O impacto dos aditivos do tabaco na toxicidade da fumaça do cigarro: uma avaliação crítica dos estudos patrocinados pela indústria do fumo / El impacto de los aditivos del tabaco en la toxicidad del humo del cigarrillo: una evaluación crítica de los estudios de la industria del tabaco / The impact of tobacco additives on cigarette smoke toxicity: a critical appraisal of tobacco industry studies

Resumo: A produção de cigarros envolve uma série de substâncias e materiais além do próprio tabaco, do papel e do filtro. Os aditivos do tabaco incluem conservantes, flavorizantes, intensificadores, umectantes, açúcares e compostos de amônio. Embora as empresas produtoras de tabaco aleguem que os aditivos não aumentam a toxicidade da fumaça e não tornam os cigarros mais atraentes ou viciantes, tais alegações são contestadas por pesquisadores independentes. Os autores realizaram uma revisão dos estudos sobre os efeitos dos aditivos sobre a composição química e toxicidade da fumaça. Os aditivos elevam os níveis de formaldeído e causam pequenas alterações nos níveis de outros analitos medidos na fumaça. Estudos toxicológicos (testes de mutagenicidade e de citotoxicidade em células de mamíferos, estudos da exposição por 90 dias por via inalatória em ratos e ensaios do micronúcleo em células da medula óssea) indicaram que os aditivos do tabaco não aumentam a toxicidade da fumaça. Entretanto, é conhecido que os estudos em roedores falham em predizer o potencial carcinogênico da fumaça do cigarro, e os testes realizados tiveram poder estatístico insuficiente para detectar diferenças pequenas, porém relevantes do ponto de vista toxicológico, entre cigarros experimentais (com aditivos) e controles (sem aditivos). Em conclusão, esta revisão da literatura mostrou que o impacto dos aditivos na toxicidade da fumaça do tabaco ainda permanece por ser esclarecido.

Resumen: La producción de cigarrillos involucra un número de sustancias y materiales diferentes al tabaco en sí, papel y filtro. Los aditivos del tabaco incluyen aromas artificiales, potenciadores del sabor, humectantes, azúcares, y compuestos de amonio. A pesar de que las compañías sostienen que los aditivos del tabaco no aumentan la toxicidad del humo y no hacen los cigarrillos más atractivos y adictivos, estas afirmaciones son cuestionadas por investigadores independientes. Este trabajo ha revisado los estudios sobre los efectos de los aditivos del tabaco en la química del humo y su toxicidad. Los aditivos del tabaco conllevan niveles más altos de formaldehído y otros cambios menores en los análisis realizados del humo. Estudios toxicológicos (tests de mutagenicidad en bacterias y citotoxicidad en mamíferos, ensayos de inhalación en ratas 90 días y células del micronúcleo de la médula ósea) mostraron que los aditivos del tabaco no aumentaron la toxicidad del humo. Los ensayos de roedores, sin embargo, no predijeron adecuadamente la carcinogenicidad del humo del tabaco, y no eran claramente suficientes para dar a conocer, sin embargo, las pequeñas, pero toxicológicamente relevantes, diferencias entre el test (con/aditivos del tabaco) y control (sin/aditivos del tabaco) en cigarrillos. Esta revisión de la literatura nos lleva a la conclusión de que el impacto dañino de los aditivos del tabaco en el humo continúa estando poco claro.

Abstract: Cigarette production involves a number of substances and materials other than just tobacco, paper and a filter. Tobacco additives include flavorings, enhancers, humectants, sugars, and ammonium compounds. Although companies maintain that tobacco additives do not enhance smoke toxicity and do not make cigarettes more attractive or addictive, these claims are questioned by independent researchers. This study reviewed the studies on the effects of tobacco additives on smoke chemistry and toxicity. Tobacco additives lead to higher levels of formaldehyde and minor changes in other smoke analytes. Toxicological studies (bacterial mutagenicity and mammalian cytoxicity tests, rat 90 days inhalation studies and bone-marrow cell micronucleus assays) found that tobacco additives did not enhance smoke toxicity. Rodent assays, however, poorly predicted carcinogenicity of tobacco smoke, and were clearly underpowered to disclose small albeit toxicologically relevant differences between test (with tobacco additives) and control (without tobacco additives) cigarettes. This literature review led to the conclusion that the impact of tobacco additives on tobacco smoke harmfulness remains unclear.

Toxicity in food flavorings at the cellular level associated with each other at different doses / Toxicidade em nível celular de aromatizantes alimentares associados entre si em diferentes doses

This study aimed to examine the cytotoxicity and genotoxicity of synthetic flavorings, nature identical, Chocolate, Strawberry and Condensed Milk. This evaluation was performed in root meristem cells of Allium cepa L., in exposure times of 24 and 48 hours and using doses of 0.2; 0.4 and 0.6 mL, in combination, in which one of the three doses of a flavoring was combined with a different dose of one of the two other flavor additives studied. Roots were fixed in Carnoys solution, hydrolyzed in hydrochloric acid, stained with acetic orcein and then analyzed, under light microscopy, 5,000 cells for each treatment. For data analysis, it was used Chi-square test at 5%. All the treatments with combinations between the flavorings Chocolate/Strawberry and Strawberry/Condensed Milk reduced, in both exposure times considered, cell division of A. cepa roots, proving to be cytotoxic. In turn, the treatments with the association of Chocolate/Condensed Milk did not change significantly the mitotic index of the cells analyzed. The Strawberry flavoring was the most cytotoxic among the additives tested. None of the evaluated associations was genotoxic under the study conditions.

Objetivou-se nesta pesquisa avaliar a citoxicidade e genotoxicidade de aromatizantes alimentares sintéticos de chocolate, morango e leite condensado. Esta avaliação ocorreu por meio das células meristemáticas de raízes de A. cepa L., nos tempos de exposição de 24 e 48h e nas doses de 0,2; 0,4 e 0,6 mL, em associação, em que para uma das três doses de um dos aromatizantes associou-se uma dose diferente de um dos outros dois aditivos de aroma em estudo. Em seguida, as raízes foram fixadas em solução de Carnoy, hidrolisadas em ácido clorídrico e coradas com orceína acética. Analisaram-se, em microscópio óptico, 5.000 células para cada grupo tratamento, e utilizou-se o teste estatístico Qui-quadrado a 5% para análise dos dados. A partir dos resultados, verificou-se que todos os tratamentos decorrentes das associações entre chocolate/morango e morango/leite condensado reduziram, nos dois tempos de exposição considerados, a divisão celular das raízes A. cepa, mostrando-se citotóxicos. Já os tratamentos provenientes da associação chocolate/leite condensado não alteraram de forma significativa os índices mitóticos das células do tecido em análise. Foi possível inferir que o aditivo de morango foi o mais citotóxico dos aditivos em estudo. Nenhuma das associações avaliadas foi genotóxica nestas condições de estudo.

Occurrence of Brettanomyces/Dekkera in Brazilian red wines and its correlation with ethylphenols

The yeast Brettanomyces/Dekkeracan cause important spoilage in wines, with the production of ethylphenols and other off-flavor compounds. This study aimed at determining the presence of this yeast and the ethylphenols produced by them in Brazilian red wines, establishing their relationship with other chemical characteristics. Isolates of Brettanomyces/Dekkerawere quantified by plating 126 samples of dry red wine in selective culture medium, while ethylphenols were analyzed by solid phase extraction and GC/FID. Free and total SO2, alcohol, total dry extract, residual sugar, total and volatile acidity, and pH were also determined. Brettanomyces/Dekkerawas present in 27% of samples. Ethylphenols were detected in most samples, with amounts higher than the threshold limit of 426 mg/L found in 46.03% of samples. The majority of wine samples showed inadequate levels of SO2and residual sugars, facts that might facilitate microbial spoilage. The passage in barrels and the grape varieties (Cabernet Sauvignon and Merlot), did not show any influence on the levels of contamination or ethylphenols contents. The prevalence of Brettanomyces/Dekkeraand the concentrations of ethylphenols were high considering the sensory impact they can cause. The growth of Brettanomyces/Dekkerawas dependent on the levels of SO2and alcohol of wines. Knowledge of the contamination, the presence of ethylphenols, and their relationship with the chemical characteristics of wines can entice effective measures to prevent Brettanomyces/Dekkeraand contribute to improve the general quality of Brazilian red wines.

Excipientes de medicamentos e as informações da bula / Pharmaceutical excipients and the information on drug labels

OBJETIVO: Avaliar a presença de conservantes, corantes, adoçantes e aromatizantes em 73 apresentações farmacêuticas de 35 medicamentos para uso oral, e as informações da bula sobre excipientes. MÉTODOS: Selecionamos 35 medicamentos, de venda livre ou sob prescrição médica, comercializados no Brasil. A amostra incluiu: analgésicos/antitérmicos, antimicrobianos, mucolíticos, antitussígenos, descongestionantes, anti-histamínicos, broncodilatadores, corticosteróides, antiinflamatórios e suplementos vitamínicos. Foram analisadas 73 apresentações desses fármacos, anotando-se as informações da bula sobre conservantes, corantes, adoçantes e aromatizantes. RESULTADOS: A bula de um medicamento (1,3 por cento) não mencionava os ingredientes inativos. Os conservantes mais encontrados nos medicamentos foram metilparabeno e propilparabeno (43 por cento e 35,6 por cento respectivamente). Os adoçantes mais usados foram: sacarose (açúcar) (53,4 por cento), sacarina sódica (38,3 por cento) e sorbitol (36,9 por cento). Vinte e um produtos (28,7 por cento) continham dois adoçantes. Predominaram os medicamentos sem corante (43,8 por cento), seguidos pelos coloridos por amarelo crepúsculo (amarelo FD&C no. 6) (15 por cento). Cinco produtos (6,8 por cento) continham mais de um corante. A tartrazina (amarelo FD&C no. 5) foi encontrada em sete formulações (9,5 por cento). Os aromatizantes mais usados foram os de frutas (83 por cento). Constatamos a freqüente omissão das bulas sobre o teor exato de açúcar dos produtos (77 por cento). Duas das quatro bulas de medicamentos contendo aspartame não mencionavam as precauções no uso por fenilcetonúricos. CONCLUSÕES: A omissão e a imprecisão das informações da bula sobre os excipientes farmacêuticos expõem os indivíduos suscetíveis ao risco de reações adversas dos conservantes e corantes. Também podem ocorrer complicações do uso inadvertido de medicamentos contendo açúcar pelos pacientes diabéticos, ou de fármacos adoçados com aspartame pelos fenilcetonúricos.

AIM: to evaluate the presence of preservatives, dyes, sweeteners and flavouring substances in 73 pharmaceutical preparations of 35 medicines for oral administration, according to drug labeling information about the excipients. METHODS: 35 medications were selected, both over-the-counter and prescription durgs, marketed in Brazil. The sample included: analgesic/antipyretic, antimicrobial, mucoregulatory, cough and cold, decongestant, antihistamine, bronchodilator, corticosteroid, antiinflammatory and vitamin medications. We collected data on 73 preparations of these drugs, according to drug labeling information regarding preservatives, dyes, sweeteners and flavourings. RESULTS: Methylparaben and propylparaben were the most common preservatives found (43 percent and 35.6 percent respectively). The most common sweeteners were: sucrose (sugar) (53.4 percent), sodium saccharin (38.3 percent) and sorbitol (36.9 percent). Twenty-one medicines (28,7 percent) contained two sweeteners. Colourless medicines predominated (43.8 percent), followed by those with sunset yellow dye (FD&C yellow no. 6) (15 percent). Five products (6.8 percent) contained more than one colour agent. Tartrazine (FD&C yellow no. 5) was present in seven preparations (9.5 percent). Fruit was the most common flavouring found (83 percent). Labelings of drugs which contained sugar frequently omitted its exact concentration (77 percent). Of the four labelings of medicines which contained aspartame, two did not warn patients regarding phenylketonuria. CONCLUSION: Omission and inacuracy of drug labeling information on pharmaceutical excipients may expose susceptible individuals to adverse reactions caused by preservatives and dyes. Complications of inadvertent intake of sugar-containing medicines by diabetics, or aspartame intake by patients with phenylketonuria may also occur.

Estimation of iodine in salt fortified with iodine & iron.

BACKGROUND & OBJECTIVE: The National Institute of Nutrition (NIN), Hyderabad has developed double fortified salt (DFS) containing both iodine and iron to control the twin problems of iodine deficiency disorders (IDD) and iron deficiency anaemia (IDA). When the iodine content of DFS was estimated by the conventional iodometric titration using sulphuric acid (H(2)SO(4)), problems such as wide variation between duplicate analysis and under/overestimations of iodine content were encountered, which led to inconsistent results. This study was undertaken to develop a modified method for the estimation of iodine in DFS so as to get reliable iodine content of DFS. METHODS: A modified method was developed using orthophosphoric acid (H(3)PO(4)) and the sensitivity of the method was confirmed by estimating the iodine content of potassium iodate (KIO(3)) standard at different concentrations of iodine (0 to 100 ppm). The iodine content of DFS and iodized salt (IS) from local market and factory was estimated by the modified method as well as the conventional iodometric titration and the results were compared. RESULTS: The pH of DFS was acidic. The time gap between the additions of acid and potassium iodide (KI) played a crucial role in getting the actual iodine content of DFS. The H(2)SO(4) and ferrous sulphate (FeSO(4)) interfered with the estimation of iodine in DFS resulting in underestimation or overestimation of iodine. Modified method (H(3)PO(4)) produced consistent and reliable iodine content of DFS. Both H(2)SO(4) and H(3)PO(4) gave same results when tested with KIO(3) standard, Reference salt and IS (both experimental and purchased from local market). Actually 0.50 ml of 1 per cent KI was sufficient to estimate the iodine content of DFS or IS. INTERPRETATION & CONCLUSION: The results of the present study showed that the conventional method using H(2)SO(4) was not suitable for the estimation of iodine in DFS. The modified method using H(2)PO(4) was ideally suited for the estimation of iodine in DFS. Also, iron from DFS did not interfere during estimation of iodine by this method. As both the conventional and the modified methods gave the same results for the iodine content of IS, it is practically prudent to use the modified method (H(2)PO(4)) for both DFS and IS instead of following one method (H(3)PO(4)) for DFS and another (H(2)SO(4)) for IS. The quantity of KI is also reduced and the order of additions of reagents is changed in the modified procedure.