2019
DOI: 10.1080/1061186x.2019.1567738
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Paclitaxel-loaded multifunctional nanoparticles for the targeted treatment of glioblastoma

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Cited by 42 publications
(23 citation statements)
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“…In a recent study, Ucakar B. et al [34] found no significant difference between the brain accumulation of T80-coated and uncoated SPION-paclitaxel PNP in an orthotopic GBM model. However, in a subsequent study by the same authors [34,35], the magnetic targeting was found to enhance the brain accumulation of these NP, their antitumor efficacy and the survival rate. A significant prolongation in the survival rates of mice was obtained using a longer targeting time (4h vs. 1h), a stronger magnet (1.4 T vs. 0.4 T) and a larger number of doses (6 vs. 2).…”
Section: Survival Ratementioning
confidence: 98%
“…In a recent study, Ucakar B. et al [34] found no significant difference between the brain accumulation of T80-coated and uncoated SPION-paclitaxel PNP in an orthotopic GBM model. However, in a subsequent study by the same authors [34,35], the magnetic targeting was found to enhance the brain accumulation of these NP, their antitumor efficacy and the survival rate. A significant prolongation in the survival rates of mice was obtained using a longer targeting time (4h vs. 1h), a stronger magnet (1.4 T vs. 0.4 T) and a larger number of doses (6 vs. 2).…”
Section: Survival Ratementioning
confidence: 98%
“…Current chemotherapy often leaves debilitating and life altering side effects since most drugs on the market that target the rapidly dividing cancer cells also inadvertently damage cells that are vital for normal life processes (Rizvi and Saleh, 2018). Actively targeting PLGA nanoparticles are able to circumvent this; Moku et al (2019) have shown increased drug loading and efficacy against lung cancer by using transactivator of transcription (TAT) peptide ligands to target mesenchymal stem cells while Ganipineni et al (2019) found that magnetically targeted paclitaxel-and SPIO-loaded PLGA-based nanoparticles effected increased cellular uptake in glioblastoma cells compared to the non-targeted carriers. Another type of nanoparticle targeting is the use of 'smart' carriers that are engineered to respond to a stimulus (Kapoor et al, 2015).…”
Section: Actively Targeted Chemotherapeuticsmentioning
confidence: 99%
“…Gold nanoparticles (2 nm) that were coated with functional derivatives of thiolated PEG have shown invisibility towards the immune system provided by PEG [106], but also enabled attaching other moieties to provide specific targeting. The surface of the nanocarriers was thus modified with the ligand RGD-a peptide with a relatively high and specific affinity for the integrins overexpressed in tumor neovasculature [107,108]. A mice model of single-nodule lung adenocarcinoma [109] was used to establish which route of administration, either inhalation or intravenous delivery, would be more effective on adenocarcinoma targeting using the nanocarriers.…”
Section: Applications In Cancer Therapymentioning
confidence: 99%