2016
DOI: 10.1016/j.jssc.2016.02.040
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A porphyrin-based metal–organic framework as a pH-responsive drug carrier

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Cited by 95 publications
(46 citation statements)
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“…More interestingly, they reported the first example of PCN‐221 MOF as an oral drug carrier . PCN‐221 was prepared from 5,10,15,20‐tetrakis (4‐carboxyphenyl) porphyrin (TCPP) and ZrCl 4 , and then the anticancer drug methotrexate (MTX) was encapsulated by immersing PCN‐221 in MTX solution.…”
Section: Stimuli‐responsive Mofs For Drug Deliverymentioning
confidence: 99%
“…More interestingly, they reported the first example of PCN‐221 MOF as an oral drug carrier . PCN‐221 was prepared from 5,10,15,20‐tetrakis (4‐carboxyphenyl) porphyrin (TCPP) and ZrCl 4 , and then the anticancer drug methotrexate (MTX) was encapsulated by immersing PCN‐221 in MTX solution.…”
Section: Stimuli‐responsive Mofs For Drug Deliverymentioning
confidence: 99%
“…This allows reducing the amount of nonactive undesirable compounds to be administered at the benefit of an anticipated decrease of toxicity. Numerous active ligands have been proposed to date to produce bioMOFs: peptides (metal peptide frameworks), nucleobases, carbohydrates, porphyrines, as well as some active ingredients . Unfortunately, most of these bioMOFs are still at their initial stages of development and a very few of them have undergone in vivo preclinical evaluation.…”
Section: Toxicity: From In Vitro To In Vivo Evaluationmentioning
confidence: 99%
“…Comparisons were made between the amorphous and crystalline forms of UiO-66, and the amorphous material was found to sustain release of calcein for up to 30 days, compared with the 2 days afforded by the crystalline counterpart. In comparison, Lin et al have loaded anti-cancer drug methotrexate into Zr-based porphyrin framework PCN-221 [ 86 ]. High drug loading and pH-responsive release was observed, allowing for limited drug release in undesirable biological areas.…”
Section: Host–guest Chemistry In Mofsmentioning
confidence: 99%