2023
DOI: 10.1016/j.arabjc.2023.105086
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Development of a new vesicular formulation for delivery of Ifosfamide: Evidence from in vitro, in vivo, and in silico experiments

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Cited by 11 publications
(3 citation statements)
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“…Hajinezhad and et al designed a novel encapsulate ifosfamide (IFO) niosomal nanometric size range with a high drug-loading capacity and evaluate the anticancer effectiveness of the encapsulate IFO. They result showed that niosomal IFO had desirable anticancer activity against breast cancer (MCF7) and neuroblastoma (SH-SY5Y) cells with a high potential in the controlled release of IFO [ 28 ].…”
Section: Discussionmentioning
confidence: 99%
“…Hajinezhad and et al designed a novel encapsulate ifosfamide (IFO) niosomal nanometric size range with a high drug-loading capacity and evaluate the anticancer effectiveness of the encapsulate IFO. They result showed that niosomal IFO had desirable anticancer activity against breast cancer (MCF7) and neuroblastoma (SH-SY5Y) cells with a high potential in the controlled release of IFO [ 28 ].…”
Section: Discussionmentioning
confidence: 99%
“…Furthermore, Anu et al synthesized selenium nanoparticles (SeNPs) as green biogenesis NPs from Cassia auriculata and shown their effectiveness against leukemia cancer cells in vitro, as well as greater solubility and decreased toxicity on normal cells [ 91 ]. Niosomal formulations to encapsulate ifosfamide, alkylating anticancer drug, was developed to control its release and alleviate its toxicity [ 92 ]. Nanocarriers for efficient delivery of anti-leukemia drugs are summarized in Table 2 .…”
Section: Nanotechnology Approachesmentioning
confidence: 99%
“…Niosomes are slightly different from liposomes as the bilayers are formed by non-ionic surfactants. The oxazaphosphorine family of alkylating drugs, Ifosfamide (IFO), when loaded with niosomes, showed potent activity with IC 50 of < 0.2 µg/ml against neuroblastoma SH-SY5Y cells [ 29 ] along with improved biochemical parameters against rat model of cancer with intravenous delivery of 0.2 mg/Kg of body weight. For liposomes, the stimuli-responsive drug delivery, where the stimuli can be pH-, redox-, enzyme-, light-, thermo-, and magneto-sensitive, is another advantage.…”
Section: Liposomementioning
confidence: 99%