Nature of drugs that we should know
INTRODUCTION
Everybody in their
lifetime has taken drugs not the illegal ones but the drugs that a doctor
prescribes us when we fall ill. Maybe we sometimes self prescribe our drugs and
end up having some OTC drugs. Many of the drugs we use have different natures
like we can say they have different properties. So here we may learn about a
few of them to get a view of the nature of some of the drugs that we might have
taken.
1. Nature
of drugs
Drugs are basically
substances that bring about a chemical reaction in our body be it beneficial or
harmful. Now one might ask how these chemical reactions are triggered by a simple pill that we take.
Well, it's by the chemicals
that they contain ie. The chemical in the pill we take can be an agonist or an
antagonist.
Agonists are
those chemicals which bind to the receptors in our body and activate the
chemical pathway again which might have been disturbed. Antagonists do the opposite ie. They inhibit the chemical process
that is going on in the body by binding to their receptors.
Now one might think then
we need to take drugs to keep our bodily reactions going on, but no the
substances that are needed to maintain these functions are naturally produced
in the body. Which means our body does produce drugs for smooth functioning and
they can be enzymes, hormones, etc.
We only need drugs or
those substances when the body is not producing them in a balanced manner.
Another nature of drugs is
that they can be toxic to the body and they are called poisons and there is a
dedicated field of study for that called toxicology which studies about drugs
that are harmful to the body.
2. Physical
nature of drugs
Now the drugs are
available in a pharmacy and we can say that the pharmacies are lit shops. The drugs
come in very different shape sizes and often colors. Scientifically speaking
the drugs have different sizes, shapes, atomic composition, chemical composition
and even the way they are administered to the body is different.
So why is there so much
diversity in drugs?
Because it all comes to
the usefulness of the drug must reach to the action site to perform the function
that it’s taken for and then it should stay there for the appropriate time and can
be excreted with minimum or no complications.
At room temperature, various drugs can be present in all the three states ie. Solid (aspirin, atropine),
liquid(nicotine and ethanol) or gas(nitrous oxide) and these states can also
decide the way of administering a drug.
Other forms of drugs can
be inorganic (lithium, iron), organic acid-base, etc.
3. Size and
shape of the drugs
The size of the drug varies
greatly as of lithium mw=7 and that of Ateplase= 59050 (it’s a protein). But most
drugs vary from 100 to 1000 in molecular weight. Besides that there are other
factors like the shape (it should fit the receptor), the charge on the molecule
all should be accurate and thus the most cases the MW is 100.
Now, our body has a
function called diffusion and thus dugs of large molecular size like more than
1000 cannot pass through the compartments so they are directly administered to
the site of requirement. Like, let us take Ateplase which is a clot-dissolving a protein having very large MW is directly infused in the vascular compartments.
So, the size of the drug
may define how the drug is administered to the body.
4. Drug reactivity and drug-receptor bonds
The drug that goes into the body makes different types of bonds with the receptors
of which are covalent bonds which are the strongest. Covalent
bonds are very strong and in many cases not reversible under biologic
conditions. Thus, the covalent bond formed between the acetyl group of
acetylsalicylic acid (aspirin) and cyclooxygenase, its enzyme target in
platelets, is not readily broken. And the platelets need to synthesize new
enzymes which might take several days.
Next
types of bonds are the electrostatic bonds which are less strong and other than
that are the hydrophobic bonds which are present between lipids.
Now
all this talk about the bonds of the molecule of the drug and the receptor is of
little importance, because what we know is that the drugs that bind through
weak bonds are more selective than strong bond drugs.
But
why and how does it matter?
Its
because if we have a highly selective short-acting drug then the receptors
that fit the drug are very few. If we make a strong bond then it will be
hard to break then the weak ones.
5.
Rational
drug design
Its
basically about the molecular structure of the drug that is made to fit its
biologic receptor. For a drug to work on mechanism weather be for
activation or inhibition the drug should be fit to the receptor. It’s not so
much of an explored area as till recently drugs were based on the chemical
reactions. This field has been achieved by computer designs of drugs in the
last few decades and more designs might come in the future.
6.
Receptor
nomenclature
In
the recent times the discoveries of the receptors of the drugs have contributed
to a very confusing naming pattern of the same. So the IUPHAR has been the suggestion
for the drug classification and naming receptors and it’s widely used.
Conclusion
So
the drugs that we take have nature a particular property and they do have
some function in the body and there is a mechanism of action of the drug. Nature
says that drugs whether prescribed or not interfere with the body mechanism to
either make it better or worse.
That’s
why it’s always advised to take drugs after prescribed by a qualified personnel
only.
So
be wise and take care!!!!!
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