Topical hydrocortisone

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Topical hydrocortisone
Clinical data
Trade namesAla-Cort, Aquanil HC, Beta HC, others [1]
Other namesCortisol; 11β,17α,21-Trihydroxypregn-4-ene-3,20-dione
AHFS/Drugs.comMonograph
MedlinePlusa682793
License data
Pregnancy
category
Routes of
administration		Topical
Drug classCorticosteroid; Glucocorticoid; Mineralocorticoid
ATC code
Legal status
Legal status
Identifiers
  • (8S,9S,10R,11S,13S,14S,17R)-11,17-Dihydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-3-one
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
Chemical and physical data
FormulaC21H30O5
Molar mass362.466 g·mol−1
3D model (JSmol)
  • O=C4\C=C2/[C@]([C@H]1[C@@H](O)C[C@@]3([C@@](O)(C(=O)CO)CC[C@H]3[C@@H]1CC2)C)(C)CC4
  • InChI=1S/C21H30O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h9,14-16,18,22,24,26H,3-8,10-11H2,1-2H3/t14-,15-,16-,18+,19-,20-,21-/m0/s1 checkY
  • Key:JYGXADMDTFJGBT-VWUMJDOOSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Topical hydrocortisone is a drug under the class of corticosteroids, which is used for the treatment of skin inflammation, itchiness and allergies.[10] Some examples include insect bites, dermatitis and rash.[11][12][13]

Hydrocortisone was discovered by Nobel laureates Edward C. Kendall and Philip S. Hench in the 1930s while they were conducting research on rheumatoid arthritis.[14][15][16] Its topical use was first recorded in the 1950s.[17][18]

The most common adverse effects after the application of topical hydrocortisone are burning and stinging sensations.[10][11] Side effects after long-term usage include eyesight damage, elevated blood sugar levels and adrenal gland disorders.[12]

Topical hydrocortisone is available in several dosage forms such as solution, lotion, cream, ointment and spray.[19] Some brand names for topical hydrocortisone include Anusol HC, Cortizone 10, and Synacort.[19]

Medical uses[edit]

Topical hydrocortisone is indicated for relieving swelling, irritation and redness in a number of skin conditions, including insect bites, heat rash, eczema, psoriasis, contact dermatitis and nappy rash.[12][19][20][21] It could be formulated as a single active ingredient in some medications, e.g. Cortaid®, which is applied for anal itchiness.[13][22][23] On some occasions, this drug may be used in combination with other types of drugs to alleviate skin problems.[13][24] For example, it could be used together with antibiotics such as polymyxin, neomycin and bacitracin to improve dermal conditions.[24]

Adverse effects[edit]

Possible adverse effects of topical hydrocortisone

Some common side effects include burning and stinging sensations.[10][11][21][25] Colour change of the skin, bump formation on the skin and additional hair growth could also occur.[11][19] Consult a doctor if these side effects persist or become worse.[11][19]

Some severe side effects are severe rash, swelling of the skin, and skin infection.[19] Rare but serious allergic reactions, also known as anaphylaxis, could also occur.[12] If you encounter any of these side effects, you should approach a doctor immediately.[19]

Adverse effects after a long-term use of topical hydrocortisone include adrenal gland disorders.[25] This problem can be more severe when you use excess topical hydrocortisone for a prolonged period of time.[25] Other adverse effects include blurry vision, dizziness, fainting, unusual heartbeat, thirsty sensation, frequent urination, and fatigue.[25] Please inform your doctor if you experience any of these symptoms.[25]

The impact of ingestion (eating) of such products has not been reported systematically, but a case report published in 2022 suggests this can lead to hospitalization and be potentially life threatening.[26]

Pharmacology[edit]

Pharmacodynamics[edit]

Hydrocortisone would bind to glucocorticoid receptors in the human body, which reduces the production of inflammatory transcription factors, phospholipase A2, and NF-kappa B, as well as increases the expression of anti-inflammatory genes.[14] In addition, hydrocortisone has a relatively wide therapeutic window,[14] implying that toxicity is less likely to occur.

Topical hydrocortisone contributes to inflammatory-reducing activity in various ways.[27] Firstly, hydrocortisone can bind to glucocorticoid receptors in the cytoplasm, causing alterations in the conformation of the receptors.[27][28] This promotes the exchange and binding of proteins at the site of the receptors.[28] The activated receptors then enter the nucleus to upregulate genes for reducing inflammation such as lipocortin.[27][28] Next, lipocortin inhibits phospholipase A2, an enzyme preventing the synthesis of prostaglandins and lipoxygenases from arachidonic acid.[27][28] After that, hydrocortisone stabilises the lysosomes in neutrophils, which are a type of white blood cell.[27] Hence, the neutrophils would not degranulate, preventing inflammation.[27] Eventually, mRNA segments are destabilized, affecting gene transcription and interrupting the gene production of cytokines, chemokines, cyclooxygenase-2, etc.[27]

Pharmacokinetics[edit]

Topical hydrocortisone has minimal absorption into the body: Only 4-19% of the topical hydrocortisone cream applied would be absorbed into the human bloodstream.[14] After a certain extent of absorption, it undergoes distribution, metabolism and elimination pathways that are similar to systemic hydrocortisone.[29] Regarding the distribution of topical hydrocortisone, it binds to plasma proteins such as globulin and albumin, then the drug is mainly metabolized in the liver, and the metabolite will be excreted through bile or by kidneys.[29]

Chemistry[edit]

This is a chemical structure of hydrocortisone with markings of the functional groups that contribute to its glucocorticoid activity.

Structure-activity relationship[edit]

Hydrocortisone, or 17-hydroxycorticosterone, is under the class of glucocorticoids, which are steroids synthesized in the adrenal cortex of the kidneys.[30][31] In order to illustrate its glucocorticoid activity, the A ring of hydrocortisone has a keto group in the 3rd carbon and a double bond between the 4th and 5th carbon.[32] For the C ring of the compound, the 11th carbon has a beta hydroxyl substitution, which is also necessary for the drug to demonstrate glucocorticoid effects.[32]

pKa[edit]

The estimated pKa values of hydrocortisone are 12.59 and -2.8 respectively.[14]

Solubility[edit]

The log P value of hydrocortisone is 1.61, which was derived from experiments done by pharmacologist Corwin Hansch and his research team.[14] In addition, the predicted water solubility of hydrocortisone is 0.199 mg/mL.[14] These values indicate that hydrocortisone has a low solubility in water and is more soluble in organic solvents.

For other chemical information of topical hydrocortisone, please refer to the 'Topical hydrocortisone' table.

Formulations[edit]

Topical hydrocortisone cream available in the United States
available in Hong Kong
Topical hydrocortisone cream with neomycin available in Hong Kong

Topical hydrocortisone is formulated as liquid, solution, lotion, cream, gel, ointment, foam, and spray.[33] The strength of topical hydrocortisone products ranges from 0.1% to 2.5%, which means there could be 1 mg to 25 mg hydrocortisone in 1g of the products.[12] Some formulations for topical hydrocortisone include hydrocortisone 0.5% cream or ointment, hydrocortisone 1% cream or ointment, and hydrocortisone 2.5% cream or ointment.[34] Regarding the method of applying the medications, please refer to the package insert or consult a pharmacist.

Some less common forms of topical hydrocortisone are also available in the market. For example, hydrocortisone butyrate is a relatively potent topical hydrocortisone cream that can only be purchased when you have a valid prescription.[12] Besides, some forms of topical hydrocortisone are mixed with antimicrobial drugs to treat bacterial or fungal problems of the skin.[12]

History[edit]

In the 1930s, hydrocortisone was found by biochemist Edward C. Kendall and rheumatologist Philip S. Hench, who were both Nobel laureates.[14][15][16] When they were investigating therapies for rheumatoid arthritis, they discovered that female patients of the disease would experience an alleviation of their condition if they were pregnant at the same time.[15][16] It was also found that patients suffering from both rheumatoid arthritis and jaundice would have fewer symptoms associated with rheumatoid arthritis.[15][16] Following this finding, they extracted different hormones from the adrenal cortex of cows in search of a suitable drug.[15][16][18] They first identified cortisone to be one of the possible drugs, and further research led them to discover an effective drug for human dermal problems, which was hydrocortisone.[15][16][18]

After the discovery of hydrocortisone, the earliest application of hydrocortisone as a topical form in humans was recorded in 1952.[16][17][18] Its successful utilization facilitated more research on topical corticosteroids, which helped the development of similar drugs with higher activity.[16][17][18]

References[edit]

  1. ^ "Hydrocortisone topical Uses, Side Effects & Warnings". Drugs.com. Retrieved 11 March 2023.
  2. ^ "Hydrocortisone topical Pregnancy and Breastfeeding Warnings". drugs.com. Retrieved 26 February 2023.
  3. ^ "Part A - Interim decisions on matters referred to an expert advisory committee: ACMS#14 (1.1-1.3)". Australian Government. Retrieved 13 April 2023.
  4. ^ "Rules for the sale, supply and administration of medicines for specific healthcare professionals". National Health Service UK. Retrieved 13 April 2023.
  5. ^ "Hydrocortisone Notice of enforcement policy" (PDF). U.S. Food and Drug Administration. Retrieved 13 April 2023.
  6. ^ "Ala-cort- hydrocortisone cream". DailyMed. U.S. National Library of Medicine. Retrieved 13 April 2023.
  7. ^ "Ala-scalp- hydrocortisone lotion". DailyMed. U.S. National Library of Medicine. Retrieved 13 April 2023.
  8. ^ "Anusol HC- hydrocortisone acetate suppository". DailyMed. U.S. National Library of Medicine. Retrieved 13 April 2023.
  9. ^ "Patterns of OTC use in the Netherlands". The Pharma Letter. London. Retrieved 13 April 2023.
  10. ^ a b c "Pandel (hydrocortisone probutate topical) dosing, indications, interactions, adverse effects, and more". Medscape. WebMD LLC. Retrieved 2023-02-26.
  11. ^ a b c d e "Hydrocortisone Topical: Uses, Side Effects, Interactions, Pictures, Warnings & Dosing - WebMD". WebMD LLC. Retrieved 2023-02-26.
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  14. ^ a b c d e f g h "Hydrocortisone". go.drugbank.com. Retrieved 2023-02-26.
  15. ^ a b c d e f "The Nobel Prize in Physiology or Medicine 1950". NobelPrize.org. Retrieved 2023-03-04.
  16. ^ a b c d e f g h Saenger AK (August 2010). "Discovery of the wonder drug: from cows to cortisone. The effects of the adrenal cortical hormone 17-hydroxy-11-dehydrocorticosterone (Compound E) on the acute phase of rheumatic fever; preliminary report. Mayo Clin Proc 1949;24:277-97". Clinical Chemistry. 56 (8): 1349–1350. doi:10.1373/clinchem.2010.149120. PMID 20538878. S2CID 1784993.
  17. ^ a b c Mukhopadhyay S, Kwatra G (2018). "Evolution and Development of Topical Corticosteroids". In Lahiri K (ed.). A Treatise on Topical Corticosteroids in Dermatology: Use, Misuse and Abuse. Singapore: Springer. pp. 1–9. doi:10.1007/978-981-10-4609-4_1. ISBN 978-981-10-4609-4.
  18. ^ a b c d e Mehta AB, Nadkarni NJ, Patil SP, Godse KV, Gautam M, Agarwal S (2016-07-01). "Topical corticosteroids in dermatology". Indian Journal of Dermatology, Venereology and Leprology. 82 (4): 371–378. doi:10.4103/0378-6323.178903. PMID 27279294. S2CID 37156776.
  19. ^ a b c d e f g "Hydrocortisone Topical". MedlinePlus Drug Information. U.S. National Library of Medicine. Retrieved 2023-02-26.
  20. ^ "Hydrocortisone: a steroid used to treat many health conditions". nhs.uk. 2019-03-26. Retrieved 2023-02-26.
  21. ^ a b "Topical Corticosteroids". Drug Office, Department of Health, Hong Kong. Retrieved 2023-03-04.
  22. ^ "Pruritus Ani (Anal Itch)". Section of Colon and Rectal Surgery. 2015-01-26. Retrieved 2023-03-04.
  23. ^ "Cortaid (Hydrocortisone Cream and Ointment 1.0%): Uses, Dosage, Side Effects, Interactions, Warning". RxList. Retrieved 2023-03-04.
  24. ^ a b "Neomycin, Polymyxin, Bacitracin, and Hydrocortisone Topical". MedlinePlus Drug Information. U.S. National Library of Medicine. Retrieved 2023-03-04.
  25. ^ a b c d e "Hydrocortisone (Topical Application Route) Side Effects". Mayo Clinic. Retrieved 2023-03-04.
  26. ^ Saha A, Balakrishnan S, Trivedi N, Agraham GM (21 October 2022). "Hypertension and Severe Hypokalemia Associated With Oral Ingestion of Topical Hydrocortisone Cream". AACE Clinical Case Reports. 9 (1): 2–4. doi:10.1016/j.aace.2022.10.004. PMC 9837079. PMID 36654996.
  27. ^ a b c d e f g Kwatra G, Mukhopadhyay S (2018). "Topical corticosteroids: pharmacology.". In Lahiri K (ed.). A Treatise on Topical Corticosteroids in Dermatology: Use, Misuse and Abuse. Springer. pp. 11–22. doi:10.1007/978-981-10-4609-4_2. ISBN 978-981-10-4609-4.
  28. ^ a b c d "glucocorticoid_pharmacology [TUSOM | Pharmwiki]". tmedweb.tulane.edu. Retrieved 2023-04-13.
  29. ^ a b "Hydrocortisone Cream: Package Insert / Prescribing Information". Drugs.com. Retrieved 2023-02-26.
  30. ^ Chourpiliadis C, Aeddula NR (2023). "Physiology, Glucocorticoids". StatPearls. Treasure Island (FL): StatPearls Publishing. PMID 32809732.
  31. ^ "Hydrocortisone". PubChem. U.S. National Library of Medicine. Retrieved 2023-04-13.
  32. ^ a b Buchwald P, Bodor N (May 2004). "Soft glucocorticoid design: structural elements and physicochemical parameters determining receptor-binding affinity". Die Pharmazie. 59 (5): 396–404. PMID 15212309.
  33. ^ "Hydrocortisone (Topical Application Route) Description and Brand Names". Mayo Clinic. Retrieved 2023-02-26.
  34. ^ "Search results for hydrocortisone". Electronic Medicines Compendium. Datapharm. Retrieved 2023-02-26.
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