2016
DOI: 10.1016/j.ijpharm.2016.06.117
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Tat peptide and hexadecylphosphocholine introduction into pegylated liposomal doxorubicin: An in vitro and in vivo study on drug cellular delivery, release, biodistribution and antitumor activity

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Cited by 26 publications
(15 citation statements)
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“…The linkage efficacy was monitored by silica thin layer chromatography (TLC) with a developing solvent of chloroform/methanol/water (90/10/2) and iodine vapor exposure. Then, the solvents were removed under a warmed nitrogen stream and the tube’s content was freeze-dried overnight 46 . The resulting white powder was re-suspended in an appropriate amount of deionized water.…”
Section: Methodsmentioning
confidence: 99%
“…The linkage efficacy was monitored by silica thin layer chromatography (TLC) with a developing solvent of chloroform/methanol/water (90/10/2) and iodine vapor exposure. Then, the solvents were removed under a warmed nitrogen stream and the tube’s content was freeze-dried overnight 46 . The resulting white powder was re-suspended in an appropriate amount of deionized water.…”
Section: Methodsmentioning
confidence: 99%
“…The antitumor effect of doxorubicin has been introduced for the selection of this compound in order to deal with a range of cancers, such as leukemia, lymphoma, and solid tumors in humans (3). However, the limiting factor in the use of doxorubicin in the treatment of cancer is its toxic effects on vital organs, such as the heart, kidneys, and liver (4,5).…”
Section: Doxorubicinmentioning
confidence: 99%
“…The PEG moiety limits the interactions of the micelles with reticuloendothelial systems and the low critical micelle concentration confers micellar stability in the circular system when they are diluted in blood following intravenous (i.v.) administration (Liu et al, ; Teymouri et al, ). The drug loading capacity of the polymeric micelle was much higher (∼10%) than the previously mentioned liposomes.…”
Section: Cellular and Molecular Targets Of Dimc Causing Cancer Cell Amentioning
confidence: 99%
“…This indicates that the issue of DiMC‐nanoparticulation still needs further investigation and improvement. As Dox and DiMC share ROS cellular alteration as one of their cellular features (Barenholz, ; Kunwar et al, ), their combined nanoparticles administration might provide a superior anti‐tumor activity with diminished side effect (Liu et al, ; Teymouri et al, ).…”
Section: Cellular and Molecular Targets Of Dimc Causing Cancer Cell Amentioning
confidence: 99%