Literature DB >> 21899541

Novel gel formulations with catanionic aggregates enable prolonged drug release and reduced skin permeation.

Noel Dew1, Katarina Edsman, Erik Björk.   

Abstract

OBJECTIVES: The aim of this study was to investigate skin permeation rates of a drug substance when applied in novel gel formulations with catanionic aggregates.
METHODS: Reference gel without catanionic aggregates was compared with formulations with catanionic aggregates composed of tetracaine and either sodium dodecyl sulphate (SDS) or capric acid. Carbomer and SoftCAT were used to compare the effect of different gel types to elucidate if physically cross-linked, 'self-destructing' systems had benefits compared with classical, covalently cross-linked, gels. KEY
FINDINGS: The rheological investigation showed that the interactions between the SoftCAT polymer and tetracaine/SDS aggregates were stronger than when the tetracaine/capric acid aggregates were used. The skin permeation was measured ex vivo in horizontal Ussing chambers and the permeation of tetracaine was significantly lower when formulations with tetracaine/SDS aggregates were applied (P < 0.001), but not statistically different from the reference when capric acid was used.
CONCLUSIONS: No morphological differences could be distinguished between the skin samples exposed to the different formulations or the reference. Skin permeation was compared with silicone sheet permeation and the results indicated that silicone sheets could be used as a model of skin when using these formulations.
© 2011 The Authors. JPP © 2011 Royal Pharmaceutical Society.

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Year:  2011        PMID: 21899541     DOI: 10.1111/j.2042-7158.2011.01339.x

Source DB:  PubMed          Journal:  J Pharm Pharmacol        ISSN: 0022-3573            Impact factor:   3.765


  2 in total

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Journal:  RSC Adv       Date:  2020-12-23       Impact factor: 3.361

2.  Formation of Drug-Participating Catanionic Aggregates for Extended Delivery of Non-Steroidal Anti-Inflammatory Drugs from Contact Lenses.

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  2 in total

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