Furosemide/Non-Steroidal Anti-Inflammatory Drug–Drug Pharmaceutical Solids: Novel Opportunities in Drug Formulation

The design of drug–drug multicomponent pharmaceutical solids is one the latest drug development approaches in the pharmaceutical industry. Its purpose is to modulate the physicochemical properties of active pharmaceutical ingredients (APIs), most of them already existing in the market, achieving imp...

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Main Authors: Francisco Javier Acebedo-Martínez, Carolina Alarcón-Payer, Lucía Rodríguez-Domingo, Alicia Domínguez-Martín, Jaime Gómez-Morales, Duane Choquesillo-Lazarte
Format: Article
Language:English
Published: MDPI AG 2021-11-01
Series:Crystals
Subjects:
Online Access:https://www.mdpi.com/2073-4352/11/11/1339
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author Francisco Javier Acebedo-Martínez
Carolina Alarcón-Payer
Lucía Rodríguez-Domingo
Alicia Domínguez-Martín
Jaime Gómez-Morales
Duane Choquesillo-Lazarte
author_facet Francisco Javier Acebedo-Martínez
Carolina Alarcón-Payer
Lucía Rodríguez-Domingo
Alicia Domínguez-Martín
Jaime Gómez-Morales
Duane Choquesillo-Lazarte
author_sort Francisco Javier Acebedo-Martínez
collection DOAJ
description The design of drug–drug multicomponent pharmaceutical solids is one the latest drug development approaches in the pharmaceutical industry. Its purpose is to modulate the physicochemical properties of active pharmaceutical ingredients (APIs), most of them already existing in the market, achieving improved bioavailability properties, especially on oral administration drugs. In this work, our efforts are focused on the mechanochemical synthesis and thorough solid-state characterization of two drug–drug cocrystals involving furosemide and two different non-steroidal anti-inflammatory drugs (NSAIDs) commonly prescribed together: ethenzamide and piroxicam. Besides powder and single crystal X-ray diffraction, infrared spectroscopy and thermal analysis, stability, and solubility tests were performed on the new solid materials. The aim of this work was evaluating the physicochemical properties of such APIs in the new formulation, which revealed a solubility improvement regarding the NSAIDs but not in furosemide. Further studies need to be carried out to evaluate the drug–drug interaction in the novel multicomponent solids, looking for potential novel therapeutic alternatives.
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spelling doaj.art-2dbd11e4465a4bdf88ead726879edd452023-11-22T22:58:10ZengMDPI AGCrystals2073-43522021-11-011111133910.3390/cryst11111339Furosemide/Non-Steroidal Anti-Inflammatory Drug–Drug Pharmaceutical Solids: Novel Opportunities in Drug FormulationFrancisco Javier Acebedo-Martínez0Carolina Alarcón-Payer1Lucía Rodríguez-Domingo2Alicia Domínguez-Martín3Jaime Gómez-Morales4Duane Choquesillo-Lazarte5Laboratorio de Estudios Cristalográficos, IACT, CSIC-Universidad de Granada, Avda. de las Palmeras 4, 18100 Armilla, SpainServicio de Farmacia, Hospital Universitario Virgen de las Nieves, 18014 Granada, SpainLaboratorio de Estudios Cristalográficos, IACT, CSIC-Universidad de Granada, Avda. de las Palmeras 4, 18100 Armilla, SpainDepartment of Inorganic Chemistry, Faculty of Pharmacy, University of Granada, 18071 Granada, SpainLaboratorio de Estudios Cristalográficos, IACT, CSIC-Universidad de Granada, Avda. de las Palmeras 4, 18100 Armilla, SpainLaboratorio de Estudios Cristalográficos, IACT, CSIC-Universidad de Granada, Avda. de las Palmeras 4, 18100 Armilla, SpainThe design of drug–drug multicomponent pharmaceutical solids is one the latest drug development approaches in the pharmaceutical industry. Its purpose is to modulate the physicochemical properties of active pharmaceutical ingredients (APIs), most of them already existing in the market, achieving improved bioavailability properties, especially on oral administration drugs. In this work, our efforts are focused on the mechanochemical synthesis and thorough solid-state characterization of two drug–drug cocrystals involving furosemide and two different non-steroidal anti-inflammatory drugs (NSAIDs) commonly prescribed together: ethenzamide and piroxicam. Besides powder and single crystal X-ray diffraction, infrared spectroscopy and thermal analysis, stability, and solubility tests were performed on the new solid materials. The aim of this work was evaluating the physicochemical properties of such APIs in the new formulation, which revealed a solubility improvement regarding the NSAIDs but not in furosemide. Further studies need to be carried out to evaluate the drug–drug interaction in the novel multicomponent solids, looking for potential novel therapeutic alternatives.https://www.mdpi.com/2073-4352/11/11/1339drug–drug cocrystalfurosemideethenzamidepiroxicammechanochemical synthesis
spellingShingle Francisco Javier Acebedo-Martínez
Carolina Alarcón-Payer
Lucía Rodríguez-Domingo
Alicia Domínguez-Martín
Jaime Gómez-Morales
Duane Choquesillo-Lazarte
Furosemide/Non-Steroidal Anti-Inflammatory Drug–Drug Pharmaceutical Solids: Novel Opportunities in Drug Formulation
Crystals
drug–drug cocrystal
furosemide
ethenzamide
piroxicam
mechanochemical synthesis
title Furosemide/Non-Steroidal Anti-Inflammatory Drug–Drug Pharmaceutical Solids: Novel Opportunities in Drug Formulation
title_full Furosemide/Non-Steroidal Anti-Inflammatory Drug–Drug Pharmaceutical Solids: Novel Opportunities in Drug Formulation
title_fullStr Furosemide/Non-Steroidal Anti-Inflammatory Drug–Drug Pharmaceutical Solids: Novel Opportunities in Drug Formulation
title_full_unstemmed Furosemide/Non-Steroidal Anti-Inflammatory Drug–Drug Pharmaceutical Solids: Novel Opportunities in Drug Formulation
title_short Furosemide/Non-Steroidal Anti-Inflammatory Drug–Drug Pharmaceutical Solids: Novel Opportunities in Drug Formulation
title_sort furosemide non steroidal anti inflammatory drug drug pharmaceutical solids novel opportunities in drug formulation
topic drug–drug cocrystal
furosemide
ethenzamide
piroxicam
mechanochemical synthesis
url https://www.mdpi.com/2073-4352/11/11/1339
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