Cetirizine

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Cetirizine
File:Cetirizine10.JPG
File:Cetirizine structure.svg
Systematic (IUPAC) name
(±)-[2-[4-[(4-chlorophenyl)phenylmethyl]-1- piperazinyl]ethoxy]acetic acid
Clinical data
[[Regulation of therapeutic goods |Template:Engvar data]]
Pregnancy
category
  • US: B (No risk in non-human studies)
Routes of
administration		 Oral
Legal status
Legal status
Pharmacokinetic data
Bioavailability well absorbed
Protein binding 93% avg
Metabolism Probable major agent: CYP3A43 (Cytochrome P450 3A43); Minor agent: CYP3A4 (Cytochrome P450 3A4)
Biological half-life 8.3 Hours
Excretion Hepatic, urine or excrement (Small amounts)
Identifiers
CAS Number 83881-51-0
ATC code R06AE07 (WHO)
PubChem CID 2678
IUPHAR/BPS 1222
DrugBank APRD00630
ChemSpider 2577
Synonyms Alatrol, Alzene, Cetirizina, Cetirin, Cetzine, Cetirizin, Cezin, Humex, Letizen, Razene, Reactine, Zyrtec, Zirtec, Zodac, Zirtek, Zynor, Zyrlek, Zyllergy
Chemical data
Formula C21H25ClN2O3
Molar mass 388.89[[Script error: No such module "String".]]
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Cetirizine (pronounced /sɛˈtɪrɨziːn/), a second-generation antihistamine, is a major metabolite of hydroxyzine, and a racemic selective H1 receptor inverse agonist used in the treatment of allergies, hay fever, angioedema, and urticaria. The structural similarity of cetirizine to hydroxyzine, and its derivation from piperazine, attribute similar adverse reactions and properties to other piperazine derivatives.[citation needed]

Formerly prescription-only in the US and Canada, cetirizine is now available over-the-counter in both countries as Zyrtec and Reactine respectively. Zyrtec was the top new non-food product of 2008 in the US, generating sales of $315.9 million.[1] It is also available as a generic drug. In Australia, Zyrtec is available over-the-counter in pharmacies and in the UK cetirizine can be sold in limited quantities off-the-shelf in any outlet and is often available in supermarkets. In India, Zyrtec and Cetzine are popular antihistamines and are available without prescription[citation needed]. As of 2009 in Germany many generic drugs containing cetirizine are available in pharmacies without prescription.[2] Norway, Sweden[3] and Finland also recognize Cetirizine as an over-the-counter medicine.

The levorotary enantiomer of cetirizine is known as levocetirizine.

Pharmacology

Cetirizine crosses the blood-brain barrier only slightly, eliminating the sedative side-effect common with older antihistamines; however it still causes mild drowsiness.[4] It has also been shown to inhibit eosinophil chemotaxis and LTB4 release. At a dosage of 20 mg, Boone et al. found that it inhibited the expression of VCAM-1 in patients with atopic dermatitis.[5]

Administration method and metabolism

Chewable, non-chewable, and syrup forms of cetirizine are similarly absorbed rapidly and effectively, with absorbed food minutely affecting the absorption rate which yields a peak serum level one hour after administration;[6] in a study of healthy volunteers prescribed 10 mg tablets, once daily for 10 days, a mean peak serum level of 311 ng/mL was observed.[7] The metabolic effects of cetirizine are long acting, remaining in the system for a maximum of 21 hours before being excreted; the average elimination half-life is 8 hours.[6][7] 70% of the drug is excreted or eliminated by kidney function within 72 hours, and 10% is removed through urine or excrement;[6][7] of which half is observed as unchanged cetirizine compound.[6][7]

Like many other antihistamine medications, cetirizine is commonly prescribed in combination with pseudoephedrine hydrochloride, a decongestant. These combinations are marketed using the same brand name as the cetirizine with a "-D" suffix (Zyrtec-D, Virlix-D, etc.)

Formerly only available by a prescription, both Zyrtec and Zyrtec-D in November 2007 became available over-the-counter in the United States.[8]

Indications

Rhinovirus infection

File:Cetirizine structure racemic.svg
L-Stereosimer (top) and D-stereoisomer of cetirizine

Interleukin 6 and interleukin 8 have been shown to be elevated in acute respiratory distress syndrome.[9] Cetirizine contains L- and D-stereoisomers. Chemically, levocetirizine is the active L-enantiomer of cetirizine. In a recent study of airway epithelial cells the following was observed: Levocetirizine inhibits the production of intercellular adhesion molecule ICAM-1 and secretion of interleukin (IL)-6 and IL-8, which may have beneficial effects on the pathophysiologic changes related to human rhinovirus (HRV) infection. Levocetirizine treatment inhibited the HRV-induced increase in ICAM-1 mRNA and protein levels, as well as the HRV-induced expression of IL-6 and IL-8 mRNA and protein levels. Viral titer, as measured by culture in MRC-5 cells, was reduced by levocetirizine. Levocetirizine treatment also reduced the increased nuclear factor-kappa B (NF-κB) expression seen with HRV infection. Levocetirizine inhibited the expression of Toll-like receptor 3 (TLR3) mRNA and protein levels. These findings indicate that, in HNEC and A549 cells, levocetirizine inhibits HRV replication and HRV-induced upregulation of ICAM-1, IL-6, and IL-8, TLR3 expression and NF-κB activation. The results of this study suggest that levocetirizine may have a possible clinical application in the treatment of airway inflammation caused by HRV infection.[10] Airway inflammation caused from a cytokine storm secondary to acute respiratory distress syndrome could also theoretically benefit.

Kimura's disease

Cetirizine is an effective agent in treating the symptoms of Kimura's disease, which mostly occurs in young Asian men, affecting the lymph nodes and soft tissue of the head and neck in the form of tumor-like lesions. Cetirizine's properties of being effective both in the treatment of pruritus (itching) and as an anti-inflammatory agent make it suitable for the treatment of the pruritus associated with these lesions.[11] In a 2005 study, the American College of Rheumatology conducted treatments initially using prednisone, followed by steroid dosages and azathioprine, omeprazole, and calcium and vitamin D supplements over the course of two years.[11] The skin condition of the patient began to improve and the skin lesions lessened. However, there were symptoms of cushingoid and hirsutism observed before the patient was removed from the courses of steroids and placed on 10 mg/day of cetirizine to prevent skin lesions;[11] an agent suitable for the treatment of pruritus associated with such lesions.[11] Asymptomatically, the patient's skin lesions disappeared after treatment with cetirizine, blood eosinophil counts became normal,[11] corticosteroid effects were resolved,[11] and a remission began within a period of two months.[11] It is also thought that the inhibition of eosinophils may be the key to treatment of Kimura's disease due to the role of eosinophils, rather than other cells with regards to the lesions of the skin.[11]

Synthesis

The following synthesis of this compound was reported in 1985:[12]

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References

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Books and journals

  1. Anderson, P. O., Knoben, J. E., et al. (2002) Handbook of clinical drug data 10th ed. McGraw-Hill International
  2. Pfizer Inc, et al. (2006) ZYRTEC (cetirizine hydrochloride) Tablets, Chewable Tablets and Syrup For Oral Use Pfizer Incorporated publications
  3. Chetrit, E. B., Amir, G., Shalit, M. (2005). Cetirizine: an effective agent in Kimura's Disease Arthritis & Rheumatism (Arthritis care & research) Vol 53, p117-118

External links

Aminoalkyl ethers
Substituted alkylamines
Substituted ethylenediamines
Phenothiazine derivatives
Piperazine derivatives
Others for systemic use
For topical use
Antiallergic agents excluding corticosteroids
Other antiallergics
da:Cetirizin

de:Cetirizin fr:Cétirizine it:Cetirizina ka:პარლაზინი hu:Cetirizin nl:Cetirizine ja:セチリジン pl:Cetyryzyna pt:Cetirizina ru:Цетиризин fi:Setiritsiini th:เซทิไรซีน tr:Setirizin

zh:盐酸西替利嗪
  1. ↑ Elliott, Stuart (24 March 2009). "A Strategy When Times Are Tough: "It's New!"". The New York Times. Retrieved 26 March 2009. 
  2. ↑ "Cetirizin". 
  3. ↑ "Cetirizin". 
  4. ↑ Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  5. ↑ Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  6. ↑ 6.0 6.1 6.2 6.3 Anderson, Philip; Knoben, James E.; Troutman, William G. (2002). Handbook of clinical drug data. New York: McGraw-Hill. p. 807. ISBN 0-07-136362-9. 
  7. ↑ 7.0 7.1 7.2 7.3 "Zyrtec prescribing information" (PDF). May 2006. Retrieved 2009-11-19. 
  8. ↑ Payne, January W (2008-01-09). "Over-the-Counter Zyrtec: a Money-Saver?". U.S. News & World Report. 
  9. ↑ Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  10. ↑ Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  11. ↑ 11.0 11.1 11.2 11.3 11.4 11.5 11.6 11.7 Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  12. ↑ Baltes, E.; De Lannoy, J.; Rodriguez, L.; 1985, U.S. Patent 4,525,358.
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