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The current study assessed the efficacy of Acyclovir (ACV) and Ivermectin (IVM) as monotherapies and combined treatments for intestinal and muscular stages of Trichinella spiralis infection. One-hundred Swiss albino mice received orally 250 ± 50 infectious larvae and were divided into infected-untreated (Group-1), IVM-treated (Group-2), ACV-treated (Group-3), combined IVM+ACV (Group-4), and healthy controls (Group-5). Each group was subdivided into subgroup-A-enteric phase (10 mice, sacrificed day-7 p.i.) and subgroup-B-muscular phase (10 mice, sacrificed day-35 p.i.). Survival rate and body weight were recorded. Parasite burden and intestinal histopathology were assessed. In addition, immunohistochemical expression of epithelial CDX2 in the intestinal phase and CyclinD1 as well as CD34 in the muscular phase were evaluated. Compared, IVM and ACV monotherapies showed insignificant differences in the amelioration of enteric histopathology, except for lymphocytic counts. In the muscle phase, monotherapies showed variable disruptions in the encapsulated larvae. Compared with monotherapies, the combined treatment performed relatively better improvement of intestinal inflammation and reduction in the enteric and muscular parasite burden. CDX2 and CyclinD1 positively correlated with intestinal inflammation and parasite burden, while CD34 showed a negative correlation. CDX2 positively correlated with CyclinD1. CD34 negatively correlated with CDX2 and CyclinD1. IVM +ACV significantly ameliorated CDX2, CyclinD1, and CD34 expressions compared with monotherapies. Conclusion. T. spiralis infection-associated inflammation induced CDX2 and CyclinD1 expressions, whereas CD34 was reduced. The molecular tumorigenic effect of the nematode remains questionable. Nevertheless, IVM +ACV appeared to be a promising anthelminthic anti-inflammatory combination that, in parallel, rectified CDX2, CyclinD1, and CD34 expressions.
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Alzheimer's disease (AD) causes dementia in both young and old people affecting more than 40 million people worldwide. The two neuropathological hallmarks of the disease, amyloid beta (Aß) plaques and neurofibrillary tangles consisting of protein tau are considered the major contributors to the disease. However, a more complete picture reveals significant neurodegeneration and decreased cell survival, neuroinflammation, changes in protein and energy homeostasis and alterations in lipid and cholesterol metabolism. In addition, gene and cell therapies for severe neurodegenerative disorders have recently improved technically in terms of safety and efficiency and have translated to the clinic showing encouraging results. Here, we review broadly current data within the field for potential targets that could modify AD through gene and cell therapy strategies. We envision that not only Aß will be targeted in a disease-modifying treatment strategy but rather that a combination of treatments, possibly at different intervention times may prove beneficial in curing this devastating disease. These include decreased tau pathology, neuronal growth factors to support neurons and modulation of neuroinflammation for an appropriate immune response. Furthermore, cell based therapies may represent potential strategies in the future.
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Doença de Alzheimer/terapia , Terapia Baseada em Transplante de Células e Tecidos/métodos , Terapia Genética/métodos , Doença de Alzheimer/genética , Peptídeos beta-Amiloides/genética , Terapia Combinada , Expressão Gênica/genética , Humanos , Neprilisina/genética , Neurogênese/fisiologia , Proteínas tauRESUMO
Millions of people worldwide receive agents targeting the renin-angiotensin system (RAS) to treat hypertension or statins to lower cholesterol. The RAS and cholesterol metabolic pathways in the brain are autonomous from their systemic counterparts and are interrelated through the cholesterol metabolite 27-hydroxycholesterol (27-OHC). These systems contribute to memory and dementia pathogenesis through interference in the amyloid-beta cascade, vascular mechanisms, glucose metabolism, apoptosis, neuroinflammation and oxidative stress. Previous studies examining the relationship between these treatments and cognition and dementia risk have produced inconsistent results. Defining the blood-brain barrier penetration of these medications has been challenging, and the mechanisms of action on cognition are not clearly established. Potential biases are apparent in epidemiological and clinical studies, such as reverse epidemiology, indication bias, problems defining medication exposure, uncertain and changing doses, and inappropriate grouping of outcomes and medications. This review summarizes current knowledge of the brain cholesterol and RAS metabolism and the mechanisms by which these pathways affect neurodegeneration. The putative mechanisms of action of statins and medications inhibiting the RAS will be examined, together with prior clinical and animal studies on their effects on cognition. We review prior epidemiological studies, analysing their strengths and biases, and identify areas for future research. Understanding the pathophysiology of the brain cholesterol system and RAS and their links to neurodegeneration has enormous potential. In future, well-designed epidemiological studies could identify potential treatments for Alzheimer's disease (AD) amongst medications that are already in use for other indications.
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Encéfalo/metabolismo , Colesterol/metabolismo , Demência/tratamento farmacológico , Inibidores de Hidroximetilglutaril-CoA Redutases/uso terapêutico , Sistema Renina-Angiotensina/efeitos dos fármacos , Encéfalo/fisiopatologia , Colesterol/fisiologia , Cognição/efeitos dos fármacos , Demência/metabolismo , Demência/fisiopatologia , Humanos , Sistema Renina-Angiotensina/fisiologiaRESUMO
Integrative approaches that combine multiple forms of data can more accurately capture pathway associations and so provide a comprehensive understanding of the molecular mechanisms that cause complex diseases. Association analyses based on single nucleotide polymorphism (SNP) genotypes, copy number variant (CNV) genotypes, and gene expression profiles are the 3 most common paradigms used for gene set/pathway enrichment analyses. Many work has been done to leverage information from 2 types of data from these 3 paradigms. However, to the best of our knowledge, there is no work done before to integrate the 3 paradigms all together. In this article, we present an integrated analysis that combine SNP, CNV, and gene expression data to generate a single gene list. We present different methods to compare this gene list with the other 3 possible lists that result from the combinations of the following pairs of data: SNP genotype with gene expression, CNV genotype with gene expression, and SNP genotype with CNV genotype. The comparison is done using 3 different cancer datasets and 2 different methods of comparison. Our results show that integrating SNP, CNV, and gene expression data give better association results than integrating any pair of 3 data.
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Variações do Número de Cópias de DNA , Expressão Gênica , Estudos de Associação Genética , Predisposição Genética para Doença , Polimorfismo de Nucleotídeo Único , Estudos de Casos e Controles , Biologia Computacional/métodos , Bases de Dados Genéticas , Estudos de Associação Genética/métodos , HumanosRESUMO
The rise of 2D materials since the discovery of graphene has been exponential. Their mechanical, electrical and optical properties are exceptional, similar to their 3D counterparts. In this paper, an α-In2Se3 crystal is mechanically exfoliated and transferred directly onto a fiber ferrule to serve as a saturable absorber (SA). A thulium-doped fluoride fiber is used as a gain medium to generate mode-locked pulses together with the In2Se3-based SA. The SA has a modulation depth of 14.6% and a saturation intensity of 0.4 kW/cm2. The passively generated mode-locked pulses have a repetition rate of 6.93 MHz and a pulse width of 5.79 ps. The mode-locked pulses also have a signal-to-noise ratio of 65.4 dB and a time-bandwidth product of 0.36. The pulse energy and peak power are 0.179 nJ and 27.2 W, respectively.
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Nanomaterials have ignited new interest due to their distinctive electronic, mechanical, and optical properties. Zinc oxide nanostructures are fabricated into thin film and then inserted between two fiber ferrules to act as a saturable absorber (SA). The modulation depth and insertion loss of the SA are 5% and 3.5 dB, respectively. When the ZnO-SA is incorporated into the laser cavity, a stable Q-switched pulse tunable from 1536 to 1586 nm (50 nm range) with pulse energy up to 46 nJ was observed. Our result suggests that ZnO is a promising broadband SA to generate passively Q-switched fiber lasers.
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We demonstrate a Q-switched erbium-doped fiber laser using tungsten disulfide (WS2) as a saturable absorber. The WS2 is deposited onto fiber ferrules using a drop-casting method. Passive Q-switched pulses operating in the C-band region with a central wavelength of 1560.7 nm are successfully generated by a tunable pulse repetition rate ranging from 27.2 to 84.8 kHz when pump power is increased from 40 to 220 mW. At the same time, the pulse width decreases from a maximum value of 3.84 µs to a minimum value of 1.44 µs. The signal-to-noise ratio gives a stable value of 43.7 dB. The modulation depth and saturation intensity are measured to be 0.99% and 36.2 MW/cm², respectively.
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Jung and Lee have made comments [Appl. Opt.53, 553-554 (2014)] on "Mode-locked thulium bismuth codoped fiber laser using Graphene saturable absorber in ring cavity" [Appl. Opt.52, 1226-1229 (2013)]. The answer for the comment is provided in this report.
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Cadmium (Cd) is an environmental pollutant known as endocrine disruptor . Cd has been reported to induce perturbations of the testicular functions and the subsequent decline of the male fertility of both animals and humans. Chlorella vulgaris (ChV) a species of green microalga has been reported to have multiple beneficial activities such as anti-inflammatory, antioxidant, and antiapoptotic effects. Thus, this work was conducted to declare the benefits of Chlorella vulgaris (ChV) (500 mg/kg doses) against cadmium chloride CdCl2 (2 mg/kg doses) toxicity on the main and accessory reproductive organs' weight, structure, and function of male rats. Briefly, 40 adult male rats in 4 groups (n = 10) were used as follows; control, ChV, CdCl2, and CdCl2+ChV. (i) The 1st group was kept as control fed on pellet chow and water ad libitum. (ii) The second group is Chlorella vulgaris (ChV) group fed with C. vulgaris alga for 10 days (500 mg/kg BW). (iii) The third group was administrated CdCl2 (2mg/kg BW) via subcutaneous injection (S/C) daily for 10 days. (iv) The fourth group administered both CdCl2 and ChV with the abovementioned doses daily for successive 10 days. Our observations declared that cadmium exhibited an adverse influence on the testes and prostate gland architecture indicated by seminiferous tubule destruction, testicular edema, degeneration of Leydig cells, and prostate acini damage. All together affect the epididymal semen quality and quantity including sperm viability, motility, and count. Interestingly, ChV could restore the testicular architecture and spermatozoa regeneration accompanied by semen quality improvement and increased reproductive hormones including testosterone. On the other side, ChV suppresses reactive oxygen species (ROS) formation via enhancement the antioxidant-related genes in the testicular tissue including SOD, CAT, GSH, and MDA and maintaining spermatocyte survival via suppression of apoptotic related genes including caspase3 and activating steroidogenic related genes including StAR and HSD17ß3 in the cadmium-treated testes. In this study, ChV could enhance male fertility under normal or stressful conditions and ameliorate the adverse effects of hazardous heavy metals that are widely distributed in our environment.
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Cloreto de Cádmio , Chlorella vulgaris , Estresse Oxidativo , Espermatogênese , Masculino , Animais , Chlorella vulgaris/química , Chlorella vulgaris/efeitos dos fármacos , Cloreto de Cádmio/toxicidade , Estresse Oxidativo/efeitos dos fármacos , Ratos , Espermatogênese/efeitos dos fármacos , Infertilidade Masculina/induzido quimicamente , Infertilidade Masculina/tratamento farmacológico , Infertilidade Masculina/metabolismo , Testículo/efeitos dos fármacos , Testículo/metabolismo , Testículo/patologia , Ratos WistarRESUMO
We demonstrate mode locking of a thulium-bismuth codoped fiber laser (TBFL) operating at 1901.6 nm, using a graphene-based saturable absorber (SA). In this work, a single layer graphene is mechanically exfoliated using the scotch tape method and directly transferred onto the surface of a fiber pigtail to fabricate the SA. The obtained Raman spectrum characteristic indicates that the graphene on the core surface has a single layer. At 1552 nm pump power of 869 mW, the mode-locked TBFL self starts to generate an optical pulse train with a repetition rate of 16.7 MHz and pulse width of 0.37 ps. This is a simple, low-cost, stable, and convenient laser oscillator for applications where eye-safe and low-photon-energy light sources are required, such as sensing and biomedical diagnostics.
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Técnicas Biossensoriais , Bismuto/química , Túlio/química , Absorção , Desenho de Equipamento , Grafite/química , Lasers , Fibras Ópticas , Oscilometria/métodos , Análise Espectral Raman/métodos , Propriedades de Superfície , Fatores de TempoRESUMO
The objective of this research is to produce oil from the catalytic pyrolysis of waste polypropylene (WPP) using a low-cost natural catalyst. Three natural catalysts were examined, i.e. Kaolin, Hematite, and white sand. Different catalyst-to-plastic ratios were examined, i.e. 1:1, 1:2, 1:4, 1:6, and 1:8. The utilized catalysts were elementally analyzed using the XRF analysis and the surface area was analyzed by the BET multi-point method. The WPP thermal degradation behavior was investigated by the thermogravimetric analysis (TGA), then the generated liquid oil was analyzed using the gas chromatography-mass spectrometry (GC-MS) and the differential scanning calorimetry (DSC). Thermal cracking without a catalyst produced a yield of 70 wt% of liquid oil, and the maximum oil yield in case of using Hematite and white sand as a catalysts were 70 wt% and 68 wt%, respectively. However, the ratio of 1:2 of the Kaolin to the WPP produced the highest oil yield of 80.75 wt%, and the ratio of 1:8 of the white sand to the WPP produced the highest gas yield, i.e. 44 wt%. Using Kaolin in the catalytic pyrolysis of WPP produced oil with the lowest percentage of heavy oils, i.e. 25.98%, and the highest percentage of light oils, which is 25.37%, when compared to other catalysts such as Hematite and white sand. Kaolin has the lowest cost of oil production compared to Hematite and white sand, which is 0.28 $/kg of oil. Kaolin is an economical catalyst that improves the quality, as well as the quantity of the produced oil in comparison to Hematite, white sand and the non-catalytic case.
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In the present research work we have theoretically examined the biosensing capabilities of proposed one dimensional defective photonic crystal for swift detection of malignant brain tissues. The transfer matrix formulation and MATLAB computational tool have been used to examine the transmission properties of proposed structure. The identical buffer layers of nanocomposite superconducting material have been used either side of cavity region to enhance the interaction between incident light and different brain tissue samples poured into the cavity region. All the investigations have been carried out under normal incidence to suppress the experimental liabilities involved. We have investigated the biosensing performance of the proposed design by changing the values of two internal parameters (1) the cavity layer thickness (d4) and (2) volume fraction (η) of nanocomposite buffer layers one by one to get the optimum biosensing performance from the structure. It has been found that the sensitivity of the proposed design becomes 1.42607 µm/RIU when the cavity region of thickness 15dd is loaded with lymphoma brain tissue. This value of sensitivity can be further increased to 2.66136 µm/RIU with η = 0.8. The findings of this work are very beneficial for designing of various bio-sensing structures composed of nanocomposite materials of diversified biomedical applications.
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Aves , Nanocompostos , Animais , Compostos de Bário , EncéfaloRESUMO
Inhibition of copper corrosion by some pyrimidinone derivatives, namely; (E)-N-(3-((1,3-dimethyl-2,4,6-trioxohexahydropyrimidin-5-yl)diazenyl)-2,5-diethoxyphenyl)benzamide (MA-975) and(E)-6-(4-((4-chlorophenyl)diazenyl)-3-methyl-5-oxo-4,5-dihydro-1H-pyrazol-1-yl)-1,3 dimethylpyrimidine-2,4(1H,3H)-dione (MA-978C) in 1.0 M nitric acid (HNO3) was studied using weight loss (WL), electrochemical impedance spectroscopy (EIS), and potentiodynamic polarization (PP) measurements. The efficiency of inhibition increases as the concentration of inhibitor increases, and it also increases as the temperature increases. With the addition of the examined inhibitors, significant corrosion protection was obtained, and (MA-975) showed a very promising % IE (89.59%) at 21 × 10-6 M using the (WL) method. The polarization data revealed that these compounds act as mixed-type compounds and are adsorbed on the copper surface following Langmuir adsorption isotherm forming a protective thin film protecting the metal in the corrosive media. Scanning electron microscopy (SEM) and Energy Dispersive X-ray were used to examine the surface morphology of copper samples. Quantum calculations and Monte Carlo simulation techniques were applied with informative yields and the results matched the experimental findings.
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Cáusticos , Cobre , Benzamidas , Corrosão , Ácido Nítrico , Pirimidinonas , Aço/químicaRESUMO
Oil spills and oily wastewater have become a major environmental problem in recent years, directly impacting the environment and biodiversity. Several techniques have been developed to solve this problem, including biological degradation, chemicals, controlled burning, physical absorption and membrane separation. Recently, biopolymeric aerogels have been proposed as a green solution for this problem, and they possess superior selective oil absorption capacity compared with other approaches. Several modification strategies have been applied to nanocellulose-based aerogel to enhance its poor hydrophobicity, increase its oil absorption capacity, improve its selectivity of oils and make it a compressible and elastic magnetically responsive aerogel, which will ease its recovery after use. This review presents an introduction to nanocellulose-based aerogel and its fabrication approaches. Different applications of nanocellulose aerogel in environmental, medical and industrial fields are presented. Different strategies for the modification of nanocellulose-based aerogel are critically discussed in this review, presenting the most recent works in terms of enhancing the aerogel performance in oil absorption in addition to the potential of these materials in near future.
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Due to limited efficacy and considerable toxicity, the therapy for Chagas' disease is far from being ideal, and thus new compounds are desirable. Diamidines and related compounds such as arylimidamides have promising trypanocidal activity against Trypanosoma cruzi. To better understand the mechanism of action of these heterocyclic cations, we investigated the kinetoplast DNA (kDNA) binding properties and trypanocidal efficacy against T. cruzi of 13 compounds. Four diamidines (DB75, DB569, DB1345, and DB829), eight arylimidamides (DB766, DB749, DB889, DB709, DB613, DB1831, DB1852, and DB2002), and one guanylhydrazone (DB1080) were assayed in thermal denaturation (T(m)) and circular dichroism (CD) studies using whole purified T. cruzi kDNA and a conserved synthetic parasite sequence. The overall CD spectra using the whole kDNA were similar to those found for the conserved sequence and were indicative of minor groove binding. Our findings showed that some of the compounds that exhibited the highest trypanocidal activities (e.g., DB766) caused low or no change in the T(m) measurements. However, while some active compounds, such as DB766, induced profound alterations of kDNA topology, others, like DB1831, although effective, did not result in altered T(m) and CD measurements. Our data suggest that the strong affinity of amidines with kDNA per se is not sufficient to generate and trigger their trypanocidal activity. Cell uptake differences and possibly distinct cellular targets need to be considered in the final evaluation of the mechanisms of action of these compounds.
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Amidinas/metabolismo , Amidinas/farmacologia , DNA de Cinetoplasto/metabolismo , Tripanossomicidas/metabolismo , Tripanossomicidas/farmacologia , Trypanosoma cruzi/efeitos dos fármacos , Amidinas/química , Sequência Conservada , DNA de Cinetoplasto/química , Relação Dose-Resposta a Droga , Testes de Sensibilidade Parasitária , Relação Estrutura-Atividade , Termodinâmica , Tripanossomicidas/químicaRESUMO
Trypanosoma cruzi is the etiological agent of Chagas disease, an important neglected illness affecting about 12-14 million people in endemic areas of Latin America. The chemotherapy of Chagas disease is quite unsatisfactory mainly due to its poor efficacy especially during the later chronic phase and the considerable well-known side effects. These facts emphasize the need to search for find new drugs. Diamidines and related compounds are minor groove binders of DNA at AT-rich sites and present excellent anti-trypanosomal activity. In the present study, six novel aromatic amidine compounds (arylimidamides and diamidines) were tested in vitro to determine activity against the infective and intracellular stages of T. cruzi, which are responsible for sustaining the infection in the mammalian hosts. In addition, their selectivity and toxicity towards primary cultures of cardiomyocyte were evaluated since these cells represent important targets of infection and inflammation in vivo. The aromatic amidines were active against T. cruzi in vitro, the arylimidamide DB1470 was the most effective compound presenting a submicromolar LD(50) values, good selectivity index, and good activity at 4 °C in the presence of blood constituents. Our results further justify trypanocidal screening assays with these classes of compounds both in vitro and in vivo in experimental models of T. cruzi infection.
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Amidinas/farmacologia , Tripanossomicidas/farmacologia , Trypanosoma cruzi/efeitos dos fármacos , Amidinas/química , Animais , Doença de Chagas/tratamento farmacológico , Doença de Chagas/parasitologia , Relação Dose-Resposta a Droga , Dose Letal Mediana , Camundongos , Miócitos Cardíacos/efeitos dos fármacos , Miócitos Cardíacos/parasitologia , Parasitemia/tratamento farmacológico , Parasitemia/parasitologia , Pentamidina/química , Pentamidina/farmacologia , Tripanossomicidas/químicaRESUMO
No vaccines or safe chemotherapy are available for Chagas disease. Pentamidine and related di-cations are DNA minor groove-binders with broad-spectrum anti-protozoal activity. Therefore our aim was to evaluate the in vitro efficacy of di-cationic compounds - DB1645, DB1582, DB1651, DB1646, DB1670 and DB1627 - against bloodstream trypomastigotes (BT) and intracellular forms of Trypanosoma cruzi. Cellular targets of these compounds in treated parasites were also analysed by fluorescence and transmission electron microscopy (TEM). DB1645, DB1582 and DB1651 were the most active against BT showing IC50 values ranging between 0.15 and 6.9 microm. All compounds displayed low toxicity towards mammalian cells and DB1645, DB1582 and DB1651 were also the most effective against intracellular parasites, with IC50 values ranging between 7.3 and 13.3 microm. All compounds localized in parasite nuclei and kDNA (with greater intensity in the latter structure), and DB1582 and DB1651 also concentrated in non-DNA-containing cytoplasmic organelles possibly acidocalcisomes. TEM revealed alterations in mitochondria and kinetoplasts, as well as important disorganization of microtubules. Our data provide further information regarding the activity of this class of compounds upon T. cruzi which should aid future design and synthesis of agents that could be used for Chagas disease therapy.
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Amidinas/farmacologia , Antiprotozoários/farmacologia , Núcleo Celular/metabolismo , DNA de Cinetoplasto/metabolismo , Frações Subcelulares/metabolismo , Trypanosoma cruzi/efeitos dos fármacos , Amidinas/química , Animais , Antiprotozoários/química , Doença de Chagas/tratamento farmacológico , Citoplasma/metabolismo , Citoplasma/ultraestrutura , DNA de Cinetoplasto/genética , Concentração Inibidora 50 , Microscopia Eletrônica de Transmissão , Microscopia de Fluorescência , Microtúbulos/metabolismo , Mitocôndrias/metabolismo , Organelas/metabolismo , Testes de Sensibilidade Parasitária/métodos , Trypanosoma cruzi/fisiologia , Trypanosoma cruzi/ultraestruturaRESUMO
Two new series of pyrimidinone derivatives linked to arylpiperazine moieties and 2'-carbethoxy-biphenylmethyl moieties were designed, synthesized and biologically evaluated for their in vivo hypotensive activities. The design of arylpiperazine analogues (IIa-f, IIIa-c, VIIa.b, IX) was based upon structural modification of the newly discovered selective alpha1-AR antagonist drug; Urapidil. Compare/fit studies of these molecules with the previously generated and validated alpha1-AR antagonist hypothesis showed that these molecules have comparable affinities for the alpha1-AR antagonist hypothesis while compound IIIc had the highest fitting value. The in vivo biological evaluation of these compounds for their effects on blood pressure of normotensive cats in comparison to the lead compound prazosin, was consistent with the results of molecular modeling fit values. As expected, compound IIIc exhibited the highest hypotensive activity among the test set compounds. Meanwhile, the design of 2'-carbethoxy-biphenylylmethyl analogues (XIa,b) was based upon the molecular modeling simulation fitting of their carboxylic acid bioprecursors with the previously generated and validated Ang II receptor antagonist hypothesis. Such compare/fit studies predicted that the designed compounds (XIa,b) showed comparable fitting affinities between their de-esterified analogues and the Ang II antagonist pharmacophore. In vivo biological evaluation of these compounds for their effects on blood pressure of normotensive cats showed that compound Xla exhibited hypotensive activity more or less similar to losartan.
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Antagonistas de Receptores Adrenérgicos alfa 1/síntese química , Antagonistas de Receptores Adrenérgicos alfa 1/farmacologia , Bloqueadores do Receptor Tipo 1 de Angiotensina II/síntese química , Bloqueadores do Receptor Tipo 1 de Angiotensina II/farmacologia , Compostos de Bifenilo/química , Compostos de Bifenilo/síntese química , Desenho Assistido por Computador , Desenho de Fármacos , Piperazinas/química , Pirimidinas/síntese química , Pirimidinas/farmacologia , Pirimidinonas/química , Pirimidinonas/síntese química , Animais , Pressão Sanguínea/efeitos dos fármacos , Simulação por Computador , Indicadores e Reagentes , Modelos Moleculares , Conformação Proteica , Ratos , Software , Relação Estrutura-AtividadeRESUMO
A novel chemically guanyl-modified cellulose (Gu-MC) - material has been synthesized for the adsorption of Cu2+, Cd2+, Hg2+, Pb2+ and Zn2+ metal ions from aqueous solution. Cellulose was pretreated with periodate prior to its condensation with aminoguanidine for the formation of cellulose aldehyde-guanyl Schiff's. The synthesized material was characterized by Fourier transform infrared spectra (FTIR), elemental analysis, scanning electron microscope (SEM) and thermogravimetric analysis (TGA). Moreover, the effect of contact time, pH, adsorbent dosage, interfering ions and initial concentration of metal ions on the adsorption capacity were investigated. At optimum conditions, the adsorption capacities of Cu2+, Zn2+, Cd2+, Pb2+ and Hg2+ were 83, 78, 68, 52, and 48mgg-1, respectively. The kinetic of adsorption adopted to the second-order model and kinetic model showed that the chemical adsorption is the rate limiting step. The proposed material has been successfully applied for the adsorption of the target metal ions from different real samples with satisfactory results.