Abstract

The review covers some issues related to the role of auxiliary components of pharmaceutical preparations. It is emphasized that these components must be studied in many respects before the development of a new pharmaceutical product, including the compliance with the production standards, their influence on the physical, pharmacological, and microbiological characteristics of the final product; the impact on the therapeutic efficacy and safety of a parent drug (i.e., the drug release, bioavailability, etc.). The aspects studied in this article lead to a conclusion that a complex approach is required for the correct assessment of the role of auxiliary components in ensuring the pharmaceutical and therapeutic properties of drugs.

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