Mussel Valner A F S N, Ferreira Max P, Marques Maria B F, Yoshida Maria I, Almeida Mariana R, Rodrigues Bernardo L, Mussel Wagner N
Departamento de Química, ICEx, Universidade Federal de Minas Gerais - UFMG, Av. Antônio Carlos 6627, 31270-901 Belo Horizonte, MG, Brazil.
CNEN-CDTN, Comissão Nacional de Energia Nuclear - Centro de Desenvolvimento da Tecnologia Nuclear, Av. Antônio Carlos, 6627 Belo Horizonte, MG, Brazil.
J Pharm Anal. 2018 Jun;8(3):194-201. doi: 10.1016/j.jpha.2018.01.005. Epub 2018 May 24.
Thalidomide was indicated as a sedative and antiemetic and prescribed for pregnant women. Its tragic teratogenic effects culminated in withdrawal from the market. Since the discovery of its anti-angiogenic and anti-inflammatory actions, thalidomide has been used in the treatment of leprosy and multiple myeloma, which justify studies of its stability. We investigated the effects of irradiation of thalidomide up to 100 kGy (fourfold the usual sterilizing dose for pharmaceutics). The β polymorph of thalidomide was obtained in an isothermal experiment at 270 °C. All samples underwent gamma irradiation for specific times. At different doses, decomposition of the pharmaceutical was not observed up to 100 kGy. The observed effect was angle turning between the phthalimide and glutarimide rings modulated by repulsion towards the carbonyl group, leading to a stable energetic configuration, as measured by the equilibrium in the torsion angle after irradiation. The thalidomide molecule has a center of symmetry, so a full turn starting from 57.3° will lead to an identical molecule. Further irradiation will start the process again. Samples irradiated at 30 and 100 kGy have more compact unit cells and a lower volume, which leads to an increase in the intermolecular hydrogen interaction within the unit cell, resulting in higher thermal stability for polymorph α.
沙利度胺曾被用作镇静剂和止吐药,并被开给孕妇服用。其悲惨的致畸作用最终导致该药物退出市场。自从发现其抗血管生成和抗炎作用以来,沙利度胺已被用于治疗麻风病和多发性骨髓瘤,这使得对其稳定性的研究变得合理。我们研究了高达100 kGy(药剂学常用灭菌剂量的四倍)的辐射对沙利度胺的影响。沙利度胺的β多晶型物是在270 °C的等温实验中获得的。所有样品均接受了特定时间的伽马辐射。在不同剂量下,直至100 kGy均未观察到药物分解。观察到的效应是邻苯二甲酰亚胺环和戊二酰亚胺环之间的角度转变,这是由对羰基的排斥作用调节的,从而导致一种稳定的能量构型,这通过辐射后扭转角的平衡来衡量。沙利度胺分子具有对称中心,因此从57.3°开始完整旋转一圈将得到相同的分子。进一步辐射将再次启动该过程。在30和100 kGy下辐照的样品具有更紧密的晶胞和更小的体积,这导致晶胞内分子间氢键相互作用增加,从而使多晶型α具有更高的热稳定性。