Development of a controlled release formulation by continuous twin screw granulation: Influence of process and formulation parameters

[Display omitted] The aim of this study was to evaluate the potential of twin screw granulation for the continuous production of controlled release formulations with hydroxypropylmethylcellulose as hydrophilic matrix former. Metoprolol tartrate was included in the formulation as very water soluble m...

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Veröffentlicht in:International journal of pharmaceutics 2016-05, Vol.505 (1-2), p.61-68
Hauptverfasser: Vanhoorne, V., Vanbillemont, B., Vercruysse, J., De Leersnyder, F., Gomes, P., Beer, T. De, Remon, J.P., Vervaet, C.
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container_end_page 68
container_issue 1-2
container_start_page 61
container_title International journal of pharmaceutics
container_volume 505
creator Vanhoorne, V.
Vanbillemont, B.
Vercruysse, J.
De Leersnyder, F.
Gomes, P.
Beer, T. De
Remon, J.P.
Vervaet, C.
description [Display omitted] The aim of this study was to evaluate the potential of twin screw granulation for the continuous production of controlled release formulations with hydroxypropylmethylcellulose as hydrophilic matrix former. Metoprolol tartrate was included in the formulation as very water soluble model drug. A premix of metoprolol tartrate, hydroxypropylmethylcellulose and filler (ratio 20/20/60, w/w) was granulated with demineralized water via twin screw granulation. After oven drying and milling, tablets were produced on a rotary Modul™ P tablet press. A D-optimal design (29 experiments) was used to assess the influence of process (screw speed, throughput, barrel temperature and screw design) and formulation parameters (starch content of the filler) on the process (torque), granule (size distribution, shape, friability, density) and tablet (hardness, friability and dissolution) critical quality attributes. The torque was dominated by the number of kneading elements and throughput, whereas screw speed and filling degree only showed a minor influence on torque. Addition of screw mixing elements after a block of kneading elements improved the yield of the process before milling as it resulted in less oversized granules and also after milling as less fines were present. Temperature was also an important parameter to optimize as a higher temperature yielded less fines and positively influenced the aspect ratio. The shape of hydroxypropylmethylcellulose granules was comparable to that of immediate release formulations. Tensile strength and friability of tablets were not dependent on the process parameters. The use of starch as filler was not beneficial with regard to granule and tablet properties. Complete drug release was obtained after 16–20h and was independent of the design’s parameters.
doi_str_mv 10.1016/j.ijpharm.2016.03.058
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A D-optimal design (29 experiments) was used to assess the influence of process (screw speed, throughput, barrel temperature and screw design) and formulation parameters (starch content of the filler) on the process (torque), granule (size distribution, shape, friability, density) and tablet (hardness, friability and dissolution) critical quality attributes. The torque was dominated by the number of kneading elements and throughput, whereas screw speed and filling degree only showed a minor influence on torque. Addition of screw mixing elements after a block of kneading elements improved the yield of the process before milling as it resulted in less oversized granules and also after milling as less fines were present. Temperature was also an important parameter to optimize as a higher temperature yielded less fines and positively influenced the aspect ratio. The shape of hydroxypropylmethylcellulose granules was comparable to that of immediate release formulations. Tensile strength and friability of tablets were not dependent on the process parameters. The use of starch as filler was not beneficial with regard to granule and tablet properties. 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A D-optimal design (29 experiments) was used to assess the influence of process (screw speed, throughput, barrel temperature and screw design) and formulation parameters (starch content of the filler) on the process (torque), granule (size distribution, shape, friability, density) and tablet (hardness, friability and dissolution) critical quality attributes. The torque was dominated by the number of kneading elements and throughput, whereas screw speed and filling degree only showed a minor influence on torque. Addition of screw mixing elements after a block of kneading elements improved the yield of the process before milling as it resulted in less oversized granules and also after milling as less fines were present. Temperature was also an important parameter to optimize as a higher temperature yielded less fines and positively influenced the aspect ratio. The shape of hydroxypropylmethylcellulose granules was comparable to that of immediate release formulations. Tensile strength and friability of tablets were not dependent on the process parameters. The use of starch as filler was not beneficial with regard to granule and tablet properties. Complete drug release was obtained after 16–20h and was independent of the design’s parameters.</description><subject>Chemistry, Pharmaceutical - methods</subject><subject>Continuous production</subject><subject>Controlled release</subject><subject>Delayed-Action Preparations</subject><subject>Drug Liberation</subject><subject>Excipients - chemistry</subject><subject>Hydroxypropylmethylcellulose</subject><subject>Hypromellose Derivatives - chemistry</subject><subject>Metoprolol - administration &amp; dosage</subject><subject>Metoprolol - chemistry</subject><subject>Particle Size</subject><subject>Process variables</subject><subject>Solubility</subject><subject>Starch - chemistry</subject><subject>Tablets</subject><subject>Technology, Pharmaceutical - methods</subject><subject>Temperature</subject><subject>Tensile Strength</subject><subject>Twin screw granulation</subject><subject>Water - chemistry</subject><subject>Wet granulation</subject><issn>0378-5173</issn><issn>1873-3476</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1u1TAQhS1URG8LjwDyspukdvwTh01VFWgrVeoG1pbjTMBXjh3spFUfgPeub-8FiVVXI4--OTM-B6GPlNSUUHm-rd12_mXSVDflWRNWE6HeoA1VLasYb-UR2hDWqkrQlh2jk5y3hBDZUPYOHTct4ZQ2bIP-fIEH8HGeICw4jthgG8OSovcw4AQeTAY8xjSt3iwuBtw_vRAurHHNeHl0AWeb4BH_TCYcoM_4Nox-hWBhpzmnaCFnbMLwn9RskplggZTfo7ej8Rk-HOop-vHt6_erm-ru_vr26vKusqxTS8WtMnzoheqJ4oIT2sFomOxGwbueMCmtMEOveAOSUtuZ0lOKimLD0DEJgp2is71uOen3CnnRk8sWvDcBync0VUTJjgvSvo62qu1e5Asq9qhNMecEo56Tm0x60pToXVh6qw9h6V1YmjBdwipznw4r1n6C4d_U33QKcLEHoHjy4CDpbN3O1cElsIseontlxTMnrKrF</recordid><startdate>20160530</startdate><enddate>20160530</enddate><creator>Vanhoorne, V.</creator><creator>Vanbillemont, B.</creator><creator>Vercruysse, J.</creator><creator>De Leersnyder, F.</creator><creator>Gomes, P.</creator><creator>Beer, T. 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Temperature was also an important parameter to optimize as a higher temperature yielded less fines and positively influenced the aspect ratio. The shape of hydroxypropylmethylcellulose granules was comparable to that of immediate release formulations. Tensile strength and friability of tablets were not dependent on the process parameters. The use of starch as filler was not beneficial with regard to granule and tablet properties. Complete drug release was obtained after 16–20h and was independent of the design’s parameters.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>27041123</pmid><doi>10.1016/j.ijpharm.2016.03.058</doi><tpages>8</tpages></addata></record>
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1873-3476
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source MEDLINE; Elsevier ScienceDirect Journals Complete
subjects Chemistry, Pharmaceutical - methods
Continuous production
Controlled release
Delayed-Action Preparations
Drug Liberation
Excipients - chemistry
Hydroxypropylmethylcellulose
Hypromellose Derivatives - chemistry
Metoprolol - administration & dosage
Metoprolol - chemistry
Particle Size
Process variables
Solubility
Starch - chemistry
Tablets
Technology, Pharmaceutical - methods
Temperature
Tensile Strength
Twin screw granulation
Water - chemistry
Wet granulation
title Development of a controlled release formulation by continuous twin screw granulation: Influence of process and formulation parameters
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