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Cetirizine dihydrochloride interaction with some diclofenac complexes
Ihsan M Kenawi1, Barsoum N Barsoum, Maha A Youssef
1Department of Chemistry, Faculty of Science, Cairo University, Giza, Egypt. ihsanata77@hotmail.com
Summary
Cetirizine dihydrochloride and diclofenac sodium form stable, high molecular weight adducts. These interactions create new ternary and quaternary compounds, even with metal-bound diclofenac.
Area of Science:
- Pharmaceutical Chemistry
- Coordination Chemistry
- Analytical Chemistry
Background:
- Cetirizine dihydrochloride is a widely used antihistamine.
- Diclofenac sodium is a common non-steroidal anti-inflammatory drug (NSAID).
- Understanding drug-drug interactions and their complex formation is crucial for pharmaceutical development.
Purpose of the Study:
- To investigate the interaction between cetirizine dihydrochloride and diclofenac sodium.
- To characterize the adducts formed, particularly in the presence of metal ions.
- To elucidate the bonding interactions and structural features of the resulting complexes.
Main Methods:
- Infrared (IR) spectroscopy
- Proton Nuclear Magnetic Resonance (1H NMR) spectroscopy
- Mass spectrometry
- Thermogravimetric (TG) analysis
- Elemental analysis
Main Results:
- Strong adduct formation between cetirizine dihydrochloride and diclofenac sodium was observed.
- Stable ternary (with divalent metals like Ca, Mg, Zn) and quaternary (with trivalent iron) compounds were formed.
- Ionic bonding occurred between diclofenac's carbonyl ion and cetirizine's piperazine ring.
- Coordination was confirmed at the NH of diphenylamine via shifts in IR bands (nuNH, deltaNH, nuC-N).
- Results were corroborated by TG and elemental analysis.
Conclusions:
- Cetirizine dihydrochloride and diclofenac sodium form stable complexes with significant molecular weight.
- These interactions are robust and can occur even when diclofenac is coordinated to metal ions.
- The study provides insights into the chemical interactions and structural characteristics of these drug adducts.