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What is the Difference Between Celecoxib and Ibuprofen

November 15, 2023 Posted by Dr Neelaka M

The key difference between Celecoxib and Ibuprofen is that Celecoxib is a selective COX-2 inhibitor and does not cause gastrointestinal ulcers, while Ibuprofen is a non-selective COX-1 and COX-2 inhibitor and thereby causes gastrointestinal ulcers.

Celecoxib and Ibuprofen are two common nonsteroidal anti-inflammatory drugs (NSAIDs) that are effective in treating a variety of conditions, including osteoarthritis, rheumatoid arthritis, and menstrual cramps (or dysmenorrhea). They work by blocking the production of prostaglandins, chemicals that play a role in inflammation and pain. Overall, celecoxib and ibuprofen are both effective NSAIDs, but they have different risks and benefits. Therefore, talking to a doctor about which drug is right for individual conditions is important.

CONTENTS

1. Overview and Key Difference
2. What is Celecoxib  
3. What is Ibuprofen
4. Similarities – Celecoxib and Ibuprofen
5. Celecoxib vs. Ibuprofen in Tabular Form
6. FAQ – Celecoxib vs. Ibuprofen
7. Summary – Celecoxib vs. Ibuprofen

What is Celecoxib?

Celecoxib is a nonsteroidal anti-inflammatory drug (NSAID) that selectively inhibits cyclooxygenase-2 (COX-2) when treating adult osteoarthritis (OA) and rheumatoid arthritis (RA). It may be combined with tramadol when managing acute pain in adults. Unlike other NSAIDs, it does not increase the risk of gastrointestinal bleeding and, therefore, was granted FDA approval in 1998.  Celecoxib has also been evaluated for its potent anticancer activities in clinical trials against various cancers. Interestingly, Celecoxib selectively inhibits only COX-2, which is heavily expressed in inflamed tissues. The inhibition of COX-2 reduces the synthesis of prostaglandin E2 (PGE2), prostacyclin (PGI2), thromboxane (TXA2), prostaglandin D2 (PGD2), and prostaglandin F2 (PGF2), which cause pain.

Celecoxib and Ibuprofen - Side by Side Comparison

Figure 01: Chemical Structure of Celecoxib

Celecoxib is rapidly absorbed in the gastrointestinal tract and reaches the peak plasma level within 3 hours after oral administration. However, the absorption is significantly lower in patients with renal impairments. Celecoxib is primarily bound to plasma albumin and widely distributed into various tissues. Therefore, it is not advisable to use Celecoxib when having renal impairments since it leads to increased serum concentration and toxicity. The drug is extensively metabolized in the liver and excreted in both urine and feces with an elimination half-life of 11 hours. The symptoms of Celecoxib overdose include breathing difficulties, coma, drowsiness, gastrointestinal bleeding, high blood pressure, kidney failure, nausea, stomach pain, sluggishness, and vomiting. During Celecoxib treatment, avoiding alcohol is recommended to decrease the risk of gastrointestinal irritation. The commonly found brand names of Celecoxib include Celebrex, Elyxyb, and Seglentis.

What is Ibuprofen?

Ibuprofen is another NSAID derived from propionic acid and was initially developed in 1960 as a safer alternative to aspirin. It is a common over-the-counter medication widely used as an analgesic, anti-inflammatory, and antipyretic drug. Ibuprofen is a non-selective inhibitor of COX-1 and COX-2, leading to decreased synthesis of prostaglandins and thromboxane. However, it causes gastrointestinal ulcers due to the inhibition of COX-1.

Celecoxib vs Ibuprofen in Tabular Form

Figure 02: Chemical Structure of Ibuprofen

Ibuprofen is well absorbed in the gastrointestinal tract and reaches the peak plasma concentration within 1-2 hours after oral administration. Absorption is slightly impaired if the drug is taken immediately after a meal. More than 99% of the absorbed drug remains bound to plasma proteins and distributed in the tissues with an apparent volume of distribution of 0.1 L/kg. Ibuprofen is extensively metabolized in the liver to hydroxylated and carboxylated derivatives and eliminated in the urine with an elimination half-life of 1-2 hours. The elimination of Ibuprofen is not affected by age and renal impairments. However, the half-life can be prolonged to 3-4 hours in patients with compromised liver functions. The symptoms of Ibuprofen overdose include headache, tinnitus, loss of consciousness, CNS depression, and seizures. The brand names of Ibuprofen include Addaprin, Advil, Alivio, Caldolor, and Cedaprin.

What are the similarities between Celecoxib and Ibuprofen?

  • Celecoxib and ibuprofen are both nonsteroidal anti-inflammatory drugs.
  • They are used to treat pain and inflammation.
  • Both celecoxib and ibuprofen work by blocking the production of prostaglandins.
  • They effectively treat various conditions, including osteoarthritis, rheumatoid arthritis, menstrual cramps, and acute pain.
  • Celecoxib and ibuprofen are both relatively affordable medications.

What is the Difference Between Celecoxib and Ibuprofen?

Celecoxib and ibuprofen are both nonsteroidal anti-inflammatory drugs (NSAIDs), but they have some important differences. Celecoxib is a selective COX-2 inhibitor, suggesting it primarily inhibits the COX-2 enzyme. In contrast, Ibuprofen is a nonselective NSAID inhibiting COX-1 and COX-2 enzymes. Celecoxib is less likely to cause gastrointestinal side effects, such as stomach bleeding and ulcers. In comparison, Ibuprofen is more likely to cause gastrointestinal side effects than celecoxib. Celecoxib has a longer half-life than ibuprofen, suggesting that it needs to be taken less often. Furthermore, ibuprofen is more effective at reducing fever than celecoxib.

Below is a summary of the difference between Celecoxib and Ibuprofen in tabular form for side-by-side comparison. All these differences should be considered when deciding the best NSAID for individual cases.

FAQ: Celecoxib and Ibuprofen

What is celecoxib used to treat?

Celecoxib is a nonsteroidal anti-inflammatory drug (NSAID) that selectively inhibits cyclooxygenase-2 (COX-2) when treating adult osteoarthritis (OA) and rheumatoid arthritis (RA).

What should I avoid while taking celecoxib?

During Celecoxib treatment, avoiding alcohol is recommended to decrease the risk of gastrointestinal irritation.

What is ibuprofen mainly used for?

Ibuprofen is widely used as an analgesic, anti-inflammatory and antipyretic drug.

Summary – Celecoxib vs. Ibuprofen

In summary, the difference between Celecoxib and Ibuprofen lies in their mechanisms of action and associated side effects. Celecoxib is a selective COX-2 inhibitor compared to Ibuprofen, a non-selective COX-1 and COX-2 inhibitor. Although both drugs effectively treat pain and inflammation, the selectivity of Celecoxib makes it advantageous for those prone to gastrointestinal complications. Ibuprofen, available over the counter and as a prescription, however, is associated with a higher risk of gastrointestinal side effects. Celecoxib has a longer half-life than ibuprofen, suggesting that it needs to be taken less often. Ibuprofen is more effective at reducing fever than celecoxib. Consulting with a healthcare professional is critical for personalized recommendations and optimal outcomes when choosing NSAIDs.

Reference:

1. Gong, Li, et al. “Celecoxib pathways.” Pharmacogenetics and Genomics, vol. 22, no. 4, 2012, pp. 310–318.
2. Rainsford, K. D. “Ibuprofen: Pharmacology, efficacy and safety.” Inflammopharmacology, vol. 17, no. 6, 2009, pp. 275–342.

Image Courtesy:

1. “Celecoxib” By User:Acdx – Own work, based on File:Celecoxib structure.png (Public Domain) via Commons Wikimedia
2. “(RS)-Ibuprofen Structural Formula V1” By Denwet – Own work (Public Domain) via Commons Wikimedia

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Filed Under: Nutrients & Drugs

About the Author: Dr Neelaka M

Dr. Neelaka Molagoda is a dedicated Drug Development and Pharmaceutical Biotechnology Lecturer, who earned his PhD in Life Sciences from Jeju National University, focusing on the pharmaceutical potential of the dietary flavonoid fisetin. His exceptional research earned him the Dean's Award for Excellent PhD Research. He has extensive experience in mammalian cell culture, zebrafish handling, bacterial transformation, siRNA-mediated gene silencing, PCR, western blot analysis, flow cytometry, enzyme activity assays, and confocal microscopy. His research delves into the mechanisms of drug action in nutraceuticals, with a focus on anti-inflammatory, anti-oxidative, anti-cancer, anti-melanogenic, and anti-angiogenic activities, as well as their effect on osteoblast differentiation and growth promotion.
Dr. Molagoda is a skilled and passionate researcher committed to advancing innovative treatments for various diseases.

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