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Home > Micro-Analysis of Aflatoxin M 1 in Dairy Products at Trace Levels and its Elimination

Micro-Analysis of Aflatoxin M 1 in Dairy Products at Trace Levels and its Elimination

Thesis Info

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Author

Hussain, Imtiaz

Program

PhD

Institute

University of the Punjab

City

Lahore

Province

Punjab

Country

Pakistan

Thesis Completing Year

2009

Thesis Completion Status

Completed

Subject

Chemistry

Language

English

Link

http://prr.hec.gov.pk/jspui/handle/123456789/1118

Added

2021-02-17 19:49:13

Modified

2024-03-24 20:25:49

ARI ID

1676726637417

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Milk is a complex mixture of fat, protein, carbohydrate, and mineral components and it has been a source of human food since the recorded history. Aflatoxin M 1 is excreted in milk of those lactating animals which have ingested aflatoxin B 1 contaminated feed. Aflatoxin B 1 (AFB 1 ) is metabolized to aflatoxin M 1 in liver and then excreted in milk and urine. Aflatoxin B 1 is a potent carcinogen and aflatoxin M 1 (AFM 1 ), being the metabolite of AFB 1, has toxic properties similar to AFB 1 . Several researches have demonstrated the potential toxicity of exposure to AFM 1 . Aflatoxin M 1 is present in milk and milk products. This study includes the determination of contamination of aflatoxin M 1 in milk and milk products and contamination of aflatoxin B 1 in dairy feed in the Punjab province of Pakistan. The analytical techniques used in the determination of AFM 1 were high performance liquid chromatography (HPLC), fluorometry (using Fluorometer), and enzyme linked immunosorbent assay (ELISA). For the determination of AFB 1 , HPLC was used. Immunoaffinity columns were used to accomplish cleanup step during HPLC and fluorometric determination. A total of 977 samples of milk, cheese, and yoghurt were analyzed for AFM 1 contamination. Whereas a total of 260 samples of feed commodities (concentrate feed, cottonseed cake, wheat bran, bread, paddy straw, and wheat straw) were analyzed for AFB 1 contamination. In the first phase of study 168 sample of raw milk from fourteen districts, were analyzed by using immunoaffinity columns and Fluorometer. All the samples were found contaminated with AFM 1 , however in 96.4% samples the level of contamination was below the US tolerance limit of 0.5 μg/ L. Only 3% samples showed AFM 1 contamination higher than the US tolerance limit. While considering EU maximum permissible limit (0.05 μg/ L), 99.4% samples exceeded this limit. Seasonal effect was also studied on the presence of AFM 1 contamination in milk. ANOVA analysis indicated significant difference (p < 0.01) in AFM 1 concentration in milk in different seasons. The AFM 1 contamination was higher in winter as compared to summer and this was supported by previous studies. During the study of AFM 1 contamination in raw milk taken from different localities, variation in levels of AFM 1 was found in raw milk from different localities in the central areas of the Punjab, Pakistan. Total 480 milk samples of buffaloes and cows xviifrom different localities (urban, semi-urban, and rural) were analyzed by using HPLC with prior clean-up step applying immunoaffinity columns. The percentage of AFM 1 contamination in buffalo and cow milk was 42.5% and 52.5% respectively. In both types of milk, level of AFM 1 contamination was higher in milk samples obtained from urban and semi-urban areas and it was minimal in milk samples taken from rural areas. The AFM 1 contamination in buffalo milk was studied statistically with respect to herd-size variation also. The results showed significant variations with respect to herd-size (F= 6.631, p= 0.001). Milk samples in case of small herd-size (1-5 cattle) and medium herd- size (6-10 cattle) showed higher AFM 1 concentration as compared to large herd-size (more than 10 cattle). Another study was conducted to investigate the AFM 1 contamination in the milk of five mammalian species namely buffalo, cow, goat, sheep, and camel from the area of Faisalabad district of the Punjab province, Pakistan. Analysis was made by using HPLC with fluorescence detection. Immunoaffinity columns, which are based on the principle of affinity chromatography, were used for clean-up purposes. Total 169 milk samples were analyzed. The percentage of AFM 1 contamination in buffalo milk, cow milk, goat milk, and sheep milk was found to be 34.5%, 37.5%, 20%, and 16.7% respectively. AFM 1 contamination was not detected in camel milk in this area. Although there is massive use of fresh milk in Pakistan, but still significant consumption occurs after milk has been processed. As AFM 1 concentration is not affected by normal milk processes, AFM 1 is also present in milk products like cheese and yoghurt. The milk product samples including 80 cheese samples and 80 yoghurt samples were analyzed by using ELISA technique. The percentage of AFM 1 contamination was found to be 87.5% and 70% in cheese and yoghurt samples respectively. Because of the possibility of presence of aflatoxin B 1 , feed plays a major role in the occurrence of aflatoxin M 1 in milk. The monitoring of AFB 1 contamination in dairy feed is compulsory to ensure safety of milk consumers. The study on the contamination of AFB 1 in the dairy feed samples showed high contamination of AFB 1 in cotton-seed cake samples and concentrate feed samples. Total 260 samples of different commodities, used as dairy feed, were analyzed for AFB 1 contamination by HPLC. The average AFB 1 contamination levels in cottonseed cake, concentrate feed, wheat bran, bread pieces, and paddy straw were found to be 242, 176, 98, 23, and 37 μg/ Kg respectively. contamination level was high as compared to US tolerance i.e., 20 μg/ Kg.
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" وَنَزَّلْنَا عَلَيْكَ ٱلْكِتَابَ تِبْيَاناً لِّكُلِّ شَيْءٍ وَهُدًى وَرَحْمَةً وَبُشْرَىٰ لِلْمُسْلِمِينَ "[[1]]

"ہم نے یہ کتاب تم پر نازل کر دی ہے جو ہر چیز کی صاف صاف وضاحت کرنے والی ہے اور ہدایت و رحمت اور بشارت ہے اُن لوگوں کے لیے جنہوں نے سر تسلیم خم کر دیا ہے" ۔

قرآن کا مخاطب انسان ہے اور یہ اپنے مخاطب کو منفرد انداز سے خطاب کرتا ہے، قرآن مجید میں اللہ تعالیٰ کا انسان...

Significance of Philadelphia Chromosome in Chronic Myeloid Leukemia Patients of Anmol Hospital, Lahore, Pakistan

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Studies on the Factors Affecting the Macrobenthic Community Structure of the Exposed Sandy Beaches Near Karachi, Pakistan

The principal objective of the research conducted during this study is to provide a profound knowledge of the ecological status and functioning of exposed sandy beaches of Karachi coast. This assessment was established on the basis of functionally important benthic community structure in response to environmental conditions which is the first comprehensive study at studied beaches at Karachi coast. In chapter 1, macrobenthic community structure of the exposed sandy beaches of Sandspit and Hawksbay in relation to physicochemical parameters and sediment characteristics is studied during 2013-2014. A total of 96 samples were collected in duplicate by quadrat (0.25 m-2) method from high tide (HT) and low tide (LT) mark for macrofauna abundance and sediment analysis from four stations (S1, S2, H1 and H2). Water samples were analyzed for temperature, salinity, pH, dissolved oxygen and nutrients analysis (NH4, NO3, PO4) by applying standard methods. Sediment samples were divided into three layers, each layer was analyzed for moisture and organic content and grain size analysis. A total of 1307 organisms 0.25m-2 belong to 83 macrobenthic species recorded during this study out of which 12 species are first records from Pakistan. A sum of 662 organisms 0.25m-2 were recorded from Sandspit and 645 organisms 0.25m-2 from Hawksbay. The most diversified macrobenthic groups of species were polychaeta (38%) followed by gastropoda (24%), crustacea (19%) and bivalvia (12%) respectively. Whereas, the most abundant faunal groups were polychaeta (44 %), crustacea (25 %), bivalvia (14 %) and gastropoda (11%). Euterpina acutifrons, Glycera alba, Donax hanlyanus, Prionospio sp. were the most dominant species at studied beaches. SIMPER analysis showed average similarity 37.5% between sites. The highest macrobenthic abundance was recorded in NEMS (414 0.25m-2) and PRMS (379 0.25m-2) and lowest during SWMS (211 macrobenthos 0.25m-2). ANOVA showed impact of different environmental parameters such as salinity, temperature, dissolved oxygen and moisture content on macrofaunal assemblages. The species composition and abundance showed a clear separation between studied sites during monsoon seasons indicating the significant impact of monsoon on macrofaunal diversity and abundance at studied beaches. xviii In chapter II, benthic foraminifera in relation to habitat conditions and seasonal influences was studied for the first time from Pakistani coast, based on 48 core samples collected monthly with the help of hand corer (diameter =3 cm) from stations as discussed for Chapter I. For this study the top 0-2 cm sediment slice was analyzed for both living and dead foraminiferal assemblages. A total of 6615 cm-2 specimens consisting of 3451 cm-2 dead tests and 3164 cm-2 living specimens were recorded which belong to 66 species out of which 47% species are miliolina, 42% rotaliina, 9% textulariina and 2% are spirillina. At Sandspit 3197 cm-2 specimens were recoded while a sum of 3418 cm-2 specimen were recorded from Hawksbay. The highest abundance was exhibited by rotaliina, milolina and textulariina respectively. The most dominant rotaliina species were Ammonia beccari, Pararotalia stellata, P. vensuta, Elphidium crispum and E. advenum respectively and Quinqueloculina bicarinata, Q. vulgaris, Miliolinella subrotunda, Spiroloculina antillarum and Miliamina sp. were abundant miliolina species. SIMPER showed that average dissimilarity between foraminifera abundance at Sandspit and Hawksbay is 18.51 %. The stations within sites showed similarity (82.83 % at Sandspit and 84.65 % at Hawksbay). A. beccari and P. stellata are the most similar species within stations at both Sandspit and Hawksbay. The highest foraminifera abundance was recorded in NEMS (3232 cm-2) and SWMS (1984 cm-2) and the lowest during PRMS (398 cm-2). pH, salinity, organic content and nutrients appeared to effect the foraminiferal assemblages. Benthic community structure of exposed sandy beaches of Sandspit and Hawksbay do not affected by a single physicochemical and environmental factor but multiple factors are controlling spatial and temporal distribution of macrofaunal and foaraminferal assemblages at these beaches. The most significant and governing factor for benthic abundance and diversity at these beaches is the monsoon season. Faunal assemblages on each site point out a variability in domination of species during studied seasons. Northeast monsoon was the most biologically productive season which provided a suitable environment for growth of both macrobenthic communities and foraminiferal assemblages. This is the first comprehensive study about ecological status of these highly dynamic environments which will be helpful in management of these beaches in future.