Araya-Sibaja Andrea Mariela, Fandaruff Cinira, Guevara-Camargo Ana María, Vargas-Huertas Felipe, Zamora William J, Vega-Baudrit José Roberto, Guillén-Girón Teodolito, Navarro-Hoyos Mirtha, Paoli Paola, Rossi Patrizia, Jones William
Laboratorio Nacional de Nanotecnología LANOTEC-CeNAT-CONARE, Pavas, 1174-1200 San José, Costa Rica.
Universidade Federal de Santa Catarina, Campus Universitário, Trindade, CCS, Bloco J/K, 89040970 Florianópolis, Brazil.
ACS Omega. 2022 Apr 19;7(17):14897-14909. doi: 10.1021/acsomega.2c00545. eCollection 2022 May 3.
The design of new pharmaceutical solids with improved physical and chemical properties can be reached through in-detail knowledge of the noncovalent intermolecular interactions between the molecules in the context of crystal packing. Although crystallization from solutions is well-known for obtaining new solids, the effect of some variables on crystallization is not yet thoroughly understood. Among these variables, solvents are noteworthy. In this context, the present study aimed to investigate the effect of ethanol (EtOH), acetonitrile (MeCN), and acetone (ACTN) on obtaining irbesartan (IBS) crystal forms with 2,3-dibromosuccinic acid. Crystal structures were solved by single-crystal diffraction, and the intermolecular interactions were analyzed using the Hirshfeld surfaces analysis. The characterization of physicochemical properties was carried out by powder X-ray diffraction, Fourier transform infrared spectroscopy (FT-IR), thermal analysis, and solution-state NMR techniques. Two different IBS salts were obtained, one from MeCN and ACTN (compound ) and a different one from EtOH (compound ). The experimental results were in agreement with the findings obtained through quantum mechanics continuum solvation models. Compound crystallized as a monoclinic system 2/, whereas compound in a triclinic system 1̅. In both structures, a net of strong hydrogen bonds is present, and their existence was confirmed by the FT-IR results. In addition, the IBS cation acts as a H-bond donor through the N1 and N6 nitrogen atoms which interact with the bromide anion and the water molecule O1W in compound . Meanwhile, N1 and N6 nitrogen atoms interact with the oxygen atoms provided by two symmetry-related 2,3-dibromo succinate anions in compound . Solution-state NMR data agreed with the protonation of the imidazolone ring in the crystal structure of compound 1. Both salts presented a different thermal behavior not only in melting temperature but also in thermal stability.
通过深入了解晶体堆积中分子间的非共价相互作用,可以设计出具有改善物理和化学性质的新型药物固体。尽管从溶液中结晶是获得新固体的常用方法,但一些变量对结晶的影响尚未得到充分理解。在这些变量中,溶剂值得关注。在此背景下,本研究旨在探究乙醇(EtOH)、乙腈(MeCN)和丙酮(ACTN)对与2,3 - 二溴琥珀酸形成厄贝沙坦(IBS)晶型的影响。通过单晶衍射解析晶体结构,并使用 Hirshfeld 表面分析来分析分子间相互作用。通过粉末 X 射线衍射、傅里叶变换红外光谱(FT - IR)、热分析和溶液态核磁共振技术对物理化学性质进行表征。得到了两种不同的 IBS 盐,一种来自 MeCN 和 ACTN(化合物 ),另一种来自 EtOH(化合物 )。实验结果与通过量子力学连续介质溶剂化模型获得的结果一致。化合物 结晶为单斜晶系 2/,而化合物 为三斜晶系 1̅。在这两种结构中,都存在强氢键网络,FT - IR 结果证实了它们的存在。此外,IBS 阳离子通过 N1 和 N6 氮原子作为氢键供体,在化合物 中与溴离子和水分子 O1W 相互作用。同时,在化合物 中,N1 和 N6 氮原子与两个对称相关的 2,3 - 二溴琥珀酸阴离子提供的氧原子相互作用。溶液态核磁共振数据与化合物 1 晶体结构中咪唑酮环的质子化情况相符。两种盐不仅在熔点温度上,而且在热稳定性方面都呈现出不同的热行为。