Solid lipid microparticles: an approach for improving oral bioavailability of aspirin - Article

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Solid lipid microparticles: an approach for improving oral bioavailability of aspirin
The objectives of the work were to develop a lipid based delivery system for aspirin and to evaluate its physicochemical and the pharmacodynamic properties. Aspirin-loaded solid lipid microparticles (SLMs) were formulated by hot homogenization and analysed for their encapsulation efficiency (EE%), in vitro release, particle size, anti-inflammatory and ulcer inhibition properties
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