1. Opiates
Essential idea: Potent medical drugs prepared by chemical modification of natural products can be addictive and become substances of abuse.

2. Action of opiates
Opiates, such as morphine, diamorphine (heroin) and codeine, are natural strong analgesics as they reduce severe pain by temporarily bonding to receptor sites in the brain or other parts of the central nervous system, CNS, such as the spinal cord.
This prevents the brain and the CSN receiving any pain impulses (prevent perception) and therefore prevents the transmission of pain impulses but without depressing the CNS.

3. Action of opiates
To be able to bond with the opioid receptors the opiates need to cross the blood-brain barrier and how well they do this depends on their solubility in water (blood) and lipids (brain) and on their chemical structure.

4. Structures of morphine, diamorphine, codeine
diamorphine/heroin
codeine
arene
tertiary amine
alkenyl
ether
hydroxyl (2)
ester (2)
ether (2)
hydroxyl

5. Morphine, heroin and codeine

6. Synthesis of opiates
Opiates compounds are derived from opium which is an extract obtained from the seeds of a poppy plant.
Morphine is the main drug extracted from opium.
Codeine and diamorphine are derived from morphine and are called semi-synthetic opiates.

7. Synthesis of heroin: esterification
Diamorphine’s structure is only slightly different from morphine.
Both the hydroxyl groups in the morphine molecule have been converted into ester groups.
This is achieved by reacting the morphine with ethanoic acid (2 molecules); as a result an esterification occurs during which also water is produced.
The esterification makes diamorphine less polar and therefore more soluble in lipids and therefore more potent as a pain killer but also more addictive.

8. Synthesis of codeine: methylation
In the synthesis of codeine from morphine one of the hydroxyl groups on the morphine is converted into a methyl ether group through a process called methylation.
This methylation makes codeine less polar but more lipid soluble although it results in less binding with the opioid receptors – weaker analgesic.

9. Summary

10. Advantages of using morphine and its derivatives as analgesics
Strong analgesics and therefore can relieve extreme pain
Fast acting as can be administered intravenously
Relieves anxiety
Induces relaxation/feeling of well-being.
High bioavailability.

11. Disadvantages of using morphine and its derivatives as analgesics
Addictive/habit-forming or physical dependence which leads to withdrawal symptoms.
As heroin is often taken by injections many addicts get infections such as HIV and hepatitis as a result of sharing needles.
Tolerance can become an issue with this type of drug as more of the drug needs to be taken to achieve the same effect; in order to achieve the desired effect heroin users may take doses which exceed the lethal dose

12. More disadvantages: side effects and addiction of using morphine and its derivatives
Constipation, loss of sex drive, poor appetite, induce sleep, addictive, constriction of pupil in the eye, depression, kidney and liver disorder, …
Addiction – withdrawal symptoms
Perspiration, diarhoea, cramps, acute feelings of distress, fever.

13. Increased potency of heroin
Diamorphine has greater potency (reaches brain faster and in higher concentration) as a painkiller than morphine and also gives a greater feeling of euphoria. This is because diamorphine is less polar than morphine as it does not have two polar hydroxyl group anymore as they have been replaced by two less polar ester groups.
As a result diamorphine (heroin) cannot form any hydrogen bonds and is therefore less soluble in polar substances such as water but more soluble in non-polar fatty tissue which makes up the central nervous system. As a result diamorphine can cross the blood-brain barrier faster/more easily than morphine.
Lower polarity in diamorphine makes it more soluble in fatty tissue and ensure a more rapid uptake into the brain.
Increased polarity makes a medicine more soluble in water and less so in fatty tissue.