Development of an anti-infection nano-hydroxypatite drug delivery microsphere and its drug-release in vitro / 南方医科大学学报
Journal of Southern Medical University
; (12): 754-756, 2006.
Article
ي Zh
| WPRIM
| ID: wpr-282925
المكتبة المسؤولة:
WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To develop an anti-infection nano-hydroxypatite (nano-HA) microsphere for local drug delivery for treating osteomyelitis.</p><p><b>METHODS</b>The nano-HA was used as the core carrier to load gentamicin (GM) and coated with poly(-hydroxybutyrate-co- hydroxyvalerate)/polyethylene glycol (PHBV/PEG), which was degradable and biocompatible, to prepare nano-HA-PHBV/PEG-GM microsphere. The surface structure and in vitro drug-release of the microsphere were studied.</p><p><b>RESULTS</b>The microsphere had good drug delivery capability. The samples weighing 90 mg each were soaked in PBS and gentamicin release within the first day was 165.2 microg/ml, which maintained a low release rate in the following days. After 28 days, gentamicin release declined to 8.5 microg/ml, which was higher than the minimal inhibitory concentration of gentamicin (2 microg/ml).</p><p><b>CONCLUSION</b>The local drug delivery system has good drug-release performance in vitro and may possess potential value in clinical management of osteomyelitis.</p>
النص الكامل:
1
الفهرس:
WPRIM
الموضوع الرئيسي:
Polyesters
/
Pharmacokinetics
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Gentamicins
/
Chemistry
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Drug Delivery Systems
/
Delayed-Action Preparations
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Microscopy, Electron, Transmission
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Nanoparticles
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Hydroxyapatites
/
Microspheres
اللغة:
Zh
مجلة:
Journal of Southern Medical University
السنة:
2006
نوع:
Article