In vitro cytotoxicity assay of Fucoidan extracted from Turbinaria conoides against cancer cell lines MCF7, A549, and normal cell line L929

Abstract The main aim of the study is to quantify the cytotoxic property of the Fucoidan extracted from the Turbinaria conoides using the MTT assay with the standard fucose. Fucoidan was extracted using the soaked water method and it was determined using the HPLC procedure the obtained Test sample Fucoidan extracted from the Turbinaria conoides and standard fucose was subjected to the cytotoxicity assay against the MCF7 Human breast cancer cell line, A549 lung cancer cell line, and L929 normal mouse fibroblast cell line. From the results it was found that the Test sample showed good IC50 value for MCF7 cell line then A549 with an increasing concentration 24 hours incubation at 37°C The IC50 for MCF7 was 115.21 µg/ml and A549 396.46µg/ml and the Fucoidan extract was checked for its cytotoxicity against the normal mouse fibroblast cell line L929, Fucoidan was found non-lethal to the L929 mouse fibroblast normal cell line. Standard fucose also gave a significant result towards MCF7 and against the L929. This indicates that the Fucoidan extracted from Tubinaria conoides shows better anticancer potential in it. Hence its application can be further extended in the pharmacological fields.

Antioxidant and cytotoxic properties of protein hydrolysates obtained from enzymatic hydrolysis of Klunzinger's mullet (Liza klunzingeri) muscle

Today, consumers are looking for functional foods that promote health and prevent certain diseases in addition to provide nutritional requirements. This study aimed to evaluate the antioxidant and cytotoxic properties of Liza klunzingeri protein hydrolysates. Fish protein hydrolysates (FPHs) were prepared from L. klunzingeri muscle using enzymatic hydrolysis with papain at enzyme/substrate ratios of 1:25 and 1:50 for 45, 90 and 180 min. The antioxidant activities of the FPHs were investigated through five antioxidant assays. The cytotoxic effects on 4T1 carcinoma cell line were also evaluated. The amino acid composition and molecular weight distribution of the hydrolysate with the highest antioxidant activity were determined by HPLC. All six FPHs exhibited good scavenging activity on ABTS (IC50=0.60-0.12 mg/mL), DPPH (IC50= 3.18-2.08 mg/mL), and hydroxyl (IC50=4.13-2.07 mg/mL) radicals. They also showed moderate Fe+2 chelating capacity (IC50=2.12-12.60 mg/mL) and relatively poor ferric reducing activity (absorbance at 70 nm= 0.01-0.15, 5 mg/mL). In addition, all hydrolysates showed cytotoxic activities against the 4T1 cells (IC50=1.62-2.61 mg/mL). 94.6% of peptide in hydrolysate with the highest antioxidant activity had molecular weight less than 1,000 Da. L. klunzingeri protein hydrolysates show significant antioxidant and anticancer activities in vitro and are suggested to be used in animal studies.

Larvicidal, cytotoxic and genotoxic effects of aqueous leaf extract ofJatropha mollissima (Pohl) Baill / Efeitos larvicida, citotóxico e genotóxico do extrato aquoso das folhas de Jatrophamollissima (Pohl) Baill

The present study aimed to evaluate the larvicidal effect of aqueous leaf extract fromJatropha mollissima on the larvae of Aedes aegypti and analyze its cytotoxic and genotoxic activity in the Alliumcepa test. Larvae of the mosquito were exposed to the negative and positive controls (distilled water anddiflubenzuron, 0.003 mg mL-1, respectively) and to leaf extract concentrations of 0.001, 0.005, 0.01, 0.02,0.04, 0.06, 0.08 and 0.1 mg mL-1. The mortality rate was evaluated every 24 hours over five days. For thecytotoxic and genotoxic analyses, roots of A. cepa were exposed to the negative (distilled water) and positivecontrol (trifluralin, 0.84 ppm) and to different leaf extract concentrations (0.01, 0.1, 1 and 10 mg mL-1) for24 hours. The statistical analyses were performed by Kruskal-Wallis test (p < 0.05). The leaf extractpresented promising larvicidal activity at the concentrations of 0.08 and 0.1 mg mL-1, and none of theconcentrations evaluated in A. cepa exhibited cytotoxic or genotoxic effect. Since the larvicidal action of J.mollissima and the absence of cellular toxicity have been demonstrated, further studies are recommended todetermine the mechanism of action of the extract as a possible natural larvicide.

O presente estudo teve como objetivo avaliar o efeito larvicida do extrato aquoso das folhas deJatropha mollissima sobre as larvas de Aedes aegypti e analisar sua atividade citotóxica e genotóxica no testeAllium cepa. As larvas do mosquito foram expostas aos controles negativo e positivo (água destilada ediflubenzuron, 0,003 mg mL-1, respectivamente) e ao extrato foliar nas concentrações de 0,001; 0,005; 0,01;0,02; 0,04; 0,06; 0,08 e 0,1 mg mL-1. A taxa de mortalidade foi avaliada a cada 24horas durante cinco dias.Para as análises citotóxica e genotóxica, as raízes de A. cepa foram expostas ao controle negativo (águadestilada) e positivo (trifluralina, 0,84 ppm) e nas concentrações (0,01; 0,1; 1 e 10 mg mL-1) do extrato foliarpor 24 horas. Análises estatísticas foram realizadas pelo teste de Kruskal-Wallis (p < 0,05). O extrato foliarapresentou atividade larvicida promissora nas concentrações de 0,08 e 0,1 mg mL-1, e nenhuma dasconcentrações avaliadas em A. cepa exibiu efeito citotóxico ou genotóxico. Uma vez demonstrada a açãolarvicida de J. mollissima e a ausência de toxicidade celular, mais estudos são recomendados para determinaro mecanismo de ação do extrato como um possível larvicida natural.

Synthesis and evaluation of platinum complexes with potential antitumor activity

Abstract A novel series of platinum (II) complexes was synthesized and the complexes were evaluated for their in vitro cytotoxicity against four human cancer cells lines. Five platinum complexes showed activity against at least one tumor cell line. Complexes 3 and 6 were promising, being active, at micromolar concentrations, against all the assayed tumor cell lines. Compound 3 was selected for further studies in mice with Ehrlich solid tumors and it was able to reduce the rate of tumor growth significantly during the first seven days. However, at the end of the experiments, there was no significant difference between the group of animals treated with 3 and the control group. The low solubility of the compound in the assay conditions can explain, at least in part, these results.

Evaluation of cytotoxic potential of latex of Calotropis procera and Podophyllotoxin in Allum cepa root model

In the present study we have utilized the Allium cepa root tip meristem model to evaluate the cytotoxic and anti-mitotic activities of latex of Calotropis procera (DL) and podophyllotoxin. Standard cyto-toxic drug cyclophosphamide and non-cytotoxic drugs cyproheptadine and aspirin served as controls. Like cyclophosphamide, both DL and podophyllotoxin significantly inhibited the growth of roots and mitotic activity in a dose-dependent manner. However, podophyllotoxin was more potent in this regard and produced root decay. Cyproheptadine and aspirin, on the other hand, showed a marginal effect on the root growth and mitotic activity at much higher concentrations

Anthrax: pathological aspects in autopsy cases in Shiraz, Islamic Republic of Iran, 1960-2001

Anthrax, like tuberculosis, shows a new epidemic spread in industrialized countries, revealing some ambiguous aspects to the disease and providing new challenges to medicine. Shiraz University of Medical Sciences has records of 7130 autopsies performed in the past 40 years, 33 of which are anthrax cases. We reviewed all the pathology slides of these cases and classified the organs involved in a search for unrecognized microscopic findings. The most common cause of death was sepsis, caused by organ involvement and direct cytotoxicity of Bacillus anthracis, in addition to its exotoxin production. Novel findings included hyaline membrane formation in respiratory system cases that is similar to acute [adult] respiratory distress syndrome and evidence of primary gastrointestinal involvement, showing the ability of the organism to pass the gastric barrier

Estudo citogenético in vivo e in vitro do efeito do fator citotóxico necrosante (CNF) de E. coli / Cytogenetic study in vivo and in vitro the effect of cytotoxic necrotizing factor (CNF) E. coli

Para testar o efeito clastogênico, aneugênico e tóxico do CNF (cytotoxic necrotizing factor) de E. coli foram realizados estudos citogenéticos em dois sistemas: in vivo, utilizando-se células de medula óssea de camundongos e in vitro, em cultura temporária de linfócitos humanos. Quarenta e oito animais foram utilizados para o estudo in vivo. Quatro grupos de doze animais foram submetidos a quatro tratamentos diferentes: o grupo CSM (controle com manipulaçao) nao recebeu extrato sonicado de E. coli, linhagem C-600, que nao produz o fator tóxico CNF, considerado controle negativo. O grupo T+ recebeu extrato sonicado contendo a toxina positiva de E. coli ISS-51, na menor diluiçao, enquanto o grupo T++ recebeu a mesma toxina na maior diluiçao. No sistema in vitro cinco doadores foram utilizados. Três amostras de cada indivíduo foram submetidas aos três tratamentos: CSM, CCM e T+. Preparaçoes citológicas para os estudos citogenéticos foram montadas para análise microscópica de: falhas ou "gaps", aberraçoes cromossômicas, índice mitótico e eritróticos micronucleares...