Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, 52074 Aachen, Germany.
Department of Chemistry, University of Oxford, Oxford OX1 3TA, U.K.
Anal Chem. 2024 Aug 13;96(32):13166-13173. doi: 10.1021/acs.analchem.4c02025. Epub 2024 Aug 2.
For the approval of a drug, the stability data must be submitted to regulatory authorities. Such analyses are often time-consuming and cost-intensive. Forced degradation studies are mainly carried out under harsh conditions in the dissolved state, often leading to extraneous degradation profiles for a solid drug. Oxidative mechanochemical degradation offers the possibility of generating realistic degradation profiles. In this study, a sustainable mechanochemical procedure is presented for the degradation of five active pharmaceutical ingredients (APIs) from the sartan family: losartan potassium, irbesartan, valsartan, olmesartan medoxomil, and telmisartan. High-resolution mass spectrometry enabled the detection of impurities already present in untreated APIs and allowed the elucidation of degradation products. Significant degradation profiles could already be obtained after 15-60 min of ball milling time. Many of the identified degradation products are described in the literature and pharmacopoeias, emphasizing the significance of our results and the applicability of this approach to predict degradation profiles for drugs in the solid state.
对于药物的批准,必须向监管机构提交稳定性数据。这些分析通常既耗时又耗费成本。强制降解研究主要在溶解状态下的恶劣条件下进行,这往往会导致固体药物出现外来降解谱。氧化机械化学降解为生成现实的降解谱提供了可能性。在这项研究中,提出了一种可持续的机械化学程序,用于降解沙坦类五种活性药物成分(API):氯沙坦钾、厄贝沙坦、缬沙坦、奥美沙坦酯和替米沙坦。高分辨率质谱法能够检测到未经处理的 API 中已经存在的杂质,并能够阐明降解产物。在球磨 15-60 分钟后,就能获得显著的降解谱。许多已鉴定的降解产物在文献和药典中都有描述,这强调了我们研究结果的重要性以及该方法在预测固体药物降解谱方面的适用性。