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Experimental Determination and Correlation of Artemisinin's Solubility in Supercritical Carbon Dioxide

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Bibliographic Details
Summary:The measurement and correlation of the experimental solubility of the antimalarial artemisinin (Artemisia annua L.) in supercritical carbon dioxide is reported. Results were obtained using a static analytical method at 308.2, 318.2, and 328.2 K, and in a pressure range from 10.0 up to 25.0 MPa. Solubility experimental data were correlated with three density-based models (Chrastil, Bartle, and Méndez-Santiago−Teja models) and with two cubic equation of state (EOS) models, namely, the Peng−Robinson EOS and the Soave−Redlich−Kwong EOS, together with the conventional van der Waals mixing and combining rules. Good correlation results were obtained between the calculated and the experimental solubility to all fitted models. Results clearly show the feasibility of processing this antimalarial drug using supercritical fluid technologies and processes.
Main Authors:Coimbra, Patrícia
Other Authors:Blanco, Miguel R.; Silva, Hélio S. R. Costa; Gil, Maria H.; Sousa, Hermínio C. de
Year:2006
Country:Portugal
Document type:article
Access type:open access
Associated institution:Universidade de Coimbra
Language:English
Origin:Estudo Geral - Universidade de Coimbra
Description
Summary:The measurement and correlation of the experimental solubility of the antimalarial artemisinin (Artemisia annua L.) in supercritical carbon dioxide is reported. Results were obtained using a static analytical method at 308.2, 318.2, and 328.2 K, and in a pressure range from 10.0 up to 25.0 MPa. Solubility experimental data were correlated with three density-based models (Chrastil, Bartle, and Méndez-Santiago−Teja models) and with two cubic equation of state (EOS) models, namely, the Peng−Robinson EOS and the Soave−Redlich−Kwong EOS, together with the conventional van der Waals mixing and combining rules. Good correlation results were obtained between the calculated and the experimental solubility to all fitted models. Results clearly show the feasibility of processing this antimalarial drug using supercritical fluid technologies and processes.

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