New Metformin–Citric Acid Pharmaceutical Molecular Salt: Improving Metformin Physicochemical Properties
Metadatos
Mostrar el registro completo del ítemAutor
Verdugo Escamilla, Cristóbal; Alarcón Payer, Carolina; Acebedo Martínez, Francisco Javier; Domínguez Martín, Alicia; Choquesillo Lazarte, DuaneEditorial
MDPI
Materia
Metformin Mechanochemistry API Molecular salt
Fecha
2022-12-02Referencia bibliográfica
Verdugo-Escamilla, C... [et al.]. New Metformin–Citric Acid Pharmaceutical Molecular Salt: Improving Metformin Physicochemical Properties. Crystals 2022, 12, 1748. [https://doi.org/10.3390/cryst12121748]
Patrocinador
MCIU/AEI/FEDER, UE PGC2018-102047-B-I00; FEDER-Universidad de Granada, Spain B-FQM-478-UGR20Resumen
Crystal engineering and, more specifically, the development of multicomponent materials
has become an effective technique to rationally modify important physicochemical properties of solids,
such as solubility and thermal stability. In this work, in order to overcome some of the problems that
metformin has as a pharmaceutical, a new metformin base salt with citric acid (MTF–CIT) has been
developed, which improves the thermal stability and solubility (two-fold) compared to metformin
base (MTF). A complete characterization of the new crystalline form through PXRD, DSC, SCXRD,
and FT–IR was conducted to ensure the purity of the new phase and provide a comprehensive
view of its physicochemical behavior, thus correlating the improvement in stability and solubility
with the crystal structure. The MTF–CIT salt crystallizes in the monoclinic P21/c1 spacegroup with
z0 = 1. Intermolecular interactions found in MTF–CIT structure and simulated crystal morphology
suggest a steric protection effect on the metformin ion that leads to the enhancement of stability in
several orders of magnitude compared with MTF, as well as an improvement in solubility due to the
exposition of polar groups in the biggest facets, making this new multicomponent salt a promising
pharmaceutical solid.