Preparation and characterization of drug-solution-dropping tablet

This study is an attempt to improve dissolution rate of a poorly watersoluble drug from tablet by drug-solution-dropping technique. Diazepam was used as a model drug. Absolute alcohol and dichloromethane were used to prepare diazepam solution. The 50 μl solution (5 mg diazepam) was dropped on blank...

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Main Authors: Orawan Chitvanich, Busaban Sirithunyalug, Siriporn Okonogi, Sirivipa Piyamongkol, Jakkapan Sirithunyalug
Format: Journal
Published: 2018
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http://cmuir.cmu.ac.th/jspui/handle/6653943832/49492
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Institution: Chiang Mai University
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spelling th-cmuir.6653943832-494922018-08-16T02:19:24Z Preparation and characterization of drug-solution-dropping tablet Orawan Chitvanich Busaban Sirithunyalug Siriporn Okonogi Sirivipa Piyamongkol Jakkapan Sirithunyalug Multidisciplinary This study is an attempt to improve dissolution rate of a poorly watersoluble drug from tablet by drug-solution-dropping technique. Diazepam was used as a model drug. Absolute alcohol and dichloromethane were used to prepare diazepam solution. The 50 μl solution (5 mg diazepam) was dropped on blank tablet by using microsyringe. Two kinds of blank tablets were prepared by direct compression (DC) and wet granulation (WG) methods, using dicalcium phosphate dihydrate and lactose as diluents, respectively, with 1000, 1400 or 1800 kg compression force. The surfaces of diazepam-solution-dropping tablets were characterized by Scanning electron microscope (SEM). Their morphologies revealed the smoother surface than that of blank tablet, particularly from wet granulation method of higher compression force but not being clear to point out diazepam particles on the surface. X-ray diffraction by monochromator (single crystal) mode was also used to point out the crystalline or amorphous form of the drug. X-ray monochromator analysis could not be used to confirm the crystallinity of diazepam on the surface of prepared tablet. Differential scanning calorimetry thermatogram showed the peak of diazepam only in the tablet prepared from wet granulaion blank tablet. Dissolution profiles of the prepared tablet from the two kinds of blank tablets were compared to diazepam tablet prepared by the conventional direct compression and wet granulation technique. The result profiles revealed that this drug-solution-dropping technique could be applied especially to poorly-water-soluble drug such as diazepam by using blank tablet at 1000 kg compression force. The dissolution rate of drug-solution-dropping tablet (DSDT) from blank tablet prepared by WG method was faster than that of DSDT from blank tablet prepared by DC method. Certainly, more uniformity of active ingredient is also an advantage of the drug-solution-dropping tablet prepared. 2018-08-16T02:19:24Z 2018-08-16T02:19:24Z 2009-07-01 Journal 16851994 2-s2.0-77953766709 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=77953766709&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/49492
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Multidisciplinary
spellingShingle Multidisciplinary
Orawan Chitvanich
Busaban Sirithunyalug
Siriporn Okonogi
Sirivipa Piyamongkol
Jakkapan Sirithunyalug
Preparation and characterization of drug-solution-dropping tablet
description This study is an attempt to improve dissolution rate of a poorly watersoluble drug from tablet by drug-solution-dropping technique. Diazepam was used as a model drug. Absolute alcohol and dichloromethane were used to prepare diazepam solution. The 50 μl solution (5 mg diazepam) was dropped on blank tablet by using microsyringe. Two kinds of blank tablets were prepared by direct compression (DC) and wet granulation (WG) methods, using dicalcium phosphate dihydrate and lactose as diluents, respectively, with 1000, 1400 or 1800 kg compression force. The surfaces of diazepam-solution-dropping tablets were characterized by Scanning electron microscope (SEM). Their morphologies revealed the smoother surface than that of blank tablet, particularly from wet granulation method of higher compression force but not being clear to point out diazepam particles on the surface. X-ray diffraction by monochromator (single crystal) mode was also used to point out the crystalline or amorphous form of the drug. X-ray monochromator analysis could not be used to confirm the crystallinity of diazepam on the surface of prepared tablet. Differential scanning calorimetry thermatogram showed the peak of diazepam only in the tablet prepared from wet granulaion blank tablet. Dissolution profiles of the prepared tablet from the two kinds of blank tablets were compared to diazepam tablet prepared by the conventional direct compression and wet granulation technique. The result profiles revealed that this drug-solution-dropping technique could be applied especially to poorly-water-soluble drug such as diazepam by using blank tablet at 1000 kg compression force. The dissolution rate of drug-solution-dropping tablet (DSDT) from blank tablet prepared by WG method was faster than that of DSDT from blank tablet prepared by DC method. Certainly, more uniformity of active ingredient is also an advantage of the drug-solution-dropping tablet prepared.
format Journal
author Orawan Chitvanich
Busaban Sirithunyalug
Siriporn Okonogi
Sirivipa Piyamongkol
Jakkapan Sirithunyalug
author_facet Orawan Chitvanich
Busaban Sirithunyalug
Siriporn Okonogi
Sirivipa Piyamongkol
Jakkapan Sirithunyalug
author_sort Orawan Chitvanich
title Preparation and characterization of drug-solution-dropping tablet
title_short Preparation and characterization of drug-solution-dropping tablet
title_full Preparation and characterization of drug-solution-dropping tablet
title_fullStr Preparation and characterization of drug-solution-dropping tablet
title_full_unstemmed Preparation and characterization of drug-solution-dropping tablet
title_sort preparation and characterization of drug-solution-dropping tablet
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=77953766709&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/49492
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