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Octreotide impurities are removed through a combination of purification techniques, such as chromatography, crystallization, and filtration.
Octreotide impurities are identified using analytical techniques such as high-performance liquid chromatography (HPLC), and liquid chromatography-mass spectrometry (LC-MS).
The synthesis of Octreotide impurities involves the use of various chemical reactions, such as peptide coupling, esterification, and protection/deprotection steps.
Impurities can have a significant impact on the safety, efficacy, and stability of Octreotide. They can affect the drug's pharmacological properties, increase the risk of adverse reactions, and reduce the shelf life of the drug.
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