Synthesis and characterization of orotic acid loaded chitosan inclusion complex

Background: Polymeric inclusion complex has been used frequently as a drug delivery system due to controlled release, non-toxic properties and high bioavailability. Objective: The current study aims to improve drug release properties of orotic acid loaded with chitosan inclusion complex (OA/CS). Mat...

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Main Authors: Hassani, Abdelkader, Azad, Abul Kalam, Mia, Abdur Rashid, Helaluddin, Abul Bashar Mohammed
Format: Conference or Workshop Item
Language:English
English
Published: 2019
Subjects:
Online Access:http://irep.iium.edu.my/77755/
http://irep.iium.edu.my/77755/1/AIPC2019BookofAbstracts-1.pdf
http://irep.iium.edu.my/77755/7/AIPC%202019%20helal.pdf
id iium-77755
recordtype eprints
spelling iium-777552020-01-28T03:19:18Z http://irep.iium.edu.my/77755/ Synthesis and characterization of orotic acid loaded chitosan inclusion complex Hassani, Abdelkader Azad, Abul Kalam Mia, Abdur Rashid Helaluddin, Abul Bashar Mohammed QD Chemistry RS192 Materia Medica-Pharmaceutical Technology RS403 Materia Medica-Pharmaceutical Chemistry Background: Polymeric inclusion complex has been used frequently as a drug delivery system due to controlled release, non-toxic properties and high bioavailability. Objective: The current study aims to improve drug release properties of orotic acid loaded with chitosan inclusion complex (OA/CS). Material and methods: The OA/CS inclusion complex were synthesized using freeze drying technique. The characterization of inclusion OA/CS was carried out using Fourier Transform Infrared Spectroscopy (FTIR), X-ray Diffractometry (XRD), Differential Scanning Calorimetry (DSC), Zeta sizer, and Transmission Electron Microscopy (TEM). Results: The FTIR peaks of orotic acid have almost vanished in the OA/CS spectrum due to the restriction of OA vibration upon loading in CS cavity. The diffraction peaks of the OA/CS are completely diffused due to the amorphous state and the lack of crystallinity of inclusion complex. The DSC marked changes are indicative of the amorphous phase of solid dispersion, as well OA encapsulation into the nanocavity of CS. The size of OA/CS ranged between 58 nm and 200 nm and the zeta potential was 30 mV. In addition, transmission electron microscopy (TEM) showed that OA/CS sizes were ranged from 20 to 45 nm. Conclusion: Thus, this study indicates that OA/CS has promising future to further develop a carrier for drug delivery systems. 2019 Conference or Workshop Item PeerReviewed application/pdf en http://irep.iium.edu.my/77755/1/AIPC2019BookofAbstracts-1.pdf application/pdf en http://irep.iium.edu.my/77755/7/AIPC%202019%20helal.pdf Hassani, Abdelkader and Azad, Abul Kalam and Mia, Abdur Rashid and Helaluddin, Abul Bashar Mohammed (2019) Synthesis and characterization of orotic acid loaded chitosan inclusion complex. In: AIMST International Pharmacy Conference (AIPC) 2019: Challenges and Opportunities in Pharmaceutical Sciences, Technology and Practice, 30 November - 1 December 2019, Faculty of Pharmacy, AIMST University, Semeling, Kedah. (Unpublished)
repository_type Digital Repository
institution_category Local University
institution International Islamic University Malaysia
building IIUM Repository
collection Online Access
language English
English
topic QD Chemistry
RS192 Materia Medica-Pharmaceutical Technology
RS403 Materia Medica-Pharmaceutical Chemistry
spellingShingle QD Chemistry
RS192 Materia Medica-Pharmaceutical Technology
RS403 Materia Medica-Pharmaceutical Chemistry
Hassani, Abdelkader
Azad, Abul Kalam
Mia, Abdur Rashid
Helaluddin, Abul Bashar Mohammed
Synthesis and characterization of orotic acid loaded chitosan inclusion complex
description Background: Polymeric inclusion complex has been used frequently as a drug delivery system due to controlled release, non-toxic properties and high bioavailability. Objective: The current study aims to improve drug release properties of orotic acid loaded with chitosan inclusion complex (OA/CS). Material and methods: The OA/CS inclusion complex were synthesized using freeze drying technique. The characterization of inclusion OA/CS was carried out using Fourier Transform Infrared Spectroscopy (FTIR), X-ray Diffractometry (XRD), Differential Scanning Calorimetry (DSC), Zeta sizer, and Transmission Electron Microscopy (TEM). Results: The FTIR peaks of orotic acid have almost vanished in the OA/CS spectrum due to the restriction of OA vibration upon loading in CS cavity. The diffraction peaks of the OA/CS are completely diffused due to the amorphous state and the lack of crystallinity of inclusion complex. The DSC marked changes are indicative of the amorphous phase of solid dispersion, as well OA encapsulation into the nanocavity of CS. The size of OA/CS ranged between 58 nm and 200 nm and the zeta potential was 30 mV. In addition, transmission electron microscopy (TEM) showed that OA/CS sizes were ranged from 20 to 45 nm. Conclusion: Thus, this study indicates that OA/CS has promising future to further develop a carrier for drug delivery systems.
format Conference or Workshop Item
author Hassani, Abdelkader
Azad, Abul Kalam
Mia, Abdur Rashid
Helaluddin, Abul Bashar Mohammed
author_facet Hassani, Abdelkader
Azad, Abul Kalam
Mia, Abdur Rashid
Helaluddin, Abul Bashar Mohammed
author_sort Hassani, Abdelkader
title Synthesis and characterization of orotic acid loaded chitosan inclusion complex
title_short Synthesis and characterization of orotic acid loaded chitosan inclusion complex
title_full Synthesis and characterization of orotic acid loaded chitosan inclusion complex
title_fullStr Synthesis and characterization of orotic acid loaded chitosan inclusion complex
title_full_unstemmed Synthesis and characterization of orotic acid loaded chitosan inclusion complex
title_sort synthesis and characterization of orotic acid loaded chitosan inclusion complex
publishDate 2019
url http://irep.iium.edu.my/77755/
http://irep.iium.edu.my/77755/1/AIPC2019BookofAbstracts-1.pdf
http://irep.iium.edu.my/77755/7/AIPC%202019%20helal.pdf
first_indexed 2023-09-18T21:49:39Z
last_indexed 2023-09-18T21:49:39Z
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