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1.
Molecules ; 25(24)2020 Dec 11.
Artículo en Inglés | MEDLINE | ID: mdl-33322297

RESUMEN

The potential of plant extracts as bioinsecticides has been described as a promising field of agricultural development. In this work, the extracts of Punica granatum (pomegranate), Phytolacca americana (American pokeweed), Glandora prostrata (shrubby gromwell), Ulex europaeus (gorce), Tagetes patula (French marigold), Camellia japonica red (camellia), Ruta graveolens (rue or herb-of-grace) were obtained, purified, and their activity against Spodoptera frugiperda (Sf9) insect cells was investigated. From the pool of over twenty extracts obtained, comprising different polarities and vegetable materials, less polar samples were shown to be more toxic towards the insect cell line Sf9. Among these, a dichloromethane extract of R. graveolens was capable of causing a loss of viability of over 50%, exceeding the effect of the commercial insecticide chlorpyrifos. This extract elicited chromatin condensation and the fragmentation in treated cells. Nanoencapsulation assays of the cytotoxic plant extracts in soybean liposomes and chitosan nanostructures were carried out. The nanosystems exhibited sizes lower or around 200 nm, low polydispersity, and generally high encapsulation efficiencies. Release assays showed that chitosan nanoemulsions provide a fast and total extract release, while liposome-based systems are suitable for a more delayed release. These results represent a proof-of-concept for the future development of bioinsecticide nanoformulations based on the cytotoxic plant extracts.


Asunto(s)
Agentes de Control Biológico/química , Plaguicidas/química , Extractos Vegetales/química , Hojas de la Planta/química , Animales , Camellia , Quitosano/química , Fabaceae , Insectos , Insecticidas/análisis , Liposomas/química , Lithospermum , Nanoestructuras , Phytolacca americana , Granada (Fruta) , Ruta , Solventes , Glycine max/efectos de los fármacos , Tagetes
2.
Molecules ; 25(7)2020 Apr 10.
Artículo en Inglés | MEDLINE | ID: mdl-32290240

RESUMEN

The reaction between organic azides and alkyne derivatives via the Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) is an efficient strategy to combine phthalocyanines and analogues with different materials. As examples of such materials, it can be considered the following ones: graphene oxide, carbon nanotubes, silica nanoparticles, gold nanoparticles, and quantum dots. This approach is also being relevant to conjugate phthalocyanines with carbohydrates and to obtain new sophisticated molecules; in such way, new systems with significant potential applications become available. This review highlights recent developments on the synthesis of phthalocyanine, subphthalocyanine, and porphyrazine derivatives where CuAAC reactions are the key synthetic step.


Asunto(s)
Azidas/química , Indoles/química , Azidas/síntesis química , Catálisis , Técnicas de Química Sintética , Química Clic , Electrodos , Indoles/síntesis química , Isoindoles , Estructura Molecular , Polímeros/química
3.
Molecules ; 25(7)2020 Apr 03.
Artículo en Inglés | MEDLINE | ID: mdl-32260294

RESUMEN

Azides and porphyrinoids (such as porphyrin and corrole macrocycles) can give rise to new derivatives with significant biological properties and as new materials' components. Significant synthetic approaches have been studied. A wide range of products (e.g., microporous organic networks, rotaxane and dendritic motifs, dendrimers as liquid crystals, as blood substitutes for transfusions and many others) can now be available and used for several medicinal and industrial purposes.


Asunto(s)
Azidas/química , Porfirinas/química , Estructura Molecular
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