.
Article in English | MEDLINE | ID: mdl-23435584

ABSTRACT

Micronic cage structures of squarate based metal-organic coordination frameworks (MOCFs) have been fabricated for the first time by specific anion selective etching of metal squarate cubes. Time and stoichiometry dependent synthesis and the corresponding microscopic studies have provided mechanistic insight into the cage formation. Furthermore, a non-covalent post-synthetic strategy has been adopted to functionalize the micronic cubes or cages with chromophores rendering the resulting hybrids green fluorescent.


Subject(s)
Cyclobutanes/chemistry , Fluorescent Dyes/chemistry , Metals/chemistry , Nanostructures/chemistry , Nanostructures/ultrastructure , Organometallic Compounds/chemistry , Cyclobutanes/chemical synthesis , Fluorescent Dyes/chemical synthesis , Metals/chemical synthesis , Models, Molecular , Nanotechnology , Organometallic Compounds/chemical synthesis , Povidone/chemical synthesis , Povidone/chemistry , Surface Properties
SELECTION OF CITATIONS
SEARCH DETAIL
...