2021
DOI: 10.1007/s12247-021-09551-8
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Mitoxantrone-Loaded PLGA Nanoparticles for Increased Sensitivity of Glioblastoma Cancer Cell to TRAIL-Induced Apoptosis

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Cited by 9 publications
(3 citation statements)
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“…In this study, the percentage of DEE of CQD-MTX complex was calculated, and the cumulative release of MTX from CQD-MTX complex was investigated at pH 7.4 and 5.2 after 48 h. Based on the results, the percentage of DEE of CQD-MTX complex was obtained 97 %, while, in studies conducted by Hashemi et al and Wang et al , the percentages of DEE of prepared complexes were 68 %, 91.36 %, respectively [ 3 , 9 ]. In addition, in this research, the cumulative release of MTX from CQD-MTX complex was 8 % and 11 % at pH 7.4 and 5.2 after 48 h, respectively, while, in study conducted by Darvish et al , the percentages of released MTX from chitosan-MTX after 48 h were about 45 % and 67 % at pH 7.4 and 5.2, respectively.…”
Section: Discussionmentioning
confidence: 99%
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“…In this study, the percentage of DEE of CQD-MTX complex was calculated, and the cumulative release of MTX from CQD-MTX complex was investigated at pH 7.4 and 5.2 after 48 h. Based on the results, the percentage of DEE of CQD-MTX complex was obtained 97 %, while, in studies conducted by Hashemi et al and Wang et al , the percentages of DEE of prepared complexes were 68 %, 91.36 %, respectively [ 3 , 9 ]. In addition, in this research, the cumulative release of MTX from CQD-MTX complex was 8 % and 11 % at pH 7.4 and 5.2 after 48 h, respectively, while, in study conducted by Darvish et al , the percentages of released MTX from chitosan-MTX after 48 h were about 45 % and 67 % at pH 7.4 and 5.2, respectively.…”
Section: Discussionmentioning
confidence: 99%
“…The percentage of drug entrapment efficiency (DEE) was 68 %. Also, at pH 7.4 after 48 h, the percentage of cumulative release of MTX from PLGA was about 30 %, while, at pH 5.5 after 48 h, it was about 60 % [ 9 ]. Based on the study conducted by Wang et al , MTX-preloaded phospholipid-amorphous calcium carbonate hybrid nanoparticles (PL-ACC-MTX) that surface modified with PL shell (containing shielding polymer polyethylene glycol (PEG) and targeting moiety folic acid) were prepared.…”
Section: Introductionmentioning
confidence: 99%
“…The evasion of apoptosis by glioblastoma cells could be explained by the extrinsic death receptor pathway that is related to Fas/FasL signal transduction being inhibited, especially at the stage of caspase-8 activation [ 116 ]. It was also shown that one of the members of the TNF family of proteins—the tumor necrosis factor-related, apoptosis-inducing ligand (TRAIL)—induces apoptosis in glioblastoma cells through binding to its death receptors, DR4 and DR5 [ 117 , 118 , 119 ]. In glioblastoma cells, the overexpression of anti-apoptotic proteins (Bcl-2) was observed.…”
Section: The Main Regulators Of Apoptosis In Glioblastoma Cellsmentioning
confidence: 99%