the kidney. not sure why
the more ionized the drug is the less absorption
Veterinary drug absorption is the uptake of a drug after administration so that it can cause some sort of alteration in the body.
Drug testing happens at random and it usually takes place in a laboratory or a restroom.
if Pka value is more for acidic drug,best side for absorption will be throughout the G.i.Tract.
The process that brings a drug from the administration site into the bloodstream is called absorption. It refers to the movement of a drug from its site of administration into the bloodstream for distribution throughout the body. Factors such as route of administration, drug formulation, and physiological properties can affect drug absorption.
Yes. Drug testing takes place first upon enlistment and at random intervals thereafter.
A target organ is an organ that is targeted by a drug or hormone. These drugs usually stimulate the organ to produce its own hormones or react positively and function in response to the drug, such as adrenaline to the heart.
The liver is responsible for drug detoxification and bile production. The liver processes drugs and toxins to make them easier for the body to eliminate, and it also produces bile which helps in the digestion and absorption of fats in the digestive system.
decrease
pKa of a drug is the pH at which the drug is 50% ionized and 50% non-ionized. This can affect drug absorption as the ionized form may have different solubility and permeability properties compared to the non-ionized form. Understanding the pKa of a drug can help predict its behavior in different pH environments and optimize absorption.
Probenecid (a drug treating gout) impairs riboflavin absorption, and propantheline bromide (a drug treating peptic ulcers) reportedly both delays and increases absorption.
Drug absorption through the skin, also known as transdermal absorption, occurs when a drug penetrates the skin layers and enters the bloodstream. Factors that influence this process include the drug's molecular size, lipophilicity (ability to dissolve in fats), skin thickness, blood flow to the skin, and the presence of enhancers or barriers on the skin.