Characterization and in vitro release study of artesunateloaded microparticles prepared using crosslinked-chitosan and its derivatives
Purpose: To determine the effect of crosslinking on the physical characteristics, recovery, and release of artesunate-loaded chitosan and carboxymethyl chitosan microparticles. Methods: The artesunate microparticles were prepared by means of ionic gelation-spray drying methods involving the use of...
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Pharmacotherapy Group
2020
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id-langga.1237102023-04-16T06:00:48Z https://repository.unair.ac.id/123710/ Characterization and in vitro release study of artesunateloaded microparticles prepared using crosslinked-chitosan and its derivatives Retno Sari Meta Dian Feriza Amani Syarahil Andang Miatmoko Dwi Setyawan R Medicine RS Pharmacy and materia medica RS1-441 Pharmacy and materia medica RS200-201 Pharmaceutical dosage forms Purpose: To determine the effect of crosslinking on the physical characteristics, recovery, and release of artesunate-loaded chitosan and carboxymethyl chitosan microparticles. Methods: The artesunate microparticles were prepared by means of ionic gelation-spray drying methods involving the use of a crosslinking agent i.e. tripolyphosphate for chitosan and CaCl2 for carboxymethyl chitosan. The drug-polymer solution mixture was introduced into the crosslinker solution and stirred for two hours at 500 rpm prior to drying at a temperature of 100ºC, a pressure of 2 mbar and a flow speed of 6.0 mL/min. The resulting microparticles were subsequently evaluated for their morphology, physical state, drug content and in vitro drug release. Results: The results showed that the type of chitosan and crosslinking affected particle shape, surface roughness, drug recovery, and drug release. The artesunate microparticles prepared with cross-linked polymer demonstrated a lower encapsulation efficiency due to the barriers presented by the crosslinking agents. The use of carboxymethyl chitosan increased the release rate of the artesunate from the microparticles by up to 1.2 times (16.78 mg/ml.min½), while chitosan decreased it 0.7 times (9.12 mg/ml.min½) compared to artesunate alone (13.54 mg/ml.min½). Conclusion: The use of crosslinking agents and chitosan type affects the physical characteristics of artesunate in addition to its release rate from microparticles. Pharmacotherapy Group 2020-11-13 Article PeerReviewed text en https://repository.unair.ac.id/123710/1/C-19%20Artikel.pdf text en https://repository.unair.ac.id/123710/2/C-19%20Kualitas%20Karil.pdf text en https://repository.unair.ac.id/123710/3/C-19%20Similarity.pdf Retno Sari and Meta Dian Feriza and Amani Syarahil and Andang Miatmoko and Dwi Setyawan (2020) Characterization and in vitro release study of artesunateloaded microparticles prepared using crosslinked-chitosan and its derivatives. Tropical Journal of Pharmaceutical Research, 19 (6). pp. 1139-1146. ISSN 1596-5996 https://www.ajol.info/index.php/tjpr/article/view/201590 https://doi.org/10.4314/tjpr.v19i6.3 |
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R Medicine RS Pharmacy and materia medica RS1-441 Pharmacy and materia medica RS200-201 Pharmaceutical dosage forms Retno Sari Meta Dian Feriza Amani Syarahil Andang Miatmoko Dwi Setyawan Characterization and in vitro release study of artesunateloaded microparticles prepared using crosslinked-chitosan and its derivatives |
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Purpose: To determine the effect of crosslinking on the physical characteristics, recovery, and release of artesunate-loaded chitosan and carboxymethyl chitosan microparticles.
Methods: The artesunate microparticles were prepared by means of ionic gelation-spray drying methods involving the use of a crosslinking agent i.e. tripolyphosphate for chitosan and CaCl2 for carboxymethyl chitosan. The drug-polymer solution mixture was introduced into the crosslinker solution and stirred for two hours at 500 rpm prior to drying at a temperature of 100ºC, a pressure of 2 mbar and a flow speed of 6.0 mL/min. The resulting microparticles were subsequently evaluated for their morphology, physical state, drug content and in vitro drug release.
Results: The results showed that the type of chitosan and crosslinking affected particle shape, surface roughness, drug recovery, and drug release. The artesunate microparticles prepared with cross-linked polymer demonstrated a lower encapsulation efficiency due to the barriers presented by the crosslinking agents. The use of carboxymethyl chitosan increased the release rate of the artesunate from the microparticles by up to 1.2 times (16.78 mg/ml.min½), while chitosan decreased it 0.7 times (9.12 mg/ml.min½) compared to artesunate alone (13.54 mg/ml.min½).
Conclusion: The use of crosslinking agents and chitosan type affects the physical characteristics of artesunate in addition to its release rate from microparticles. |
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Article PeerReviewed |
author |
Retno Sari Meta Dian Feriza Amani Syarahil Andang Miatmoko Dwi Setyawan |
author_facet |
Retno Sari Meta Dian Feriza Amani Syarahil Andang Miatmoko Dwi Setyawan |
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Retno Sari |
title |
Characterization and in vitro release study of artesunateloaded microparticles prepared using crosslinked-chitosan and its derivatives |
title_short |
Characterization and in vitro release study of artesunateloaded microparticles prepared using crosslinked-chitosan and its derivatives |
title_full |
Characterization and in vitro release study of artesunateloaded microparticles prepared using crosslinked-chitosan and its derivatives |
title_fullStr |
Characterization and in vitro release study of artesunateloaded microparticles prepared using crosslinked-chitosan and its derivatives |
title_full_unstemmed |
Characterization and in vitro release study of artesunateloaded microparticles prepared using crosslinked-chitosan and its derivatives |
title_sort |
characterization and in vitro release study of artesunateloaded microparticles prepared using crosslinked-chitosan and its derivatives |
publisher |
Pharmacotherapy Group |
publishDate |
2020 |
url |
https://repository.unair.ac.id/123710/1/C-19%20Artikel.pdf https://repository.unair.ac.id/123710/2/C-19%20Kualitas%20Karil.pdf https://repository.unair.ac.id/123710/3/C-19%20Similarity.pdf https://repository.unair.ac.id/123710/ https://www.ajol.info/index.php/tjpr/article/view/201590 https://doi.org/10.4314/tjpr.v19i6.3 |
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1764209107521241088 |