Influence of Chitin Source and Polymorphism on Powder Compression and Compaction: Application in Drug Delivery
The objective of the research reported herein is to compare the compaction properties of three different chitin extracts from the organisms most used in the seafood industry; namely crabs, shrimps and squids. The foregoing is examined in relation to their polymorphic forms as well as compression and...
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doaj-abb8add8c39146d9bcb61f058afe82ac2020-11-25T04:06:13ZengMDPI AGMolecules1420-30492020-11-01255269526910.3390/molecules25225269Influence of Chitin Source and Polymorphism on Powder Compression and Compaction: Application in Drug DeliveryLinda Al-Hmoud0Deeb Abu Fara1Iyad Rashid2Babur Z. Chowdhry3Adnan A. Badwan4Chemical Engineering Department, School of Engineering, University of Jordan, Amman 11942, JordanChemical Engineering Department, School of Engineering, University of Jordan, Amman 11942, JordanResearch and Innovation Centre, The Jordanian Pharmaceutical Manufacturing Company (JPM), P.O. Box 94, Naor 11710, JordanSchool of Science, Faculty of Engineering & Science, University of Greenwich, Medway Campus, Chatham Maritime, Kent ME4 4TB, UKResearch and Innovation Centre, The Jordanian Pharmaceutical Manufacturing Company (JPM), P.O. Box 94, Naor 11710, JordanThe objective of the research reported herein is to compare the compaction properties of three different chitin extracts from the organisms most used in the seafood industry; namely crabs, shrimps and squids. The foregoing is examined in relation to their polymorphic forms as well as compression and compaction behavior. Chitin extracted from crabs and shrimps exhibits the α-polymorphic form whilst chitin extracted from squid pins displays a β-polymorphic form. These polymorphs were characterized using FTIR, X-ray powder diffraction and scanning electron microscopy. Pore diameter and volume differ between the two polymorphic powder forms. The β form is smaller in pore diameter and volume. Scanning electron microscopy of the two polymorphic forms shows clear variation in the arrangement of chitin layers such that the α form appears more condensed due to the anti-parallel arrangement of the polymer chains. True, bulk and tapped densities of these polymorphs and their mixtures indicated poor flowability. Nevertheless, compression and compaction properties obtained by applying Heckle and Kawakita analyses indicated that both polymorphs are able to be compacted with differences in the extent of compaction. Chitin compacts, regardless of their origin, showed a very high crushing strength with very fast dissolution which makes them suitable for use as fast mouth dissolving tablets. Moreover, when different chitin powders are granulated with two model drugs, i.e., metronidazole and spiramycin they yielded high crushing strength and their dissolution profiles were in accordance with compendial requirements. It is concluded that the source of chitin extraction is as important as the polymorphic form when compression and compaction of chitin powders is carried out.https://www.mdpi.com/1420-3049/25/22/5269chitinpolymorphschitin sourceschitin characterizationdisintegrationdissolution |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Linda Al-Hmoud Deeb Abu Fara Iyad Rashid Babur Z. Chowdhry Adnan A. Badwan |
spellingShingle |
Linda Al-Hmoud Deeb Abu Fara Iyad Rashid Babur Z. Chowdhry Adnan A. Badwan Influence of Chitin Source and Polymorphism on Powder Compression and Compaction: Application in Drug Delivery Molecules chitin polymorphs chitin sources chitin characterization disintegration dissolution |
author_facet |
Linda Al-Hmoud Deeb Abu Fara Iyad Rashid Babur Z. Chowdhry Adnan A. Badwan |
author_sort |
Linda Al-Hmoud |
title |
Influence of Chitin Source and Polymorphism on Powder Compression and Compaction: Application in Drug Delivery |
title_short |
Influence of Chitin Source and Polymorphism on Powder Compression and Compaction: Application in Drug Delivery |
title_full |
Influence of Chitin Source and Polymorphism on Powder Compression and Compaction: Application in Drug Delivery |
title_fullStr |
Influence of Chitin Source and Polymorphism on Powder Compression and Compaction: Application in Drug Delivery |
title_full_unstemmed |
Influence of Chitin Source and Polymorphism on Powder Compression and Compaction: Application in Drug Delivery |
title_sort |
influence of chitin source and polymorphism on powder compression and compaction: application in drug delivery |
publisher |
MDPI AG |
series |
Molecules |
issn |
1420-3049 |
publishDate |
2020-11-01 |
description |
The objective of the research reported herein is to compare the compaction properties of three different chitin extracts from the organisms most used in the seafood industry; namely crabs, shrimps and squids. The foregoing is examined in relation to their polymorphic forms as well as compression and compaction behavior. Chitin extracted from crabs and shrimps exhibits the α-polymorphic form whilst chitin extracted from squid pins displays a β-polymorphic form. These polymorphs were characterized using FTIR, X-ray powder diffraction and scanning electron microscopy. Pore diameter and volume differ between the two polymorphic powder forms. The β form is smaller in pore diameter and volume. Scanning electron microscopy of the two polymorphic forms shows clear variation in the arrangement of chitin layers such that the α form appears more condensed due to the anti-parallel arrangement of the polymer chains. True, bulk and tapped densities of these polymorphs and their mixtures indicated poor flowability. Nevertheless, compression and compaction properties obtained by applying Heckle and Kawakita analyses indicated that both polymorphs are able to be compacted with differences in the extent of compaction. Chitin compacts, regardless of their origin, showed a very high crushing strength with very fast dissolution which makes them suitable for use as fast mouth dissolving tablets. Moreover, when different chitin powders are granulated with two model drugs, i.e., metronidazole and spiramycin they yielded high crushing strength and their dissolution profiles were in accordance with compendial requirements. It is concluded that the source of chitin extraction is as important as the polymorphic form when compression and compaction of chitin powders is carried out. |
topic |
chitin polymorphs chitin sources chitin characterization disintegration dissolution |
url |
https://www.mdpi.com/1420-3049/25/22/5269 |
work_keys_str_mv |
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