TY - JOUR
T1 - Biocompatible Zr-based nanoscale MOFs coated with modified poly ($varepsilon$-caprolactone) as anticancer drug carriers
AU - Vandichel, Matthias
AU - Filippousi, Maria
AU - Turner, Stuart
AU - Leus, Karen
AU - Siafaka, Panoraia I.
AU - Tseligka, Eirini D.
AU - Nanaki, Stavroula G.
AU - Vizirianakis, Ioannis S.
AU - Bikiaris, Dimitrios N.
AU - Van Der Voort, Pascal
AU - Van Tendeloo, Gustaaf
N1 - Publisher Copyright:
© 2016 Elsevier B.V.
PY - 2016/7/25
Y1 - 2016/7/25
N2 - Nanoscale Zr-based metal organic frameworks (MOFs) UiO-66 and UiO-67 were studied as potential anticancer drug delivery vehicles. Two model drugs were used, hydrophobic paclitaxel and hydrophilic cisplatin, and were adsorbed onto/into the nano MOFs (NMOFs). The drug loaded MOFs were further encapsulated inside a modified poly(ε-caprolactone) with D-α-tocopheryl polyethylene glycol succinate polymeric matrix, in the form of microparticles, in order to prepare sustained release formulations and to reduce the drug toxicity. The drugs physical state and release rate was studied at 37 °C using Simulated Body Fluid. It was found that the drug release depends on the interaction between the MOFs and the drugs while the controlled release rates can be attributed to the microencapsulated formulations. The in vitro antitumor activity was assessed using HSC-3 (human oral squamous carcinoma; head and neck) and U-87 MG (human glioblastoma grade IV; astrocytoma) cancer cells. Cytotoxicity studies for both cell lines showed that the polymer coated, drug loaded MOFs exhibited better anticancer activity compared to free paclitaxel and cisplatin solutions at different concentrations.
AB - Nanoscale Zr-based metal organic frameworks (MOFs) UiO-66 and UiO-67 were studied as potential anticancer drug delivery vehicles. Two model drugs were used, hydrophobic paclitaxel and hydrophilic cisplatin, and were adsorbed onto/into the nano MOFs (NMOFs). The drug loaded MOFs were further encapsulated inside a modified poly(ε-caprolactone) with D-α-tocopheryl polyethylene glycol succinate polymeric matrix, in the form of microparticles, in order to prepare sustained release formulations and to reduce the drug toxicity. The drugs physical state and release rate was studied at 37 °C using Simulated Body Fluid. It was found that the drug release depends on the interaction between the MOFs and the drugs while the controlled release rates can be attributed to the microencapsulated formulations. The in vitro antitumor activity was assessed using HSC-3 (human oral squamous carcinoma; head and neck) and U-87 MG (human glioblastoma grade IV; astrocytoma) cancer cells. Cytotoxicity studies for both cell lines showed that the polymer coated, drug loaded MOFs exhibited better anticancer activity compared to free paclitaxel and cisplatin solutions at different concentrations.
KW - ADF-STEM
KW - Drug delivery
KW - Metal-organic frameworks/UiO-66
KW - Polymer
KW - SEM
KW - UiO-67
UR - http://www.scopus.com/inward/record.url?scp=84975795954&partnerID=8YFLogxK
U2 - 10.1016/j.ijpharm.2016.05.048
DO - 10.1016/j.ijpharm.2016.05.048
M3 - Article
C2 - 27235556
AN - SCOPUS:84975795954
SN - 0378-5173
VL - 509
SP - 208
EP - 218
JO - International Journal of Pharmaceutics
JF - International Journal of Pharmaceutics
IS - 1-2
ER -