Nanoparticles-in-beads made of alginate and chitosan derivatives as oral insulin carrier / Mulham Alfatama
This project aimed to design nanoparticles-in-beads made of alginate, chitosan and their derivatives as oral insulin carrier. In the first part of the study, the calcium alginate beads were prepared using the vibratory nozzle extrusion microencapsulation technique through concurrent core and coat fo...
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| Format: | Book Section |
| Language: | English |
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Institute of Graduate Studies, UiTM
2018
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| Online Access: | https://ir.uitm.edu.my/id/eprint/20555/1/ABS_MULHAM%20ALFATAMA%20TDRA%20VOL%2013%20IGS%2018.pdf |
| _version_ | 1825735415390273536 |
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| author | Alfatama, Mulham |
| author_facet | Alfatama, Mulham |
| author_sort | Alfatama, Mulham |
| collection | UITM |
| description | This project aimed to design nanoparticles-in-beads made of alginate, chitosan and their derivatives as oral insulin carrier. In the first part of the study, the calcium alginate beads were prepared using the vibratory nozzle extrusion microencapsulation technique through concurrent core and coat formation with chlorpheniramine maleate as a model drug. These beads were coated with chitosan/chitosan-oleic acid conjugate of which the latter was synthesized via covalent reaction. The formability of beads was optimized through varying alginate solution concentration, alginate/chitosan solution flow rate and nozzle vibrational frequency. The size, shape, morphology, swelling, erosion, water uptake, drug content, drug release and matrix molecular profiles of beads were characterized. Spherical discrete coated beads were produced through critical interplay of nozzle vibrational frequency and polymeric solution flow rate. The conjugate-coated beads had their swelling and water uptake tendency negated through the introduction of tripolyphosphate ions as a crosslinking agent to attract the conjugate to the alginate core interface for coacervation to take place. The drug release propensity of tripolyphosphate-crosslinked, chitosan-oleic acid conjugate-coated beads was unexpectedly higher than the uncoated beads. This was attributed to reduced drug-alginate interaction as a result of alginate coacervating with chitosan-oleic acid conjugate and loss of calcium alginate crosslinkage to tripolyphosphate species. In the second part of the study, nanoparticles of simple calcium alginate, calcium alginatestearic acid, and calcium alginate-C18 conjugate were prepared by nanospray drying technique… |
| first_indexed | 2024-03-06T01:46:46Z |
| format | Book Section |
| id | uitm.eprints-0555 |
| institution | Universiti Teknologi MARA |
| language | English |
| last_indexed | 2024-03-06T01:46:46Z |
| publishDate | 2018 |
| publisher | Institute of Graduate Studies, UiTM |
| record_format | dspace |
| spelling | uitm.eprints-05552018-07-06T05:52:36Z https://ir.uitm.edu.my/id/eprint/20555/ Nanoparticles-in-beads made of alginate and chitosan derivatives as oral insulin carrier / Mulham Alfatama Alfatama, Mulham Bioactive compounds This project aimed to design nanoparticles-in-beads made of alginate, chitosan and their derivatives as oral insulin carrier. In the first part of the study, the calcium alginate beads were prepared using the vibratory nozzle extrusion microencapsulation technique through concurrent core and coat formation with chlorpheniramine maleate as a model drug. These beads were coated with chitosan/chitosan-oleic acid conjugate of which the latter was synthesized via covalent reaction. The formability of beads was optimized through varying alginate solution concentration, alginate/chitosan solution flow rate and nozzle vibrational frequency. The size, shape, morphology, swelling, erosion, water uptake, drug content, drug release and matrix molecular profiles of beads were characterized. Spherical discrete coated beads were produced through critical interplay of nozzle vibrational frequency and polymeric solution flow rate. The conjugate-coated beads had their swelling and water uptake tendency negated through the introduction of tripolyphosphate ions as a crosslinking agent to attract the conjugate to the alginate core interface for coacervation to take place. The drug release propensity of tripolyphosphate-crosslinked, chitosan-oleic acid conjugate-coated beads was unexpectedly higher than the uncoated beads. This was attributed to reduced drug-alginate interaction as a result of alginate coacervating with chitosan-oleic acid conjugate and loss of calcium alginate crosslinkage to tripolyphosphate species. In the second part of the study, nanoparticles of simple calcium alginate, calcium alginatestearic acid, and calcium alginate-C18 conjugate were prepared by nanospray drying technique… Institute of Graduate Studies, UiTM 2018 Book Section PeerReviewed text en https://ir.uitm.edu.my/id/eprint/20555/1/ABS_MULHAM%20ALFATAMA%20TDRA%20VOL%2013%20IGS%2018.pdf Nanoparticles-in-beads made of alginate and chitosan derivatives as oral insulin carrier / Mulham Alfatama. (2018) In: The Doctoral Research Abstracts. IGS Biannual Publication, 18 (18). Institute of Graduate Studies, UiTM, Shah Alam. |
| spellingShingle | Bioactive compounds Alfatama, Mulham Nanoparticles-in-beads made of alginate and chitosan derivatives as oral insulin carrier / Mulham Alfatama |
| title | Nanoparticles-in-beads made of alginate and chitosan derivatives as oral insulin carrier / Mulham Alfatama |
| title_full | Nanoparticles-in-beads made of alginate and chitosan derivatives as oral insulin carrier / Mulham Alfatama |
| title_fullStr | Nanoparticles-in-beads made of alginate and chitosan derivatives as oral insulin carrier / Mulham Alfatama |
| title_full_unstemmed | Nanoparticles-in-beads made of alginate and chitosan derivatives as oral insulin carrier / Mulham Alfatama |
| title_short | Nanoparticles-in-beads made of alginate and chitosan derivatives as oral insulin carrier / Mulham Alfatama |
| title_sort | nanoparticles in beads made of alginate and chitosan derivatives as oral insulin carrier mulham alfatama |
| topic | Bioactive compounds |
| url | https://ir.uitm.edu.my/id/eprint/20555/1/ABS_MULHAM%20ALFATAMA%20TDRA%20VOL%2013%20IGS%2018.pdf |
| work_keys_str_mv | AT alfatamamulham nanoparticlesinbeadsmadeofalginateandchitosanderivativesasoralinsulincarriermulhamalfatama |