The Prospects of Carrying and Releasing Drugs Via Biodegradable Magnesium Foam

Powder metallurgy technology was used to produce magnesium foams in order to evaluate their ability to perform as a solid biodegradable platform for drug delivery. The amount and delivery time of the released drug (gentamicin) was controlled by the level of space‐holding particles (spacer) that was...

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Bibliographic Details
Published inAdvanced engineering materials Vol. 12; no. 8; pp. B374 - B379
Main Authors Aghion, Eli, Yered, Tal, Perez, Yifat, Gueta, Yael
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 01.08.2010
WILEY‐VCH Verlag
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Summary:Powder metallurgy technology was used to produce magnesium foams in order to evaluate their ability to perform as a solid biodegradable platform for drug delivery. The amount and delivery time of the released drug (gentamicin) was controlled by the level of space‐holding particles (spacer) that was mixed with the magnesium powder prior to the sintering process. Metallurgical examination of the magnesium foams was carried out using optical and scanning electron microscopy (SEM) and X‐ray diffraction analysis. Microtomography CT analysis was used to evaluate the structural characteristics of the magnesium foams and their internal interconnected porosity configuration. The corrosion behavior of the magnesium foams was evaluated by immersion test in a simulated physiological environment (PBS solution). The absorption of gentamicin was obtained by immersing magnesium foams in concentrated gentamicin solutions within a vacuum chamber, followed by water evaporation. The detection of gentamicin in PBS solution was carried out using a Fluorescence Polarimetry analyzer. The results show that the release profile of gentamicin from magnesium foam with 10 and 25% spacer in PBS solution was in accord with common dissolution kinetics of an active ingredient from polymeric drug delivery systems. Magnesium foams were produced by powder metallurgy in order to evaluate their ability to perform as a biodegradable platform for drug delivery. The amount and delivery time of the released drug (gentamicin) was controlled by the level of space‐holding particles (spacer). The results show that the release profile of gentamicin from magnesium foams in PBS solution was in accord with common dissolution kinetics of an active ingredient from polymeric drug delivery systems.
Bibliography:The authors would like to thank Dr. David Eglin from AO Research Institute, Davos, Switzerland, for his kind assistance in the microtomography CT analysis and Mr. Amir Arnon from Ben-Gurion University for his assistance in the experimental work.
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ArticleID:ADEM200980044
The authors would like to thank Dr. David Eglin from AO Research Institute, Davos, Switzerland, for his kind assistance in the microtomography CT analysis and Mr. Amir Arnon from Ben‐Gurion University for his assistance in the experimental work.
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
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ISSN:1438-1656
1527-2648
1527-2648
DOI:10.1002/adem.200980044