4.7 Article

Oromucosal Alginate Films with Zein Nanoparticles as a Novel Delivery System for Digoxin

Journal

PHARMACEUTICS
Volume 13, Issue 12, Pages -

Publisher

MDPI
DOI: 10.3390/pharmaceutics13122030

Keywords

oromucosal films; sodium alginate; nanoparticle drug carriers; digoxin; zein; heart failure

Funding

  1. Portuguese Foundation for Science and Technology/MCTES [UIDB/00709/2020, UIDP/00709/2020]
  2. project APIMedOlder - FEDER, through COMPETE2020-Programa Operacional Competitividade e Internacionalizacao [PTDC/MEDFAR/31598/2017, POCI-01-0145FEDER-031598]
  3. project ZAPGO - FEDER, through COMPETE2020-Programa Operacional Competitividade e Internacionalizacao [POCI-01-0145FEDER-031598, PTDC/NAN-MAT/28989/2017]
  4. national funds (OE), through the Portuguese Foundation for Science and Technology (FCT/MCTES)
  5. European Union/ERDF, ESF, European Regional Development Fund ERDF under the Interreg V A SpainPortugal (POCTEP) 2014-2020 program [0633_BIOIMPACE_4_A]
  6. Fundação para a Ciência e a Tecnologia [PTDC/NAN-MAT/28989/2017] Funding Source: FCT

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The study demonstrated the potential of sodium alginate films with zein nanoparticles loaded with digoxin for buccal drug delivery, aiming to reduce dosing frequency and facilitate quick onset of action. The innovative formulation showed promising properties for drug delivery application and may offer a safer alternative for digoxin administration compared to existing dosage forms on the market.
Digoxin is a hydrophobic drug used for the treatment of heart failure that possesses a narrow therapeutic index, which raises safety concerns for toxicity. This is of utmost relevance in specific populations, such as the elderly. This study aimed to demonstrate the potential of the sodium alginate films as buccal drug delivery system containing zein nanoparticles incorporated with digoxin to reduce the number of doses, facilitating the administration with a quick onset of action. The film was prepared using the solvent casting method, whereas nanoparticles by the nanoprecipitation method. The nanoparticles incorporated with digoxin (0.25 mg/mL) exhibited a mean size of 87.20 +/- 0.88 nm, a polydispersity index of 0.23 +/- 0.00, and a zeta potential of 21.23 +/- 0.07 mV. Digoxin was successfully encapsulated into zein nanoparticles with an encapsulation efficiency of 91% (+/- 0.00). Films with/without glycerol and with different concentrations of ethanol were produced. The sodium alginate (SA) films with 10% ethanol demonstrated good performance for swelling (maximum of 1474%) and mechanical properties, with a mean tensile strength of 0.40 +/- 0.04 MPa and an elongation at break of 27.85% (+/- 0.58), compatible with drug delivery application into the buccal mucosa. The current study suggests that SA films with digoxin-loaded zein nanoparticles can be an effective alternative to the dosage forms available on the market for digoxin administration.

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