Practical: Drug stocks, solutions and dilutons Flashcards
Beer-Lambert law + define symbols
A = log10 (Io/I) = ϵcl
A = absorbance of light
Io = intensity of beam before passing through sample
I = intensity of beam of light emerging from sample
ϵ = absoption coefficient
c = concentration
l = pathlength
what does a greater absorption coefficient mean?
more light absorbed
what’s the relationship between the concentration of a substance and the absorbance?
linear
what does a longer pathlength l mean?
more light absorbed
what’s used to measure absorbance?
spectrophotometer
what can we use absorbance to calculate?
the concentration of the sample solution
how long should we switch on a colorimeter for before using?
15 mins
what do we zero a colorimeter with?
distilled water
is it more accurate to pipette small or large volumes?
large volumes
what’s the standard method for diluting in pharmacology and why?
serial dilutions - accurate
what’s the method of choice for preparing drug solutions and why?
serial solutions
it uses volumes that don’t differ by more than 10x (less likely to have experimental errors)
disadvantage of serial dilutions
irreversible (start again if you get a step wrong)
which pipettes use a blue tip?
P1000
which pipettes use a yellow tip?
P20 and P200
what’s more accurate - using serial dilutions or making each dilution separately from a starting stock solution?
serial dilutions