The Optimum Conditions of Carboxymethyl Chitosan Synthesis on Drug Delivery Application and Its Release of Kinetics Study

In this paper, carboxymethyl chitosan (CMC) was synthesized and studied as a carrier to encapsulate vitamin (as drug model) and controlled release. Chitosan (CS) is a polycationic derivated from chitin, which suitable for active substance carrier system on biomedical function. CS has good properties...

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Main Authors: Parsaoran Siahaan, Nadira Cahyaning Mentari, Ustera Octovindra Wiedyanto, Dwi Hudiyanti, Suci Zulaikha Hildayani, Marlyn Dian Laksitorini
Format: Article
Language:English
Published: Department of Chemistry, Universitas Gadjah Mada 2017-07-01
Series:Indonesian Journal of Chemistry
Subjects:
Online Access:https://jurnal.ugm.ac.id/ijc/article/view/24252
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author Parsaoran Siahaan
Nadira Cahyaning Mentari
Ustera Octovindra Wiedyanto
Dwi Hudiyanti
Suci Zulaikha Hildayani
Marlyn Dian Laksitorini
author_facet Parsaoran Siahaan
Nadira Cahyaning Mentari
Ustera Octovindra Wiedyanto
Dwi Hudiyanti
Suci Zulaikha Hildayani
Marlyn Dian Laksitorini
author_sort Parsaoran Siahaan
collection DOAJ
description In this paper, carboxymethyl chitosan (CMC) was synthesized and studied as a carrier to encapsulate vitamin (as drug model) and controlled release. Chitosan (CS) is a polycationic derivated from chitin, which suitable for active substance carrier system on biomedical function. CS has good properties such as non-toxic, biodegradable, and biocompatible. However, CS insoluble in an aqueous solvent so CS was modified chemically into CMC. CMC was formed by reacting CS and monochloroacetic acid with sodium hydroxide (NaOH) as a catalyst. Optimation was performed by varying the NaOH concentration during alkalizing the CS and the temperature reaction. The functional group and crystallinity of CS and CMC were estimated by FTIR and XRD. The degree substitution of carboxymethylation has an average value of 0.60. The results show optimum temperature reaction and NaOH concentration were 60 °C and 40% (w/v). The nicotinamide (NA), a hydrophilic vitamin, was loaded within CMC matrix system through in vitro precipitation method. To confirm the encapsulation of NA in CMC and the release kinetics of NA from CMC in distilled water was studied through UV-Vis spectrophotometry. The release profile of NA from CMC matrix system carried out for 3 h and 12 h. The rate of NA release from CMC increases with increasing time and the follows a zero order, Higuchi, and Korsmeyer-Peppas kinetics rules.
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spelling doaj.art-b68e8a181b5b4c1c9ac1c6c83f0c62dc2022-12-21T21:34:36ZengDepartment of Chemistry, Universitas Gadjah MadaIndonesian Journal of Chemistry1411-94202460-15782017-07-0117229130010.22146/ijc.2425217281The Optimum Conditions of Carboxymethyl Chitosan Synthesis on Drug Delivery Application and Its Release of Kinetics StudyParsaoran Siahaan0Nadira Cahyaning Mentari1Ustera Octovindra Wiedyanto2Dwi Hudiyanti3Suci Zulaikha Hildayani4Marlyn Dian Laksitorini5Diponegoro UniversityDepartment of Chemistry, Diponegoro UniversityDepartment of Chemistry, Diponegoro UniversityDepartment of Chemistry, Diponegoro UniversityDepartment of Chemistry, Diponegoro UniversityDepartment of Pharmaceutics, Faculty of Pharmacy, Universitas Gadjah MadaIn this paper, carboxymethyl chitosan (CMC) was synthesized and studied as a carrier to encapsulate vitamin (as drug model) and controlled release. Chitosan (CS) is a polycationic derivated from chitin, which suitable for active substance carrier system on biomedical function. CS has good properties such as non-toxic, biodegradable, and biocompatible. However, CS insoluble in an aqueous solvent so CS was modified chemically into CMC. CMC was formed by reacting CS and monochloroacetic acid with sodium hydroxide (NaOH) as a catalyst. Optimation was performed by varying the NaOH concentration during alkalizing the CS and the temperature reaction. The functional group and crystallinity of CS and CMC were estimated by FTIR and XRD. The degree substitution of carboxymethylation has an average value of 0.60. The results show optimum temperature reaction and NaOH concentration were 60 °C and 40% (w/v). The nicotinamide (NA), a hydrophilic vitamin, was loaded within CMC matrix system through in vitro precipitation method. To confirm the encapsulation of NA in CMC and the release kinetics of NA from CMC in distilled water was studied through UV-Vis spectrophotometry. The release profile of NA from CMC matrix system carried out for 3 h and 12 h. The rate of NA release from CMC increases with increasing time and the follows a zero order, Higuchi, and Korsmeyer-Peppas kinetics rules.https://jurnal.ugm.ac.id/ijc/article/view/24252carboxymethyl chitosantemperature reactionNaOH concentrationencapsulationrelease kinetics
spellingShingle Parsaoran Siahaan
Nadira Cahyaning Mentari
Ustera Octovindra Wiedyanto
Dwi Hudiyanti
Suci Zulaikha Hildayani
Marlyn Dian Laksitorini
The Optimum Conditions of Carboxymethyl Chitosan Synthesis on Drug Delivery Application and Its Release of Kinetics Study
Indonesian Journal of Chemistry
carboxymethyl chitosan
temperature reaction
NaOH concentration
encapsulation
release kinetics
title The Optimum Conditions of Carboxymethyl Chitosan Synthesis on Drug Delivery Application and Its Release of Kinetics Study
title_full The Optimum Conditions of Carboxymethyl Chitosan Synthesis on Drug Delivery Application and Its Release of Kinetics Study
title_fullStr The Optimum Conditions of Carboxymethyl Chitosan Synthesis on Drug Delivery Application and Its Release of Kinetics Study
title_full_unstemmed The Optimum Conditions of Carboxymethyl Chitosan Synthesis on Drug Delivery Application and Its Release of Kinetics Study
title_short The Optimum Conditions of Carboxymethyl Chitosan Synthesis on Drug Delivery Application and Its Release of Kinetics Study
title_sort optimum conditions of carboxymethyl chitosan synthesis on drug delivery application and its release of kinetics study
topic carboxymethyl chitosan
temperature reaction
NaOH concentration
encapsulation
release kinetics
url https://jurnal.ugm.ac.id/ijc/article/view/24252
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