Jasbir Singh Bedi

Determination of Organochlorine Pesticide Residues in Freshwater Fish Species in Punjab, India

The levels of organochlorine pesticides residues were determined in five freshwater fish species in Punjab State, India. These species were selected in view of their importance to local human fish consumer. DDTs were the predominant organochlorine contaminants in all species with pp DDT and pp DDE as the main pollutants. Other organochlorines, such as HCH isomers and dieldrin were also found at lower levels in fish species. The α-HCH was the dominant isomer of HCH in all fish species followed by γ-, β- and δ-HCH. The residues of aldrin, chlordane, heptachlor and endosulphan were not detected in any fish sample. The levels of organochlorines detected in present study were below the tolerance limits recommended at National and International standards.

Electrospinning of poly(methyl methacrylate) nanofibers in a pump-free process

Abstract The effects of processing parameters, including solution concentration, viscosity, nozzle diameter, voltage bias and the nozzle to collector distance, on the morphology and diameters of poly(methyl methacrylate) (PMMA) fibers have been systematically investigated, using a unique pump-free electrospinning method. For PMMA solution concentrations less than the critical entanglement concentration, ce, prolate spheroid-shaped droplets or beads with fibers were formed, whereas at concentrations above ce, good quality bead-free fibers were formed. Quantitative analysis revealed a linear dependence between the solution viscosity and fiber diameter. Larger fiber diameters were achieved by increasing the nozzle diameter and voltage bias. Increasing the bias voltage has the additional effect of broadening the diameter distribution, as a result of splaying and splitting. By contrast, when the strength of the electrical field was reduced by increasing the distance between the nozzle and collector, the overall fiber diameter was reduced.

Emerging issue of antibiotic resistance from food producing animals in India: Perspective and legal framework

ABSTRACT Intensification of the animal husbandry sector in India has coincided with increased administration of antibiotics in food-producing animals for the treatment and prevention of diseases or to promote growth and enhance productivity. Antibiotics are an important tool for the livestock sector to meet the increased domestic demand of food for the burgeoning human population. The irrational use of antibiotics in food-producing animals has resulted in the occurrence of the residues in milk, meat, eggs, etc., and may lead to adverse health effects in consumers. Also there is growing concern that nonprudent use of antibiotics is linked with the escalating emergence of human infections with antibiotic-resistant pathogens of zoonotic importance. Regulations controlling the use of antibiotics in human and animal medicine in India are very weak and in its initial phases. The aim of this review is to investigate the Indian scenario with regards to the occurrence of antibiotics residues and emergence of antibiotic-resistant pathogens from foods of animal origin. Studies conducted in various parts of the country revealed varying concentrations of antibiotic residues and varying occurrence of antibiotic-resistant pathogens in animal-originated foods highlighting the need of effective control strategies for combating this potentially serious problem.

In utero exposure of neonatal buffalo calves to pesticide residues and the alterations within their reproductive tract.

In utero exposure of neonates to pesticide residues could be damaging to the reproductive tract. Hence, the present study assessed the circulating concentrations of pesticide residues in buffalo and their neonatal calves as well as in the reproductive tract tissue samples of same calves. Also, histopathological alterations were revealed in the reproductive tract of calves. Pesticide residues were high (P<0.05) in the reproductive tract of calves (119.5 ± 20.2 ng/g, 35% positive) in comparison to their blood (32.1 ± 8.4 ng/ml, 15% positive) or blood of their dams (41.5 ± 8.3 ng/ml, 25% positive). The number of histopathological alterations were high (P<0.05) in the reproductive tract of a calf contaminated with high concentrations of pesticide residues (3.43 ± 1.29) in comparison to a tract positive for low residue concentrations (1.57 ± 0.60) or pesticide negative tract (0.28 ± 0.10). In conclusion, in utero exposure of neonatal buffalo calves to pesticide residues may be associated with damaging alterations in their reproductive tract.

Sensorial and physicochemical analysis of Indian honeys for assessment of quality and floral origins

In the present study, sensory and physicochemical properties of raw honey samples originating from different floral sources of India were investigated. Sensory analysis was carried out by quantitative descriptive analysis method. Samples having higher scores for flowery aroma, amber colour together with less crystallization were perceived to be more desirable with greater acceptability. The values obtained for electrical conductivity (0.28-1.0 mS/cm), moisture content (18.37-22%), HMF content (3.65-23.16 mg/kg), free acidity (14.83-40.17 meq/kg), pH (3.81-4.85), ash (0.08-0.49%), specific gravity (1.39-1.42 g/cm2), total reducing sugars (64.91-71.39%) and protein content (0.16-0.70%) were within the criteria set by International regulations of quality. To classify and differentiate unifloral honeys originating from nine botanical origins, the data matrix was also subjected to principal component analysis. The overall results revealed that both the sensory and physicochemical properties of honey can be used as indicators not only of quality but also of origin.

Persistent organic pollutants (POPs) in fresh water farm fish species from Punjab (India) and evaluation of their dietary intake for human risk assessment

ABSTRACT In India, persistent organic pollutants (POPs) have been used extensively in both agricultural and industrial sectors, resulting in deterioration of terrestrial and aquatic environment. In the present study, analysis of POPs in fresh water ecosystem comprising samples of fish, sediments, and water was done from fish farms in Punjab, India. POP residues comprising lindane, p,p’-DDE, p,p’-DDD, endosulfan sulfate, and polychlorinated biphenyl (PCB) congeners (PCB-28, PCB-138, PCB-180) were detected in fish samples. Residues of p,p’ DDE and p,p’ DDD were recorded utmost in fish flesh with mean levels of 13.8 and 5.8 ng g−1, respectively. PCB residues were estimated in 20 fish samples with values in the range ND–46.3 ng g−1. The mean residue levels detected in this study were lower than the recommended maximum residue limits (MRLs) described by EU-MRLs, Italian-MRLs, FDA-2001, and FAO-1983. At the current levels of POP residues in fish flesh, the human health risk assessment based on both deterministic (mean residue levels) and probabilistic (95th percentile upper bound limit) approaches, reflected that cancer and non-cancer risks were within United States Environmental Protection Agency (USEPA) prescribed limits. The presence of POP residues in fish farm sediments and water elucidated the relationship between occurrence of POP residues in fish and its aquatic environment.

Validation of HPLC Multi-residue Method for Determination of Fluoroquinolones, Tetracycline, Sulphonamides and Chloramphenicol Residues in Bovine Milk

The occurrence of antibiotic residues in milk constitutes a potential risk to the health of consumers. The present study describes the optimisation and validation of a high-performance liquid chromatographic (HPLC) method for the simultaneous determination of sulphadiazine (SDZ), sulphamethoxazole (SMX), oxytetracycline (OTC), doxycycline (DOX), tetracycline (TC), enrofloxacin (ENRO) and chloramphenicol (CLP) residues in bovine milk using colchicine (COL) as internal standard. The determination of these antimicrobials was carried out on C18 analytical column using high-performance liquid chromatographic-diode array detection (HPLC-DAD). The extraction method involving deproteinisation of the milk sample followed by a solid-phase extraction (SPE) clean-up of antibiotic residues has been developed. The method was validated according to the European Commission Decision 2002/657/EC and applied for the analysis of antibiotic residues in 21 raw milk samples collected from Ludhiana, Punjab, India. The recoveries for the studied antibiotics ranged from 83.3–111.8% with relative standard deviations between 3.5 and 16.2%. The limits of quantification for these antibiotics, with the exception of chloramphenicol, were below the maximum residue limits (MRLs), making the method suitable for performing routine analysis.