Transdermal analgesic patch: Difference between revisions
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== History == |
== History == |
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Transdermal drug delivery was influenced by topical drug delivery. Sherman Kramer and Dale Wurster, his teacher, were both based in pharmacology and are credited with the beginning stages of transdermal patch delivery in 1961. By attaching a diffusion cell to the volunteers and monitoring their levels of the drug administered, it was discovered that the levels of the drug could be affected by the absorption of the skin and the diffusion area of the patch. 10 years later, Alejandro Zaffaroni filed a patent for transdermal drug delivery through a rate-controlling membrane. Arnold Beckett, a British pharmacist, held experiments with a patch system that were studied and proven to maintain steady blood levels through administration of the drug.<ref |
Transdermal drug delivery was influenced by topical drug delivery. Sherman Kramer and Dale Wurster, his teacher, were both based in pharmacology and are credited with the beginning stages of transdermal patch delivery in 1961. By attaching a diffusion cell to the volunteers and monitoring their levels of the drug administered, it was discovered that the levels of the drug could be affected by the absorption of the skin and the diffusion area of the patch. 10 years later, Alejandro Zaffaroni filed a patent for transdermal drug delivery through a rate-controlling membrane. Arnold Beckett, a British pharmacist, held experiments with a patch system that were studied and proven to maintain steady blood levels through administration of the drug.<ref>{{Cite journal |last=Pastore |first=Michael N |last2=Kalia |first2=Yogeshvar N |last3=Horstmann |first3=Michael |last4=Roberts |first4=Michael S |date=May 2015 |title=Transdermal patches: history, development and pharmacology: History of transdermal patches |url=https://onlinelibrary.wiley.com/doi/10.1111/bph.13059 |journal=British Journal of Pharmacology |language=en |volume=172 |issue=9 |pages=2179–2209 |doi=10.1111/bph.13059 |pmc=PMC4403087 |pmid=25560046}}</ref> These discoveries laid the foundation for transdermal patch systems and individual research with specific drugs for transdermal patch systems followed. |
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==See also== |
==See also== |
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Revision as of 11:57, 27 April 2023
A transdermal analgesic or pain relief patch is a medicated adhesive patch used to relieve minor to severe pain. There are three primary types of analgesic patches. First are patches containing counterirritants, which are used to treat mild to moderate pain. Second are patches containing opioids, such as Buprenorphine and Fentanyl, narcotics used to relieve moderate to severe pain. Fentanyl is often used for opioid-tolerant patients. Most obscure of all are patched containing Nitroglycerin, also known as glyceryl trinitrate (GTN), a medication used for heart failure, high blood pressure, anal fissures, painful periods, and to treat and prevent chest pain.
Counterirritant patches
Counterirritant patches contain ingredients such as capsaicin, methyl salicylate, camphor, or menthol, which are thought to mask pain signals by causing other sensations (itching, warmth, or cooling) in the areas they are applied to.[1] In the United States, patches sold under the brand name Salonpas are approved by the Food and Drug Administration under a New Drug Application (NDA) for the treatment of mild to moderate pain caused by soft tissue injury (e.g., strains, sprains), arthritis, or backache. While Salonpas patches may provide some relief, the effects are not strong and the evidence supporting their efficacy is weak.[2]
Other products, including Bengay and Mentholatum, which are not covered by NDA, indicate relief of minor pain.[1] Counterirritant patches are sold over-the-counter and do not require a prescription. Other over-the-counter products marketed for the relief of minor injury or arthritis pain include Absorbine Jr. Pain Relief, Excedrin Cooling Pads, and Icy Hot Patches.[3]
In Japan, Salonpas, produced by Hisamitsu Pharmaceutical, remains a popular brand. Other manufacturers, including Yutoku Pharmaceutical, SS Pharmaceutical, and Suzuki Nippondo also produce similar over-the-counter patches containing methyl salicylate or glycol salicylate.[4]
In Australia, patches sold under the brand names Eco Pain and Dencorub are approved by the Therapeutic Goods Administration and listed on the Australian Register for Therapeutic Goods (ARTG) as a Class 1 Medical Device. They are approved for sale over-the-counter for the treatment of mild pain caused by soft tissue injury (e.g., strains, sprains), arthritis, or backache.
Fentanyl patches
Fentanyl transdermal patches are sold under the brand name Duragesic or as generic equivalents. Fentanyl is an opioid with rapid onset of pain relief; it is often used to treat breakthrough pain. Fentanyl patches release fentanyl through the skin and may provide pain relief for up to 72 hours.[5]
Several deaths or life-threatening overdoses have been linked to misuse of fentanyl patches.[6] Fentanyl patches are indicated only for patients with moderate to severe chronic pain who have been taking regular narcotic pain medication for more than a week and who are considered opioid-tolerant. Overdose can occur when patients use more patches than prescribed, change the patches too frequently, or expose the patches to extreme heat.[6]
Nitroglycerin
History
Transdermal drug delivery was influenced by topical drug delivery. Sherman Kramer and Dale Wurster, his teacher, were both based in pharmacology and are credited with the beginning stages of transdermal patch delivery in 1961. By attaching a diffusion cell to the volunteers and monitoring their levels of the drug administered, it was discovered that the levels of the drug could be affected by the absorption of the skin and the diffusion area of the patch. 10 years later, Alejandro Zaffaroni filed a patent for transdermal drug delivery through a rate-controlling membrane. Arnold Beckett, a British pharmacist, held experiments with a patch system that were studied and proven to maintain steady blood levels through administration of the drug.[7] These discoveries laid the foundation for transdermal patch systems and individual research with specific drugs for transdermal patch systems followed.
See also
- Manufacturers
- Products
References
- ^ a b Pray, W. Steven (1 September 2008). "The pharmacist's role in the appropriate selection of a nonprescription product for pain relief". U.S. Pharmacist. Retrieved 2010-03-24.
- ^ Hall, Harriet. "Salonpas". Science-Based Medicine. Archived from the original on 13 April 2021. Retrieved 14 April 2021.
{{cite web}}:|archive-date=/|archive-url=timestamp mismatch; 5 February 2021 suggested (help) - ^ Levy, Sandra (10 December 2001). "External painkillers lead sales in analgesics market". Drug Topics. Retrieved 2010-03-24.
- ^ Ghosh, Tapash K.; William R. Pfister; Su Il Yum (1997). Transdermal and Topical Drug Delivery Systems. Informa Health Care. ISBN 1-57491-041-8.
- ^ American Society of Health-System Pharmacists, Inc. (15 January 2021). "Fentanyl Transdermal Patch". MedlinePlus. Retrieved 3 August 2021.
- ^ a b US Department of Health and Human Services (21 December 2007). "Information for Healthcare Professionals: Fentanyl Transdermal System (marketed as Duragesic and generics)". US Food and Drug Administration Postmarket Drug Safety Information for Patients and Providers. Retrieved 2010-03-24.
- ^ Pastore, Michael N; Kalia, Yogeshvar N; Horstmann, Michael; Roberts, Michael S (May 2015). "Transdermal patches: history, development and pharmacology: History of transdermal patches". British Journal of Pharmacology. 172 (9): 2179–2209. doi:10.1111/bph.13059. PMC 4403087. PMID 25560046.
{{cite journal}}: CS1 maint: PMC format (link)