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| Content Provider | PubMed Central |
|---|---|
| Author | Li, Feng-qian Yan, Cheng Bi, Juan Lv, Wei-lin Ji, Rui-rui Chen, Xu Su, Jia-can Hu, Jin-hong |
| Copyright Year | 2011 |
| Abstract | Scopolamine hydrobromide (SH)-loaded microparticles were prepared from a colloidal fluid containing ionotropic-gelated chitosan nanoparticles using a spray-drying method. The spray-dried microparticles were then formulated into orally disintegrating tablets (ODTs) using a wet granulation tablet formation process. A drug entrapment efficiency of about 90% (w/w) and loading capacity of 20% (w/w) were achieved for the microparticles, which ranged from 2 μm to 8 μm in diameter. Results of disintegration tests showed that the formulated ODTs could be completely dissolved within 45 seconds. Drug dissolution profiles suggested that SH is released more slowly from tablets made using the microencapsulation process compared with tablets containing SH that is free or in the form of nanoparticles. The time it took for 90% of the drug to be released increased significantly from 3 minutes for conventional ODTs to 90 minutes for ODTs with crosslinked microparticles. Compared with ODTs made with noncrosslinked microparticles, it was thus possible to achieve an even lower drug release rate using tablets with appropriate chitosan crosslinking. Results obtained indicate that the development of new ODTs designed with crosslinked microparticles might be a rational way to overcome the unwanted taste of conventional ODTs and the side effects related to SH’s intrinsic characteristics. |
| Related Links | http://dx.doi.org/10.2147/ijn.s17900 |
| Ending Page | 904 |
| Starting Page | 897 |
| File Format | |
| ISSN | 11782013 |
| e-ISSN | 11782013 |
| Journal | International Journal of Nanomedicine |
| Volume Number | 6 |
| Language | English |
| Publisher | Dove Medical Press |
| Publisher Date | 2011-04-01 |
| Access Restriction | Open |
| Rights Holder | Dove Medical Press |
| Subject Keyword | Research in Higher Education |
| Content Type | Text |
| Resource Type | Article |
| Subject | Nanoscience and Nanotechnology Organic Chemistry Medicine Drug Discovery Biomaterials Biophysics Bioengineering Pharmaceutical Science |
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