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Gastric Irritation and Bioavailability of Pyroxicam β-Cyclodextrin Inclusion Complex

Pyroxicam is a nonsteroidal anti-inflammatory drug (NSAID) used for the treatment of pain and inflammation associated with various conditions such as arthritis. However, its oral administration often leads to gastric irritation due to its acidic nature. To overcome this limitation and improve its bioavailability, pyroxicam has been formulated into inclusion complexes with β-cyclodextrin.

 

The inclusion of pyroxicam into β-cyclodextrin complexes offers several advantages. Firstly, it reduces gastric irritation commonly associated with the oral administration of pyroxicam. The complexation with β-cyclodextrin masks the acidic groups of pyroxicam, making it less irritating to the gastric mucosa. This results in improved gastrointestinal tolerability and patient compliance.

 

Moreover, the β-cyclodextrin inclusion complex enhances the solubility and dissolution rate of pyroxicam in the gastrointestinal tract. This leads to improved bioavailability of the drug, as more pyroxicam molecules are available for absorption into the bloodstream. The increased bioavailability ensures that therapeutic concentrations of pyroxicam are achieved more rapidly and consistently, leading to better efficacy in pain and inflammation management.

 

Additionally, the β-cyclodextrin complexation may also contribute to the stability of pyroxicam in the gastrointestinal environment. By encapsulating pyroxicam molecules within the hydrophobic cavity of β-cyclodextrin, the complex protects the drug from degradation by gastric acid and enzymes. This results in prolonged residence time in the stomach and enhanced absorption in the small intestine, further improving bioavailability.

 

In conclusion, the formulation of pyroxicam as a β-cyclodextrin inclusion complex offers significant benefits in terms of reducing gastric irritation and enhancing bioavailability. This innovative approach not only improves patient comfort and compliance but also ensures optimal therapeutic outcomes. Further research into the pharmacokinetics and pharmacodynamics of pyroxicam β-cyclodextrin complexes is warranted to fully elucidate their potential in clinical practice.

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