2016
DOI: 10.1016/j.ijpharm.2016.05.048
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Biocompatible Zr-based nanoscale MOFs coated with modified poly(ε-caprolactone) as anticancer drug carriers

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Cited by 108 publications
(59 citation statements)
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“…173 It is of interest to use MOFs as carriers for the delivery of chemotherapeutic drugs for the cancer therapy, such as 5-FU, DOX, CPT, platinum drugs and methotrexate (MTX). 165,166,[174][175][176][177][178] Thus, 5-FU-loaded MOFs exhibit excellent anticancer activity against human spinal cord tumor cells. 179 DOX-loaded nano-sized MOFs (UiO-68) were modied with folic acid (FA) as a targeting agent and were used to effectively treat hepatoma by intravenous injection.…”
Section: Metal-organic Frameworkmentioning
confidence: 98%
“…173 It is of interest to use MOFs as carriers for the delivery of chemotherapeutic drugs for the cancer therapy, such as 5-FU, DOX, CPT, platinum drugs and methotrexate (MTX). 165,166,[174][175][176][177][178] Thus, 5-FU-loaded MOFs exhibit excellent anticancer activity against human spinal cord tumor cells. 179 DOX-loaded nano-sized MOFs (UiO-68) were modied with folic acid (FA) as a targeting agent and were used to effectively treat hepatoma by intravenous injection.…”
Section: Metal-organic Frameworkmentioning
confidence: 98%
“…Additionally, Tendeloo and co‐workers were able to fabricate poly(ε‐caprolactone) coated Zr‐based MOFs for anticancer drug carriers . In this work, poly(ε‐caprolactone)–tocopheryl poly(ethylene glycol)‐succinate (PCL–TPGS) copolymer was engineered on the surface of UiO‐66 and UiO‐67 MOFs due to its biocompatibility and non‐toxicity.…”
Section: Multifunctional Mofs For Cancer Theranosticsmentioning
confidence: 99%
“…To the best of our knowledge, this approach has not been used for the surface functionalisation of zirconium MOFs, possibly because their water stability is higher than for other MOF systems. Zr MOFs coated with poly(ξ-caprolactone) in the form of microparticles have recently been reported [103]. The authors investigated UiO-66 and UiO-67 microencapsulation with a copolymer of poly(ξ-caprolactone) and D-α-tocopherol polyethylene glycol 1000 succinate (PCL-TPGS), a derivate of vitamin E and PEG.…”
Section: Postsynthetic Noncovalent Modificationmentioning
confidence: 99%
“…Encapsulation of MOF nanoparticles in polymer microspheres can also control release. UiO-66 and UiO-67 were loaded with cisplatin (4.8% w/w and 1% w/w, respectively) and taxol (14% w/w and 10% w/w, respectively) before microencapsulation in modified poly(ξcaprolactone), and their release kinetics in PBS (pH 7.4) were investigated [103]. Burst release of cisplatin from uncoated UiO-66 and UiO-67 was observed (70% and 90% release, respectively, after 5 h of exposure) followed by slow release of the remainder, either as a consequence of the majority of the drug being bound to the surfaces of the MOFs rather than stored in their pores, or to carrier instability.…”
Section: Controlling Cargo Releasementioning
confidence: 99%