alexa Fentanyl - A Potent Opioid Analgesic: A Review | Open Access Journals
ISSN: 2329-6631
Journal of Developing Drugs
Make the best use of Scientific Research and information from our 700+ peer reviewed, Open Access Journals that operates with the help of 50,000+ Editorial Board Members and esteemed reviewers and 1000+ Scientific associations in Medical, Clinical, Pharmaceutical, Engineering, Technology and Management Fields.
Meet Inspiring Speakers and Experts at our 3000+ Global Conferenceseries Events with over 600+ Conferences, 1200+ Symposiums and 1200+ Workshops on
Medical, Pharma, Engineering, Science, Technology and Business

Fentanyl - A Potent Opioid Analgesic: A Review

Ashok Kumar Sharma*, Maniratna Nareda, Sanaa Aziz, Deepak Sharma and Dr. Shiv Kumar Garg

Maharishi Arvind College of Pharmacy, Ambabari, Jaipur, Rajasthan, India

*Corresponding Author:
Ashok Kumar Sharma
Research Scholar, Maharishi Arvind College of Pharmacy
Ambabari, Jaipur, Rajasthan, India
Tel: +91-9887593534
Email: Ashoksharma3332@yahoo.in

Received date: September 09, 2016; Accepted date: October 06, 2016; Published date: October 14, 2016

Citation: Sharma AK, Nareda M, Aziz S, Sharma D, Garg S (2016) Fentanyl - A Potent Opioid Analgesic: A Review. J Dev Drugs 5:162. doi: 10.4172/2329-6631.1000162

Copyright: © 2016 Sharma AK, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

 

Visit for more related articles at Journal of Developing Drugs

Abstract

Fentanyl is a potent analgesic that is almost a hundred times accented than morphine, the use of fentanyl is pain allayer and anesthetic was adopted in the medical primed. Fentanyl was first introduced by Dr. Jansen in 1959. Many type of fentanyl derivatives have been developed by adding respective substituents to the canonic molecule inorder to alter the potency, some of the ensunting molecules may exist as isomers. (The isomers of 3-methylfentanyl), which have different types of analgesic potencies depends on which is used. Bever reported that the 3rd position of a methyl group (-CH3) into the piperidine ring, increases analgesic potency. The Trans isomer was slightly more active agent than fentanyl, but its respective cis form was eight folds more active. They found that activity of the cis (+) 3-methylfentanyl more potent than fentanyl, whereas the cis negative form was less potent.

Introduction

Fentanyl is a potent analgesic that is almost a hundred times accented than morphine, the use of fentanyl is pain allayer and anesthetic was adopted in the medical primed. Fentanyl was first introduced by Dr. Jansen in 1959 [1-4].

Many type of fentanyl derivatives have been developed by adding respective substituents to the canonic molecule inorder to alter the potency, some of the ensunting molecules may exist as isomers. (The isomers of 3-methylfentanyl), which have different types of analgesic potencies depends on which is used [5-8].

Bever reported that the 3rd position of a methyl group (-CH3) into the piperidine ring, increases analgesic potency.

The Trans isomer was slightly more active agent than fentanyl, but its respective cis form was eight folds more active. They found that activity of the cis (+) 3-methylfentanyl more potent than fentanyl, whereas the cis negative form was less potent [9-15].

Chemistry

Fentanyl is a synthetic opioid related phenyl piperidine opioid agonist with the analgesic and anesthetic properties. Fentanyl acts on the mu-receptor in the central nervous system. Fentanyl stimulates the exchanges of GTP for GDP on the G-protein complex inhibits adenylate cyclase, results in a decrease in intracellular cAMP and leads the reduction in release of neurotransmitters substance like GABA, dopamine, acetylcholine and noradrenaline. The analgesic activity of fentanyl is due to the its metabolite morphine, show stimulation the opening of G-PC (G-protein coupled receptor inwardly regenerated potassium channels and blocks the opening of N-type voltage gated calcium channels resulting in hyperpolarization and reduced neuronal votability.

Fentanyl is a piperidine derivative opioid analgesic. The systematic IUPAC name is N-(1-(2-phenethyl)-4-piperidinyl-N-phenylpropanamide.

Fentanyl having its two forms as follows.

Fentanyl citrate

developing-drugs

Molecular formula: C22H28N2O.C6H8O7

Molecular weight: 528.59 gm/mol

Melting point: 154-156°C

Solubility: Fentanyl is the white colour crystalline powder soluble in water.

Fentanyl HCl

developing-drugs

Molecular formula: C22H28N2O.HCl

Molecular weight: 372.93 gm/mol

Melting point: 232°C

Solubility: White in colour

Crystalline in nature, partially soluble in water.

Analogues: The fentanyl which is the most potent analgesic in the field of medical and healthcare, which leads to the development of different type of formulation fentanyl analogues. Several fentanyl analogues used as recreational drugs by the drug abusers including β- hydroxy-3-methylfentanyl 3-Methylfentanyl, Acetyl-α-methylfentanyl, α-methylfentanyl, β-hydroxyfentanyl, thiofentanyl, α– methylthiofentanyl 3-Methylthiofentanyl.

Physical characteristic which can be used for the identification of fentanyl and its salts is that appears as white crystalline powder, due its water-soluble action fentanyl citrate is mostly used for the oral buccal dosage form (buccal lozenges) and transdermal patches, transmucosal [14-16].

Pharmacodynamics/Mechanism of Action

Fentanyl is the potent opioid analgesic. Fentanyl interacts with the opioid mu-receptor and binds with kappa (κ) and delta-type opioid receptors also. These mu-binding sites are broadly distributed in the human spinal cord, brain, and other tissues. In clinical Fentanyl show its principal pharmacologic action on the central nervous system. Its therapeutic action values are analgesia and sedation. Fentanyl depresses the respiratory centers, depresses the cough reflex, and constricts the pupils as binding the mu (μ) receptor [17-22].

Fentanyl is a pure opioid agonist, acts as interacting with opioid mureceptors located in the brain, spinal cord and smooth muscles. The primary site of therapeutic action is the central nervous system (CNS). Clinically use of fentanyl pharmacologic consequence of the interaction of fentanyl with mu-receptors is analgesic and sedative [23-26].

Opioids increase the muscle tone action and decrease the contraction of the smooth muscle in the GI tract. This the results of prolongation of GI transit time and responsible for the constipating effect of opioids. The opioids increase biliary tract pressure and some patients with biliary colic may undergo declension of pain.

Opiate receptors coupled with G-protein receptors and act as both positive and negative regulators for synaptic transmission G-proteins that activate effective proteins. Receptor binding of the opiate stimulates exchange of GTP to GDP on the G-protein complex. As system is adenylate cyclase and cAMP situated at the endo surface of the plasma membrane, opioids decrease intracellular cAMP by inhibiting adenylate cyclase. Opioids also show the inhibitory action the release of vasopressin, somatostatin, glucagon and insulin. The most analgesic activity of the fentanyl is due to its conversion to morphine [27-30].

Pharmacokinetics

The pharmacokinetics as absorption of fentanyl drug from the oral transmucosal drug delivery is a combination of an initial rapid absorption from buccal mucosa and more prolonged absorption of the swallowed fentanyl from the GI tract. Both the blood profile and the bioavailability of fentanyl will depend the fraction of the dose that absorbed through the oral mucosa and the fraction swallowed. The onset of action as IV (Intra venous) administration is rapid, the analgesia peak occurs within several minutes and the duration of analgesia action is 30-60 minutes after a single dose up to 100 μg [31-36].

Generally, ¼ part (25%) of the total dose of fentanyl is rapidly absorbed in the bucal mucosa and show the systemically availability. The left over ¾ parts (75%) of the total drug dose is swallowed in the saliva and slowly absorbed from the GI tract. About 25% of this amount (¼ of the total dose) escapes hepatic and intestinal first-pass elimination and able for systemically availability. Thus, generally observed 50% bioavailability of the oral transmucosal fentanyl citrateis divided between rapid transmucosal and slower GI tract absorption [37,38].

Less than 7-8% of the drug dose is excreted unchanged by the urine and only around 1% is excreted unchanged by the feces. The metabolites mainly excreted in the urine. The total plasma clearance for fentanyl was observed 0.5 Ltr/hr/kg (range 0.3 to 0.7 Ltr/hr/kg) [38-41].

Route of elimination

Fentanyl metabolized in human cytochrome P450 3A4 in isoenzyme system and eliminated by urinary system, after intravenously rout of Fentanyl approximately 75% (3/4 part) of drug is excreted by the urinary system within 72 hours [42-44].

Medicinal uses

Analgesia: The analgesic activity of fentanyl depends on the blood plasma drug level. These are the indicates for the relief of mild to severe pain [45,46].

Acute pain: Opioids are the most effective agents for the treatment of acute and severe pain for short term relief and it also controls to severe acute pain treatment. They have also been found to be important in treatment of rheumatoid arthritis and Cancer pain [47,48].

Central nervous system: Fentanyl depresses the cough reflex by the suppressing cough center in the medulla. Antitussive effects occur with the doses lower than the dose required for analgesia.

Gastrointestinal system: Fentanyl causes reduction in motility increase in muscle tone in the antrum of the stomach and duodenum. Digestion for foods is delayed in the small intestine and the propulsive contractions are decreased. Propulsive peristaltic waves in the colon are decreased the tone may increase to the point of spasm results in constipation.

Respiratory system: All the mu-receptor agonists show respiratory depression.

Intranasal: The intranasal bioavailability of fentanyl is about 80-90% but there is imprecision due to clotted pharyngeal swallow nostrils, and incorrect administration [49-52].

Side effects

Fentanyl having the following side effects [50-54].

More common:

• Blurred vision

• Chest pain

• Sore throat

• Loss of appetite

• Decreased urine

• Lightheadedness

• Rapid breathing

• Convulsions

• Increased thirst

• Lower back or side pain

• Difficult or labored breathing

• Nausea or vomiting

• Confusion

• Dry mouth

• Irregular heartbeat

Less common:

• Change in walking and balance

• Slow or fast heartbeat

• Rhythmic movement of the muscles

• Pounding in the ears

• Stomach pain

• Unsteadiness

• Decreased frequency of urination

• Shakiness in the legs, arms, hands, or feet

• Thinking abnormalities

Side Effects: Post Treatment

• Restlessness

• Weakness

• Stomach cramps

• Speech disorder

• Fentanyl Interactions

Fentanyl may interact with:

• Fentanyl shows the interaction with the mono amino oxidase inhibitors. Like isocarboxazid (Marplan) and phenelzine [55,56].

• Antagonist activity against pentazocine and butorphanol.

• Partial agonist analgesics, such as buprenorphine.

Show the interaction with the anticholinergics agents.

Fentanyl and alcohol

Use of the fentanyl with alcohol may cause of low blood pressure, sedation, respiratory depression, coma, and death.

Fentanyl and grapefruit

Potentially respiratory depression may occur if the consumption of grape fruit juice. Respiratory depression also occurs if fentanyl using with cytochrome inhibitors.

Fentanyl dosage

Fentanyl comes in five strengths which deliver fentanyl as different rates like-12 micrograms per hour (mcg/h), 25 mcg/hour, 50 mcg/ hour, 75 mcg/hour, and 100 mcg/hour.

Fentanyl overdose

Fentanyl having the following symptoms on its overdose [57].

• Difficulties breathing

• Coma

• Extreme sleepiness

• Difficulty thinking, talking, or walking

• Contraction of pupils

• Dizziness and Faintness

• Confusion

References

Select your language of interest to view the total content in your interested language
Post your comment

Share This Article

Recommended Conferences

Article Usage

  • Total views: 8440
  • [From(publication date):
    December-2016 - Aug 17, 2017]
  • Breakdown by view type
  • HTML page views : 8298
  • PDF downloads :142
 
 

Post your comment

captcha   Reload  Can't read the image? click here to refresh

Peer Reviewed Journals
 
Make the best use of Scientific Research and information from our 700 + peer reviewed, Open Access Journals
International Conferences 2017-18
 
Meet Inspiring Speakers and Experts at our 3000+ Global Annual Meetings

Contact Us

Agri, Food, Aqua and Veterinary Science Journals

Dr. Krish

agrifoodaquavet@omicsonline.com

1-702-714-7001 Extn: 9040

Clinical and Biochemistry Journals

Datta A

clinical_biochem@omicsonline.com

1-702-714-7001Extn: 9037

Business & Management Journals

Ronald

business@omicsonline.com

1-702-714-7001Extn: 9042

Chemical Engineering and Chemistry Journals

Gabriel Shaw

chemicaleng_chemistry@omicsonline.com

1-702-714-7001 Extn: 9040

Earth & Environmental Sciences

Katie Wilson

environmentalsci@omicsonline.com

1-702-714-7001Extn: 9042

Engineering Journals

James Franklin

engineering@omicsonline.com

1-702-714-7001Extn: 9042

General Science and Health care Journals

Andrea Jason

generalsci_healthcare@omicsonline.com

1-702-714-7001Extn: 9043

Genetics and Molecular Biology Journals

Anna Melissa

genetics_molbio@omicsonline.com

1-702-714-7001 Extn: 9006

Immunology & Microbiology Journals

David Gorantl

immuno_microbio@omicsonline.com

1-702-714-7001Extn: 9014

Informatics Journals

Stephanie Skinner

omics@omicsonline.com

1-702-714-7001Extn: 9039

Material Sciences Journals

Rachle Green

materialsci@omicsonline.com

1-702-714-7001Extn: 9039

Mathematics and Physics Journals

Jim Willison

mathematics_physics@omicsonline.com

1-702-714-7001 Extn: 9042

Medical Journals

Nimmi Anna

medical@omicsonline.com

1-702-714-7001 Extn: 9038

Neuroscience & Psychology Journals

Nathan T

neuro_psychology@omicsonline.com

1-702-714-7001Extn: 9041

Pharmaceutical Sciences Journals

John Behannon

pharma@omicsonline.com

1-702-714-7001Extn: 9007

Social & Political Science Journals

Steve Harry

social_politicalsci@omicsonline.com

1-702-714-7001 Extn: 9042

 
© 2008-2017 OMICS International - Open Access Publisher. Best viewed in Mozilla Firefox | Google Chrome | Above IE 7.0 version