Calculating the equivalent dose for intraperitoneal injection

In summary, the conversation discusses the differences in administering a drug, specifically Propionic Acid, through intracerebroventricular and intraperitoneal methods. It is noted that intracerebroventricular administration is uncommon and may not have established formulations, making it difficult to calculate the equivalent dosage for intraperitoneal use. The effect of the drug on the brain can also be affected by the difficulty of crossing the blood-brain barrier. Further research on specific drugs and their dosages for both methods is recommended.
  • #1
Eagle9
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Hello guys :cool:

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? :rolleyes:
 
  • #3
Intracerebroventricular administration of drugs are very uncommon to begin with and most drugs don't have formulations for that method already established. So, converting them to use for intraperitoneal route would be pointless, the formulas for most drugs that can be injected in that manner will already be published by the pharmaceutical industry. You should be able to find what you already need. Also, some drugs are injected into the brain in the first place because of difficulties crossing the blood-brain barrier, massive doses of some drugs may not be effective regardless. If you want to know about a specific drug that is commonly used in animal testing via the intracerebroventricular route, then you could possibly find some methods of calculating the equivalent dosage via the intraperitoneal route, if it is already a common practice of doing so. Really, the specific drug needs to be known to fully answer your question.

http://www.ncbi.nlm.nih.gov/pubmed/19558257
 
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Likes Laroxe

1. What is the purpose of calculating the equivalent dose for intraperitoneal injection?

The equivalent dose for intraperitoneal injection is used to determine the amount of a substance that needs to be injected into the peritoneal cavity in order to achieve a similar effect as a given dose of the same substance administered through a different route.

2. How is the equivalent dose for intraperitoneal injection calculated?

The equivalent dose for intraperitoneal injection is calculated by taking into account the bioavailability and absorption rate of the substance through the intraperitoneal route compared to the other route of administration.

3. Why is the equivalent dose for intraperitoneal injection important in research?

The equivalent dose for intraperitoneal injection is important in research as it allows for a more accurate comparison of the effects of a substance when administered through different routes, which can vary greatly in terms of bioavailability and absorption rate.

4. Can the equivalent dose for intraperitoneal injection be used interchangeably with other routes of administration?

No, the equivalent dose for intraperitoneal injection should only be used as a guide for comparison and should not be used as an exact conversion for dosages between different routes of administration.

5. How can the equivalent dose for intraperitoneal injection be adjusted for different substances?

The equivalent dose for intraperitoneal injection can be adjusted for different substances by taking into account their unique pharmacokinetic properties, such as molecular weight, solubility, and metabolism rate.

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