scholarly journals Analysis of organochlorine DDT residue along with its metabolites in dry fishes from some selected markets of Dhaka city

2021 ◽  
Vol 5 (2) ◽  
pp. 79-84
Author(s):  
M Amin Uddin ◽  
Md Abdur Rahman ◽  
M Alamgir Zaman Chowdhury ◽  
Md Harunur Rashid ◽  
Zeenath Fardous ◽  
...  

A study was investigated to estimate the current status of health hazardous organochlorine insecticide DDT and its metabolites DDE and DDD in different species of dry fish. To achieve the goal of this experiment, ten different sun-dried fish samples were collected from different markets of Dhaka city. The concentration of DDT, DDE and DDD was determined using the capillary column coupled to Gas Chromatograph with Electron Captured Detector (GC-ECD). Most of the dry fishes, seven out of ten samples, were found to be contaminated with DDT along with its metabolites DDE and DDD ranging from 0.029-1.22 mg/kg which is a serious concern because of the nature of long persistency and bioaccumulation of DDT in the environment. The highest concentration of DDT (1.22 mg/kg) was observed in Pampus chinensis dry fish whereas low concentration was detected in Otolithoides pama (0.029 mg/kg). Asian Australas. J. Food Saf. Secur. 2021, 5 (2), 79-84

2017 ◽  
Vol 1 ◽  
pp. 264
Author(s):  
Md Didarul Islam ◽  
Ashiqur Rahaman ◽  
Fahmida Jannat

This study was based on to determine the concentration of macro and micro nutrients as well as toxic and nontoxic heavy metals present in the chicken feed available in Dhaka city of Bangladesh. All macro nutrients, if present in the feed at high concentration have some adverse effect, at the same time if this nutrient present in the feed at low concentration this have some adverse effect too. So that this nutrient level should be maintained at a marginal level. On the other side toxic heavy metals if present in the feed at very low concentration those can contaminate the total environment of the ecosystem. In this study six brand samples (starter, grower, finisher and layer) which was collected from different renowned chicken feed formulation industry in Bangladesh. Those samples were prepared for analysis by wet ashing and then metals were determined by Atomic Absorption Spectroscopy. It was found that 27.7 to 68.4, 57.3 to 121.9, 0.21 to 4.1, 0.32 to 2.1, 0.11 to 1.58, 0.28 to 2.11 and 0.28 to 1.78 for zinc, iron, copper, mercury, cadmium, nickel and cobalt respectively. It was found that essential macro and micro nutrients were present in the feed in low concentration on the other side mercury was present in high concentration in the feed samples.


2016 ◽  
Vol 44 (1) ◽  
pp. 1-8
Author(s):  
Maria Zaman ◽  
Nasim Sultana ◽  
Mozaffar Husain ◽  
M Niamul Naser

Pesticide residues, specially the persistent organic pollutant (POP) were analyzed from some fish species of Rangpur floodplain, Bangladesh. Fish samples were extracted with ethyl acetate, cleaned by sulphuric acid and analyzed by gas chromatograph and gas chromatograph-mass spectrometer. Presence of endrin was detected in Taki fish (Channa punctatus) samples. Traces of other pesticides were also evident. This confirms the use of banned pesticide in the northwestern Bangladesh. We discussed some consequences of public health issues if these contaminantspasses through in the higher food chain from the wetland ecosystem.Bangladesh J. Zool. 44(1): 1-8, 2016


Author(s):  
G.P. Morie ◽  
C.H. Sloan

AbstractA gas chromatographic method was developed for the determination of N-nitrosodimethylamine (NDMA) in cigarette smoke. The NDMA in the smoke of 200 cigarettes was trapped in a solution of sodium hydroxide and separated from most of the smoke components by distillation from acidic and basic solutions. The aqueous solution was extracted for 8 hr. into ethyl ether in a Dean Stark apparatus. To concentrate the solution of NDMA, the ether was distilled until only 5 ml of the solution remained. An aliquot of this solution was analysed by means of a gas chromatograph equipped with a 200-ft. glass capillary column coated with Carbowax 20-M poly(ethylene glycoI). An alkali metal flame ionization detector with a selectivity of 10*/1 for nitrogen compounds to normal hydrocarbons was used. Small amounts (2 ng) of nitrosamines in the presence of large amounts of other compounds were easily detected. N-nitrosodimethylamine-C


2020 ◽  
Vol 5 (1) ◽  
pp. 28-40
Author(s):  
Walter C. John ◽  
Binta A. Buba ◽  
Timothy T. Ayisa ◽  
Olusolape Oke ◽  
Temitope A. Ihum ◽  
...  

Purpose: This research was conducted to determine the occurrence of aflatoxin producing fungi in smoke-dried fish in Bida.Methodology: The study was carried out at the Microbiology Laboratory Federal Polytechnic, Bida, Niger state. Smoke dried fish samples were collected randomly from three major markets in Bida town. Fungi isolation was done after serial dilution using Potato dextrose agar. Total fungal load per sample was obtained from plate counts and expressed as colony-forming units per gram (cfu/g). The isolates were identified microscopically using Lactophenol cotton blue stain. Aflatoxigenicity text was done using coconut extract agar and exposed to 365 nm ultra violet light. Data collected were analysed by one-way analysis of variance (ANOVA) at P < 0.05.Findings: The results showed maximum mean fungal load of smoke-dried fish of 9.54x105±1.83x106 cfu/g. Fungi associated with the smoked dried fish belong to five genera: Aspergillus, Penicillium, Candida, Acremonium and Rhizopus. Comparatively, the assessment showed that smoke-dried fish from old market were the most contaminated followed by samples from small market and modern markets. Aspergillus flavus had the highest prevalence of 32.88 %. Only strains of Aspergillus flavus gave positive to aflatoxins, out of the 24 Aspergillus flavus studied, only 25 % were positive to aflatoxins. Old market exhibited the highest of aflatoxin producing fungi.Unique contribution to theory, practice and policy: In view of this results, there is need to adopt hygienic practices during smoke dried fish processing and storage in Bida to avoid increase risk of aflatoxin poisoning.


1983 ◽  
Vol 66 (6) ◽  
pp. 1443-1446
Author(s):  
Ray H Liu ◽  
Warren W Ku ◽  
Mary P Fitzgerald

Abstract A gas chromatograph-mass spectrometer-data system equipped with a capillary column is used to analyze commonly abused amine drug mixtures. Enantiomeric amines are analyzed as N-trifluoroacetyl- I-prolyl chloride derivatives. The 10 compounds included in this study are amphetamine, methamphetamine, norephedrine, ephedrine, 3,-4-methylenedioxyamphetamine, N,N-dimethyltryptamine, N,N-diethyltryptamine, N,N-dimethyl-5-methoxytryptamine, mescaline, and caffeine. All compounds, including possible enantiomers, are resolved and identified by the described method.


1984 ◽  
Vol 30 (10) ◽  
pp. 1672-1674 ◽  
Author(s):  
N B Smith

Abstract In this method for detection and quantification of volatile alcohols by capillary gas chromatography, the serum sample is deproteinized, then directly injected into the gas chromatograph with 1-propanol as the internal standard. The capillary column is a 30-m bonded methylsilicone-coated, fused-silica column. With helium as the carrier gas, the injector inlet is set at a split ratio of 1/30 and the average linear velocity in the column is 25 cm/s. Injector and flame-ionization detector temperatures are 280 degrees C, oven temperature 35 degrees C. Chromatography time is less than 3 min.


2008 ◽  
Vol 62 (2) ◽  
Author(s):  
Žofia Krkošová ◽  
Róbert Kubinec ◽  
Helena Jurdáková ◽  
Jaroslav Blaško ◽  
Ivan Ostrovský ◽  
...  

AbstractAn overview of the existing methods for minimization of the analysis time in gas chromatography (GC) is presented and a new system for fast temperature programming and very fast cooling down is evaluated. In this study, a system of coaxial tubes, a heating/cooling module (HC-M), was developed and studied with a capillary column placed inside the HC-M. The module itself was heated by a GC oven and cooled down by an external cooling medium. The HC-M was heated at rates of up to 330 °C min−1 and cooled at the rate of 6000 °C min−1. The GC system was prepared for the next run within a few seconds. The HC-M permits good separation reproducibility, comparable with that of a conventional GC, expressed in terms of relative retention times and peak areas of analytes reproducibilities. The HC-M can be used within any commercial gas chromatograph.


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