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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Nalawade, Pravin | - |
| dc.contributor.author | Kadam, Vilasrao | - |
| dc.contributor.author | Hirlekar, Rajashree | - |
| dc.date.accessioned | 2010-03-30T07:07:52Z | - |
| dc.date.available | 2010-03-30T07:07:52Z | - |
| dc.date.issued | 2010-04 | - |
| dc.identifier.issn | 0975-1084 (Online); 0022-4456 (Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/7716 | - |
| dc.description | 295-299 | en_US |
| dc.description.abstract | This study presents improvement in solubility and
dissolution rate of valsartan (VAL) using  -cyclodextrin (CD) and hydroxypropyl--cyclodextrin (HP-CD). Formation and characterization of solid inclusion
complexes were investigated by DSC, FTIR, SEM, 1HNMR and in-vitro dissolution studies.
Preparation method influenced physical properties of binary mixtures. Inclusion
complexes obtained by co-evaporation method showed higher in vitro drug dissolution rates. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | CSIR | en_US |
| dc.source | JSIR Vol.69(04) [April 2010] | en_US |
| dc.subject | Co-evaporation method | en_US |
| dc.subject | Drug dissolution | en_US |
| dc.subject | Inclusion complexes | en_US |
| dc.title | Study of inclusion complexes of valsartan with -cyclodextrin and hydroxypropyl -cyclodextrin | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | JSIR Vol.69(04) [April 2010] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| JSIR 69(4) 295-299.pdf | 131.93 kB | Adobe PDF | View/Open |
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