Thermal Compatibility of New ACEI Derivatives with Popular Excipients Used to Produce Solid Pharmaceutical Formulations.

IF 4.3 3区 医学 Q2 CHEMISTRY, MEDICINAL Pharmaceuticals Pub Date : 2024-10-03 DOI:10.3390/ph17101323
Mateusz Broncel, Anna Juszczak, Wojciech Szczolko, Daniele Silvestri, Agnieszka Białek-Dratwa, Stanisław Wacławek, Oskar Kowalski, Paweł Ramos
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Abstract

Background/Objectives: Increasing drugs' stability and adequately protecting them against degradation will ensure a decrease in their price and broader availability of pharmaceutical substances. This is of great importance, especially for drugs used to treat the most common diseases in the population, such as hypertension. The study examined two newly synthesized substances from the angiotensin I-converting enzyme inhibitor (ACEI) group as potential drugs. ACEIs are among the leading drugs used in the treatment of hypertension in the world. The chemical modifications of the tested substances applied concerned the places most susceptible to degradation. The presented work analyzed the compatibility of new derivatives with selected excipients used in pharmacy. Methods: Thermogravimetric (TGA) and differential thermal analyses (c-DTA) were used as the main methods. In addition, non-thermal methods such as colorimetry analysis, Fourier-transform infrared (FTIR) and UV spectroscopy were used. Results: Based on the conducted studies, it can be concluded that the incompatibility of IND-1 with glucose anhydrous and lactose monohydrate occurs only when the mixture is stored at higher temperatures. For the remaining IND-1 and IND-2 mixtures with excipients, compatibility was demonstrated. Conclusions: The obtained results confirmed the usefulness of the applied thermal analyses (TGA and c-DTA) for assessing the compatibility of the tested potential drugs with excipients. However, in the case of incompatibility reactions of substances occurring under the influence of elevated temperatures, such as the Maillard reaction, it is necessary to use non-thermal methods to obtain the right result.

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新型 ACEI 衍生物与用于生产固体药物制剂的常用辅料的热相容性。
背景/目标:提高药物的稳定性,充分保护药物,防止药物降解,将确保降低药物价格,扩大药物的供应范围。这一点非常重要,尤其是对于治疗高血压等最常见疾病的药物而言。这项研究将血管紧张素 I 转换酶抑制剂(ACEI)类的两种新合成物质作为潜在药物进行了研究。血管紧张素转换酶抑制剂是世界上治疗高血压的主要药物之一。所测试物质的化学修饰涉及最容易降解的地方。本研究分析了新衍生物与选定的药用辅料的相容性。研究方法主要采用热重分析法(TGA)和差热分析法(c-DTA)。此外,还使用了比色分析、傅立叶变换红外(FTIR)和紫外光谱等非热分析方法。研究结果根据所进行的研究,可以得出结论:IND-1 与无水葡萄糖和一水乳糖的不相容性仅发生在混合物储存温度较高的情况下。其余 IND-1 和 IND-2 与辅料的混合物则表现出相容性。结论所得结果证实了应用热分析(TGA 和 c-DTA)评估受测潜在药物与辅料相容性的实用性。不过,如果物质在高温影响下发生不相容反应,如 Maillard 反应,则有必要使用非热分析方法来获得正确的结果。
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来源期刊
Pharmaceuticals
Pharmaceuticals Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
6.10
自引率
4.30%
发文量
1332
审稿时长
6 weeks
期刊介绍: Pharmaceuticals (ISSN 1424-8247) is an international scientific journal of medicinal chemistry and related drug sciences.Our aim is to publish updated reviews as well as research articles with comprehensive theoretical and experimental details. Short communications are also accepted; therefore, there is no restriction on the maximum length of the papers.
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