Reinvestigation of the paracetamol–caffeine, aspirin–caffeine, and paracetamol–aspirin phase equilibria diagrams
Many drug candidates are poorly soluble. The formation of solid dispersion can improve their solubility, consequently their bioavailability. For this purpose, the use of eutectic mixtures is well known in the pharmaceutical field. At the eutectic composition, both components are in reduced particle...
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description | Many drug candidates are poorly soluble. The formation of solid dispersion can improve their solubility, consequently their bioavailability. For this purpose, the use of eutectic mixtures is well known in the pharmaceutical field. At the eutectic composition, both components are in reduced particle size and well dispersed. In this work, we focus on the combination of paracetamol, aspirin, and caffeine, which is highly effective for the treatment of migraine headache pain. We have reinvestigated the paracetamol–caffeine, aspirin–caffeine, and paracetamol–aspirin phase equilibria diagrams taking into account the polymorphism of caffeine, paracetamol, and aspirin. The three phase diagrams are determined using X-ray diffraction and the differential scanning calorimetry from the binary mixtures. It is concluded that the paracetamol–caffeine and aspirin–caffeine systems are similar and exhibit two invariants, one eutectic and one metatectic. The paracetamol–aspirin phase diagram reveals the formation of one eutectic. The composition of the three eutectics formed is confirmed by the related Tamman’s triangles. No compound formation is found in the three systems. |
doi_str_mv | 10.1007/s10973-017-6855-6 |
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The formation of solid dispersion can improve their solubility, consequently their bioavailability. For this purpose, the use of eutectic mixtures is well known in the pharmaceutical field. At the eutectic composition, both components are in reduced particle size and well dispersed. In this work, we focus on the combination of paracetamol, aspirin, and caffeine, which is highly effective for the treatment of migraine headache pain. We have reinvestigated the paracetamol–caffeine, aspirin–caffeine, and paracetamol–aspirin phase equilibria diagrams taking into account the polymorphism of caffeine, paracetamol, and aspirin. The three phase diagrams are determined using X-ray diffraction and the differential scanning calorimetry from the binary mixtures. It is concluded that the paracetamol–caffeine and aspirin–caffeine systems are similar and exhibit two invariants, one eutectic and one metatectic. The paracetamol–aspirin phase diagram reveals the formation of one eutectic. The composition of the three eutectics formed is confirmed by the related Tamman’s triangles. No compound formation is found in the three systems.</description><identifier>ISSN: 1388-6150</identifier><identifier>EISSN: 1588-2926</identifier><identifier>DOI: 10.1007/s10973-017-6855-6</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Acetaminophen ; Analgesics ; Analytical Chemistry ; Aspirin ; Binary mixtures ; Bioavailability ; Caffeine ; Chemistry ; Chemistry and Materials Science ; Condensed Matter ; Eutectic composition ; Headache ; Inorganic Chemistry ; Materials Science ; Measurement Science and Instrumentation ; Migraine ; Pain ; Phase diagrams ; Phase equilibria ; Physical Chemistry ; Physics ; Polymer Sciences ; Polymorphism ; Triangles</subject><ispartof>Journal of thermal analysis and calorimetry, 2018-03, Vol.131 (3), p.2141-2155</ispartof><rights>Akadémiai Kiadó, Budapest, Hungary 2017</rights><rights>COPYRIGHT 2018 Springer</rights><rights>Copyright Springer Science & Business Media 2018</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c488t-a0aaf975a831e7002dbe949c8f8c5c155744a4c24e41904003fe4baae7bd912a3</citedby><cites>FETCH-LOGICAL-c488t-a0aaf975a831e7002dbe949c8f8c5c155744a4c24e41904003fe4baae7bd912a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10973-017-6855-6$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10973-017-6855-6$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,780,784,885,27922,27923,41486,42555,51317</link.rule.ids><backlink>$$Uhttps://hal.science/hal-01674789$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Dichi, Emma</creatorcontrib><creatorcontrib>Sghaier, Mehrez</creatorcontrib><creatorcontrib>Guiblin, Nicolas</creatorcontrib><title>Reinvestigation of the paracetamol–caffeine, aspirin–caffeine, and paracetamol–aspirin phase equilibria diagrams</title><title>Journal of thermal analysis and calorimetry</title><addtitle>J Therm Anal Calorim</addtitle><description>Many drug candidates are poorly soluble. The formation of solid dispersion can improve their solubility, consequently their bioavailability. For this purpose, the use of eutectic mixtures is well known in the pharmaceutical field. At the eutectic composition, both components are in reduced particle size and well dispersed. In this work, we focus on the combination of paracetamol, aspirin, and caffeine, which is highly effective for the treatment of migraine headache pain. We have reinvestigated the paracetamol–caffeine, aspirin–caffeine, and paracetamol–aspirin phase equilibria diagrams taking into account the polymorphism of caffeine, paracetamol, and aspirin. The three phase diagrams are determined using X-ray diffraction and the differential scanning calorimetry from the binary mixtures. It is concluded that the paracetamol–caffeine and aspirin–caffeine systems are similar and exhibit two invariants, one eutectic and one metatectic. The paracetamol–aspirin phase diagram reveals the formation of one eutectic. The composition of the three eutectics formed is confirmed by the related Tamman’s triangles. No compound formation is found in the three systems.</description><subject>Acetaminophen</subject><subject>Analgesics</subject><subject>Analytical Chemistry</subject><subject>Aspirin</subject><subject>Binary mixtures</subject><subject>Bioavailability</subject><subject>Caffeine</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Condensed Matter</subject><subject>Eutectic composition</subject><subject>Headache</subject><subject>Inorganic Chemistry</subject><subject>Materials Science</subject><subject>Measurement Science and Instrumentation</subject><subject>Migraine</subject><subject>Pain</subject><subject>Phase diagrams</subject><subject>Phase equilibria</subject><subject>Physical Chemistry</subject><subject>Physics</subject><subject>Polymer Sciences</subject><subject>Polymorphism</subject><subject>Triangles</subject><issn>1388-6150</issn><issn>1588-2926</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kt9qFDEUxgexYK0-gHcDXhWcepLJTJLLpVhbWBBqvQ5nMyezKfOvyeyid30H39AnMcsUy4qSixw-fl_Id_iy7B2DCwYgP0YGWpYFMFnUqqqK-kV2yiqlCq55_TLNZZprVsGr7HWM9wCgNbDTbH9LfthTnH2Lsx-HfHT5vKV8woCWZuzH7tfjT4vOJY4-5BgnH_xwrA3NX_wTlU9bjJTTw853fhM85o3HNmAf32QnDrtIb5_us-zb1ae7y-ti_eXzzeVqXVih1FwgIDotK1QlIwnAmw1poa1yylaWVZUUAoXlggTTIABKR2KDSHLTaMaxPMvOl3e32Jkp-B7DDzOiN9ertTlowGoppNJ7ltj3CzuF8WGXVmLux10Y0vcMTysWqixF-Uy12JHxgxvnlLz30ZpVxVXNOOeQqIt_UOk01Hs7DuR80o8M50eGxMz0fW5xF6O5-Xp7zLKFtWGMMZD7k4yBObTBLG1I4aQ5tMHUycMXT0zs0FJ4Dvd_02-zCrkC</recordid><startdate>20180301</startdate><enddate>20180301</enddate><creator>Dichi, Emma</creator><creator>Sghaier, Mehrez</creator><creator>Guiblin, Nicolas</creator><general>Springer Netherlands</general><general>Springer</general><general>Springer Nature B.V</general><general>Springer Verlag</general><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>1XC</scope></search><sort><creationdate>20180301</creationdate><title>Reinvestigation of the paracetamol–caffeine, aspirin–caffeine, and paracetamol–aspirin phase equilibria diagrams</title><author>Dichi, Emma ; Sghaier, Mehrez ; Guiblin, Nicolas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c488t-a0aaf975a831e7002dbe949c8f8c5c155744a4c24e41904003fe4baae7bd912a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Acetaminophen</topic><topic>Analgesics</topic><topic>Analytical Chemistry</topic><topic>Aspirin</topic><topic>Binary mixtures</topic><topic>Bioavailability</topic><topic>Caffeine</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Condensed Matter</topic><topic>Eutectic composition</topic><topic>Headache</topic><topic>Inorganic Chemistry</topic><topic>Materials Science</topic><topic>Measurement Science and Instrumentation</topic><topic>Migraine</topic><topic>Pain</topic><topic>Phase diagrams</topic><topic>Phase equilibria</topic><topic>Physical Chemistry</topic><topic>Physics</topic><topic>Polymer Sciences</topic><topic>Polymorphism</topic><topic>Triangles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dichi, Emma</creatorcontrib><creatorcontrib>Sghaier, Mehrez</creatorcontrib><creatorcontrib>Guiblin, Nicolas</creatorcontrib><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Journal of thermal analysis and calorimetry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dichi, Emma</au><au>Sghaier, Mehrez</au><au>Guiblin, Nicolas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reinvestigation of the paracetamol–caffeine, aspirin–caffeine, and paracetamol–aspirin phase equilibria diagrams</atitle><jtitle>Journal of thermal analysis and calorimetry</jtitle><stitle>J Therm Anal Calorim</stitle><date>2018-03-01</date><risdate>2018</risdate><volume>131</volume><issue>3</issue><spage>2141</spage><epage>2155</epage><pages>2141-2155</pages><issn>1388-6150</issn><eissn>1588-2926</eissn><abstract>Many drug candidates are poorly soluble. The formation of solid dispersion can improve their solubility, consequently their bioavailability. For this purpose, the use of eutectic mixtures is well known in the pharmaceutical field. At the eutectic composition, both components are in reduced particle size and well dispersed. In this work, we focus on the combination of paracetamol, aspirin, and caffeine, which is highly effective for the treatment of migraine headache pain. We have reinvestigated the paracetamol–caffeine, aspirin–caffeine, and paracetamol–aspirin phase equilibria diagrams taking into account the polymorphism of caffeine, paracetamol, and aspirin. The three phase diagrams are determined using X-ray diffraction and the differential scanning calorimetry from the binary mixtures. It is concluded that the paracetamol–caffeine and aspirin–caffeine systems are similar and exhibit two invariants, one eutectic and one metatectic. The paracetamol–aspirin phase diagram reveals the formation of one eutectic. The composition of the three eutectics formed is confirmed by the related Tamman’s triangles. No compound formation is found in the three systems.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><doi>10.1007/s10973-017-6855-6</doi><tpages>15</tpages></addata></record> |
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subjects | Acetaminophen Analgesics Analytical Chemistry Aspirin Binary mixtures Bioavailability Caffeine Chemistry Chemistry and Materials Science Condensed Matter Eutectic composition Headache Inorganic Chemistry Materials Science Measurement Science and Instrumentation Migraine Pain Phase diagrams Phase equilibria Physical Chemistry Physics Polymer Sciences Polymorphism Triangles |
title | Reinvestigation of the paracetamol–caffeine, aspirin–caffeine, and paracetamol–aspirin phase equilibria diagrams |
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