Formation of encapsulated mefenamic acid-beta cyclodextrin and unencapsulated mefenamic acid using electrospray technique / Nurul Karimah Zolkepali
The potential of using electrostatic atomizer or electrospray in producing fine and encapsulated particle of Mefenamic Acid (MA) form I with β-cyclodextrin (βCD) was demonstrated in this study. Encapsulated MA-βCD with a molar ratio of 1:2 was prepared in water-ethanol suspension, followed by the el...
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| Format: | Thesis |
| Language: | English |
| Published: |
2016
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| Online Access: | https://ir.uitm.edu.my/id/eprint/17913/2/TM_NURUL%20KARIMAH%20ZOLKEPALI%20EH%2016_5.pdf |
| _version_ | 1796900719902588928 |
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| author | Zolkepali, Nurul Karimah |
| author_facet | Zolkepali, Nurul Karimah |
| author_sort | Zolkepali, Nurul Karimah |
| collection | UITM |
| description | The potential of using electrostatic atomizer or electrospray in producing fine and encapsulated particle of Mefenamic Acid (MA) form I with β-cyclodextrin (βCD) was demonstrated in this study. Encapsulated MA-βCD with a molar ratio of 1:2 was prepared in water-ethanol suspension, followed by the electrospray process to atomize the droplet into fine dried particles. The working distance (WD) between the electrospray needle tip and the substrate were varied from 15 to 25 cm. Using FE-SEM and ImageJ software, the sizes of encapsulated MA-βCD particles were found to decrease from 91±26 to 42±35 nm as the WD increased. The dissolution rate of encapsulated particles of MA-βCD was found to be higher compared to the particles of as-received MA and the unencapsulated MA. The presence of the encapsulated MA-βCD was proven by the DSC result with the disappearance of MA peak after the atomization process. The XRD and FTIR analysis showed that the encapsulation occurred with the existence of new solid phase that was expected from the interaction between MA and βCD at 11.30°, 17.60°, 18.18°, 20.36°, 31.32° (2θ) and the appearance of C=C at wavelength 1513 cm⁻¹ to 1642.26 cm⁻¹. Further analysis by TEM showed the size and morphology of MA- βCD particles when immersed in water and acetone. Encapsulated MA-βCD particles were solubilized in water but suspended as a spherical shape in acetone. |
| first_indexed | 2024-03-06T01:39:29Z |
| format | Thesis |
| id | oai:ir.uitm.edu.my:17913 |
| institution | Universiti Teknologi MARA |
| language | English |
| last_indexed | 2024-03-06T01:39:29Z |
| publishDate | 2016 |
| record_format | dspace |
| spelling | oai:ir.uitm.edu.my:179132022-04-14T02:24:12Z https://ir.uitm.edu.my/id/eprint/17913/ Formation of encapsulated mefenamic acid-beta cyclodextrin and unencapsulated mefenamic acid using electrospray technique / Nurul Karimah Zolkepali Zolkepali, Nurul Karimah The potential of using electrostatic atomizer or electrospray in producing fine and encapsulated particle of Mefenamic Acid (MA) form I with β-cyclodextrin (βCD) was demonstrated in this study. Encapsulated MA-βCD with a molar ratio of 1:2 was prepared in water-ethanol suspension, followed by the electrospray process to atomize the droplet into fine dried particles. The working distance (WD) between the electrospray needle tip and the substrate were varied from 15 to 25 cm. Using FE-SEM and ImageJ software, the sizes of encapsulated MA-βCD particles were found to decrease from 91±26 to 42±35 nm as the WD increased. The dissolution rate of encapsulated particles of MA-βCD was found to be higher compared to the particles of as-received MA and the unencapsulated MA. The presence of the encapsulated MA-βCD was proven by the DSC result with the disappearance of MA peak after the atomization process. The XRD and FTIR analysis showed that the encapsulation occurred with the existence of new solid phase that was expected from the interaction between MA and βCD at 11.30°, 17.60°, 18.18°, 20.36°, 31.32° (2θ) and the appearance of C=C at wavelength 1513 cm⁻¹ to 1642.26 cm⁻¹. Further analysis by TEM showed the size and morphology of MA- βCD particles when immersed in water and acetone. Encapsulated MA-βCD particles were solubilized in water but suspended as a spherical shape in acetone. 2016-01 Thesis NonPeerReviewed text en https://ir.uitm.edu.my/id/eprint/17913/2/TM_NURUL%20KARIMAH%20ZOLKEPALI%20EH%2016_5.pdf Formation of encapsulated mefenamic acid-beta cyclodextrin and unencapsulated mefenamic acid using electrospray technique / Nurul Karimah Zolkepali. (2016) Masters thesis, thesis, Universiti Teknologi MARA. <http://terminalib.uitm.edu.my/17913.pdf> |
| spellingShingle | Zolkepali, Nurul Karimah Formation of encapsulated mefenamic acid-beta cyclodextrin and unencapsulated mefenamic acid using electrospray technique / Nurul Karimah Zolkepali |
| title | Formation of encapsulated mefenamic acid-beta cyclodextrin and unencapsulated mefenamic acid using electrospray technique / Nurul Karimah Zolkepali |
| title_full | Formation of encapsulated mefenamic acid-beta cyclodextrin and unencapsulated mefenamic acid using electrospray technique / Nurul Karimah Zolkepali |
| title_fullStr | Formation of encapsulated mefenamic acid-beta cyclodextrin and unencapsulated mefenamic acid using electrospray technique / Nurul Karimah Zolkepali |
| title_full_unstemmed | Formation of encapsulated mefenamic acid-beta cyclodextrin and unencapsulated mefenamic acid using electrospray technique / Nurul Karimah Zolkepali |
| title_short | Formation of encapsulated mefenamic acid-beta cyclodextrin and unencapsulated mefenamic acid using electrospray technique / Nurul Karimah Zolkepali |
| title_sort | formation of encapsulated mefenamic acid beta cyclodextrin and unencapsulated mefenamic acid using electrospray technique nurul karimah zolkepali |
| url | https://ir.uitm.edu.my/id/eprint/17913/2/TM_NURUL%20KARIMAH%20ZOLKEPALI%20EH%2016_5.pdf |
| work_keys_str_mv | AT zolkepalinurulkarimah formationofencapsulatedmefenamicacidbetacyclodextrinandunencapsulatedmefenamicacidusingelectrospraytechniquenurulkarimahzolkepali |