0000000001018864

AUTHOR

L. I. Giannola

showing 5 related works from this author

Transbuccal tablets of carbamazepine: formulation, release and absorption pattern.

2006

Tranbsuccal drug administration is an attractive method, as it has several advantages especially with respect to peroral delivery. Here we report: i) the aptitude of carbamazepine (CBZ) to penetrate porcine buccal mucosa and reconstituted human oral (RHO) epithelium; ii) three different tablet formulations for transbuccal administration; iii) the drug release rate from tablets. CBZ permeation through the buccal mucosa was investigated by using two different bi-compartmental open models: Franz cells for porcine buccal mucosa and Transwell diffusion cells system for RHO epithelium. Results, expressed as drug flux (Js) and permeability coefficients (Kp), indicated that CBZ well penetrates the …

CarbamazepineCheekSolubilitySwineSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoChemistry PharmaceuticalSettore MED/50 - Scienze Tecniche Mediche ApplicateMouth MucosaAdministration BuccalAnimalsbuccal permeation modelling transbuccal drug delivery carbamazepine polyacrylic acid microspheres tablets matrices tabletsAbsorptionTablets
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3D OSCC model: effects following topical 5-FU delivery by drug-loaded tablets

2012

Settore MED/28 - Malattie OdontostomatologicheOral drug delivery
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Current status in buccal drug delivery

2008

This article overviews the progress made in buccal drug delivery research during the last five years and reports a new high-tech approach to achieve controlled delivery.

Drug permeationSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoBuccal drug deliverySettore MED/50 - Scienze Tecniche Mediche ApplicateIntelliDrug deviceBuccal drug delivery; Drug permeation; Promoting buccal absorption; IntelliDrug devicePromoting buccal absorption
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New horizons for OSCC chemotherapy: transmucosal permeability of 5-fluorouracil throughout porcine buccal mucosa

2007

buccal drug delivery5-fluouracilchemotherapytransmucosal permeability
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N-valproyl-aminoacids as new potential antiepileptic drugs: Synthesis, characterization and in vitro studies on stability

2015

Epilepsy, affecting at least 50 million persons worldwide, is one of the most common neurological disorders. Despite the significant advances in understanding epileptogenic mechanisms and in counteracting their pathological consequences, this clinical condition still has to be faced of treating more effectively the symptoms (epileptic seizures) and of preventing their unfavourable evolution. So far, research has been unsuccessful involved in developing effective antiepileptic drugs (AEDs) capable of preventing the development of the pathogenic process, set in motion by different etiological factors, that leads ultimately to chronic epilepsies .[1, 2] So, a substantial need remains to develo…

Biochemistry Genetics and Molecular Biology (all)Settore CHIM/09 - Farmaceutico Tecnologico ApplicativoBiochemistry (medical)Plant Scienceantiepileptic drugsAminoacidic conjugateBiochemistry Genetics and Molecular Biology (all); Biochemistry (medical); Plant ScienceValproyl derivative
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