In situ fluidized hot melt granulation using a novel meltable binder: Effect of formulation variables on granule characteristics and controlled release tablets

In situ fluidized hot melt granulation (FHMG) for different (ternary) formulations based on glyceryl palmito-stearate as non-conventional meltable binder and ibuprofen as model drug was examined for controlled release applications. The process was robust, lasted only 15. min, and enabled to attain h...

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Autores principales: Prado, H.J., Bonelli, P.R., Cukierman, A.L.
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_00325910_v264_n_p498_Prado
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spelling todo:paper_00325910_v264_n_p498_Prado2023-10-03T14:45:17Z In situ fluidized hot melt granulation using a novel meltable binder: Effect of formulation variables on granule characteristics and controlled release tablets Prado, H.J. Bonelli, P.R. Cukierman, A.L. Controlled release Fluidized hot melt granulation Gelucires Glyceryl palmito-stearate Tablets Binders Drug products Fluidization Lubricants Controlled release Fluidized hot melt granulation Gelucires Glyceryl palmito-stearate Tablets Granulation glycerol palmitostearate ibuprofen lubricating agent article controlled release formulation crystal structure drug granulation drug granule fluidized hot melt granulation infrared spectroscopy particle size phase transition scanning electron microscopy tablet compression tablet formulation temperature measurement X ray diffraction In situ fluidized hot melt granulation (FHMG) for different (ternary) formulations based on glyceryl palmito-stearate as non-conventional meltable binder and ibuprofen as model drug was examined for controlled release applications. The process was robust, lasted only 15. min, and enabled to attain high yields (95-98. wt.%). The obtained granules presented a bimodal size distribution, having the major mode of 200. μm and good flow properties, thus avoiding the necessity to add other lubricants for tablet compaction. The crystalline structure of ibuprofen and of the non meltable excipients was retained, and that of glyceryl palmito-stearate was recovered in the final granules. The resulting ibuprofen tablets had good pharmacotechnical properties. The granulation process did not modify release profiles from the tablets. The main factor influencing the release profiles was the content of glyceryl palmito-stearate in the formulations. A high drug load (50. wt.%), which is particularly important in the case of high dose active pharmaceutical ingredients, was achieved. Glyceryl palmito-stearate performed a triple function in the tablet formulation: as a meltable binder, as a controlled release matrix and as a lubricant. © 2014 Elsevier B.V. Fil:Prado, H.J. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Bonelli, P.R. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Cukierman, A.L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00325910_v264_n_p498_Prado
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Controlled release
Fluidized hot melt granulation
Gelucires
Glyceryl palmito-stearate
Tablets
Binders
Drug products
Fluidization
Lubricants
Controlled release
Fluidized hot melt granulation
Gelucires
Glyceryl palmito-stearate
Tablets
Granulation
glycerol palmitostearate
ibuprofen
lubricating agent
article
controlled release formulation
crystal structure
drug granulation
drug granule
fluidized hot melt granulation
infrared spectroscopy
particle size
phase transition
scanning electron microscopy
tablet compression
tablet formulation
temperature measurement
X ray diffraction
spellingShingle Controlled release
Fluidized hot melt granulation
Gelucires
Glyceryl palmito-stearate
Tablets
Binders
Drug products
Fluidization
Lubricants
Controlled release
Fluidized hot melt granulation
Gelucires
Glyceryl palmito-stearate
Tablets
Granulation
glycerol palmitostearate
ibuprofen
lubricating agent
article
controlled release formulation
crystal structure
drug granulation
drug granule
fluidized hot melt granulation
infrared spectroscopy
particle size
phase transition
scanning electron microscopy
tablet compression
tablet formulation
temperature measurement
X ray diffraction
Prado, H.J.
Bonelli, P.R.
Cukierman, A.L.
In situ fluidized hot melt granulation using a novel meltable binder: Effect of formulation variables on granule characteristics and controlled release tablets
topic_facet Controlled release
Fluidized hot melt granulation
Gelucires
Glyceryl palmito-stearate
Tablets
Binders
Drug products
Fluidization
Lubricants
Controlled release
Fluidized hot melt granulation
Gelucires
Glyceryl palmito-stearate
Tablets
Granulation
glycerol palmitostearate
ibuprofen
lubricating agent
article
controlled release formulation
crystal structure
drug granulation
drug granule
fluidized hot melt granulation
infrared spectroscopy
particle size
phase transition
scanning electron microscopy
tablet compression
tablet formulation
temperature measurement
X ray diffraction
description In situ fluidized hot melt granulation (FHMG) for different (ternary) formulations based on glyceryl palmito-stearate as non-conventional meltable binder and ibuprofen as model drug was examined for controlled release applications. The process was robust, lasted only 15. min, and enabled to attain high yields (95-98. wt.%). The obtained granules presented a bimodal size distribution, having the major mode of 200. μm and good flow properties, thus avoiding the necessity to add other lubricants for tablet compaction. The crystalline structure of ibuprofen and of the non meltable excipients was retained, and that of glyceryl palmito-stearate was recovered in the final granules. The resulting ibuprofen tablets had good pharmacotechnical properties. The granulation process did not modify release profiles from the tablets. The main factor influencing the release profiles was the content of glyceryl palmito-stearate in the formulations. A high drug load (50. wt.%), which is particularly important in the case of high dose active pharmaceutical ingredients, was achieved. Glyceryl palmito-stearate performed a triple function in the tablet formulation: as a meltable binder, as a controlled release matrix and as a lubricant. © 2014 Elsevier B.V.
format JOUR
author Prado, H.J.
Bonelli, P.R.
Cukierman, A.L.
author_facet Prado, H.J.
Bonelli, P.R.
Cukierman, A.L.
author_sort Prado, H.J.
title In situ fluidized hot melt granulation using a novel meltable binder: Effect of formulation variables on granule characteristics and controlled release tablets
title_short In situ fluidized hot melt granulation using a novel meltable binder: Effect of formulation variables on granule characteristics and controlled release tablets
title_full In situ fluidized hot melt granulation using a novel meltable binder: Effect of formulation variables on granule characteristics and controlled release tablets
title_fullStr In situ fluidized hot melt granulation using a novel meltable binder: Effect of formulation variables on granule characteristics and controlled release tablets
title_full_unstemmed In situ fluidized hot melt granulation using a novel meltable binder: Effect of formulation variables on granule characteristics and controlled release tablets
title_sort in situ fluidized hot melt granulation using a novel meltable binder: effect of formulation variables on granule characteristics and controlled release tablets
url http://hdl.handle.net/20.500.12110/paper_00325910_v264_n_p498_Prado
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AT cukiermanal insitufluidizedhotmeltgranulationusinganovelmeltablebindereffectofformulationvariablesongranulecharacteristicsandcontrolledreleasetablets
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