[Preparation and drug release of curcumin-loaded poly (α-isobutyl cyanoacrylate) microspheres].

Sheng Wu Yi Xue Gong Cheng Xue Za Zhi

Key Laboratory of Carbon Fiber and Functional Polymers, Beijing University of Chemical Technology, Beijing 100029, P. R.

Published: October 2018

AI Article Synopsis

  • Curcumin-loaded microspheres were created using a one-step emulsification method, combining α-isobutyl cyanoacrylate, poloxamer 188, and curcumin complexed with hydroxypropyl-β-cyclodextrin.
  • As the concentration of emulsifier increased, the size of the microspheres decreased while drug loading and encapsulation efficiency improved, with an optimal emulsifier concentration identified at 0.05%.
  • Higher concentrations of curcumin increased drug loading but decreased encapsulation efficiency; moreover, increased drug loading led to a lower cumulative release percentage, suggesting better wettability and bioavailability of the drug.

Article Abstract

Curcumin-loaded poly (α-isobutyl cyanoacrylate) microspheres (Cur-HP-β-CD-PiBCA) were prepared by one-step emulsification with α-isobutyl cyanoacrylate as materials, poloxamer 188 as emulsifier, and curcumin complex with hydroxypropyl-β-cyclodextrin (Cur-HP-β-CD) as drug prepared by kneading method. Effects of emulsifier and drug concentration on microspheres size and distribution, drug loading and encapsulation efficiency were investigated in detail. And the curcumin release of drug-loaded microspheres was also studied. Results showed that as the emulsifier concentration increased from 0.01% to 0.07%, particle size of the drug-loaded microspheres decreased while particle size distribution, drug loading and entrapment efficiency increased. The optimized concentration of surfactant was 0.05%. With increasing the concentration of drug from 0.03% to 0.07%, drug loading of Cur-HP-β-CD-PiBCA increased, but encapsulation efficiency decreased. Additionally, the results of drug release experiments revealed that the higher drug loading of Cur-HP-β-CD-PiBCA was, the lower cumulative release percentage was. Drug-loading of cumulative inclusions in HP-β-CD by PiBCA can improve its wettability, and increase the degree of dissolution and bioavailability.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9935258PMC
http://dx.doi.org/10.7507/1001-5515.201701045DOI Listing

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