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Selective cyclooxygenase inhibitors: current status.
Ravindran Nandakishore, Prasanna R Yalavarthi, Yengala R Kiran
1Department of Pharmaceutics, Sree Vidyanikethan College of Pharmacy, Andhra Pradesh 517102, India. Kishore.ravindran@yahoo.co.in.
Aspirin and NSAIDs cause ulcers by inhibiting COX enzymes. Selective COX-2 inhibitors (Coxibs) were developed to reduce gastrointestinal bleeding, offering a safer alternative for pain and inflammation management.
Area of Science:
- Pharmacology
- Gastroenterology
Background:
- Aspirin and NSAIDs are effective analgesics and anti-inflammatories but cause gastric ulcers via COX inhibition.
- Developing safer NSAIDs targeting COX enzymes has been a long-standing goal in drug design.
Purpose of the Study:
- To review the development and therapeutic role of selective cyclooxygenase-2 (COX-2) inhibitors.
- To discuss the physiological functions, side effects, and withdrawal reasons of COX-2 inhibitors.
Main Methods:
- Literature review of COX-2 inhibitors.
- Analysis of drug mechanisms, efficacy, and safety profiles.
Main Results:
- Selective COX-2 inhibitors (Coxibs) were developed in the late 1990s.
- Coxibs demonstrated efficacy comparable to NSAIDs with reduced gastrointestinal side effects.
Conclusions:
- COX-2 inhibitors represent a significant advancement in developing safer anti-inflammatory and analgesic drugs.
- Understanding their physiological roles and side effects is crucial for safe clinical use and future drug development.
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