Enhancing transdermal delivery of opioid antagonists and agonists using codrugs linked to bupropion or hydroxybupropion
The present invention is directed to novel codrugs comprising bupropion or hydroxybupropion and an opioid antagonist or an opioid agonist joined together by chemical bonding. The codrugs provide a significant increase in the transdermal flux across human skin, as compared to the basic opioid antagonist or opioid agonist.
1. A codrug comprising:
(a) hydroxybupropion; and
(b) an opioid antagonist or an opioid agonist selected from the group consisting of Naltrexone, Buprenorphine, Butorphanol, Codeine, Dihydrocodeine, Dihydromorphine, Ethylmorphine, Hydromorphone, Levallorphan, Levorphanol, Nalbuphine, Nalmefene, Nalorphine, Naloxone, 6-β-Naltrexol, Phenazocine, Pholcodine, and 6-α-Naltrexol;
wherein hydroxybupropion is linked via a carbonate linker to the opioid antagonist or opioid agonist to form a single chemical entity.
2. The codrug of claim 1 , wherein said carbonate linker is cleavable.
3. The codrug of claim 2 , wherein said carbonate linker is cleavable via hydrolysis and/or enzymatic digestion.
4. The codrug of claim 1 , wherein said codrug comprises Naltrexone or 6-β-Naltrexol.
5. The codrug of claim 4 , wherein said codrug comprises 6-β-Naltrexol.
6. The codrug of claim 4 , wherein said codrug comprises Naltrexone.
7. A transdermal patch comprising a substrate and a layer of the codrug of claim 1 .
8. A codrug having the following structure:
9. A codrug having the following structure:
10. A codrug having the following structure:
11. A codrug having the following structure:
12. A codrug having the following structure:
13. A codrug having the following structure: