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1.
Sci Total Environ ; 723: 138109, 2020 Jun 25.
Article in English | MEDLINE | ID: mdl-32229385

ABSTRACT

Dependence on fossil fuels such as oil, coal and natural gas are on alarming increase, thereby causing such resources to be in a depletion mode and a novel sustainable approach for bioenergy production are in demand. Successful implementation of zero waste discharge policy is one such way to attain a sustainable development of bioenergy. Zero waste discharge can be induced only through the conversion of organic wastes into bioenergy. Waste management is pivotal and considering its importance of minimizing the issue and menace of wastes, conversion strategy of organic waste is effectively recommended. Present review is concentrated on providing a keen view on the potential organic waste sources and the way in which the bioenergy is produced through efficient conversion processes. Biogas, bioethanol, biocoal, biohydrogen and biodiesel are the principal renewable energy sources. Different types of organic wastes used for bioenergy generation and its sources, anaerobic digestion-biogas production and its related process affecting parameters including fermentation, photosynthetic process and novel nano-inspired techniques are discussed. Bioenergy production from organic waste is associated with mitigation of lump waste generation and its dumping into land, specifically reducing all hazards and negativities in all sectors during waste disposal. A sustainable bioenergy sector with upgraded security for fuels, tackles the challenging climatic change problem also. Thus, intensification of organic waste conversion strategies to bioenergy, specially, biogas and biohydrogen production is elaborated and analyzed in the present article. Predominantly, persistent drawbacks of the existing organic waste conversion methods have been noted, providing consideration to economic, environmental and social development.


Subject(s)
Refuse Disposal , Waste Management , Biofuels , Fermentation
2.
Int J Biol Macromol ; 154: 390-412, 2020 Jul 01.
Article in English | MEDLINE | ID: mdl-32194126

ABSTRACT

Wide sustainability and reusability of biomacromolecules such as carbohydrates and proteins-based biopolymers pave the way for providing maximal importance in the field of generating biopolymeric nanoparticles. As compared to synthetic nanomaterials, carbohydrate and protein based biopolymeric nanomaterials offer unique advantages that include antibacterial, biocompatible, immunogenicity, and biodegradable properties. Additionally, they have the significant property of more size distribution. Carbohydrate nanoparticles are primarily derived from the polysaccharide biopolymers such as alginate and chitosan; and protein nanoparticles are made from the diverse peptide biopolymers such as albumin, keratin, sericin, fibroin, gelatin and collagen. Advanced methods such as emulsification, desolvation, electrohydrodynamic atomization and coacervation are employed for the controlled fabrication of green biomacromolecules based nanoparticles. Suitability of biopolymeric nanoparticles in plethora of biotechnological applications are quite feasible with the advent of advanced technologies such as dynamic light scattering, scanning electron microscopy, transmission electron microscopy, atomic force microscopy, X-ray diffraction, Fourier transform infrared spectroscopy, and UV visible spectroscopy etc. Applications of such biomacromolecules nanoparticles are highly prevalent in agriculture, food, and biomedical industries. Thus, contributions of biopolymeric nanoparticles derived from carbohydrates and proteins biomacromolecules and their recent trends of patents granted in the biotechnological applications are critically discussed along with a promising future scope.


Subject(s)
Biopolymers , Carbohydrates/chemistry , Nanoparticles , Proteins/chemistry , Nanotechnology
3.
J Agric Food Chem ; 66(3): 602-612, 2018 Jan 24.
Article in English | MEDLINE | ID: mdl-29276946

ABSTRACT

Zerumbone isolated from the rhizomes of Zingiber zerumbet was investigated for the mechanisms by which it exhibits antiproliferative activity in colorectal cancer cells (SW480). The results indicated that the zerumbone suppressed cell growth and enhanced cell apoptosis. Exposure to zerumbone induced generation of reactive oxygen species, reduced the cellular antioxidant status, decreased mitochondrial membrane potential, and activated caspase 3, caspase 8, and caspase 9 (p < 0.001). It was also found that there was a decrease in the expression of Bcl 2 and elevation of Bax (p < 0.001) on exposure to zerumbone. Furthermore, treatment with 50, 75, and 100 µM zerumbone resulted in cell cycle arrest at the G2/M phase with a value of 17.2 ± 0.1, 19.63 ± 0.25, and 26.66 ± 0.25, respectively, and also distorted the microfilament network and effectively inhibited cellular migration.


Subject(s)
Apoptosis/drug effects , Cell Cycle Checkpoints/drug effects , Cell Movement/drug effects , Colorectal Neoplasms/physiopathology , Plant Extracts/pharmacology , Sesquiterpenes/pharmacology , Zingiberaceae/chemistry , Caspase 3/genetics , Caspase 3/metabolism , Caspase 8/genetics , Caspase 8/metabolism , Cell Line, Tumor , Cell Proliferation/drug effects , Colorectal Neoplasms/drug therapy , Colorectal Neoplasms/genetics , Colorectal Neoplasms/metabolism , Humans , Plant Extracts/isolation & purification , Proto-Oncogene Proteins c-bcl-2/genetics , Proto-Oncogene Proteins c-bcl-2/metabolism , Sesquiterpenes/isolation & purification
4.
Chem Biol Interact ; 278: 32-39, 2017 Dec 25.
Article in English | MEDLINE | ID: mdl-28987329

ABSTRACT

A newly synthesised zerumbone pendant derivative (ZPD) was studied in human cervical cancer cells (HeLa) for its anticancer properties. ZPD significantly inhibited the growth of human cervical cancer cells with a GI50 value of 6.35 ± 1.30 µM, which also induced morphological changes and apoptosis in a dose-dependent manner. Our data indicated that ZPD actively encouraged programmed cell death in HeLa cells which were confirmed by DNA fragmentation, phosphatidylserine translocation, increased activity of caspase 3, upregulation of the expression of the pro-apoptotic protein Bax, cleaved PARP, cleaved caspase 3 and downregulation of anti-apoptotic protein Bcl-2. ZPD also inhibited cell migration of HeLa cells, decreasing the production of MMP-2,-9 and downregulation of expression of MMPs and pro-angiogenic factor VEGF. Also it is nontoxic to normal rat cardiac myoblasts. Overall, ZPD is a promising candidate for inducing cytotoxicity, apoptosis and anti-migratory effects in cervical cancer cells.


Subject(s)
Antineoplastic Agents/pharmacology , Apoptosis/drug effects , Sesquiterpenes/pharmacology , Antineoplastic Agents/chemistry , Caspase 3/metabolism , Cell Movement/drug effects , DNA Fragmentation/drug effects , Down-Regulation/drug effects , Female , HeLa Cells , Humans , Microscopy, Fluorescence , Paclitaxel/toxicity , Phosphatidylserines/metabolism , Poly(ADP-ribose) Polymerases/metabolism , Proto-Oncogene Proteins c-bcl-2/metabolism , Sesquiterpenes/chemistry , Up-Regulation/drug effects , Uterine Cervical Neoplasms/metabolism , Uterine Cervical Neoplasms/pathology , bcl-2-Associated X Protein/metabolism
5.
J Environ Biol ; 37(5): 949-54, 2016 09.
Article in English | MEDLINE | ID: mdl-29251876

ABSTRACT

In the present study, ambient air quality was monitored during July to November 2013 in the vicinity of Bellary Thermal Power Station (BTPS), Karnataka to assess the impact of pollutants emitted from power plant on the productivity of maize (Zea mays L.). Atmospheric pollutant load were measured in five different villages at varying distances and directions from thermal power plant, with the village farthest away from BTPS (Yelubenchi) as control. Maize yield was also estimated in these locations and correlated to the pollutant concentrations. It was found that, both particulate matter and SO2 which are indicators of emissions from coal-fueled power plants were highest in Thimmalapur village located in the predominant down wind direction. A significant reduction in maize yield was noticed (8197 to 6509 kg ha-1 for seed and 14041 to 9933 kg ha-1 for stover) across the gradient in distance and direction from BTPS which might be influenced by the pollutants emitted. The implications of these observations are further discussed in the paper.


Subject(s)
Air Pollutants/toxicity , Crops, Agricultural/drug effects , Power Plants , Zea mays/drug effects , India , Time Factors , Zea mays/physiology
6.
Indian J Pharmacol ; 47(1): 17-21, 2015.
Article in English | MEDLINE | ID: mdl-25821305

ABSTRACT

OBJECTIVE: Statins have anti-inflammatory effects that are not directly related to their cholesterol lowering activity. This study was carried out to evaluate the effect of simvastatin or rosuvastatin on the extent of colonic mucosal damage and on the inflammatory response in trinitrobenzene sulfonic acid (TNBS)-induced ulcerative colitis. MATERIALS AND METHODS: Ulcerative colitis was induced by single intrarectal injection of 120 mg/kg TNBS. Test groups were treated with simvastatin (10 mg/kg, p.o.) or rosuvastatin (10 mg/kg, p.o.). Colonic mucosal inflammation was evaluated clinically, biochemically, and histologically. RESULT: Disease activity index score in TNBS-treated rats, as determined by weight loss, stool consistency, fecal occult blood, were significantly lowers in simvastatin or rosuvastatin-treated rats than TNBS-treated animals. Simvastatin or rosuvastatin counteracted the reduction in colon length, decreased colon weight, neutrophil accumulation, and tumor necrosis factor-alpha level in TNBS-induced colitis. Simvastatin and rosuvastatin also inhibited the increase in oxidative stress levels after TNBS administration. CONCLUSIONS: These results suggest that simvastatin and rosuvastatin significantly ameliorate experimental colitis in rats, and these effects could be explained by their anti-inflammatory and antioxidant activity.


Subject(s)
Anti-Inflammatory Agents/pharmacology , Antioxidants/pharmacology , Colitis, Ulcerative/prevention & control , Colon/drug effects , Hydroxymethylglutaryl-CoA Reductase Inhibitors/pharmacology , Rosuvastatin Calcium/pharmacology , Simvastatin/pharmacology , Trinitrobenzenesulfonic Acid , Animals , Colitis, Ulcerative/chemically induced , Colitis, Ulcerative/metabolism , Colitis, Ulcerative/pathology , Colon/metabolism , Colon/pathology , Cytoprotection , Disease Models, Animal , Female , Glutathione/metabolism , Inflammation Mediators/metabolism , Malondialdehyde/metabolism , Neutrophil Infiltration/drug effects , Oxidative Stress/drug effects , Peroxidase/metabolism , Rats, Wistar , Superoxide Dismutase/metabolism , Tumor Necrosis Factor-alpha/metabolism
7.
Nat Prod Res ; 29(10): 947-52, 2015.
Article in English | MEDLINE | ID: mdl-25200721

ABSTRACT

Eight known phytochemicals, four sesquiterpenes and four flavonoids of Zingiber zerumbet were screened against α-glucosidase enzyme, aldose reductase enzyme and antiglycation property under in vitro conditions. The results established kaempferol-3-O-methylether as a potent inhibitor of α-glucosidase enzyme with an IC50 value of 7.88 µM. In aldose reductase enzyme inhibition assay, all the compounds except zerumbone epoxide showed good to excellent inhibition properties. Among these, the flavonoid compounds were found to be potent aldose reductase inhibitors compared with the four sesquiterpenes. In addition, compounds such as α-humulene, kaempferol, kaempferol-3-O-methylether and 3″,4″-O-diacetylafzelin displayed potent antiglycation properties. From overall results, we found that kaempferol and kaempferol-3-O-methylether are potent inhibitors of α-glucosidase enzyme, aldose reductase enzyme and glycation reaction, the three main targets of drugs for the treatment of diabetes and its complications.


Subject(s)
Aldehyde Reductase/antagonists & inhibitors , Flavonoids/chemistry , Glycoside Hydrolase Inhibitors/chemistry , Sesquiterpenes/chemistry , Zingiberaceae/chemistry , Enzyme Inhibitors/chemistry , Flavonoids/isolation & purification , Kaempferols/chemistry , Kaempferols/isolation & purification , Molecular Structure , Monocyclic Sesquiterpenes , Sesquiterpenes/isolation & purification
8.
Biol Trace Elem Res ; 161(1): 107-15, 2014 Oct.
Article in English | MEDLINE | ID: mdl-25062888

ABSTRACT

Cardiac hypertrophy has been considered as an important risk factor of morbidity and mortality. It is characterized as thickening of ventricle wall of the heart and consequent reduction in the contracting ability of the heart to pump the blood. Hyperglycemia-induced reactive oxygen species act as major mediators of diabetic complications. Inflammation plays an essential role in the development of diabetic cardiac hypertrophy. Selenium has been shown to induce insulin-like and anti-inflammatory effects in human and experimental animals. But, its mechanism of action has not been elucidated. Hence, in order to probe into its mechanism at molecular level, we designed an experiment to study the effect of selenium as sodium selenite in streptozotocin-induced diabetic rats. The rats were divided into four groups and maintained as follows: (1) controls, (2) sodium selenite-treated controls, (3) diabetic, and (4) sodium selenite-treated diabetic rats. Duration of the experiment was 30 days. Selenium supplementation enhanced the streptozotocin-induced reduction in the activities of antioxidant enzymes, decreased the serum glucose level, glycated hemoglobin content, concentration of high-sensitivity C-reactive protein, levels of lipid peroxidation products, as well as inflammatory parameters. Decrease in the phospholipase activity by selenium supplementation also contributed to the downregulation of leukotriene pathway. It also downregulated the expressions of nuclear transcription factor κB (NFκB), lipoxygenase, cyclooxygenase, 5-lipoxygenase-activating protein, and receptor for leukotriene B4. Hence, selenium decreased the production of reactive oxygen species and inhibited the activation of NFκB-mediated transcription of pro-inflammatory mediators which resulted in the downregulation of leukotriene pathway in diabetic cardiac hypertrophy.


Subject(s)
Diabetes Mellitus, Experimental/prevention & control , Diabetic Cardiomyopathies/prevention & control , Leukotrienes/metabolism , Oxidative Stress/drug effects , Signal Transduction/drug effects , Sodium Selenite/pharmacology , Analysis of Variance , Animals , Arachidonate 5-Lipoxygenase/genetics , Arachidonate 5-Lipoxygenase/metabolism , Blood Glucose/metabolism , C-Reactive Protein/metabolism , Cyclooxygenase 2/genetics , Cyclooxygenase 2/metabolism , Diabetes Mellitus, Experimental/genetics , Diabetes Mellitus, Experimental/metabolism , Diabetic Cardiomyopathies/genetics , Diabetic Cardiomyopathies/metabolism , Down-Regulation/drug effects , Gene Expression/drug effects , Glycated Hemoglobin/metabolism , Lipid Peroxidation/drug effects , Male , NF-kappa B/genetics , NF-kappa B/metabolism , Oxidative Stress/physiology , Rats, Sprague-Dawley , Reverse Transcriptase Polymerase Chain Reaction , Signal Transduction/physiology , Sodium Selenite/administration & dosage , Trace Elements/administration & dosage , Trace Elements/pharmacology
9.
Org Biomol Chem ; 12(19): 3045-61, 2014 May 21.
Article in English | MEDLINE | ID: mdl-24691752

ABSTRACT

Herein we describe our efforts on the Lewis acid catalyzed stereoselective ring-opening of pentafulvene derived diazabicyclic olefins using various ortho-functionalized aryl iodides such as 2-iodoanilines, 2-iodophenols and 2-iodobenzene thiols to access trans-1,2 disubstituted alkylidenecyclopentenes. The scope of the reaction was also explored with a range of easily available aromatic and aliphatic alcohols. Furthermore, the palladium catalyzed intramolecular Heck cyclization of trans-1,2 disubstituted alkylidenecyclopentenes would provide an easy approach for the synthesis of highly functionalized spiropentacyclic frameworks consisting of a cyclopentene fused to an indoline/benzothiophene and pyrazolidine.

10.
Org Lett ; 15(13): 3338-41, 2013 Jul 05.
Article in English | MEDLINE | ID: mdl-23782427

ABSTRACT

A palladium/Lewis acid mediated stepwise and one-pot transformation of pentafulvene derived diazabicyclic olefins is described. The reaction offers a facile strategy for the synthesis of novel spiropentacyclic motifs with indoline and pyrazolidine fused to the cyclopentene core.

11.
Indian J Pharm Sci ; 73(1): 120-2, 2011 Jan.
Article in English | MEDLINE | ID: mdl-22131637

ABSTRACT

A simple, precise and rapid RP-HPLC method was developed for the determination of doxazosin mesylate in pharmaceutical formulations. The method was carried out on a Chromolith RP-C(18) column using a mixture of potassium phosphate buffer and methanol (40:60 v/v) and detection was done at 251 nm. The linearity range was 1-5 µg/ml. The retention time of the drug was 3.8 min. The LOD and LOQ were found to be 0.1 µg/ml and 0.5 µg/ml, respectively.

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