statistical treatment for storage stability data
Posted: Tue Jul 25, 2006 4:02 am
Dear All,
Recently (last 1 year actually) I collected data for one of my experiment about the storage stability of pesticide residue in olive oil under our pre-selected storage condition.
This is the short description about the way I carried my experiment
2x20 vials of olive oil samples (5g each) were prepared from a stock of olive oil (500g) containing 0.25mg of pesticide of interest (Cypermethrin).
After this, all the samples were kept in freezer at -18 degree C (in dark).
At each sampling day (total 20 sampling days) , 2 vials were taken out from the freezer and the amount of cypermethrin was determined (with duplicate injections).
Now, I have two set of data namely set A and set B.
My questions are:
1. What should I do to determine whether the pesticide was degraded during the storage period? (In term of statistics or other ways)
2. How many replicates that normally needed for pesticide storage data?
Thanks
Recently (last 1 year actually) I collected data for one of my experiment about the storage stability of pesticide residue in olive oil under our pre-selected storage condition.
This is the short description about the way I carried my experiment
2x20 vials of olive oil samples (5g each) were prepared from a stock of olive oil (500g) containing 0.25mg of pesticide of interest (Cypermethrin).
After this, all the samples were kept in freezer at -18 degree C (in dark).
At each sampling day (total 20 sampling days) , 2 vials were taken out from the freezer and the amount of cypermethrin was determined (with duplicate injections).
Now, I have two set of data namely set A and set B.
My questions are:
1. What should I do to determine whether the pesticide was degraded during the storage period? (In term of statistics or other ways)
2. How many replicates that normally needed for pesticide storage data?
Thanks