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Drug intermediates play a crucial role in the pharmaceutical industry, serving as essential building blocks in the synthesis of active pharmaceutical ingredients (APIs). These intermediates are not intended for direct therapeutic use; instead, they are chemical compounds that undergo further transformations to produce final drug products. The importance of drug intermediates cannot be understated, as they significantly influence both the efficiency and cost-effectiveness of drug development processes.

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The stability testing of APIs generally begins during the early stages of drug formulation. APIs are the substances in pharmaceutical products that provide therapeutic effects; therefore, their stability is crucial. The primary goal is to ascertain the degradation pathway of the API and to determine the appropriate storage conditions that will maximize its shelf life. Tests typically include accelerated stability studies, where samples are subjected to higher-than-normal temperatures and humidity levels to expedite degradation processes. These studies help predict how the API will behave under regular storage conditions.

This is crucial because, without SDS, proteins of different sizes and shapes would migrate through the gel based on both size and net charge. The presence of SDS levels the playing field, allowing proteins to be separated solely by their molecular weight. Therefore, during electrophoresis, all proteins will experience the same electric field-driven force, enabling their separation based on size alone.

Vitamin C, also known as ascorbic acid, is a water-soluble vitamin that acts as a powerful antioxidant in the human body. It plays a crucial role in several physiological processes, including collagen synthesis, immune system support, and the absorption of iron. The human body cannot produce Vitamin C on its own, making it essential to obtain this nutrient through dietary sources or supplements.

5. Generic APIs