Extrusion for pharma applications: An update

Abstract This paper aims to give an overview of our current research and development on hot‐melt extrusion (HME) for pharmaceutical formulation and drug delivery. Unfortunately, a large percentage of marketed drugs (40%) and those in the development pipeline (90%) are poorly water soluble. We use a...
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Autor*in:	Maël Gallas [verfasserIn] Pascal Boulet [verfasserIn] Victoire deMargerie [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2023

Schlagwörter:	drug delivery drug formulation hot melt extrusion pharma polymers vertical extrusion

Übergeordnetes Werk:	In: SPE Polymers - Wiley, 2022, 4(2023), 1, Seite 16-23
Übergeordnetes Werk:	volume:4 ; year:2023 ; number:1 ; pages:16-23

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc

DOI / URN:	10.1002/pls2.10081

Katalog-ID:	DOAJ081587872

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spelling	10.1002/pls2.10081 doi (DE-627)DOAJ081587872 (DE-599)DOAJ0a4c83b2c65b449899222ba5d119e465 DE-627 ger DE-627 rakwb eng TP1080-1185 Maël Gallas verfasserin aut Extrusion for pharma applications: An update 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract This paper aims to give an overview of our current research and development on hot‐melt extrusion (HME) for pharmaceutical formulation and drug delivery. Unfortunately, a large percentage of marketed drugs (40%) and those in the development pipeline (90%) are poorly water soluble. We use a few examples to show that solubility of APIs can be drastically improved by using HME to mix them with different biocompatible polymers and playing with the various process parameters (extrusion temperature, screw speed, screw configuration, etc.). The advantages of this technique are then presented as well as the further development needed to make this process fully industrial for pharmaceutical purposes. drug delivery drug formulation hot melt extrusion pharma polymers vertical extrusion Polymers and polymer manufacture Pascal Boulet verfasserin aut Victoire deMargerie verfasserin aut In SPE Polymers Wiley, 2022 4(2023), 1, Seite 16-23 (DE-627)1754880401 (DE-600)3060487-4 26903857 nnns volume:4 year:2023 number:1 pages:16-23 https://doi.org/10.1002/pls2.10081 kostenfrei https://doaj.org/article/0a4c83b2c65b449899222ba5d119e465 kostenfrei https://doi.org/10.1002/pls2.10081 kostenfrei https://doaj.org/toc/2690-3857 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 4 2023 1 16-23
allfields_unstemmed	10.1002/pls2.10081 doi (DE-627)DOAJ081587872 (DE-599)DOAJ0a4c83b2c65b449899222ba5d119e465 DE-627 ger DE-627 rakwb eng TP1080-1185 Maël Gallas verfasserin aut Extrusion for pharma applications: An update 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract This paper aims to give an overview of our current research and development on hot‐melt extrusion (HME) for pharmaceutical formulation and drug delivery. Unfortunately, a large percentage of marketed drugs (40%) and those in the development pipeline (90%) are poorly water soluble. We use a few examples to show that solubility of APIs can be drastically improved by using HME to mix them with different biocompatible polymers and playing with the various process parameters (extrusion temperature, screw speed, screw configuration, etc.). The advantages of this technique are then presented as well as the further development needed to make this process fully industrial for pharmaceutical purposes. drug delivery drug formulation hot melt extrusion pharma polymers vertical extrusion Polymers and polymer manufacture Pascal Boulet verfasserin aut Victoire deMargerie verfasserin aut In SPE Polymers Wiley, 2022 4(2023), 1, Seite 16-23 (DE-627)1754880401 (DE-600)3060487-4 26903857 nnns volume:4 year:2023 number:1 pages:16-23 https://doi.org/10.1002/pls2.10081 kostenfrei https://doaj.org/article/0a4c83b2c65b449899222ba5d119e465 kostenfrei https://doi.org/10.1002/pls2.10081 kostenfrei https://doaj.org/toc/2690-3857 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 4 2023 1 16-23
allfieldsGer	10.1002/pls2.10081 doi (DE-627)DOAJ081587872 (DE-599)DOAJ0a4c83b2c65b449899222ba5d119e465 DE-627 ger DE-627 rakwb eng TP1080-1185 Maël Gallas verfasserin aut Extrusion for pharma applications: An update 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract This paper aims to give an overview of our current research and development on hot‐melt extrusion (HME) for pharmaceutical formulation and drug delivery. Unfortunately, a large percentage of marketed drugs (40%) and those in the development pipeline (90%) are poorly water soluble. We use a few examples to show that solubility of APIs can be drastically improved by using HME to mix them with different biocompatible polymers and playing with the various process parameters (extrusion temperature, screw speed, screw configuration, etc.). The advantages of this technique are then presented as well as the further development needed to make this process fully industrial for pharmaceutical purposes. drug delivery drug formulation hot melt extrusion pharma polymers vertical extrusion Polymers and polymer manufacture Pascal Boulet verfasserin aut Victoire deMargerie verfasserin aut In SPE Polymers Wiley, 2022 4(2023), 1, Seite 16-23 (DE-627)1754880401 (DE-600)3060487-4 26903857 nnns volume:4 year:2023 number:1 pages:16-23 https://doi.org/10.1002/pls2.10081 kostenfrei https://doaj.org/article/0a4c83b2c65b449899222ba5d119e465 kostenfrei https://doi.org/10.1002/pls2.10081 kostenfrei https://doaj.org/toc/2690-3857 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 4 2023 1 16-23
allfieldsSound	10.1002/pls2.10081 doi (DE-627)DOAJ081587872 (DE-599)DOAJ0a4c83b2c65b449899222ba5d119e465 DE-627 ger DE-627 rakwb eng TP1080-1185 Maël Gallas verfasserin aut Extrusion for pharma applications: An update 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract This paper aims to give an overview of our current research and development on hot‐melt extrusion (HME) for pharmaceutical formulation and drug delivery. Unfortunately, a large percentage of marketed drugs (40%) and those in the development pipeline (90%) are poorly water soluble. We use a few examples to show that solubility of APIs can be drastically improved by using HME to mix them with different biocompatible polymers and playing with the various process parameters (extrusion temperature, screw speed, screw configuration, etc.). The advantages of this technique are then presented as well as the further development needed to make this process fully industrial for pharmaceutical purposes. drug delivery drug formulation hot melt extrusion pharma polymers vertical extrusion Polymers and polymer manufacture Pascal Boulet verfasserin aut Victoire deMargerie verfasserin aut In SPE Polymers Wiley, 2022 4(2023), 1, Seite 16-23 (DE-627)1754880401 (DE-600)3060487-4 26903857 nnns volume:4 year:2023 number:1 pages:16-23 https://doi.org/10.1002/pls2.10081 kostenfrei https://doaj.org/article/0a4c83b2c65b449899222ba5d119e465 kostenfrei https://doi.org/10.1002/pls2.10081 kostenfrei https://doaj.org/toc/2690-3857 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 4 2023 1 16-23
language	English
source	In SPE Polymers 4(2023), 1, Seite 16-23 volume:4 year:2023 number:1 pages:16-23
sourceStr	In SPE Polymers 4(2023), 1, Seite 16-23 volume:4 year:2023 number:1 pages:16-23
format_phy_str_mv	Article
institution	findex.gbv.de
topic_facet	drug delivery drug formulation hot melt extrusion pharma polymers vertical extrusion Polymers and polymer manufacture
isfreeaccess_bool	true
container_title	SPE Polymers
authorswithroles_txt_mv	Maël Gallas @@aut@@ Pascal Boulet @@aut@@ Victoire deMargerie @@aut@@
publishDateDaySort_date	2023-01-01T00:00:00Z
hierarchy_top_id	1754880401
id	DOAJ081587872
language_de	englisch
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callnumber-first	T - Technology
author	Maël Gallas
spellingShingle	Maël Gallas misc TP1080-1185 misc drug delivery misc drug formulation misc hot melt extrusion misc pharma polymers misc vertical extrusion misc Polymers and polymer manufacture Extrusion for pharma applications: An update
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topic_title	TP1080-1185 Extrusion for pharma applications: An update drug delivery drug formulation hot melt extrusion pharma polymers vertical extrusion
topic	misc TP1080-1185 misc drug delivery misc drug formulation misc hot melt extrusion misc pharma polymers misc vertical extrusion misc Polymers and polymer manufacture
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title	Extrusion for pharma applications: An update
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title_sort	extrusion for pharma applications: an update
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title_auth	Extrusion for pharma applications: An update
abstract	Abstract This paper aims to give an overview of our current research and development on hot‐melt extrusion (HME) for pharmaceutical formulation and drug delivery. Unfortunately, a large percentage of marketed drugs (40%) and those in the development pipeline (90%) are poorly water soluble. We use a few examples to show that solubility of APIs can be drastically improved by using HME to mix them with different biocompatible polymers and playing with the various process parameters (extrusion temperature, screw speed, screw configuration, etc.). The advantages of this technique are then presented as well as the further development needed to make this process fully industrial for pharmaceutical purposes.
abstractGer	Abstract This paper aims to give an overview of our current research and development on hot‐melt extrusion (HME) for pharmaceutical formulation and drug delivery. Unfortunately, a large percentage of marketed drugs (40%) and those in the development pipeline (90%) are poorly water soluble. We use a few examples to show that solubility of APIs can be drastically improved by using HME to mix them with different biocompatible polymers and playing with the various process parameters (extrusion temperature, screw speed, screw configuration, etc.). The advantages of this technique are then presented as well as the further development needed to make this process fully industrial for pharmaceutical purposes.
abstract_unstemmed	Abstract This paper aims to give an overview of our current research and development on hot‐melt extrusion (HME) for pharmaceutical formulation and drug delivery. Unfortunately, a large percentage of marketed drugs (40%) and those in the development pipeline (90%) are poorly water soluble. We use a few examples to show that solubility of APIs can be drastically improved by using HME to mix them with different biocompatible polymers and playing with the various process parameters (extrusion temperature, screw speed, screw configuration, etc.). The advantages of this technique are then presented as well as the further development needed to make this process fully industrial for pharmaceutical purposes.
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title_short	Extrusion for pharma applications: An update
url	https://doi.org/10.1002/pls2.10081 https://doaj.org/article/0a4c83b2c65b449899222ba5d119e465 https://doaj.org/toc/2690-3857
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