How drugs are distributed throughout the body

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Drugs In The Body

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Biology Biology is the study of life; in this unit we talked about cells (types, what they're made up of and specialization), the cell cycle, 3 organ system, and the interactions between the different systems.

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BODY SYSTEMS Organs are classified according to their functions

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The Working Cell

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How drugs are distributed throughout the body

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Sources: https://www.sciencedirect.com/topics/neuroscience/drug-protein-binding https://www.sciencedirect.com/topics/medicine-and-dentistry/drug-receptor#:~:text=Receptors%20are%20the%20targets%20for%20drugs%20and%20endogenous,may%20determine%20the%20magnitude%20of%20the%20pharmacologic%20response. https://www.sciencedirect.com/topics/medicine-and-dentistry/drug-receptor https://www.msdmanuals.com/professional/clinical-pharmacology/pharmacokinetics/drug-absorption https://www.merckmanuals.com/home/drugs/administration-and-kinetics-of-drugs/drug-administration https://pubmed.ncbi.nlm.nih.gov/12943856/ https://derangedphysiology.com/main/cicm-primary-exam/required-reading/pharmacokinetics/Chapter%20134/gastric-drug-absorption https://www.merckmanuals.com/home/drugs/administration-and-kinetics-of-drugs/drug-distribution

Fat

Those that are fat-soluble can pass cell membranes faster than drugs that are water-soluble. Transport systems facilitate the transfer of various medications into and out of tissues.

Drugs that dissolve in fat (fat-soluble drugs), such as the antianxiety drug clorazepate, tend to concentrate in fatty tissues.

Atorvastatin (Lipitor) is a cholesterol-lowering drug that is often prescribed to persons who have excessive cholesterol or heart disease. It's also used for those who have a higher risk of heart disease, such as diabetics, even if their cholesterol levels are normal.

Fat in the circulation may act as a stumbling block to the medicine reaching its intended target, since it may hijack the drug molecules.

Stomach and Stomach acids

A sufficiently large concentration gradient to promote simple passive diffusion is another element that favours medication absorption in the stomach. This necessitates a low-potency drug (i.e. given as a very large dose). It also helps if the medicine has a tiny molecule that can easily pass through the gastrointestinal mucous barrier.

The medications, on the other hand, may be destroyed by the stomach. When a medicine is decided to be supplied through inhilator or injection, this is what happens.

Pepto-Bismol relieves upset stomach by binding with the mucoproteins in the stomach lining and providing a protective coating that soothes irritation and provides fast relief from upset stomach and indigestion.

The medication is dissolved by gastric acid in the stomach. The medication is absorbed into the circulation through the stomach lining.

Protein

Proteins take over the medicine molecule, preventing it from reaching where it's supposed to go.

Monoclonal antibodies (mAbs or MoAbs), which are man-made copies of immune system proteins, can be particularly beneficial in the treatment of cancer because they can be engineered to attack a specific component of a cancer cell and so hinder the carcinogenesis process.

Circulatory

The medications go through the circulatory system to the liver and the targeted location.

Anticoagulants are medicines that prevent the blood from clotting as quickly or as effectively as normal. Some people call anticoagulants blood thinners. However, the blood is not actually made any thinner - it just does not clot so easily whilst you take an anticoagulant.

Small intestines

In the GI tract, the small intestine has the most surface area for drug absorption, and its membranes are more porous than those in the stomach. Most medications are absorbed largely in the small intestine as a result of these factors.

Corticosteroids, or commonly just referred to as steroids, are a common medication used in the treatment of inflammatory bowel disease

Enzymes

Enzymes have these two characteristics, making them highly selective and strong medications capable of achieving therapeutic biochemistry in the body that tiny molecules cannot. Many enzyme medications for a variety of illnesses have been developed as a consequence of these properties.

Enzymes as medications have two distinct characteristics that set them apart from all other forms of pharmaceuticals. First, enzymes frequently bind and function with high affinity and specificity on their targets. Enzymes, on the other hand, are catalytic, meaning they transform several target molecules into the desired products.

For chronic pancreatitis, pancreatic enzymes are used. For these individuals, medical therapy frequently includes the prescription of pancreatic enzyme preparations. This approach is based on research that suggest pancreatic enzymes have a positive impact on a variety of outcomes, including abdominal discomfort, weight loss, painkiller usage, fatty stools, and overall quality of life.

Receptors

When receptors that target the organ grab onto the drug molecule, the medications know where to go.

When medication molecules attach to receptors that aren't meant to be binded to, adverse effects might occur.

Liver

When a medicine enters the circulation, it goes to the liver, where it may be eliminated by the enzymes that are created. Many medications are chemically altered (metabolised) by the intestinal wall and liver, reducing the quantity of drug that reaches the circulation.

Cholic acid may assist restore normal liver function by: Maintaining bile acid balance under normal physiologic settings via the farnesoid X receptor (FXR). 1 Keeping hepatotoxic atypical bile acids from accumulating and causing liver damage

Cells

The medicine gets absorbed by the cells, and it accomplishes what it is supposed to do, such as ease pain.