Recent patents on nanotechnology

Design and Testing of Solid Lipid Nanoparticles Carrying Azelnidipine for Treating High Blood Pressure

Updated

Abstract

The optimized batch of azelnidipine-loaded solid lipid nanoparticles exhibited a particle size of 166.4 nm and an entrapment efficiency of 86.21%.

  • Solid lipid nanoparticles are designed to enhance the solubility and therapeutic efficacy of poorly soluble drugs like azelnidipine.
  • Azelnidipine's effectiveness in treating high blood pressure may be limited by its high lipophilicity and poor solubility in the gastrointestinal tract.
  • The formulation process involved hot melt emulsification and ultrasonication using glyceryl monostearate and Poloxamer 188.
  • The optimized formulation demonstrated significant characteristics, including a polydispersity index of 0.40 and a zeta potential of -13.7 mV.
  • In vitro drug release tests indicated a sustained release pattern for approximately 12 hours.

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