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SIWES PRESENTATION.pptx

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Akindele122016JAMB30948_1
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SIWES PRESENTATION.pptx

  1. 1. FEDERAL UNIVERSITY DUTSE STUDENT INDUSTRIAL WORK EXPERIENCE SCHEME (SIWES) HELD AT BIORESOURCES DEVELOPMENT CENTRE KANO (BIODEC KANO) BAYERO UNIVERSITY KANO (NEW CAMPUS) PRESENTATION BY RABIU KUDIROH OMOSALEWA FSC/BCH/18/1048 SUPERVISED BY MR ADEPOJU MALIK December – May, 2022
  2. 2. HISTORY OF BIODEC KANO • Bioresources Development Center (BIODEC) Kano formerly known as Aquaculture Training Centre kano, was established by the National Biotechnology Development Agency in the year 2012 to support the agency’s delivery of indigenous bioresource and benefits. • The center was upgraded to a BIODEC center in the year 2014 in order to play a critical role in the sustainable development and use of indigenous bioresources through the application of emerging science and technology, at the same time empowering people in kano, and its neighboring states and technical skills in order to boost food production, health, job creation and wealth.
  3. 3. ORGANOGRAM OF BIODEC
  4. 4. ACUTE TOXICITY Acute toxicity is calculated using LD50. LD50 Median lethal dose, is a dose that can kill 50% of a tested population, the unit of LD50 is mg/kg, there are two methods of LD50 DETERMINATION OF THE ACUTE TOXICITY ON AN ANTI-ULCER HERBAL MEDICINE USING LORKE`S METHOD. They are two phase, phase1 and phase2 PHASE1: 9 mice were used in this phase and were grouped into three groups consisting of 3 mice each, the herbal medicine was administrated to each group Group1_10mg/kg, Group2_100mg/kg, Group3_1000mg/kg The phase one mice were observed for 24 hours to check for mortality. PHASE2: 4 mice were used in this phase, and the observation from phase 1 determine the amount of herbs to be administered to the mice in phase2.
  5. 5. RESULTS AND CONCLUSION RESULTS Phase1:After 24 hours of observation Group1_ 0/3, no mortality Group2_0/3, no mortality Group3_0/3, no mortality. Phase2: from the observation in phase one, according to LD50 table the four mice in phase were administered 1200mg/kg, 1600mgmg/kg, 2900mg/kg, 5000mg/kg. 1200mg/kg_ 0/1, no mortality 1600mg/kg_ 1/1, mortality 2900mg/kg_ 1/1, mortality 500mg/kg_ 1/1, mortality LD50”

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