Abstract
In the present work, a promising formulation of an inhaled powder based on tobramycin-loaded microparticles has been reported. Biodegradable microparticles with controlled diameters in the range of 1-5 μm and narrow size distribution were synthesized by Flow Focusing® technology. Particles production was planned and optimized with the aid of a well-established mathematic model. Close agreements between theoretical an experimental sizes were obtained. To deliver a high payload of tobramycin to the lungs, the influence of surfactant concentration, polymer-drug ratio and initial drug concentration were investigated. For chosen formulations, drug delivery profiles were also studied. In some cases, it was found a controlled drug delivery for more than ten days, which could represent an important advance in the treatment of chronic lung infections. Other particles factors affecting deposit of an aerosol in the lung were also studied, such as surface charge and density.
Keywords: Drug delivery systems, Flow Focusing®, microparticles, PLGA, pulmonary administration, tobramycin sulphate, tobramycin, Biodegradable microparticles, tobramycin-loaded microparticles, mass median aerodynamic diameter (MMAD)
Medicinal Chemistry
Title:Use of Flow Focusing® Technology to Produce Tobramycin-Loaded Plga Microparticles for Pulmonary Drug Delivery
Volume: 8 Issue: 4
Author(s): Lucia Martin-Banderas, Maria Angeles Holgado, Josefa Alvarez-Fuentes and Mercedes Fernandez- Arevalo
Affiliation:
Keywords: Drug delivery systems, Flow Focusing®, microparticles, PLGA, pulmonary administration, tobramycin sulphate, tobramycin, Biodegradable microparticles, tobramycin-loaded microparticles, mass median aerodynamic diameter (MMAD)
Abstract: In the present work, a promising formulation of an inhaled powder based on tobramycin-loaded microparticles has been reported. Biodegradable microparticles with controlled diameters in the range of 1-5 μm and narrow size distribution were synthesized by Flow Focusing® technology. Particles production was planned and optimized with the aid of a well-established mathematic model. Close agreements between theoretical an experimental sizes were obtained. To deliver a high payload of tobramycin to the lungs, the influence of surfactant concentration, polymer-drug ratio and initial drug concentration were investigated. For chosen formulations, drug delivery profiles were also studied. In some cases, it was found a controlled drug delivery for more than ten days, which could represent an important advance in the treatment of chronic lung infections. Other particles factors affecting deposit of an aerosol in the lung were also studied, such as surface charge and density.
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Cite this article as:
Martin-Banderas Lucia, Angeles Holgado Maria, Alvarez-Fuentes Josefa and Fernandez- Arevalo Mercedes, Use of Flow Focusing® Technology to Produce Tobramycin-Loaded Plga Microparticles for Pulmonary Drug Delivery, Medicinal Chemistry 2012; 8 (4) . https://dx.doi.org/10.2174/157340612801216409
DOI https://dx.doi.org/10.2174/157340612801216409 |
Print ISSN 1573-4064 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6638 |

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