RESUMEN
In the present study, we have demonstrated synthesis of agar aldehyde (Aald) from seaweed polysaccharide and its further successful application for preparation of Aald mediated solid silver nanocomposite (Aald-AgNPs). Aald-AgNPs were characterized for biophysical properties by FTIR, XRD, SEM, TEM, XPS, and UV-vis spectroscopy. Aald-AgNPs were further tested in vitro and in vivo for anticancer activity. The results of the in vitro study revealed that Aald-AgNPs exhibited activity against 3 cancer cell lines. Aald-AgNPs were found to act through causing dose dependent increase in cell size, inducing anueploidy, mitochondrial disintegration and increasing septa formation in cell cytoplasm. Results of in vivo anticancer activity against ME-180, Colon-26, and HL-60 xenograft mice tumor models showed 64 %, 27.3 % and 51 % reduction in tumor volume, respectively with 83-100 % survival rate. Aald-AgNPs exhibited excellent antibacterial activity. It was interesting to note that Aald-AgNPs did not exhibit any significant detrimental effect on viability and metabolic activity of normal bone marrow derived mesenchymal stem cells. This study opens new areas of research for chemists and biologists to use seaweed-derived polymers to develop nanocomposites for cancer therapeutics.
Asunto(s)
Agar/administración & dosificación , Aldehídos/administración & dosificación , Antineoplásicos/administración & dosificación , Biopolímeros/administración & dosificación , Nanopartículas del Metal/administración & dosificación , Nanocompuestos/administración & dosificación , Algas Marinas , Plata/administración & dosificación , Animales , Antibacterianos/administración & dosificación , Línea Celular Tumoral , Bacterias Gramnegativas/efectos de los fármacos , Bacterias Grampositivas/efectos de los fármacos , Humanos , Ratones Endogámicos BALB C , Neoplasias/tratamiento farmacológicoRESUMEN
This paper demonstrates an integrated zero liquid discharge (ZLD) process for time-dependent recovery of 5-hydroxymethyl furfural (HMF), levulinic acid (LA) and potassium, nitrogen and sulphur rich mother liquor (KNS-ML) - manure from agar/agarose containing seaweed aqueous solution using transition metal-free KHSO4 as an eco-friendly and reusable catalyst. The selectivity of HMF is higher at 115 °C in 3 h and favorable to LA in 6 h in autoclave conditions. The proposed concept could be fine-tuned for the selective production of 5-HMF (up to 91% yield) or levulinic acid (56% yield) in the presence of the KHSO4 catalyst. We have also achieved recyclability of KHSO4 up to nine (09) cycles and the gram-scale reaction has been demonstrated. The (KNS-ML) obtained after nine cycles followed by neutralization with ammonia solution utilized for manure makes the process zero-liquid discharge and more cost-effective. The efficacy of the KNS-ML after nine cycles has been tested on groundnut plants.
Asunto(s)
Furaldehído/análogos & derivados , Ácidos Levulínicos/química , Algas Marinas/química , Catálisis , Furaldehído/química , Nitrógeno/química , Extractos Vegetales/química , Potasio/química , Sulfatos/química , Azufre/químicaRESUMEN
Here, we demonstrate a successful synthesis of bio-based aldehyde namely dialdehyde-carboxymethylagarose (DCMA) using carboxymethyagarose (CMA). Further reaction parameters (i.e. reaction temperature, pH and periodate concentration) were optimized to achieve maximum aldehyde content and product yield. The synthesis of DCMA was confirmed by employing FTIR, (1)H NMR, XRD, SEM, AFM, TGA, DSC, EA and GPC techniques. To investigate the aldehyde functionality, DCMA was allowed to interact with BSA and obtained results were found to be comparable with that of synthetic aldehyde (Formaldehyde). Further interaction of DCMA with BSA was confirmed by using UV-vis, FTIR, fluorescent spectroscopy, CD and DLS analysis. Results of this study revealed that bio-based aldehyde behaves like formaldehyde. This study adds value to abundant marine biopolymers and opens the new research area for polymer researchers.
Asunto(s)
Aldehídos/síntesis química , Aldehídos/metabolismo , Algas Marinas/química , Sefarosa/análogos & derivados , Albúmina Sérica Bovina/metabolismo , Aldehídos/química , Animales , Bovinos , Técnicas de Química Sintética , Unión Proteica , Sefarosa/síntesis química , Sefarosa/química , Sefarosa/metabolismoRESUMEN
Several deep eutectic solvents prepared by the complexation of choline chloride as the hydrogen bond acceptor and hydrogen bond donors such as urea, thiourea, ethylene glycol, and glycerol were employed to partition glaucarubinone, an antimalarial compound present in roots of the plant, Simarouba glauca. Among all the solvents, the deep eutectic solvent consisting of the mixture of choline chloride and urea the most suitable to partition the antimalarial compound from the extract selectively. Analytical tools such as high-performance liquid chromatography and electrospray ionization mass spectrometry were used for characterizations, and glaucarubinone extracted from the roots of the plant by conventional solvent extraction method was used as a reference for comparison. The hydrogen and noncovalent bonds formed between glaucarubinone and the deep eutectic solvents could be responsible for the selective partition of the drug molecule.