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Research Detail

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J.A. Khatoon
Departrpent of Biochemistry Bangladesh Agricultural University, Mymensingh-2202 Banqladesh

M H-H.Khan
Departrpent of Biochemistry Bangladesh Agricultural University, Mymensingh-2202 Banqladesh

M.A. Hqssain
D.epartrpent of Biochemistry Bangladesh Agricultural University, Mymensingh-2202 Banqladesh

The  present study wheat grains were treated with 14C-malathion stored under laboratory condition in glass jar for a maximum period of 180 days and sampled at 1, 15, 30, 60, 90 120 and 180 days for the determination of the insecticide residue. The surface, extractable and bound residues were determined using radio-tracer technique. The amount of bound residues in grains at 10 and 50 ppm gradually increased to 3.8 and 4.2% respectively of the initially applied dose after 180 days. The amount of surface residues has been declined gradually and the values  were 32.2% and 33.0% at 10 and 50 ppm, respectively. The amount of extractable residues increased up to 50.9% and 52.0% for applied dose of 10 and 50 ppm, respectively. When rats were allowed to feed these 14C-bound residues, radioactivity excreted in urine counted for 34.5% and in faces 42.5% of the administered doses. In faces, 45.1% was methanol extractable and 54.0% was non-extractable. Maximum  bodnd14C-residues as found in fat bodies (3.6%) followed by liver (2.5%), kidney (1.3%), muscle (0.75%), spleen (0.48%), heart (0.30%)  and blood (0.10%).

  Bioavailability,Toxicology, Mal, Wheat
  BAU, Mymensingh
  
  
  Pest Management
  Wheat

1.To study the fate and magnitude of malathion residues in 14C-malathion treated wheat in storage

2.To investigate the reduction and distribution of the same.

Chemicals:  Malathion  (0,  0-dimethyi-S-(1-2-Dithoxy-carbonyl) [1, 2-C] phosphorodithioate), specific gravity 24.8 mci/m  mole,  radiochemical  purity 99% was obtained  from  International Atomic   Energy  Agency   (IAEA).   Non-labeled   malathion   was   also   obtained   from   IAEA. Formulated malathion was obtained from plant protection department of Bangladesh.   Grain treatment: Pesficide free wheat grains were collected from Wheat Research Center, Dinajpur. The unwanted materials,  broken as well as deformed grains were removed  from it. Then the sample was divided into three groups. Sample A was treated with 100 IJCi-malathion and 433.5 mg  of 2% non-labeled  malathion  in order to prepare  a final concentration  of 10   ppm and sample B was treated with 100 11ci 14C-malathion  and 2433.5 mg of 2% non-labeledmalathion  to produce  50 PPM whereas sample C was not treated with insecticide  and used as control.  All the samples  were tumbled  in separate glass  jars for four hours  continuously and stored at 22-25°C at relative humidity of 65-75% and moisture content of 10-12%. Sampling  and  residues  determination:  Malathion  treated  and  untreated  wheat  samples were taken at intervals of 15, 30, 60, 90, 120 and 180 days from the storage. 25 g of sample from  each  group  was  washed  three  times  with  distilled  water.  Then  the  washings  were collected  and  analyzed  for  radioactivity  in  a Hewlett  Packard  Liquid  Scintillation  Counter, Tricarb  460  C  (Surface  residues).  The  washed  grains  were  dried,  ground  thoroughly  and extracted with 95% methanol  for 24 hours in asoxhlet apparatus.  The methanol  extract was then counted  for radioactivity  (methanol  extractable  residues). 

  Bangladesh J of Agril. Sci. 30(1): 63-68, January, 2003
  
Funding Source:
  

. The amount of bound residues in grains at 10 and 50 ppm gradually increased to 3.8 and 4.2% respectively of the initially applied dose after 180 days. The amount of surface residues has been declined gradually and the values Vl!ere 32.2% and 33.0% at 10 and 50 ppm, respectively. The amo4nt of extractable resjdues increased up to 50.9% and 52.0% for applied dose of 10 and 50 ppm, respectively. When rats were allowed to feed these 14C-bound residues, radioactivity excreted in urine counted for 34.5% and in faces 42.5% of the administered doses. In faces, 45.1% was methanol extractable and 54.0% was non-extractable. Maximum bpuncj 14C-residues as found in fat bodies (3.6%) followed by liver (2.5%), kidney (1.3%), muscle (0.75%), spleen (0.48%), heart (0.30%) Cjnd blood (0.10%).

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