TY - JOUR
T1 - Site-directed drug release performance in chemically-modified FeFe2O4 and CoFe2O4 magnetic nanoparticles for controlled drug delivery systems
AU - Santos, Samuel Brito Ferreira
AU - Araújo, Pascally Maria Aparecida Guerra de
AU - Santos, Isabela Alves dos
AU - Costa, Ana Cristina Figueiredo de Melo
AU - Lima, Álvaro Silva
AU - Conrado, Líbia de Sousa
PY - 2021/7/15
Y1 - 2021/7/15
N2 - This paper proposes a novel approach to the development of magnetic nanoparticles (MNPs) for drug delivery systems. The nanocarriers are made from FeFe2O4 and CoFe2O4 MNPs that were synthesized by combustion, coated with silica derivatives, and then conjugated to ciprofloxacin. The drug release tests were performed into simulated body fluid consisted of ciprofloxacin adsorbed onto MNPs composites with various mass ratios of hydroxyapatite:FeFe2O4 (M) and hydroxyapatite:CoFe2O4 (C), evaluated by pharmacokinetic models, and regression analysis. The MNPs were characterized by morphological and structural characterizations. Drug release was measured with a discontinuous method (paddle apparatus) and with a continuous method simulating a blood vessel. XRD and FTIR showed that all of the MNPs were successfully synthesized, coated, and drug conjugated. VSM exhibited superparamagnetic characteristics, with saturation magnetization varying between 9.74 and 32.90 emu/g and 9.65–30.00 emu/g for FeFe2O4 and CoFe2O4, respectively, as a function of the MNPs mass ratio on the nanocarrier. The discontinuous method showed drug release over 80% (FeFe2O4), while the CoFe2O4-based achieved over 40%, which indicates that the incorporation of hydroxyapatite favors the carrying of ciprofloxacin. The continuous method showed a drug release under 14% and 14.5% for the FeFe2O4 and CoFe2O4 based nanocarriers respectively, and this reduction of the desorbed drug compared to the discontinuous method may have occurred due to the action of the applied magnetic field. The mathematical model provided the release speed and time to reach the maximum fraction desorbed (<4 min), highlighted for M2 (13.8%) and C3 (14.5%) drug released, with a mass ratio of 50:50 and 30:70, respectively. The proposed continuous release model showed that the action of site-directed targeting significantly affected the amount of drug released. This identifies the optimal device for the development of magnetic nanoparticulate systems for drug delivery and tissue engineering.
AB - This paper proposes a novel approach to the development of magnetic nanoparticles (MNPs) for drug delivery systems. The nanocarriers are made from FeFe2O4 and CoFe2O4 MNPs that were synthesized by combustion, coated with silica derivatives, and then conjugated to ciprofloxacin. The drug release tests were performed into simulated body fluid consisted of ciprofloxacin adsorbed onto MNPs composites with various mass ratios of hydroxyapatite:FeFe2O4 (M) and hydroxyapatite:CoFe2O4 (C), evaluated by pharmacokinetic models, and regression analysis. The MNPs were characterized by morphological and structural characterizations. Drug release was measured with a discontinuous method (paddle apparatus) and with a continuous method simulating a blood vessel. XRD and FTIR showed that all of the MNPs were successfully synthesized, coated, and drug conjugated. VSM exhibited superparamagnetic characteristics, with saturation magnetization varying between 9.74 and 32.90 emu/g and 9.65–30.00 emu/g for FeFe2O4 and CoFe2O4, respectively, as a function of the MNPs mass ratio on the nanocarrier. The discontinuous method showed drug release over 80% (FeFe2O4), while the CoFe2O4-based achieved over 40%, which indicates that the incorporation of hydroxyapatite favors the carrying of ciprofloxacin. The continuous method showed a drug release under 14% and 14.5% for the FeFe2O4 and CoFe2O4 based nanocarriers respectively, and this reduction of the desorbed drug compared to the discontinuous method may have occurred due to the action of the applied magnetic field. The mathematical model provided the release speed and time to reach the maximum fraction desorbed (<4 min), highlighted for M2 (13.8%) and C3 (14.5%) drug released, with a mass ratio of 50:50 and 30:70, respectively. The proposed continuous release model showed that the action of site-directed targeting significantly affected the amount of drug released. This identifies the optimal device for the development of magnetic nanoparticulate systems for drug delivery and tissue engineering.
KW - ciprofloxacin
KW - drug carrier
KW - hydroxyapatite
KW - iron oxide
U2 - 10.1016/j.ceramint.2021.03.300
DO - 10.1016/j.ceramint.2021.03.300
M3 - Article
AN - SCOPUS:85103991057
SN - 0272-8842
VL - 47
SP - 19622
EP - 19631
JO - Ceramics International
JF - Ceramics International
IS - 14
ER -