Opioids
[SH4:p87-p90; "Opioid receptors" CEACCP 2005 Vol 5(I) p22-25]
Overview
- Opioids is unique in its ability to produce analgesia without producing loss of touch, proprioception, or consciousness.
- Main difference between opioids are potency, and rate of equilibration
Classifications
By method of synthesis
1. Naturally-occuring opioids
- Phenanthrene
* Include morphine, codeine, thebain
* Thebain has insignificant analgesia, but can be changed to etorphine (>1000 times the morphine analgesic potency)
- Benzylisoquinolines
* Include papaverine, noscapine (both lack opioid activity)
2. Semisynthetic opioids
- Come from relatively simple modification of morphine
- Methylmorphine (codeine)
* Adding methyl group to C3 in morphine
- Diacetylmorphine (heroin)
* Adding acetyl groups (R-COCH3) to C3 and C6 in morphine
3. Synthetic opioids
Contains phenanthrene nucleus but are synthesized
- Morphine derivative (4 rings)
* Levorphanol
* Butorphanol
- Benzomorphan derivative (3 rings)
* Pentazocine
* Cyclazocine
- Phenylpiperidine derivative (2 rings)
* Pethidine (meperidine)
* Fentanyl
* Sufentanil
* Alfentanil
* Remifentanil
* Diphenoxylate (lomotil)
- Diphenylhaptene derivatvies (2 rings)
* Methadone
* Propoxyphene
By activity at receptors
1. Opioid agonists
- Morphine
- Pethidine
- Fentanyl
- Alfentanil
2. Opioid agonist-antagonists
- Pentazocine
- Buprenorphine
- Naltrexone
- Meptazinol
3. Opioid antagonists
NB:
- Phenylpiperidine derivatives are similar to amide LA in MW and pharmacokinetics
Structure
- Phenanthrene nucleus consists of 3 benzene rings (14 carbons)
- Most opioid agonists also has a 4th carbon ring (piperidine, a 5 carbon + 1 nitrogen ring)
--> N in the piperidine ring is a tertiary amine
* At pH 7.4, tertiary amine is highly ionised --> More water solubility
- Close relationship between stereochemical structure and potency
--> Levorotatory isomer is most active
Special considerations
- After 60 years of age,
* Decreased sensitivity to pain
* Increased analgesic response to opioids