The effect of β-cyclodextrin on the solubility and dissolution rate of meloxicam and investigation of the driving force for complexation using molecular modeling
✍ Scribed by Aiman A. Obaidat; Rasha A. Khanfar; Mohammad N. Khawam
- Publisher
- Springer Netherlands
- Year
- 2008
- Tongue
- English
- Weight
- 340 KB
- Volume
- 63
- Category
- Article
- ISSN
- 0923-0750
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## Abstract Gadolinium‐chelates bearing hydrophobic substituents on their surfaces form inclusion complexes with β‐cyclodextrin. When the chelate contains more than one substituent, the observed relaxation enhancement has to be analysed on the basis of the contributions arising from the actual spec
Cyclodextrins are a group of cyclic oligosaccharides with a ring, basket-like structure. These compounds are able to include several kinds of molecules into their internal cavity, leading to important modiÐcations of the properties of the guest compound. The interaction between b-cyclodextrin and t