Transdermal drug delivery of paroxetine through lipid-vesicular formulation to augment its bioavailability. [electronic resource]
Producer: 20130815Description: 307-17 p. digitalISSN:- 1873-3476
- Administration, Oral
- Animals
- Biological Availability
- Calorimetry, Differential Scanning
- Cholesterol -- chemistry
- Drug Carriers -- chemistry
- Drug Stability
- Lecithins -- chemistry
- Liposomes
- Paroxetine -- administration & dosage
- Particle Size
- Rabbits
- Selective Serotonin Reuptake Inhibitors -- administration & dosage
- Skin -- drug effects
- Skin Absorption
- Skin Irritancy Tests
- Surface Properties
- Tablets
- Transdermal Patch
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Publication Type: Journal Article
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