| Literature DB >> 33498239 |
Susana Santos Braga1, Firas El-Saleh2, Karyna Lysenko1,3, Filipe A Almeida Paz3.
Abstract
Efavirenz is an antiretroviral drug of widespread use in the management of infections with human immunodeficiency virus type 1 (HIV-1). Efavirenz is also used in paediatrics, but due to its very poor aqueous solubility the liquid formulations available resort to oil-based excipients. In this report we describe the interaction of γ-cyclodextrin with efavirenz in solution and in the solid state. In aqueous solution, the preferential host-guest stoichiometry was determined by the continuous variation method using 1H NMR, which indicated a 3:2 host-to-guest proportion. Following, the solid inclusion compound was prepared at different stoichiometries by co-dissolution and freeze-drying. Solid-state characterisation of the products using FT-IR, 13C{1H} CP-MAS NMR, thermogravimetry, and X-ray powder diffraction has confirmed that the 3:2 stoichiometry is the adequate starting condition to isolate a solid inclusion compound in the pure form. The effect of γ-cyclodextrin on the solubility of efavirenz is studied by the isotherm method.Entities:
Keywords: antiretroviral; cyclodextrin inclusion; solid state; solution-phase
Year: 2021 PMID: 33498239 PMCID: PMC7863942 DOI: 10.3390/molecules26030519
Source DB: PubMed Journal: Molecules ISSN: 1420-3049 Impact factor: 4.411