An API is the substance in a pharmaceutical drug that is biologically active. It is the element that provides the therapeutic effect, distinguishing one medication from another. For instance, in a pain relief tablet, the API might be acetaminophen, whereas the remaining ingredients, known as excipients, help to deliver the API effectively but do not exert therapeutic effects themselves.
To address these concerns, many plants have turned to alternative disinfectants like ozone and ultraviolet (UV) light. Ozone is a powerful oxidant that can inactivate a wide range of pathogens and is particularly advantageous because it leaves no residual chemicals in the treated water. UV disinfection, on the other hand, uses ultraviolet light to disrupt the DNA of microorganisms, effectively neutralizing them without adding any chemicals.
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Once APIs are formulated into FPPs, stability testing becomes even more critical. FPPs might contain various excipients that can interact with the active ingredient, influence its stability, and affect the overall product performance. For example, the choice of excipients, packaging materials, and the manufacturing process can all impact the shelf life of a medication.
The Vitamin C market is characterized by a diverse array of suppliers, ranging from large multinational corporations to smaller, specialized companies. Major players in the industry often invest heavily in research and development to create innovative products that meet consumer demands. This includes enhancing the stability of Vitamin C in formulations, improving its absorption, and exploring new delivery methods, such as liposomal and powder forms.