What is it about?
The work is to improve bioavailability, safety and antibacterial potential of clarithromycin
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Why is it important?
The major obstacles for treatment of intracellular infections with clarithromycin are poor gastrointestinal solubility, short half-life (3–4 h), low oral bioavailability and hepatotoxicity. Therefore, clarithromycin loaded solid lipid nanocarriers (CLA-SLNs) were engineered by an emulsification solvent evaporation method to improve CLA in vivo pharmacokinetics and safety.
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This page is a summary of: Implications of designing clarithromycin loaded solid lipid nanoparticles on their pharmacokinetics, antibacterial activity and safety, RSC Advances, January 2016, Royal Society of Chemistry,
DOI: 10.1039/c6ra12841f.
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