2016
DOI: 10.3109/21691401.2016.1138484
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Overall condition improvement in a rat model of nephrotic syndrome treated with CellCept nanoliposomes

Abstract: Purpose To investigate the effect of CellCept nanoliposomes on Adriamycin-induced nephrotic syndrome in rats. Methods To model nephrotic syndrome, rats were injected with 6.5 mg/kg of Adriamycin in the tail vein. The rats were randomly divided into three groups, including a control group, a free mycophenolate mofetil (MMF)-treated group, and a liposome-encapsulated MMF-treated group. Five weeks after the Adriamycin treatment, the free MMF-treated group received CellCept while the liposome-encapsulated MMF-trea… Show more

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Cited by 2 publications
(3 citation statements)
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“…After 1 week of acclimatization, apart from the 10 rats randomized into the control group with saline (1.0 mL/100 g), we intravenously administered the rest with Adriamycin (ADR, 6.5 mg/kg dissolved in saline, Shenzhen Main Luck Pharmaceuticals Inc.) to establish a NS rat model ( Teng et al, 2017 ). In other words, a nephritis model was established by injecting Adriamycin in the caudal vein only once.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…After 1 week of acclimatization, apart from the 10 rats randomized into the control group with saline (1.0 mL/100 g), we intravenously administered the rest with Adriamycin (ADR, 6.5 mg/kg dissolved in saline, Shenzhen Main Luck Pharmaceuticals Inc.) to establish a NS rat model ( Teng et al, 2017 ). In other words, a nephritis model was established by injecting Adriamycin in the caudal vein only once.…”
Section: Methodsmentioning
confidence: 99%
“…Full scan mode was adopted: scan range 80-1200 m/z. saline, Shenzhen Main Luck Pharmaceuticals Inc.) to establish a NS rat model (Teng et al, 2017). In other words, a nephritis model was established by injecting Adriamycin in the caudal vein only once.…”
Section: Uhplc-q-orbitrap Hrms Analysis Of Ybtmentioning
confidence: 99%
“…Nanotechnology has been applied to protect and precisely deliver MMF/MPA to target tissues and cells to treat inflammatory diseases and has shown promise. [14][15][16][17][18][19][20] For example, a triglyceride mimetic prodrug of MPA has been developed for targeted delivery to mesenteric lymph nodes and successfully suppressed the immune reaction to an oral ovalbumin antigen challenge in mice. 17 In addition, MMF-loaded PEG-PLGA nanoparticles (NPs) have been perfused into a donor mouse heart prior to transplantation and successfully inhibited post-transplantation inflammation.…”
Section: Introductionmentioning
confidence: 99%