Effects of pore CaCO3 form agencies on dissolution mechanisms of amoxicillin drugs encapsulated in hydrogels full-IPN chitosan N-vinyl caprolactam

Emil Budianto; Maghfira Fauzia

doi:10.1063/1.5030238

Effects of pore CaCO₃ form agencies on dissolution mechanisms of amoxicillin drugs encapsulated in hydrogels full-IPN chitosan N-vinyl caprolactam

Emil Budianto, Maghfira Fauzia

Department of Chemistry

Research output: Chapter in Book/Report/Conference proceeding › Conference contribution › peer-review

1 Citation (Scopus)

Abstract

The administration of amoxicillin trihydrate in Helicobacter pylori infection is not effective enough because the conventional preparations used have a short retention time in the stomach. To overcome this problem, amoxicillin trihydrate was encapsulated into the floating drug delivery matrix-matrix. In this study, the full-ipn acetaldehyde crosslinked hydrogel (N-vinyl caprolactam) was synthesized with a 10% CaCO3 pore forming agent and then encapsulated on amoxicillin trihydrate and studied the mechanism of drug dissolution with its kinetic kinetics approach. The K-PNVCL Hydrogel produces optimal properties which are then loaded with amoxicillin trihydrate in situ and post loading. In this research, we have got the percentage of swelling, floating time, the efficiency of in situ and post loading 873%; 3.15 minutes; 99.8% and 99.4%. The dissolution test was performed on amoxicillin trihydrate which had been encapsulated K-PNVCL hydrogel in vitro at pH 1.2 resulting in 94.5% for in situ loading and 98.5% for post loading. Results of the kinetics of drug release for post loading and in situ loading methods tend to follow the Higuchi model kinetics. The drug release mechanism occurs by Fickian diffusion. Proof of drug release mechanism from K-PNVCL hydrogel matrix is further done by Scanning Electron Microscope (SEM) instrument.

Original language	English
Title of host publication	Proceedings of the 3rd International Conference on Materials and Metallurgical Engineering and Technology, ICOMMET 2017
Subtitle of host publication	Advancing Innovation in Materials Science, Technology and Applications for Sustainable Future
Editors	Mas Irfan P. Hidayat
Publisher	American Institute of Physics Inc.
ISBN (Electronic)	9780735416406
DOIs	https://doi.org/10.1063/1.5030238
Publication status	Published - 3 Apr 2018
Event	3rd International Conference on Materials and Metallurgical Engineering and Technology: Advancing Innovation in Materials Science, Technology and Applications for Sustainable Future, ICOMMET 2017 - Surabaya, Indonesia Duration: 30 Oct 2017 → 31 Oct 2017

Publication series

Name	AIP Conference Proceedings
Volume	1945
ISSN (Print)	0094-243X
ISSN (Electronic)	1551-7616

Conference

Conference	3rd International Conference on Materials and Metallurgical Engineering and Technology: Advancing Innovation in Materials Science, Technology and Applications for Sustainable Future, ICOMMET 2017
Country/Territory	Indonesia
City	Surabaya
Period	30/10/17 → 31/10/17

Keywords

dissolution test
floating drug delivery system
full-IPN
poly (N-vinylcaprolactam)
release mechanism

Access to Document

10.1063/1.5030238

Cite this

Budianto, E., & Fauzia, M. (2018). Effects of pore CaCO₃ form agencies on dissolution mechanisms of amoxicillin drugs encapsulated in hydrogels full-IPN chitosan N-vinyl caprolactam. In M. I. P. Hidayat (Ed.), Proceedings of the 3rd International Conference on Materials and Metallurgical Engineering and Technology, ICOMMET 2017: Advancing Innovation in Materials Science, Technology and Applications for Sustainable Future Article 020016 (AIP Conference Proceedings; Vol. 1945). American Institute of Physics Inc.. https://doi.org/10.1063/1.5030238

Budianto, Emil ; Fauzia, Maghfira. / Effects of pore CaCO₃ form agencies on dissolution mechanisms of amoxicillin drugs encapsulated in hydrogels full-IPN chitosan N-vinyl caprolactam. Proceedings of the 3rd International Conference on Materials and Metallurgical Engineering and Technology, ICOMMET 2017: Advancing Innovation in Materials Science, Technology and Applications for Sustainable Future. editor / Mas Irfan P. Hidayat. American Institute of Physics Inc., 2018. (AIP Conference Proceedings).

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abstract = "The administration of amoxicillin trihydrate in Helicobacter pylori infection is not effective enough because the conventional preparations used have a short retention time in the stomach. To overcome this problem, amoxicillin trihydrate was encapsulated into the floating drug delivery matrix-matrix. In this study, the full-ipn acetaldehyde crosslinked hydrogel (N-vinyl caprolactam) was synthesized with a 10% CaCO3 pore forming agent and then encapsulated on amoxicillin trihydrate and studied the mechanism of drug dissolution with its kinetic kinetics approach. The K-PNVCL Hydrogel produces optimal properties which are then loaded with amoxicillin trihydrate in situ and post loading. In this research, we have got the percentage of swelling, floating time, the efficiency of in situ and post loading 873%; 3.15 minutes; 99.8% and 99.4%. The dissolution test was performed on amoxicillin trihydrate which had been encapsulated K-PNVCL hydrogel in vitro at pH 1.2 resulting in 94.5% for in situ loading and 98.5% for post loading. Results of the kinetics of drug release for post loading and in situ loading methods tend to follow the Higuchi model kinetics. The drug release mechanism occurs by Fickian diffusion. Proof of drug release mechanism from K-PNVCL hydrogel matrix is further done by Scanning Electron Microscope (SEM) instrument.",

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Budianto, E & Fauzia, M 2018, Effects of pore CaCO₃ form agencies on dissolution mechanisms of amoxicillin drugs encapsulated in hydrogels full-IPN chitosan N-vinyl caprolactam. in MIP Hidayat (ed.), Proceedings of the 3rd International Conference on Materials and Metallurgical Engineering and Technology, ICOMMET 2017: Advancing Innovation in Materials Science, Technology and Applications for Sustainable Future., 020016, AIP Conference Proceedings, vol. 1945, American Institute of Physics Inc., 3rd International Conference on Materials and Metallurgical Engineering and Technology: Advancing Innovation in Materials Science, Technology and Applications for Sustainable Future, ICOMMET 2017, Surabaya, Indonesia, 30/10/17. https://doi.org/10.1063/1.5030238

Effects of pore CaCO₃ form agencies on dissolution mechanisms of amoxicillin drugs encapsulated in hydrogels full-IPN chitosan N-vinyl caprolactam. / Budianto, Emil; Fauzia, Maghfira.
Proceedings of the 3rd International Conference on Materials and Metallurgical Engineering and Technology, ICOMMET 2017: Advancing Innovation in Materials Science, Technology and Applications for Sustainable Future. ed. / Mas Irfan P. Hidayat. American Institute of Physics Inc., 2018. 020016 (AIP Conference Proceedings; Vol. 1945).

Research output: Chapter in Book/Report/Conference proceeding › Conference contribution › peer-review

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N2 - The administration of amoxicillin trihydrate in Helicobacter pylori infection is not effective enough because the conventional preparations used have a short retention time in the stomach. To overcome this problem, amoxicillin trihydrate was encapsulated into the floating drug delivery matrix-matrix. In this study, the full-ipn acetaldehyde crosslinked hydrogel (N-vinyl caprolactam) was synthesized with a 10% CaCO3 pore forming agent and then encapsulated on amoxicillin trihydrate and studied the mechanism of drug dissolution with its kinetic kinetics approach. The K-PNVCL Hydrogel produces optimal properties which are then loaded with amoxicillin trihydrate in situ and post loading. In this research, we have got the percentage of swelling, floating time, the efficiency of in situ and post loading 873%; 3.15 minutes; 99.8% and 99.4%. The dissolution test was performed on amoxicillin trihydrate which had been encapsulated K-PNVCL hydrogel in vitro at pH 1.2 resulting in 94.5% for in situ loading and 98.5% for post loading. Results of the kinetics of drug release for post loading and in situ loading methods tend to follow the Higuchi model kinetics. The drug release mechanism occurs by Fickian diffusion. Proof of drug release mechanism from K-PNVCL hydrogel matrix is further done by Scanning Electron Microscope (SEM) instrument.

AB - The administration of amoxicillin trihydrate in Helicobacter pylori infection is not effective enough because the conventional preparations used have a short retention time in the stomach. To overcome this problem, amoxicillin trihydrate was encapsulated into the floating drug delivery matrix-matrix. In this study, the full-ipn acetaldehyde crosslinked hydrogel (N-vinyl caprolactam) was synthesized with a 10% CaCO3 pore forming agent and then encapsulated on amoxicillin trihydrate and studied the mechanism of drug dissolution with its kinetic kinetics approach. The K-PNVCL Hydrogel produces optimal properties which are then loaded with amoxicillin trihydrate in situ and post loading. In this research, we have got the percentage of swelling, floating time, the efficiency of in situ and post loading 873%; 3.15 minutes; 99.8% and 99.4%. The dissolution test was performed on amoxicillin trihydrate which had been encapsulated K-PNVCL hydrogel in vitro at pH 1.2 resulting in 94.5% for in situ loading and 98.5% for post loading. Results of the kinetics of drug release for post loading and in situ loading methods tend to follow the Higuchi model kinetics. The drug release mechanism occurs by Fickian diffusion. Proof of drug release mechanism from K-PNVCL hydrogel matrix is further done by Scanning Electron Microscope (SEM) instrument.

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KW - poly (N-vinylcaprolactam)

KW - release mechanism

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Budianto E, Fauzia M. Effects of pore CaCO₃ form agencies on dissolution mechanisms of amoxicillin drugs encapsulated in hydrogels full-IPN chitosan N-vinyl caprolactam. In Hidayat MIP, editor, Proceedings of the 3rd International Conference on Materials and Metallurgical Engineering and Technology, ICOMMET 2017: Advancing Innovation in Materials Science, Technology and Applications for Sustainable Future. American Institute of Physics Inc. 2018. 020016. (AIP Conference Proceedings). doi: 10.1063/1.5030238