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

<b>Background/Objectives:</b> 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 d...

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Main Authors: Mateusz Broncel (Author), Anna Juszczak (Author), Wojciech Szczolko (Author), Daniele Silvestri (Author), Agnieszka Białek-Dratwa (Author), Stanisław Wacławek (Author), Oskar Kowalski (Author), Paweł Ramos (Author)
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Published: MDPI AG, 2024-10-01T00:00:00Z.
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LEADER 00000 am a22000003u 4500
001 doaj_5ab3fec4fba04e88b58e4122bffb3ecd
042 |a dc 
100 1 0 |a Mateusz Broncel  |e author 
700 1 0 |a Anna Juszczak  |e author 
700 1 0 |a Wojciech Szczolko  |e author 
700 1 0 |a Daniele Silvestri  |e author 
700 1 0 |a Agnieszka Białek-Dratwa  |e author 
700 1 0 |a Stanisław Wacławek  |e author 
700 1 0 |a Oskar Kowalski  |e author 
700 1 0 |a Paweł Ramos  |e author 
245 0 0 |a Thermal Compatibility of New ACEI Derivatives with Popular Excipients Used to Produce Solid Pharmaceutical Formulations 
260 |b MDPI AG,   |c 2024-10-01T00:00:00Z. 
500 |a 10.3390/ph17101323 
500 |a 1424-8247 
520 |a <b>Background/Objectives:</b> 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. <b>Methods</b>: 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. <b>Conclusions</b>: 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. 
546 |a EN 
690 |a ACEI 
690 |a pharmaceutical excipients 
690 |a compatibility 
690 |a TGA 
690 |a c-DTA 
690 |a FTIR 
690 |a Medicine 
690 |a R 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceuticals, Vol 17, Iss 10, p 1323 (2024) 
787 0 |n https://www.mdpi.com/1424-8247/17/10/1323 
787 0 |n https://doaj.org/toc/1424-8247 
856 4 1 |u https://doaj.org/article/5ab3fec4fba04e88b58e4122bffb3ecd  |z Connect to this object online.