Effects of Different Formulation Methods on Drug Crystallinity, Drug-Carrier Interaction, and Ex Vivo Permeation of a Ternary Solid Dispersion Containing Nisoldipine
Solid dispersion (SD) is an established approach to increase the solubility and dissolution of BCS class II drugs. The selection of a suitable method of preparation and the suitable polymeric carrier are the two most important parameters for a successful SD. The present research is aimed to evaluate...
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| Format: | Article |
| Language: | English |
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Springer
2019
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| Online Access: | http://umpir.ump.edu.my/id/eprint/29653/ http://umpir.ump.edu.my/id/eprint/29653/1/journal%20pharma%20innovation.docx |
| _version_ | 1848823330709176320 |
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| author | Mahmood, Syed Kumar Mandal, Uttam May Kway, Oo Bapadditya, Chatterjee |
| author_facet | Mahmood, Syed Kumar Mandal, Uttam May Kway, Oo Bapadditya, Chatterjee |
| author_sort | Mahmood, Syed |
| building | UMP Institutional Repository |
| collection | Online Access |
| description | Solid dispersion (SD) is an established approach to increase the solubility and dissolution of BCS class II drugs. The selection of a suitable method of preparation and the suitable polymeric carrier are the two most important parameters for a successful SD. The present research is aimed to evaluate the effect of preparation method on drug crystallinity, drug-polymer interaction, ex vivo permeability, and SD stability. A ternary SD containing nisoldipine as drug and PVP K30, poloxamer 188 as the carrier was prepared by hot melt mixing, solvent evaporation by rotary vacuum evaporator, and lyophilization. The prepared samples were analyzed in comparison in order to meet the objectives. All three methods yielded a mixed system of the crystalline and amorphous phase with a significant increase in saturation solubility compared to the raw drug. Infra-red spectroscopy study showed the highest degree of H bonding between drug and carrier in the freeze-dried formulation. X-ray diffraction study showed maximum loss of drug crystallinity from the rotary vacuum evaporated SD (3.70% at 11.3, 2θ angle). Ex vivo permeability study showed the maximum drug permeation by freeze-dried product. But freeze-dried product was shown to be the least stable in stability analysis. In terms of product stability, melt mixing is the best out of the three methods tested. Different methods of preparation have different impacts on functional group interaction, loss of crystallinity, ex vivo permeation, and stability of ternary SD. |
| first_indexed | 2025-11-15T02:55:26Z |
| format | Article |
| id | ump-29653 |
| institution | Universiti Malaysia Pahang |
| institution_category | Local University |
| language | English |
| last_indexed | 2025-11-15T02:55:26Z |
| publishDate | 2019 |
| publisher | Springer |
| recordtype | eprints |
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| spelling | ump-296532020-10-20T06:15:01Z http://umpir.ump.edu.my/id/eprint/29653/ Effects of Different Formulation Methods on Drug Crystallinity, Drug-Carrier Interaction, and Ex Vivo Permeation of a Ternary Solid Dispersion Containing Nisoldipine Mahmood, Syed Kumar Mandal, Uttam May Kway, Oo Bapadditya, Chatterjee RS Pharmacy and materia medica Solid dispersion (SD) is an established approach to increase the solubility and dissolution of BCS class II drugs. The selection of a suitable method of preparation and the suitable polymeric carrier are the two most important parameters for a successful SD. The present research is aimed to evaluate the effect of preparation method on drug crystallinity, drug-polymer interaction, ex vivo permeability, and SD stability. A ternary SD containing nisoldipine as drug and PVP K30, poloxamer 188 as the carrier was prepared by hot melt mixing, solvent evaporation by rotary vacuum evaporator, and lyophilization. The prepared samples were analyzed in comparison in order to meet the objectives. All three methods yielded a mixed system of the crystalline and amorphous phase with a significant increase in saturation solubility compared to the raw drug. Infra-red spectroscopy study showed the highest degree of H bonding between drug and carrier in the freeze-dried formulation. X-ray diffraction study showed maximum loss of drug crystallinity from the rotary vacuum evaporated SD (3.70% at 11.3, 2θ angle). Ex vivo permeability study showed the maximum drug permeation by freeze-dried product. But freeze-dried product was shown to be the least stable in stability analysis. In terms of product stability, melt mixing is the best out of the three methods tested. Different methods of preparation have different impacts on functional group interaction, loss of crystallinity, ex vivo permeation, and stability of ternary SD. Springer 2019 Article PeerReviewed pdf en http://umpir.ump.edu.my/id/eprint/29653/1/journal%20pharma%20innovation.docx Mahmood, Syed and Kumar Mandal, Uttam and May Kway, Oo and Bapadditya, Chatterjee (2019) Effects of Different Formulation Methods on Drug Crystallinity, Drug-Carrier Interaction, and Ex Vivo Permeation of a Ternary Solid Dispersion Containing Nisoldipine. Journal of Pharmaceutical Innovation. pp. 1-15. ISSN https://link.springer.com/article/10.1007/s12247-019-09415-2. (Published) https://doi.org/10.1007/s12247-019-09415-2 https://link.springer.com/article/10.1007%2Fs12247-019-09415-2#citeas |
| spellingShingle | RS Pharmacy and materia medica Mahmood, Syed Kumar Mandal, Uttam May Kway, Oo Bapadditya, Chatterjee Effects of Different Formulation Methods on Drug Crystallinity, Drug-Carrier Interaction, and Ex Vivo Permeation of a Ternary Solid Dispersion Containing Nisoldipine |
| title | Effects of Different Formulation Methods on Drug Crystallinity, Drug-Carrier Interaction, and Ex Vivo Permeation of a Ternary Solid Dispersion Containing Nisoldipine |
| title_full | Effects of Different Formulation Methods on Drug Crystallinity, Drug-Carrier Interaction, and Ex Vivo Permeation of a Ternary Solid Dispersion Containing Nisoldipine |
| title_fullStr | Effects of Different Formulation Methods on Drug Crystallinity, Drug-Carrier Interaction, and Ex Vivo Permeation of a Ternary Solid Dispersion Containing Nisoldipine |
| title_full_unstemmed | Effects of Different Formulation Methods on Drug Crystallinity, Drug-Carrier Interaction, and Ex Vivo Permeation of a Ternary Solid Dispersion Containing Nisoldipine |
| title_short | Effects of Different Formulation Methods on Drug Crystallinity, Drug-Carrier Interaction, and Ex Vivo Permeation of a Ternary Solid Dispersion Containing Nisoldipine |
| title_sort | effects of different formulation methods on drug crystallinity, drug-carrier interaction, and ex vivo permeation of a ternary solid dispersion containing nisoldipine |
| topic | RS Pharmacy and materia medica |
| url | http://umpir.ump.edu.my/id/eprint/29653/ http://umpir.ump.edu.my/id/eprint/29653/ http://umpir.ump.edu.my/id/eprint/29653/ http://umpir.ump.edu.my/id/eprint/29653/1/journal%20pharma%20innovation.docx |