- #1
Eagle9
- 238
- 10
Hello guys
Imagine that we have got a rat and we administer a certain dose (let it be 4.0 µl of a 0.052 M solution) of some (let’s say Propionic Acid - PPA) drug in a intracerebroventricular way – directly in rat’s brain. Now imagine that we administer the same drug in intraperitoneal way – directly in body cavity. In order to achieve same physiological impact on brain the dose in second approach should be different – higher (since in the second method the PPA needs to cover more distance in order to achieve brain), but how much higher? How this can be calculated?
Imagine that we have got a rat and we administer a certain dose (let it be 4.0 µl of a 0.052 M solution) of some (let’s say Propionic Acid - PPA) drug in a intracerebroventricular way – directly in rat’s brain. Now imagine that we administer the same drug in intraperitoneal way – directly in body cavity. In order to achieve same physiological impact on brain the dose in second approach should be different – higher (since in the second method the PPA needs to cover more distance in order to achieve brain), but how much higher? How this can be calculated?