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Biopolymeric Magnetic Nanocarriers for Controlled drug release

Biopolymeric Magnetic Nanocarriers for Controlled drug releaseaf Anamika Singh
Bag om Biopolymeric Magnetic Nanocarriers for Controlled drug release

Bipolymeric magnetic nanoparticles for controlled release involve the synthesis of polymeric nanoparticles and evaluation of their drug release potential used for Magnetic drug targeting. Magnetic drug targeting is a drug delivery system that can be used in cancer treatment. Coated magnetic particles, called carriers, are very useful for delivering chemotherapeutic drugs. In the present research casein coated iron oxide nanocarriers (CCIONPs) of core shell nanostructure have been described to find application in magnetic drug targeting. The nanoparticles were loaded with cytarabine drug and its controlled release was investigated as a function of drug loading, chemical architecture of the nanocarriers, and nature of release media. Drug release data were examined by some kinetic models like zero-order, first order, and Higuchi.

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  • Sprog:
  • Engelsk
  • ISBN:
  • 9783659933547
  • Indbinding:
  • Paperback
  • Sideantal:
  • 88
  • Udgivet:
  • 24. september 2018
  • Størrelse:
  • 150x6x220 mm.
  • Vægt:
  • 149 g.
Leveringstid: 2-3 uger
Forventet levering: 19. december 2024
Forlænget returret til d. 31. januar 2025

Beskrivelse af Biopolymeric Magnetic Nanocarriers for Controlled drug release

Bipolymeric magnetic nanoparticles for controlled release involve the synthesis of polymeric nanoparticles and evaluation of their drug release potential used for Magnetic drug targeting. Magnetic drug targeting is a drug delivery system that can be used in cancer treatment. Coated magnetic particles, called carriers, are very useful for delivering chemotherapeutic drugs. In the present research casein coated iron oxide nanocarriers (CCIONPs) of core shell nanostructure have been described to find application in magnetic drug targeting. The nanoparticles were loaded with cytarabine drug and its controlled release was investigated as a function of drug loading, chemical architecture of the nanocarriers, and nature of release media. Drug release data were examined by some kinetic models like zero-order, first order, and Higuchi.

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