Quantification of oxytocin residues in dairy milk from Sindh,Pakistan

In this study, a total of 84 milk samples (60 nonbranded and 24 branded) were analysed for occurrence of oxytocin (OT) residues by ELISA. OT level was detected in the range of 39.29–456.55 pg mL^?1 with mean value of 138.53 ng L^?1. In branded milk samples, OT residues were minimal as compared to nonbranded milk samples. Nonbranded milk samples had higher prevalence of OT residues; 16.67% had OT level in the range of ≤500 ng L^?1. The average daily intake of OT was found 0.087 μg day^?1 per person. It was concluded that the OT concentration was relatively higher in samples obtained from dairy farm, dairy shop and milk man than that in ultra‐high temperature (UHT) and powder milk samples. In addition, there are no reports subjected to standardising a permissible OT level in dairy milk category, although OT is considered detrimental to both human and animal life.     

Control of milk acidity by photoluminescence

For a quality assessment of milk and dairy products, the optical methods are used. In this paper, the use possibility is investigated of the optical method of photoluminescence for the milk acidity value finding out. The spectral measurements were carried out on a diffraction spectrofluorimeter in the range of 200–500 nm. The milk acidity measurement accuracy was controlled by the titrimetric method. It is established that as far as milk sours, the excitation spectra in the range of 200–500 nm decrease; but there are qualitative changes in the range of 350–500 nm. With acidity growth, the photoluminescence flux decreases if it is excited by the radiation value λ_e = 262 nm, grows at λ_e = 385 nm and decreases at λ_e = 442 nm. It is advisable to control the milk acidity in terms of the photoluminescence fluxes ratio Φ₃₈₅/Φ₄₄₂. The linear approximation of the function Φ₃₈₅/Φ₄₄₂(K) is statistically reliable (the determination factor R² = 0.99).     

High-pressure homogenisation of raw bovine milk. Effects on fat globule size distribution and microbial inactivation

Whole raw milk was processed using a 15 L h⁻¹ homogeniser with a high-pressure (HP) valve immediately followed by a cooling heat exchanger. The influence of homogenisation pressure (100–300 MPa) and milk inlet temperature T_in (4°C, 14°C or 24°C) on milk temperature T₂ at the HP valve outlet, on fat globule size distribution and on the reduction of the endogenous flora were investigated. The T_in values of 4–24°C led to milk temperatures of 14–33°C before the HP valve, mainly because of compression heating. High T_in and/or homogenisation pressure decreased the fat globule size. At 200 MPa, the d_4.3 diameter of fat globules decreased from 3.8±0.2 (control milk) to 0.80±0.08 μm, 0.65±0.10 or 0.37±0.07 μm at T_in=4, 14°C or 24°C, respectively. A second homogenisation pass at 200 MPa (T_in=4°C, 14°C or 24°C) further decreased d_4.3 diameters to about 0.2 μm and narrowed the size distribution. At all T_in tested, an homogenisation pressure of 300 MPa induced clusters of fat globules, easily dissociated with SDS, and probably formed by sharing protein constituents adsorbed at the fat globule surface. The total endogenous flora of raw milk was reduced by more than 1 log cycle, provided homogenisation pressure was ⩾200 MPa at T_in=24°C (T₂∼60°C), 250 MPa at T_in=14°C (T₂∼62°C), or 300 MPa at T_in=4°C (T₂∼65°C). At all T_in tested, a second pass through the HP valve (200 MPa) doubled the inactivation ratio of the total flora. Microbial patterns of raw milk were also affected; Gram-negative bacteria were less resistant than Gram-positive bacteria.     

Optimisation of spray drying process parameters for low‐fat honey‐based milk powder with antioxidant activity

The purpose of this study was to optimise process parameters to prepare spray‐dried honey‐based milk powder containing functional properties of honey. Experimental design with temperature (180 to 200 °C), honey concentration (5–15%) and feed flow rate (8–10 rpm) as independent variables was studied to investigate the effect on product responses. Results showed that increasing the temperature resulted in powder with lower moisture, bulk density, antioxidant activity, total phenolic contents, total flavonoid contents and higher water solubility index. Increasing feed flow rate resulted in higher moisture, bulk density, antioxidant activity, reduced water solubility index, total phenolic content and total flavonoid content, whereas increasing honey concentration resulted in increase in antioxidant activity, total phenolic content and total flavonoid content. The moisture content, bulk density, water solubility index, DPPH scavenging activity, total phenolic content and total flavonoid content were 3.27%, 0.44 g cc^?1, 96.67 g g^?1, 17.45%, 2.54 GAE g^?1 powder and 1.40 RE g^?1 powder, respectively.     

Modification in direct analysis method: metal levels in raw milk at the region of Izmit by graphite furnace atomic absorption spectrophotometer

A simple method was developed for the determination of cadmium (Cd) and lead (Pb) in milk serum prepared by spontaneous souring, using graphite furnace atomic absorption spectrophotometry. Samples of raw milk were collected from the bulk holding tanks of thirty-six dairy farms in twelve localities in Izmit. The samples were kept at room temperature (25 °C) for 48 h in order to allow the pH to decrease below 4.6, and the casein and fat to precipitate. Milk serum was filtered and directly injected into a graphite tube. The standard addition method was employed, and 0.1% phosphoric acid was used as the matrix modifier. The mean recoveries from three added concentrations were 91.4% for Cd and 95.8% for Pb. Cadmium and Pb concentrations found in the reference standard milk powder using this method were close to the certified values. The mean Cd contents obtained from thirty-six samples were 0.257 μg L⁻¹, ranging from 0.180 to 0.398 μg L⁻¹. The mean Pb contents found were 6.83 μg L⁻¹, ranging from 5.32 to 9.94 μg L⁻¹.     

Microbiological assay with Bacillus licheniformis for the easy detection of quinolones in milk

This paper proposes a microbiological method in microtitre plates for the detection of residues of quinolones in milk. The method uses spores of Bacillus licheniformis in culture medium with a redox combination of indicators and gives a response time of 5.5 h. This method detects 92 μg L⁻¹ of ciprofloxacin, 63 μg L⁻¹ of danofloxacin, 109 μg L⁻¹ of enrofloxacin, 101 μg L⁻¹ of marbofloxacin and 109 μg L⁻¹ of sarafloxacin in milk. Therefore, the assay is easy to develop and to use in laboratory, allowing analysis of large numbers of samples at low cost. Due to its good sensitivity to quinolones, this assay can be used as a complementary test of commercial microbiological methods and thereby improve food security.     

Development of vacuum‐dried probiotic milk powder with Bacillus coagulans

The present study explored the possibilities of using Bacillus coagulans as a probiotic culture in vacuum‐dried milk powder. The operational drying temperature at 63 ± 2 °C under 0.7 kg/cm² pressure emerged as the best temperature at which to prepare dried milk powder within 4.5 h with a mean (±SEM) Bacillus coagulans B37 spore count of 8.78 ± 0.03 log cfu/g and moisture content of 4.82 ± 0.12%. The total spore counts in vacuum‐dried milk powder did not change (P > 0.10) at storage temperatures of 7 °C, 37 °C or 45 °C over a three‐month period.     

Influence of skimmed milk concentrate replacement by dry dairy products in a low fat set‐type yoghurt model system. I: Use of whey protein concentrates,milk protein concentrates and skimmed milk powder

Ten commercial samples of dry dairy products used for protein fortification in a low fat yoghurt model system at industrial scale were studied. The products employed were whey protein concentratres, milk protein concentrates, skimmed milk concentrates and skimmed milk powder which originated from different countries. The gross chemical composition of these dried products were determined, including polyacrylamide gel electrophoresis (SDS‐PAGE) and isoelectric focusing of the proteins, and minerals such as Na, Ca, K and Mg. Yoghurts were formulated using a skim milk concentrated as a milk base enriched with different dry dairy products up to a 43 g kg⁻¹ protein content. Replacement percentage of skim milk concentrated by dry dairy products in the mix was between 1.49 and 3.77%. Yoghurts enriched with milk protein concentrates did not show significantly different viscosity (35.12 Pa s) and syneresis index (591.4 g kg⁻¹) than the two control yoghurts obtained only from skimmed milk concentrates (35.6 Pa s and 565.7 g kg⁻¹) and skimmed milk powder (32.77 Pa s and 551.5 g kg⁻¹), respectively. Yoghurt fortified with the whey protein concentrates, however, was less firm (22.59 Pa s) and had less syneresis index (216 g kg⁻¹) than control yoghurts. Therefore, whey protein concentrates may be useful for drinking yoghurt production. © 1999 Society of Chemical Industry     

Impact of β-glucan on debittering,bioaccessibility and storage stability of skim milk fortified with shrimp oil nanoliposomes

Shrimp oil was encapsulated in nanoliposomes and fortified into skim milk. Shrimp oil nanoliposomes (SONL) were thermodynamically stable when added into skim milk at 10 mL 100 mL⁻¹. Mild bitterness in fortified skim milk caused by the SONL was masked by adding β-glucan at various levels (0.05–0.2 g 100 mL⁻¹). With the addition of SONL, fortified skim milk appeared more reddish in colour due to the presence of astaxanthin. Addition of β-glucan resulted in the increase in viscosity of the fortified milk by forming network of junction zones. During the storage of skim milk fortified with SONL and 0.1 g 100 mL⁻¹ β-glucan at 4 °C for 15 days, no major quality changes took place. Simulated in vitro digestion studies revealed that 45.41 g 100 g⁻¹ eicosapentaenoic acid (EPA) and 48.86 g 100 g⁻¹ docosahexaenoic acid (DHA) from shrimp oil were bioaccessible for absorption in the gut after digestion.     

Determination of Melamine in Liquid Milk and Milk Powder by Titania-Based Ligand-Exchange Hydrophilic Interaction Liquid Chromatography

A simple and rapid high-performance liquid chromatography (HPLC) procedure for the analysis of melamine in liquid milk and milk powder has been developed. Decrease of acetonitrile percentage and phosphate buffer concentration in mobile phase, and lowering of buffer pH and column temperature would benefit the retention of melamine on titania. Taking advantage of the ligand-exchange and hydrophilic interaction mixed retention mode on bare titania column, neither complex pretreatment nor ion-pair reagent was required. The whole analysis for one sample including sample pretreatment and HPLC analysis could be accomplished within 30 min. The method presented good linearity (R ² = 0.9998) in a wide range of 0.02–10 μg mL⁻¹. The limit of detection (3σ) and limit of quantification (10σ) of the method were 6 and 20 μg L⁻¹, respectively, which were equivalent to 15 and 50 μg kg⁻¹ melamine in liquid milk, 60 and 200 μg kg⁻¹ melamine in milk powder, respectively. Such sensitivity could be compared with those obtained by HPLC with solid-phase extraction or HPLC coupled with tandem mass spectrometry and was adequate for the screening of melamine in tainted dairy products. The repeatability (RSDs) of the retention times and peak areas of 11 replicate detections of 1.0 μg mL⁻¹ melamine were 0.32% and 2.5%, respectively. The intermediate precision on three consecutive days (RSDs, n = 6) of the retention times and peak areas were 1.1% and 2.3%, respectively. The recovery of spiked melamine in dairy samples ranged from 95.2% to 105%. The simplicity, sensitivity and rapidity of the proposed method make it an effective alternative detecting technique for melamine.     

Selenium supplementation of diets of dairy cows to produce Se-enriched cheese

Selenium (Se) deficiency in people and animals is a nutritional problem in many regions of the world. Ten mid-lactation Estonian Red dairy cows were supplemented for 64 days with inorganic Se [0.39 mg kg⁻¹ in total mixed ration (TMR)] followed by a 57-day period of supplementation with organic and inorganic Se (0.44 mg kg⁻¹ in TMR), according to EU directives on maximum allowed amounts. Feeding organic Se increased Se content in blood (from 186.5 to 287.9 μg kg⁻¹), milk (from 17.1 to 51.8 μg kg⁻¹) and Edam-type cheese made there from (from 146 to 361 μg kg⁻¹). Se content in milk after supplementation was high enough to produce a cheese enabling the nutrition claim “high in Se” and related health claims. The concentration of the main primary oxidation products of linoleic acid (oxylipins) was low and leukotoxin diols were found in trace amounts; the oxidative stability of cheeses was high.     

Dietary fibre extracted from different types of whole grains and beans: a comparative study

Dietary fibre (DF) from different whole grains and beans (quinoa, buckwheat, highland barley, pea and mung bean) was extracted by enzymatic action. The components, crystallinity and properties were comparatively studied. Furthermore, we evaluated correlations between DF components and their crystallinity, thermal, physicochemical and functional properties. Results showed quinoa DF had highest polyphenol (25.58 mg GAE per 100 g), pectin (4.68%) and cellulose (52.34%) contents, crystallinity value (CV, 30.24%), ΔH (185.53 J g⁻¹), water-holding capacity (WHC, 5.35 g g⁻¹), α-amylase activity inhibition ratio (α-AAIR, 13.34%) and glucose absorption capacity (GAC), but lowest protein content (9.78%) and T_p (163.05 °C). Mung bean DF had highest lignin content (33.56%), fat adsorption capacity (4.73 g g⁻¹), and T_p (176.25 °C), but lowest CV (15.26%) and ΔH (132.15 J g⁻¹). Correlation analysis showed cellulose content had positive linear correlations with CV, ΔH, WHC, α-AAIR and GAC, but a negative correlation with T_p. The structure and properties of DF are largely attributed to cellulose content.     

Immunomodulatory activities of Lactobacillus rhamnosus ZDY114 and donkey milk in BALB/c mice

The immunomodulatory activity of Lactobacillus rhamnosus ZDY114 and donkey milk in BALB/c mice was evaluated by assessing the splenic lymphocyte transformation, haemolytic complement activity, carbon clearance ability and natural killer cell activity. Results showed donkey milk (5 g kg⁻¹) in combination with L. rhamnosus ZDY114 (5 × 10⁷ cfu mL⁻¹) exhibited a significant increase in splenic lymphocyte proliferation, carbon granule engulfing ability and natural killer cell activity when compared with donkey milk or L. rhamnosus ZDY114 alone (p < 0.05). An elevated response in serum haemolytic activity was only observed when compared with L. rhamnosus ZDY114. In conclusion, donkey milk (5 g kg⁻¹) in combination with L. rhamnosus ZDY114 (5 × 10⁷ cfu mL⁻¹) was able to enhance specific immune functions.     

Predicting cutting and clotting time of coagulating goat's milk using diffuse reflectance: effect of pH,temperature and enzyme concentration

A diffuse reflectance sensor, which used optical fibres and near-infrared radiation (NIR) at 880 nm, was used to monitor goat's milk coagulation. A randomised block design replicated three times was utilized to test the effects of pH, temperature and enzyme concentration on diffuse reflectance parameters. Milk pH was adjusted to three levels (5.5, 6.0 and 6.5) and coagulated at three different temperatures (28, 32 and 36°C), using three enzyme concentrations (0.020, 0.035 and 0.050 mL kg⁻¹ of milk). A linear cutting time prediction equation, T_cut=βT_max, was found to predict visual cutting time with a standard error of prediction of 84.5 s and an R² of 0.9785. β was affected by pH, temperature and enzyme concentration. The diffuse reflectance parameter (T_max) was strongly correlated to the Berridge clotting time (R²=0.9913). Parameters generated from the diffuse reflectance profiles, with the exception of response-based parameters, were found to be a function of coagulation rate.     

Equivalent processing for pasteurization of a pineapple juice–coconut milk blend by selected nonthermal technologies

Identifying equivalent processing conditions is critical for the relevant comparison of food quality attributes. This study investigates equivalent processes for at least 5-log reduction of Escherichia coli and Listeria innocua in pineapple juice–coconut milk (PC) blends by high-pressure processing (HPP), pulsed electric fields (PEF), and ultrasound (US) either alone or combined with other preservation factors (pH, nisin, and/or heat). The two blends (pH 4 and 5) and coconut milk (pH 7) as a reference were subjected to HPP at 300–600 MPa, 20°C for 0.5–30 min; PEF at an electric field strength of 10–21 kV/cm, 40°C for 24 µs; and US at 120 µm amplitude, 25 or 45°C for 6 or 10 min. At least a 5-log reduction of E. coli was achieved at pH 4 by HPP at 400 MPa, 20°C for 1 min; PEF at 21 kV/cm, 235 Hz, 40°C for 24 µs; and US at 120 µm, 45°C for 6 min. As L. innocua showed greater resistance, a synergistic lethal effect was provided at pH 4 by HPP with 75 ppm nisin at 600 MPa, 20°C for 5 min; PEF with 50 ppm nisin at 18 kV/cm, 588 Hz, 40°C for 24 µs; and US at 45°C, 120 µm for 10 min. The total soluble solids (11.2–12.4°Bx), acidity (0.47%–0.51% citric acid), pH (3.91–4.16), and viscosity (3.55 × 10⁻³–4.0 × 10⁻³ Pa s) were not significantly affected under the identified equivalent conditions. HPP was superior to PEF and US, achieving higher ascorbic acid retention and lower color difference in PC blend compared to the untreated sample.     

Alkaline phosphatase and microbial inactivation by pulsed electric field in bovine milk

The effects of pulsed electric field (PEF) treatments at field intensities of 25–37 kV cm^− 1 and final PEF treatment temperatures of 15 °C and 60 °C on the inactivation of alkaline phosphatase (ALP), Total Plate Count (TPC), Pseudomonas and Enterobacteriaceae counts were determined in raw skim milk. At 15 °C, PEF treatments of 28 to 37 kV cm^− 1 resulted in 24–42% inactivation in ALP activity and < 1 log reduction in TPC and Pseudomonas count, while the Enterobacteriaceae count was reduced by at least 2.1 log units to below the detection limit of 1 CFU mL^− 1. PEF treatments of 25 to 35 kV cm^− 1 at 60 °C resulted in 29–67% inactivation in ALP activity and up to 2.4 log reduction in TPC, while the Pseudomonas and Enterobacteriaceae counts were reduced by at least 5.9 and 2.1 logs, respectively, to below the detection limit of 1 CFU mL^− 1. Kinetic studies suggested that the effect of field intensity on ALP inactivation at the final PEF treatment temperature of 60 °C was more than twice that at 15 °C. A combined effect was observed between the field intensity and temperature in the inactivation of both ALP enzyme and the natural microbial flora in raw skim milk.Industrial relevanceMilk has been pasteurised to ensure its safety and extend its shelf life. However, the need for retaining heat-sensitive nutrient and sensory properties of milk has resulted in interest in the application of alternative technologies. The results of the current study suggest that PEF as a non-thermal process can be employed for the treatment of raw milk in mild temperature to achieve adequate safety and shelf life while preserving the heat-sensitive enzymes, nutrients and bioactive compounds.     

Determination of the survival kinetics of Salmonella spp. on the surface of ripened raw milk cheese during storage at different temperatures

The aim of this study was to determine the survival kinetics of Salmonella enterica subsp. enterica in ripened raw milk cheese. Cheese samples inoculated with S. enterica subsp. enterica were stored at 5, 15 and 25 °C and analysed in terms of physico-chemical and microbiological characteristics. Three primary models were used to estimate the kinetic parameters of S. enterica subsp. enterica. The secondary Arrhenius model was used to establish the relationship between temperature and parameter α of the Weibull model. Additionally, prediction of S. enterica subsp. enterica survival as a function of storage temperature was made. S. enterica subsp. enterica growth was inhibited during storage, and bacteria survived for an extensive period of time at high number (60 day at 5 °C, 26 day at 25 °C). The storage temperature significantly influenced the inactivation rate of Salmonella in raw milk ripened cheese and proceeded faster at 25 °C compared to remaining storage temperature. Obtained results suggest that contamination by Salmonella in raw milk cheese might result in residual risk.     

Effects of intraruminal infusions of propionate and butyrate with two different protein supplements on milk production and blood metabolites in dairy cows receiving grass silage-based diet

Four cows were used in a balanced 4×4 Latin square with 2 week experimental periods to investigate the effects of intraruminal infusions of volatile fatty acids and protein source on milk production and blood metabolites. The four treatments in a 2×2 factorial arrangement were isoenergetic intraruminal infusions of propionate (500 g day⁻¹) or butyrate (417 g day⁻¹) each given with isonitrogenous protein supplementation of fish meal (FM) or barley protein (BP). The cows were fed restrictively with 9 kg dry matter day⁻¹ of formic acid treated grass silage and 8 kg day⁻¹ of concentrate. Propionate infusion increased milk yield (24·9 vs 23·4 kg day⁻¹; P<0·05), milk protein yield (832 vs 778 g day⁻¹; P=0·05) and milk lactose content (44·7 vs 43·5 g kg⁻¹; P<0·05) and yield (1113 vs 1023 g day⁻¹; P<0·01), whereas butyrate infusion was associated with a higher milk fat content (44·7 vs 39·4 g kg⁻¹; P<0·01) and yield (1033 vs 974 g day⁻¹; P<0·01). FM tended (P<0·10) to increase milk yield, but had no significant effects on milk composition or milk component yields compared with BP. Butyrate infusion increased blood ketones, plasma non-esterified fatty acids and glycine relative to propionate infusion. The concentrations of ammonia N in rumen fluid and urea in plasma and milk were similar for both protein supplements. The profile of amino acids in plasma was similar for both protein supplements except for the higher concentrations of phenylalanine, proline and tyrosine with BP. The results show that protein utilisation can be improved by increasing the supply of propionate from rumen fermentation in cows given a grass silage-based diet. © 1998 SCI.     

Lead excretion in milk of accidentally exposed dairy cattle

Lead (Pb) exposure in dairy cattle is associated with economic losses due to mortality and treatment costs, but with production animals there is also risk to the human food chain. The first objective of this study was to quantify the Pb concentration in milk from Pb-exposed cattle. The second objective was to correlate blood and milk Pb concentrations from individual cows. The third objective was long-term monitoring to determine the duration of milk contamination after exposure ceased. A dairy herd of more than 100 cows was accidentally exposed to Pb-contaminated feed. Milk and blood were collected for Pb analysis. Serial collection of milk samples continued for 2.5 years. The initial concentration of Pb in bulk tank milk was 0.0999 mg l^–1. The highest milk Pb concentration from an individual cow was 0.4657 mg l^–1 and the highest blood Pb concentration was 1.216 mg l^–1. One milk sample collected at the end of the study (day 922) contained 0.0117 mg Pb l^–1 of Pb. The calculated relationship between milk (y) and blood (x) Pb concentration was ln(y) = 3.4(x) – 2.21 (R² = 0.98).