Hi, i am a postgrad student who are currently doing malaria research and i will do Beta hematin inhibition assay. i would like to ask two questions.

  • what is the suitable solvent that i can use to dilute my extracts and standard drugs? is it only by using distilled water or acetate buffer?
  • i already run the experiment by using both distilled water and acetate buffer to do the serial dilution and the results seems to be quite the same. but the problem is, after i did the calculation by using the formula, my answer is negative and i think this is bacause my extracts are mostly have colour and the absrobance of the extracts is higher than the control. am i using the right formula or is there any other formula that i can use for this experiment?
  • here's the formula i used to calculate the % of inhibition.

    f = (Acontrol -Asample)/ (Acontrol –Amin)

    Acontrol is the absorbance of the heme with the absence of parasite lysate or lipid extract or an antimalarial compounds at 405nm while Asample represents the absorbance of the heme in the presence of both parasite lysate or lipid extract and crude extracts or major compounds. Amin is the absorbance of the heme with parasite lysate or lipid extract in the absence of an antimalarial compounds at 405nm. Percentage of inhibition of β-hematin by plant extracts will be calculated by the following equations

    % of inhibition = (1-f) x 100

    Thank You in advance.

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