Simple synthesis of photoluminescent carbon dots from a marine polysaccharide found in shark cartilage

BACKGROUND: For more than a decade, water-soluble, eco-friendly, biocompatible, and low-toxicity fluorescent nanomaterials have received considerable attention for their numerous in vivo and in vitro applications in biomedical imaging, disease diagnostics, and environmental monitoring. Owing to their tunable photoluminescence properties, carbon-based luminescent nanomaterials have shown great potential in bioimaging, photocatalysis, and biosensing among other applications. RESULTS: Marine environments provide excellent resources for the fabrication of these nanomaterials, because many marine organisms contain interesting trigger organic compounds that can be used as precursors. Herein, we synthesize multi-color emissive carbon dots (CDs) with an intrinsic photoluminescence quantum yield of 20.46%. These nanostructures were achieved through the one-step hydrothermal treatment of marine polysaccharide chondroitin sulfate, obtained from shark cartilage, in aqueous solution. CONCLUSIONS: We successfully demonstrate the low toxicity of our marine resource-derived CDs in zebrafish, and provide an initial assessment of their possible use as a bioimaging agent. Notably, the newly synthesized CDs localize in the intestines of zebrafish larvae, thereby indicating their biocompatibility and potential use as in vivo dyes.

Degradation of textile dyes by cyanobacteria

Abstract Dyes are recalcitrant compounds that resist conventional biological treatments. The degradation of three textile dyes (Indigo, RBBR and Sulphur Black), and the dye-containing liquid effluent and solid waste from the Municipal Treatment Station, Americana, São Paulo, Brazil, by the cyanobacteria Anabaena flos-aquae UTCC64, Phormidium autumnale UTEX1580 and Synechococcus sp. PCC7942 was evaluated. The dye degradation efficiency of the cyanobacteria was compared with anaerobic and anaerobic-aerobic systems in terms of discolouration and toxicity evaluations. The discoloration was evaluated by absorption spectroscopy. Toxicity was measured using the organisms Hydra attenuata, the alga Selenastrum capricornutum and lettuce seeds. The three cyanobacteria showed the potential to remediate textile effluent by removing the colour and reducing the toxicity. However, the growth of cyanobacteria on sludge was slow and discoloration was not efficient. The cyanobacteria P. autumnale UTEX1580 was the only strain that completely degraded the indigo dye. An evaluation of the mutagenicity potential was performed by use of the micronucleus assay using Allium sp. No mutagenicity was observed after the treatment. Two metabolites were produced during the degradation, anthranilic acid and isatin, but toxicity did not increase after the treatment. The cyanobacteria showed the ability to degrade the dyes present in a textile effluent; therefore, they can be used in a tertiary treatment of effluents with recalcitrant compounds.

Effects of intracameral brilliant blue on the corneal endothelium of swine: in vitro study / Avaliação do endotélio corneano suíno por microscopia eletrônica de varredura após aplicação de azul brilhante a 0, 05% na câmara anterior: estudo in vitro

The aim was to investigate the ultrastructural changes in the corneal endothelium of pigs induced by intracameral 0.05% brilliant blue. Twenty swine corneas were separated into two groups, the right eye bulbs (control group) and the left eye bulbs (experimental group) of the same animal. All the eye bulbs were evaluated with specular microscopy. The cornea of the right eye bulbs was excised and in the left eye bulbs 0.2ml of 0.05% brilliant blue vital dye (OPTH-blue±) was injected into the anterior chamber, where it remained for one minute. Then the anterior chamber was cleaned with a balanced salt solution injection and the cornea was excised too. All the corneas were evaluated by scanning electron microscopy to evaluate the changes on the endothelium caused by the brilliant blue dye. There were no significant differences between the right corneal endothelium cells and the left corneal endothelium cells with scanning electron microscopy after intracameral use of 0.05% brilliant blue dye. The 0.05% brilliant blue dye concentration did not cause deleterious effects for the swine corneal endothelium after intracameral use and can be a choice for safe staining of the anterior capsule of the lens in cataract surgery.(AU)

Com o objetivo de avaliar as alterações ultraestruturais no endotélio corneano suíno induzidas pela aplicação intracameral do corante azul brilhante 0,05%, vinte córneas suínas foram separadas em dois grupos: olhos direitos (grupo controle) e olhos esquerdos (grupo experimental). Inicialmente todos os bulbos oculares foram avaliados por microscopia especular. As córneas dos bulbos oculares do grupo controle foram excisadas, enquanto nos bulbos oculares do grupo experimental foram injetados 0,2ml do corante vital azul brilhante 0,05% na câmara anterior e mantido por um minuto. Após esse período a câmara anterior foi lavada com solução salina balanceada e as córneas foram excisadas. Todas as córneas excisadas foram avaliadas por microscopia eletrônica de varredura para verificar a ocorrência possíveis alterações no endotélio corneano causadas pelo corante. Não foram observadas diferenças ultraestruturais durante a avaliação endotelial por microscopia eletrônica de varredura das córneas do grupo controle e experimental após a aplicação do azul brilhante 0,05% na câmara anterior. O corante azul brilhante na concentração 0,05% não causou danos endoteliais após seu uso intracameral em suínos e pode ser uma alternativa segura para a coloração da cápsula anterior da lente na cirurgia de catarata.(AU)

Aerobiología y biodeterioro del género Aspergillus Link en depósitos de tres instituciones patrimoniales cubanas / Aerobiology and biodeterioration of the genus Aspergillus Link in repositories of three Cuban heritage intitutions

Las especies del género Aspergillus Link constituyen importantes agentes biodeteriorantes de objetos de valor constructivo, cultural y patrimonial. En ambientes laborales, sus propágulos y metabolitos pueden provocar afecciones a la salud humana. Los estudios aeromicológicos pueden contribuir a minimizar el impacto de Aspergillus spp. en el biodeterioro y la calidad de vida. Se han caracterizado de acuerdo a su potencial biodeterió- geno y patogénico representantes de Aspergillus spp. en el aire de depósitos de materiales en tres instituciones patrimoniales cubanas. Las muestras se tomaron empleando un biocolector SAS súper 100. Se evaluó cualitativamente la actividad celulolítica, amilolítica y proteolítica de los aislados; así como la excreción de pigmentos y ácidos orgánicos. Se evaluó el crecimiento a 37°C y la secreción de hemolisinas. Aspergillus spp. constituyó parte considerable de la micobiota aérea viable en los depósitos con 22 especies correspondientes a 12 secciones, las de mayor variabilidad fueron Flavi y Restricti, mientras la primera y la sección Aspergillus fueron las mejor representadas. El 74 por ciento de las cepas mostraron alta capacidad para degradar los compuestos orgánicos evaluados y secretar ácidos, mientras el 34 por ciento excretó pigmentos de amarillo a pardo oscuro, se evidenció un amplio potencial biodeteriorante en general. Más del 30 por ciento de los aislados mostraron ser patógenos oportunistas peligrosos para el hombre al crecer a 37°C, secretar hemolisinas, y presentar un tamaño conidial que posibilita la depositación en alvéolos pulmonares. Las cepas con mayor impacto biodeteriorante y patogénico fueron las correspondientes a las Secciones Flavi, Nigri y la especie Aspergillus fumigatus Fresen.

Species of the genus Aspergillus Link cause damage to objects constructive, cultural and heritage value. In work environments, their propagules and metabolites may cause disorders to human health. Aerobiological studies can help minimize the impact of Aspergillus spp. in the biodeterioration and quality of life. Aspergillus spp. strains present in the air of the repositories in three Cuban heritage institutions were characterized according to their biodeteriogenic and pathogenic potential. Each isolated was classified taxonomically, cellulolytic, amylolytic and proteolytic activity as well as excretion of pigments and organic acids was evaluated. The capacity to grow at 37°C and secrete hemolysins was qualitatively evaluated. Aspergillus spp. was significant portion of viable air micobiota in the three repositories with 22 species corresponding to 12 sections, most variability were Flavi and Restricti, while the first section and Aspergillus were the best represented. The 74 percent of the strains showed high ability to degrade organic compounds evaluated and secrete acids, while 34 percent excreted pigments from yellow to dark brown, evidenced a broad biodeteriogenic potential in general. More than 30 percent of the isolates were shown to be dangerous opportunistic pathogens for humans to grow at 37°C, secrete hemolysin, and present a conidial size which enables the deposition pulmonary alveoli. Strains higher biodeteriogenic and pathogenic impact were those corresponding to the Flavi, Nigri sections and the species Aspergillus fumigatus Fresen.

In vitro cytotoxicity of self-curing acrylic resins of different colors

OBJECTIVE: The aim of this study was to assess the in vitro cytotoxicity of acrylic resins of different colors over time. METHODS: Specimens were divided into 4 groups (n = 6) according to the color of the acrylic resin (Orto Class, Clássico, Campinas, São Paulo, Brazil): Group 1: clear acrylic resin; group 2: pink acrylic resin; group 3: blue acrylic resin and group 4: green acrylic resin. All specimens were fabricated according to the mass manipulation technique and submitted to mechanical polishing protocol. The control was performed with an amalgam specimen (C+), a glass specimen (C-) and cell control (CC). Specimens were immersed in Minimum Eagle's Medium (MEM) and incubated for 24 h at 37o C. The extracts from the experimental material were filtered and mixed with L929 fibroblast. Cytotoxicity was evaluated at 4 different times, 24, 48, 72 and 168 h. After contact, cells were incubated for 24 h and added to 100 µ of 0.01% neutral red dye. The cells were incubated for 3 h for pigment incorporation and fixed. Cells viability was determined by a spectroscopic (BioTek, Winooski, Vermont, USA) with a 492-nm wavelength λ=492 nm). RESULTS: There were no statistical differences between the experimental groups and the CC and C- groups. CONCLUSION: Clear, pink, blue and green self-curing acrylic resins fabricated by means of the mass manipulation technique and mechanically polished are not cytotoxic. Neither the pigment added to the self-curing acrylic resin nor the factor of time influenced the cytotoxicity of the material. .

OBJETIVO: avaliar, in vitro, a citotoxicidade de resinas acrílicas autopolimerizáveis, de diferentes cores, ao longo do tempo. MÉTODOS: os corpos de prova foram divididos em quatro grupos (n = 3), de acordo com a cor da resina acrílica utilizada (Orto Class, Clássico, São Paulo/SP), sendo: grupo 1, acrílica incolor; grupo 2, acrílica rosa; grupo 3, acrílica azul; e, grupo 4, acrílico verde. Todos os corpos de prova foram confeccionados pela técnica de massa e polidos mecanicamente. Um corpo de prova de amálgama, um de vidro e célula constituíram o controle positivo (C+), controle negativo (C-), e controle de célula (CC), respectivamente. Em seguida, esses foram imersos em meio mínimo essencial de Eagle (MEM) por 24h, quando se removeu o sobrenadante e colocou-os em contato com fibroblastos L929. Avaliou-se a citotoxicidade em quatro períodos: 24, 48, 72 e 168h. Após o contato com o meio, as células foram incubadas por 24h e adicionou-se 100µ do corante vermelho neutro a 0,01%. Posteriormente, as células foram incubadas por 3h, para incorporação do corante, e fixadas. A contagem das células viáveis foi realizada em espectrofotômetro (BioTek, Winooski, EUA), com um comprimento de onda de 492nm (λ = 492nm). RESULTADOS: não houve diferença estatística entre os grupos experimentais e os grupos CC e C-. CONCLUSÇÕES: as resinas acrílicas autopolimerizáveis incolor, rosa, azul e verde, manipuladas pela técnica de massa e polidas mecanicamente não são citotóxicas. O corante utilizado em resinas autopolimerizáveis e tempo não influenciam na citotoxocidade do material. .

Efeito do dióxido de titânio na decomposição fotocatalítica de substâncias persistentes no ambiente: corantes têxteis e interferentes endócrinos / Effect of titanium dioxide in the photocatalytic decomposition of persistent chemicals in the environment: textiles and dyes endocrine interfering

O objetivo do presente trabalho foi estudar a degradação fotocatalítica de três corantes e um interferente endócrino mediado pelo dióxido de titânio (TiO2). Foi estudada a degradação fotocatalítica de dois azo corantes comerciais, respectivamente o C.I Reactive Black 5 e o C.I Reactive Red 239. Para esse estudo foi utilizado o TiO2 P25 Evonik como catalisador e os experimentos foram realizados em solução aquosa com reator artificial equipado com lâmpada de vapor de mercúrio 125W. Nesse estudo,foram avaliados os seguintes parâmetros: concentração de TiO2, tempo de irradiação, pH, concentração inicial de corante, presença de diferentes concentrações de peróxido de hidrogênio e degradação em sistema bi-compartimental para os dois azo corantes. O outro corante estudado foi o Índigo Carmine (IC). Primeiramente foi investigada a descoloração do corante em efluente modelo usando processo físico e químico para sua remoção. Os experimentos de descoloração do efluente contendo o corante IC foram realizados usando carvão ativado no escuro e com irradiação. Além disso, o efeito do carvão ativado / TiO2 / UV foi avaliado pelo mesmo sistema. Os parâmetros da degradação do IC foram realizados, seguindo: concentração de TiO2, pH, concentração inicial de corante, presença de ânions inorgânicos, temperatura, concentração de peróxido de hidrogênio. A eficiência de três diferentes reatores (Reator 1 – reator do tipo batch com lâmpada vapor de mercúrio 125W; Reator 2 – reator do tipo batch equipado com 4 lâmpadas daylight 20W; Reator 3 – reator tubular de fluxo contínuo equipado com uma lâmpada daylight 20W) e reator batch com luz solar foram avaliados para degradação do IC.Além disso, otimizados experimentos foram realizados em planta piloto com compound parabolic collector reatores (CPC) na Plataforma Solar de Almería, Espanha, com TiO2 em suspensão e suportado. O IC foi estudado em diferentes tipos de águas, sendo elas: água destilada, água sintética moderadamente dura, água sintética e real de estação de tratamento de água residuária (ETAR). Testes ecotoxicológicos para o IC foram realizados em dois diferentes níveis tróficos de cadeia alimentar (Daphnia similis e Pseudokirchneriella subcapitata) e testes com minhocas Eisenia andrei. A degradação fotocatalítica do Bisfenol A (BPA) em diferentes tipos de águas na presença de TiO2 foi feita sob diferentes condições. O TiO2 em suspensão foi utilizado para comparar a eficiência da degradação do BPA (...) em batch e CPC reatores. O TiO2 foi suportado em esferas de vidro pelo método sol-gel e usado em reatores solares CPC em escala piloto para degradação do BPA (...) A influência das espécies reativas (...) foi avaliada. Testes ecotoxicológicos com minhocas Eisenia andrei também foram realizados para o BPA e seus produtos de degradação.

Chromovitrectomy: update

The basic concept for the application of vital dyes during vitreoretinal surgery is to assist in highlighting preretinal membranes and tissues which are very thin and semitransparent and thus difficult to detect. The vital dyes may be classified according to different criteria, where the most commonly applied includes chemical classification. In ophthalmic surgery, vital dyes are widely used in cataract and vitreoretinal surgery. The vital dyes, indocyanine green, infracyanine green, and brilliant blue stain the internal limiting membrane, and trypan blue and triamcinolone acetonide help to visualize epiretinal membranes and vitreous, respectively. This review exhibits the current literature regarding the properties of vital dyes, techniques of application, indications, and toxicities during vitreoretinal surgery and, also suggests that the field of chromovitrectomy represents an expanding area of research.

Citotoxicidade do corante dinitrofenilazo CI DB291: biotransformação, estresse oxidativo e alteração epigenética em células HepG2 / Cytotoxicity of the CI DB291 dinitrofenilazo dye: biotransformation, oxidative stress and epigenetic change in HepG2 cells

O produto comercial CI Disperse Blue 291 (CI DB291) é amplamente utilizado pela industria têxtil. Estudos mostram que corantes dinitrofenilazo são genotóxicos no ensaio de Ames/Salmonella, mas há poucos estudos sobre seus efeitos em células eucariontes. Este trabalho teve como objetivo investigar a genotoxicidade e citotoxicidade do corante DB291 em células humanas em cultura, bem como vias pelas quais o corante atua levando aos efeitos tóxicos. O corante comercial foi purificado por HPLC-DAD e utilizado para incubação com células HepG2 (5-100 µM por 3-72 h). A citotoxicidade foi avaliada pelos ensaios de XTT, corante cristal violeta, lactato desidrogenase extracelular e consumo de glicose. A geração de ROS intracelular foi verificada pela emissão de fluorescência da 2',7'-diclorofluoresceína. Análises de ciclo celular, fragmentação do DNA, potencial de membrana mitocondrial (Ψ) e cálcio intracelular foram realizadas por citometria de fluxo. A produção de ATP foi mensurada por quimiluminescência. Níveis de 8-oxodG e 5-mdC foram avaliados por HPLC-ESI-MS/MS e HPLC-UV, respectivamente. A expressão da enzima DNMT1 foi avaliada por western blot. Um produto de biotransformação foi identificado e caracterizado estruturalmente por MS/MS e 1H-RMN. A exposição ao corante DB291 diminuiu significativamente a sobrevivência das células em um modo tempo- e dose-dependente (IC50 = 74 µM), com a concomitante formação de um produto de biotransformação reduzido. A morte celular ocorreu sem lise da membrana plasmática. Nas células expostas, foi observado aumento da atividade enzimática mitocondrial, acompanhado por um aumento da taxa de consumo de glicose. Índices elevados de ATP, Ψ e cálcio foram verificados após a incubação das células com concentrações crescentes do corante. Alterações mitocondriais e o processo de biotransformação impeliram a aumento na produção de ROS intracelular, 8-oxodG e fragmentação do DNA. O dano ao DNA induziu a parada no ciclo...

The commercial CI Disperse Blue 291 (CI DB291) is widely used by textile industry. It is mutagenic in the Ames/S. typhimurium assay, but there are few studies showing its effects in eukaryotic cells. We evaluated here the toxicity of CI DB291 in the human HepG2 cell line. The commercial dye was purified by HPLC-DAD and used for incubation with HepG2 cells (5-100 µM for 3-72 h). Cytotoxicity was assessed by the XTT, crystal violet dye, extracellular lactate dehydrogenase and glucose consumption assays. ROS formation was assessed by 2',7'-dichlorofluorescein fluorescence. Analyses of cell cycle, DNA fragmentation, mitochondrial membrane potential (Ψ) and intracellular calcium were analyzed by flow cytometry. ATP level was measured by chemiluminescence. Levels of 8-oxodG and 5-mdC were evaluated by HPLCESI-MS/MS and HPLC-UV, respectively. DNMT1 expression was assessed by western blot. A biotransformation product was identified and structurally characterized by MS/MS and 1H-NMR. DB291 significantly decreased cell survival in a time- and dose-dependent manner (IC50 = 74 µM), with concomitant formation of a reduced biotransformation product. Plasma membrane lysis did not occur. Increased mitochondrial enzymatic activity, accompanied by increase in glucose consumption rate, was observed in cells incubated with DB291. Elevated ATP, Ψ, and intracellular calcium was verified after cell incubation with increasing dye concentrations. Mitochondrial changes and the biotransformation process accounted for the observed raise in intracellular ROS, 8-oxodG, and DNA fragmentation. DNA damage induced cell cycle arrest and DNMT1 overexpression, followed by DNA hypomethylation in the subsequent cell cycle. Results point for the first time to toxicity of the dye through biotransformation, mitochondrial changes, and oxidative stress.

Corantes vitais em cromovitrectomia / Vital dyes in chromovitrectomy

O objetivo do artigo é apresentar os dados atuais da aplicação de corantes vitais durante cirurgia vitreorretiniana, "cromovitrectomia", bem como uma revisão da literatura atual sobre o assunto no tocante às técnicas de aplicação, indicações e complicações em cromovitrectomia. Um grande número de publicações tem abordado o perfil tóxico da indocianina verde na cromovitrectomia. Dados experimentais mostram uma toxicidade dose-dependente da mesma em várias populações de células retinianas. Novas gerações de corantes incluem: azul tripan, azul patente, acetato de triancinolona, infracianina verde, fluoresceína sódica, azul de bromofenol, acetato de fluorometolona e azul brilhante. Novos instrumentos podem permitir um corar seletivo de estruturas durante a vitrectomia. Este artigo mostra que o campo da cromovitrectomia está em plena expansão de pesquisas. Os corantes de primeira linha são a indocianina verde, infracianina verde e o azul brilhante. Azul patente, azul de bromofenol e azul tripan surgem como novos adjuvantes para melhor observação da membrana epirretiniana. Demais corantes que surgiram merecem maior investigação.

The aim of this article is to present the current data with regard to the application of vital dyes during vitreoretinal surgery, "chromovitrectomy", as well as to overview the current literature regarding the properties of dyes, techniques of application, indications and complications in chromovitrectomy. A large body of published research has recently addressed the toxicity profile of indocyanine green for chromovitrectomy. Experimental data demonstrate dose-dependent toxicity of indocyanine green to various retinal cells. Newer generation vital dyes for chromovitrectomy include trypan blue, patent blue, triamcinolone acetonide, infracyanine green, sodium fluorescein, bromophenol blue, fluorometholone acetate and brilliant blue. Novel instruments may enable a selective painting of preretinal tissues during chromovitrectomy. This review suggests that the field of chromovitrectomy represents an expanding area of research. The first line agents for internal limiting membrane staining in chromovitrectomy are indocyanine green, infracyanine green, and brilliant blue. Patent blue, bromophenol blue and trypan blue arose as outstanding biostains for visualization of epiretinal membranes. Novel dyes available for chromovitrectomy deserve further investigation.

Decolorization of different textile dyes by Penicillium simplicissimum and toxicity evaluation after fungal treatment

The objective of this study was to investigate the capacity of decolorization and detoxification of the textile dyes Reactive Red 198 (RR198), Reactive Blue 214 (RB214), Reactive Blue 21 (RB21) and the mixture of the three dyes (MXD) by Penicillium simplicissimum INCQS 40211. The dye RB21, a phthalocyanine, was totally decolorized in 2 days, and the others, the monoazo RR198, the diazo RB214 and MXD were decolorized after 7 days by P. simplicissimum. Initially the dye decolorization involved dye adsorption by the biomass followed by degradation. The acute toxicity after fungal treatment was monitored with the microcrustacean Daphnia pulex and measured through Effective Concentration 50 percent (EC50). P. simplicissimum reduced efficiently the toxicity of RB21 from moderately acutely toxic to minor acutely toxic and it also reduced the toxicity of RB214 and MXD, which remained minor acutely toxic. Nevertheless, the fungus increased the toxicity of RR198 despite of the reduction of MXD toxicity, which included this dye. Thus, P. simplicissimum INCQS 40211 was efficient to decolorize different textile dyes and the mixture of them with a significant reduction of their toxicity. In addition this investigation also demonstrated the need of toxicological assays associated to decolorization experiments.

Homeopathic drugs Natrum sulphuricum and Carcinosin prevent azo dye-induced hepatocarcinogenesis in mice.

The study was undertaken to examine whether Carcinosin-200 (Car-200) could provide additional ameliorative effect, if used intermittently with Natrum sulphuricum-30 (Nat Sulph-30) against hepatocarcinogenesis induced by chronic feeding of p-dimethylaminoazobenzene (p-DAB) and phenobarbital (PB) in mice (Mus musculus). Mice were randomly divided into seven sub-groups: (i) normal untreated; (ii) normal + succussed alcohol; (iii) p-DAB (0.06%) + PB (0.05%); (iv) p-DAB + PB + succussed alcohol, (v) p-DAB + PB + Nat Sulph-30, (vi) p-DAB + PB + Car-200, and (vii) p-DAB + PB + Nat Sulph-30 + Car-200. They were sacrificed at 30, 60, 90 and 120 days for assessment of genotoxicity through cytogenetical end-points like chromosome aberrations, micronuclei, mitotic index and sperm head anomaly and cytotoxicity through assay of widely accepted biomarkers and pathophysiological parameters. Additionally, electron microscopic studies and gelatin zymography for matrix metalloproteinases (MMPs) were conducted in liver at 90 and 120 days. Results showed that administration of Nat Sulph-30 alone and in combination with Car-200 reduced the liver tumors with positive ultra-structural changes and in MMPs expression, genotoxic parameters, lipid peroxidation, -glutamyl transferase, lactate dehydrogenase, blood glucose, bilirubin, creatinine, urea and increased GSH, glucose-6-phosphate dehydrogenase, superoxide dismutase, catalase, glutathione reductase activities and hemoglobin, cholesterol, and albumin levels. Thus, intermittent use of Car-200 along with Nat Sulph-30 yielded additional benefit against genotoxicity, cytotoxicity, hepatotoxicity and oxidative stress induced by the carcinogens during hepatocarcinogenesis.

Nanofiltration process on dye removal from simulated textile wastewater

Dyestuffs removal from industrial wastewater requires special advanced technologies, since dyes are usually difficult to remove by biological methods. In this study nanofiltration process was used for removal of different dyestuffs from solutions. The rate of dye removal by spiral wound nanofiltration membrane in film thin composite MWCO=90 Dalton, was evaluated for four classes of dyes acidic, disperse, reactive and direct in red and blue dyes medium. Dye absorbance was measured by spectrophotometric method [2120 Standard Method 1998]. Effects of feed concentration, pressure and total dissolved solids concentration were also studied. Results showed that increasing dye concentration lead to higher color removal up to 98% and at different pressures for acidic and reactive blue were up to 99.7%. Different types of dyes had no effect on dye removal and permeate flux. During 2 h. of the operation time, permeate flux decline was increased. Permeate fluxes for different types of red dyes were from 16.6 to 12.6 [L/m[2]/h.] and for blue dyes were from 16.6 to 10.45 [L/m[2]/h.]. Presence of sodium chloride in dye solutions increased dye rejections nearby 100%. Chemical oxygen demand removal efficiencies for reactive blue, disperse blue, direct and disperse red dyes were also approximately 100%

Mutagenicity assessment of textile dyes from Sanganer (Rajasthan).

Sanganer town, district Jaipur (Rajasthan, India) is famous worldwide for its hand block dyeing and textile printing industries. These industries use a variety of chemicals and dyes during processing and finishing of raw materials. Most of the textile dyes used by these industries have not been evaluated for their impact on health and the environment. The workers in these industries are exposed to such dyes with no control over the length and frequency of exposure. Further, untreated and sometimes even treated effluents from these industries are released into surface waters of Amani Shah drainage or through the drainage systems, seep into the ground water and adjoining water bodies. Since many textile dyes are known carcinogens and mutagens, a complete evaluation of the safety of these dyes in the human environment must include an evaluation of their genotoxicity or mutagenicity. A total of 12 textile dyes from Sanganer were tested for their mutagenicity, by Ames Salmonella reversion assay using strain TA 100 of Salmonella typhimurium. Only 1 dye, Red 12 B showed absence of mutagenic activity. The remaining 11 dyes were all positively mutagenic.

A comparative study on the toxic effects of textile dye wastewaters (untreated and treated) on mortality and RBC of a freshwater fish Gambusia affinis (Baird and Gerard).

Comparative toxicological studies of textile dye wastewater (untreated and treated) on a freshwater fish, Gambusia affinis, revealed a marked reduction in mortality and cytotoxic effects on RBCs, measured as reduction in their counts and percent changes in their shape (poikilocytosis) and variation in their size (anisocytosis)}, after subjecting them to both physicochemical and biological treatments. On comparing the data of mortality and the cytotoxic effects on RBCs, we found poikilocytosis is a better indicator for toxicity measurement of both untreated as well as treated wastewater, especially at their lowest concentrations where percent mortality was found to be either nil or lowerer than the percentage of poikilocytic RBCs. Although percent reduction in RBC counts and changes in their size (anisocytosis) indicated toxic effects of wastewaters, but EC5o values for RBC counts were usually higher than those for poikilocytosis and mortality, and non-calculable for anisocytosis suggesting their lesser sensitivity to pollutants. In view of these findings, we recommend monitoring of toxic effects of wastewaters during fish bioassay on both mortality and variation in RBC shape.

Differential role of MAP kinase isoforms in malachite green transformed Syrian hamster embryo fibroblasts in culture.

Malachite green (MG) induces DNA damage and malignant transformation of Syrian hamster embryo (SHE) cells in primary culture. In the present study, we have studied the role of all the three isoforms of mitogen activated protein (MAP) kinases i.e. ERK (extracellular regulated kinase), JNK (JUN- N- terminal kinase) and p38 kinase during transformation of SHE cells by MG. The results showed that transformed cells were associated with a decreased expression of phosphoactive ERK and JNK and increased expression of p38 kinase as evident from the Western blot, immunofluorescence and flow cytometry studies. Also, a persistent nuclear localization of p38 kinase was observed in the transformed cells. The present study indicated that p38 kinase was present at higher levels and seemed to be associated with transformation, which suggested that inhibitors of p38 kinase could serve in general as potential agents for selective cancer therapy.

Decolorization of simulated spent reactive dye bath using solar / TiO2/H2O2

Different parameters were investigated to evaluate their effect on the process removal efficiency of reactive dye from simulated spent reactive dye bath, by solar / TiO[2] / H[2]O[2], including H[2]O[2] concentration, TiO[2] loading and pH. As a result 99% of reactive dye can be removed at a TiO[2] loading of 400mg/l, H[2]O[2] concentration of 150 mg/l and of pH: 5.2. The effect of photo-catalytic deactivation of TiO2 on reactive dye removal was studied for ten number of cycles, and found that the extent of deactivation was high for each consecutive repeated use

Evaluation of protective potentials of a potentized homeopathic drug, Chelidonium majus, during azo dye induced hepatocarcinogenesis in mice.

Several cytogenetical and enzymatic protocols were used to test if two microdoses of Chelidonium majus, namely Chelidonium-30 (Ch-30) and Chelidonium-200 (Ch-200), used as homeopathic drugs, showed anti-tumor activity and also favorably modulated genotoxic damages produced by an azo dye in mice at several intervals of fixation. Different sets of healthy mice were fed: (i) hepatocarcinogen, p-dimethylaminoazobenzene (p-DAB, initiator) + phenobarbital (PB, promoter), (ii) only p-DAB, (iii) only PB, and (iv) neither p-DAB nor PB (normal control). Mice fed with p-DAB + PB were divided into different sets that were also fed either Ch-30 (v) or Ch-200 (vi) or diluted alcohol (vii), the "vehicle" of the microdoses of Chelidonium. All mice of group (i), a few of group (ii) and group (vii) and none of groups (iii) and (iv) developed tumors in liver at the longer intervals of fixation. The frequencies of chromosome aberrations (CA), micronucleated erythrocytes (MN), mitotic index (MI) and sperm head abnormality (SHA) were much higher in groups (i) and (vii) mice than in groups (ii), (iii) and (iv) mice at all fixation intervals. However, in mice of both groups (v) and (vi), the frequencies of CA, MN, SHA were strikingly less than those of groups (i) and (vii), and moderately less than those of groups (ii) and (iii). Both Ch-30 and Ch-200 also modulated favourably some toxicity marker enzymes like acid and alkaline phosphatases, peroxidases, glutamate oxaloacetate and glutamate pyruvate transaminases in liver, kidney and spleen tissues of the carcinogen fed mice. The microdoses of Chelidonium having no visible ill effects of their own, may be strong candidates for use in delaying/protecting liver cancer.

Determinação de metais presentes em corantes e pigmentos utilizados em embalagens para alimentos / Determination of metals present in dyes and pigments used in food packaging

Entre os aditivos presentes na formulação de embalagens para alimentos, principalmente embalagens plásticas, incluem-se as substâncias que conferem coloração, classificadas como corantes ou pigmentos, dependendo de sua solubilidade ou não no polímero. Sua adição em materiais para embalagens satisfaz uma exigência estética e tecnológica. Os metais que podem estar presentes como contaminantes das substâncias corantes e portanto nas embalagens, podem migrar para o alimento, apresentando riscos à saúde. O objetivo deste trabalho foi verificar e monitorar os teores de chumbo, cádmio e zinco nestes produtos, e validar a metodologia analítica segundo os Regulamentos Técnicos do Mercosul (Resolução nº 105/99 da ANVISA/MS). A quantificação destes metais foi feita por espectrofotometria de absorção atômica com chama. Das 407 amostras analisadas 5% estavam em desacordo com os limites estipulados pela legislação vigente. Os altos teores de metais nelas encontrados justificam o controle contínuo que deve ser feito sobre estes produtos

Toxicidad en dosis repetidas del Oncidium luridum Lindl / Toxicity by repeated doses of Oncidium luridum Lindl

Se realizó un estudio de toxicidad subcrónica en ratas Wistar mediante la administración oral de una tintura de orquídea silvestre. La experiencia duró 45 días; se realizó examen físico diario individual y se controló semanalmente el consumo de agua, alimentos y peso corporal. Se midieron algunas variables sanguíneas al inicio de la experiencia y final de ésta que nos sirvieron como marcadores fisiológicos de órganos y sistemas. Se realizó necropsia a todos los animales, tomando muestras de los principales órganos para su histología. Durante la evolución no se apreciaron signos de intoxicación. Se observó disminución de la variable hemoglobina y aumento de los niveles de glucosa en sangre en todos los grupos, lo cual consideramos que no guarda relación con el producto. Además, se observó que el nivel de colesterol se mantuvo elevado en los grupos controles, no sucedió así con los grupos experimentales. La histología no arrojó lesiones tóxicas

Sublethal effects of textile dye stuff effluent on selected oxidative enzymes and tissue respiration of Cyprinus carpio (Linn.).

Toxic effects of sublethal concentration of dye stuff effluent on succinic dehydrogenase (SDH) and lactic dehydrogenase (LDH) activities and tissue respiration were studied in C. carpio. While the sublethal exposure significantly reduced SDH activity and tissue respiration, LDH activity increased in gill, brain, liver, muscle and kidney. The maximum inhibition of SDH activity (74%) was recorded in gill and the minimum (38%) in liver. The percentage reduction of oxygen consumption in the tested tissues was in the order of gill greater than brain greater than liver greater than muscle greater than kidney. The muscle showed the highest level (96%) of increase in LDH activity whereas the kidney cells showed the minimum increase. Exposure to sublethal concentration suppressed the aerobic respiration and triggered the anaerobic respiration.