Stability of Aspirin

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Experiment 4: The Stability of Aspirin Introduction Drugs are produced in various ways and they are presented in many forms, they will undergo chemical decomposition or chemical degradation in a period of time after production. This can lead to a substantial lowering of the quantity of the therapeutic agent in the dosage form.1 Therefore, it is important to find out the best storage condition for that specific drug, so that the drug can maintain its effect and quality for the longest time, thus maintaining its stability. That particular length of time is known as the shelf-life. Many factors will influence drug stability such as the pH and temperature. By understanding the kinetics of the process of the breakdown of drug, the amount of drug decomposes in a given time can be predicted. The effect of temperature on the stability of acetylsalicylic acid (aspirin) was being investigated in this experiment. The equation of the reaction of acetylsalicylic acid is: Acetylsalicylic acid Acetic acid + Salicylic acid The application considered here was the stability of aspirin in solution, and how the rate of decomposition varied with temperature. From the above equation, acetylsalicylic acid would decompose to acetic acid and salicylic acid under moist condition. To obtain the kinetic data on the stability of drug, a test known as ‘accelerated stability test’ was taken. The decomposition of the drug was speeded up during the experiment while retaining the rank order of different formulations.2 Aims UV spectroscopy was used in the experiment to obtain a number of kinetic data. Besides gaining practical experiences in assaying the equipment, the aims of the experiment were to understand the ways that temperature influenced reaction rates by determining the order of reaction with respect to acetylsalicylic acid; finding out the effect of temperature on the rate
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