Molecular dynamic investigation on the dissolution behaviour of carbamazepine form III in ethanol solution

Carbamazepine (CBZ) is well known to have low solubility, hence an understanding of crystal behaviour is vital to improve the solubility of the drugs, hence for the oral bioavailability. The objectives of this work are to assess the morphology prediction of the most stable form of CBZ, which form (I...

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Published in:Key Engineering Materials
Main Author: Yusop S.N.; Anuar N.; Md Azmi N.S.; Abu Bakar N.H.
Format: Conference paper
Language:English
Published: Trans Tech Publications Ltd 2019
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85079495488&doi=10.4028%2fwww.scientific.net%2fKEM.797.149&partnerID=40&md5=724be4b42dcfe784fb28cca2cd5d611f
id 2-s2.0-85079495488
spelling 2-s2.0-85079495488
Yusop S.N.; Anuar N.; Md Azmi N.S.; Abu Bakar N.H.
Molecular dynamic investigation on the dissolution behaviour of carbamazepine form III in ethanol solution
2019
Key Engineering Materials
797

10.4028/www.scientific.net/KEM.797.149
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85079495488&doi=10.4028%2fwww.scientific.net%2fKEM.797.149&partnerID=40&md5=724be4b42dcfe784fb28cca2cd5d611f
Carbamazepine (CBZ) is well known to have low solubility, hence an understanding of crystal behaviour is vital to improve the solubility of the drugs, hence for the oral bioavailability. The objectives of this work are to assess the morphology prediction of the most stable form of CBZ, which form (III) and to access the dissolution behaviour of the crystal. Material Studio 4.0 was used to predict the morphology of CBZ form (III) based on attachment energy calculations in vacuum condition by using the combination of MNDO charges from MOPAC with PCFF potential function. Later, predicted morphology was used for dissolution prediction in ethanol solvent using dynamic simulation with CVFF potential function. From the result, the morphology prediction of CBZ form (III) produced hexagonal – like shape with seven dominated facets; (011), (11-1), (100), (10-2), (020), (110) and (11-2) with the most morphological important is (011) face with 45.23% area while the fastest growing facet is (11-2) which only 0.91% area contributed for the whole crystal. The lattice energy calculated was-21.62 kcal/mol with only 1.36% error compared to the experimental value;-21.33 kcal/mol. The dissolution prediction result shows that small facet area with the amine and carbonyl groups exposed at the surface will dissolve readily than the other facets. This result explain that the small facet area with protruding functional groups that can form hydrogen bond to ethanol molecules will be the most favourable facet to dissolve. © 2019 Trans Tech Publications, Switzerland.
Trans Tech Publications Ltd
10139826
English
Conference paper

author Yusop S.N.; Anuar N.; Md Azmi N.S.; Abu Bakar N.H.
spellingShingle Yusop S.N.; Anuar N.; Md Azmi N.S.; Abu Bakar N.H.
Molecular dynamic investigation on the dissolution behaviour of carbamazepine form III in ethanol solution
author_facet Yusop S.N.; Anuar N.; Md Azmi N.S.; Abu Bakar N.H.
author_sort Yusop S.N.; Anuar N.; Md Azmi N.S.; Abu Bakar N.H.
title Molecular dynamic investigation on the dissolution behaviour of carbamazepine form III in ethanol solution
title_short Molecular dynamic investigation on the dissolution behaviour of carbamazepine form III in ethanol solution
title_full Molecular dynamic investigation on the dissolution behaviour of carbamazepine form III in ethanol solution
title_fullStr Molecular dynamic investigation on the dissolution behaviour of carbamazepine form III in ethanol solution
title_full_unstemmed Molecular dynamic investigation on the dissolution behaviour of carbamazepine form III in ethanol solution
title_sort Molecular dynamic investigation on the dissolution behaviour of carbamazepine form III in ethanol solution
publishDate 2019
container_title Key Engineering Materials
container_volume 797
container_issue
doi_str_mv 10.4028/www.scientific.net/KEM.797.149
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-85079495488&doi=10.4028%2fwww.scientific.net%2fKEM.797.149&partnerID=40&md5=724be4b42dcfe784fb28cca2cd5d611f
description Carbamazepine (CBZ) is well known to have low solubility, hence an understanding of crystal behaviour is vital to improve the solubility of the drugs, hence for the oral bioavailability. The objectives of this work are to assess the morphology prediction of the most stable form of CBZ, which form (III) and to access the dissolution behaviour of the crystal. Material Studio 4.0 was used to predict the morphology of CBZ form (III) based on attachment energy calculations in vacuum condition by using the combination of MNDO charges from MOPAC with PCFF potential function. Later, predicted morphology was used for dissolution prediction in ethanol solvent using dynamic simulation with CVFF potential function. From the result, the morphology prediction of CBZ form (III) produced hexagonal – like shape with seven dominated facets; (011), (11-1), (100), (10-2), (020), (110) and (11-2) with the most morphological important is (011) face with 45.23% area while the fastest growing facet is (11-2) which only 0.91% area contributed for the whole crystal. The lattice energy calculated was-21.62 kcal/mol with only 1.36% error compared to the experimental value;-21.33 kcal/mol. The dissolution prediction result shows that small facet area with the amine and carbonyl groups exposed at the surface will dissolve readily than the other facets. This result explain that the small facet area with protruding functional groups that can form hydrogen bond to ethanol molecules will be the most favourable facet to dissolve. © 2019 Trans Tech Publications, Switzerland.
publisher Trans Tech Publications Ltd
issn 10139826
language English
format Conference paper
accesstype
record_format scopus
collection Scopus
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