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Startseite » Bioavailability enhancement » Supercritical Antisolvent Process for Pharmaceutical Applications: A Review

Supercritical Antisolvent Process for Pharmaceutical Applications: A Review

12. August 2020
Conventional pharmaceutical formulations and modified-release drug delivery systems

Conventional pharmaceutical formulations and modified-release drug delivery systems

The supercritical antisolvent (SAS) technique has been widely employed in the biomedical field, including drug delivery, to obtain drug particles or polymer-based systems of nanometric or micrometric size. The primary purpose of producing SAS particles is to improve the treatment of di erent pathologies and to better the patient’s compliance. In this context, many active compounds have been micronized to enhance their dissolution rate and bioavailability. Aiming for more e ective treatments with reduced side e ects caused by drug overdose, the SAS polymer/active principle coprecipitation has mainly been proposed to o er an adequate drug release for specific therapy. The demand for new formulations with reduced side e ects on the patient’s health is still growing; in this context, the SAS technique is a promising tool to solve existing issues in the biomedical field. This updated review on the use of the SAS process for clinical applications provides useful information about the achievements, the most e ffective polymeric carriers, and parameters, as well as future perspectives.

Download the full publication here: Supercritical Antisolvent Process for Pharmaceutical Applications- A Review

or continue reading here: Franco, P.; De Marco, I. Supercritical Antisolvent Process for Pharmaceutical Applications: A Review. Processes 2020, 8, 938.

Keywords: supercritical antisolvent; micronization; coprecipitation; biomedical field; drug delivery

Tags: excipientsformulation

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