Preparation and in vitro/in vivo characterization of curcumin microspheres intended to treat colon cancer
Objective: The objective of the present investigation was to prepare colon targeted curcumin microspheres using Eudragit S100 and evaluate the same for in vitro/in vivo properties. Materials and Methods: A "O/O solvent evaporation" technique was used in the preparation of microspheres. The...
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| Format: | Article |
| Language: | English |
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Wolters Kluwer Medknow Publications
2012-01-01
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| Series: | Journal of Pharmacy and Bioallied Sciences |
| Subjects: | |
| Online Access: | http://www.jpbsonline.org/article.asp?issn=0975-7406;year=2012;volume=4;issue=2;spage=164;epage=171;aulast=Madhavi |
| _version_ | 1811262229339701248 |
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| author | M Madhavi K Madhavi A V Jithan |
| author_facet | M Madhavi K Madhavi A V Jithan |
| author_sort | M Madhavi |
| collection | DOAJ |
| description | Objective: The objective of the present investigation was to prepare colon targeted curcumin microspheres using Eudragit S100 and evaluate the same for in vitro/in vivo properties. Materials and Methods: A "O/O solvent evaporation" technique was used in the preparation of microspheres. The influence of various process variables including stirring speed, drug:polymer ratio and percentage of emulsifier on the fabrication were investigated and the formulation was optimized. Prepared microspheres were evaluated for in vitro and in vivo properties. Surface morphology, particle size, percentage drug entrapment, percentage yield, drug polymer interaction, in vitro drug release in simulated gastrointestinal transit conditions and stability were the in vitro parameters investigated. Using an optimized formulation, drug release into the systemic circulation and organ distribution were investigated as in vivo parameters. In vivo parameters were estimated in male albino rats. Results: Curcumin microspheres of Eudragit S100 were successfully prepared using o/o solvent evaporation method. Microspheres prepared using 1:2 drug:polymer ratio, with a stirring speed of 1000 rpm, and using 1.0% w/v concentration of emulsifying agent was selected as an optimized formulation. The release studies with optimized formulation demonstrated that aqueous solubility of curcumin was enhanced by 8 times with the formulation. FTIR studies demonstrated no change in drug characteristics upon microsphere fabrication. The enhancement in solubility is thus due to the increase in the surface area of the drug substance and not due to a change of drug to a different physical state. This was further confirmed by scanning electron microsphere pictures. Drug release followed Korsmeyer and Peppas release model. Accelerated stability studies indicated that the drug is stable in the formulation for a period of atleast 14 weeks at room temperature. In vivo studies demonstrated a sustained drug release into the systemic circulation after oral administration of the formulation. Further, colon target was affectively achieved using the optimized formulation. Eudragit microspheres delivered most of their drug load (79.0%) to the colon, whereas with plain drug suspension only 28.0% of the total dose reached the target site. Conclusion: This study successfully developed curcumin microspheres that can be used effectively in the treatment of the colon cancer. |
| first_indexed | 2024-04-12T19:20:13Z |
| format | Article |
| id | doaj.art-320784fad6894c57a0e9308fc1429bba |
| institution | Directory Open Access Journal |
| issn | 0975-7406 0976-4879 |
| language | English |
| last_indexed | 2024-04-12T19:20:13Z |
| publishDate | 2012-01-01 |
| publisher | Wolters Kluwer Medknow Publications |
| record_format | Article |
| series | Journal of Pharmacy and Bioallied Sciences |
| spelling | doaj.art-320784fad6894c57a0e9308fc1429bba2022-12-22T03:19:36ZengWolters Kluwer Medknow PublicationsJournal of Pharmacy and Bioallied Sciences0975-74060976-48792012-01-014216417110.4103/0975-7406.94825Preparation and in vitro/in vivo characterization of curcumin microspheres intended to treat colon cancerM MadhaviK MadhaviA V JithanObjective: The objective of the present investigation was to prepare colon targeted curcumin microspheres using Eudragit S100 and evaluate the same for in vitro/in vivo properties. Materials and Methods: A "O/O solvent evaporation" technique was used in the preparation of microspheres. The influence of various process variables including stirring speed, drug:polymer ratio and percentage of emulsifier on the fabrication were investigated and the formulation was optimized. Prepared microspheres were evaluated for in vitro and in vivo properties. Surface morphology, particle size, percentage drug entrapment, percentage yield, drug polymer interaction, in vitro drug release in simulated gastrointestinal transit conditions and stability were the in vitro parameters investigated. Using an optimized formulation, drug release into the systemic circulation and organ distribution were investigated as in vivo parameters. In vivo parameters were estimated in male albino rats. Results: Curcumin microspheres of Eudragit S100 were successfully prepared using o/o solvent evaporation method. Microspheres prepared using 1:2 drug:polymer ratio, with a stirring speed of 1000 rpm, and using 1.0% w/v concentration of emulsifying agent was selected as an optimized formulation. The release studies with optimized formulation demonstrated that aqueous solubility of curcumin was enhanced by 8 times with the formulation. FTIR studies demonstrated no change in drug characteristics upon microsphere fabrication. The enhancement in solubility is thus due to the increase in the surface area of the drug substance and not due to a change of drug to a different physical state. This was further confirmed by scanning electron microsphere pictures. Drug release followed Korsmeyer and Peppas release model. Accelerated stability studies indicated that the drug is stable in the formulation for a period of atleast 14 weeks at room temperature. In vivo studies demonstrated a sustained drug release into the systemic circulation after oral administration of the formulation. Further, colon target was affectively achieved using the optimized formulation. Eudragit microspheres delivered most of their drug load (79.0%) to the colon, whereas with plain drug suspension only 28.0% of the total dose reached the target site. Conclusion: This study successfully developed curcumin microspheres that can be used effectively in the treatment of the colon cancer.http://www.jpbsonline.org/article.asp?issn=0975-7406;year=2012;volume=4;issue=2;spage=164;epage=171;aulast=MadhaviColon targetingcurcumineudragit S100microspherespH sensitive |
| spellingShingle | M Madhavi K Madhavi A V Jithan Preparation and in vitro/in vivo characterization of curcumin microspheres intended to treat colon cancer Journal of Pharmacy and Bioallied Sciences Colon targeting curcumin eudragit S100 microspheres pH sensitive |
| title | Preparation and in vitro/in vivo characterization of curcumin microspheres intended to treat colon cancer |
| title_full | Preparation and in vitro/in vivo characterization of curcumin microspheres intended to treat colon cancer |
| title_fullStr | Preparation and in vitro/in vivo characterization of curcumin microspheres intended to treat colon cancer |
| title_full_unstemmed | Preparation and in vitro/in vivo characterization of curcumin microspheres intended to treat colon cancer |
| title_short | Preparation and in vitro/in vivo characterization of curcumin microspheres intended to treat colon cancer |
| title_sort | preparation and in vitro in vivo characterization of curcumin microspheres intended to treat colon cancer |
| topic | Colon targeting curcumin eudragit S100 microspheres pH sensitive |
| url | http://www.jpbsonline.org/article.asp?issn=0975-7406;year=2012;volume=4;issue=2;spage=164;epage=171;aulast=Madhavi |
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