2018
DOI: 10.1016/j.tibtech.2018.02.006
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Design of Polymeric Gene Carriers for Effective Intracellular Delivery

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Cited by 119 publications
(94 citation statements)
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“…Owing to their positive surface charge, the NCs were shown to condense nucleic acids during the gel retardation assay . Simply possessing the capacity of condensing nucleic acids, however, is not sufficient for gene delivery, which involves other processes such as cellular internalization and endo‐lysosomal escape . Detailed evaluation of the in vitro and in vivo transfection efficiency of the NCs is required before the application potential of the NCs for gene therapy can be more conclusively determined.…”
Section: Synthesis Of Cu Ncs As Theranostic Agentsmentioning
confidence: 99%
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“…Owing to their positive surface charge, the NCs were shown to condense nucleic acids during the gel retardation assay . Simply possessing the capacity of condensing nucleic acids, however, is not sufficient for gene delivery, which involves other processes such as cellular internalization and endo‐lysosomal escape . Detailed evaluation of the in vitro and in vivo transfection efficiency of the NCs is required before the application potential of the NCs for gene therapy can be more conclusively determined.…”
Section: Synthesis Of Cu Ncs As Theranostic Agentsmentioning
confidence: 99%
“… Diagnosis using Cu NCs is performed largely based on the detection of abnormal molecular events in the pathological site. In cancer cells, abnormal molecular events are usually manifested in terms of alternations in protein expression, changes in the level of reactive oxygen/nitrogen species, and alternations in intracellular pH . Cu NCs can possibly be developed as probes for these molecular events because some of them exhibit an aggregation‐induced emission (AIE) effect in liquid media .…”
Section: Working Principles Of Cu Ncs As Theranostic Agentsmentioning
confidence: 99%
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“…Inspired by virus strategies that use multiple attachment factors and receptors for targeting host cells in parallel or in succession, researchers have exploited various ligands conjugated to delivery systems aiming to facilitate tumor cell targeting and penetration. To date, various cell specific ligands have been employed, such as lactose, anti‐CD3 antibody, OV‐TL16, PSMA‐specific monoclonal antibody J591, HER‐2 antibody, mannose, GRP‐78‐targeting peptide, transferrin, RGD peptide and folic acid . Sun et al .…”
Section: Specificity and Infection Properties Mimic Designs For Targementioning
confidence: 99%
“…65 employed, such as lactose, anti-CD3 antibody, OV-TL16, PSMAspecific monoclonal antibody J591, HER-2 antibody, mannose, GRP-78-targeting peptide, transferrin, RGD peptide and folic acid. 75 Sun et al 76 developed a targeted gene delivery system by conjugating βcyclodextrin modified polyethylenimine (PEI-CD) and adamantyl peptide (AdGRGDS) based on host-guest interaction. In vitro and in vivo assays highlighted the importance of AdGRGDS targeting specificity to tumor cells with integrin α v β 3 overexpression and demonstrated that the PEI-CD/AdGRGDS gene delivery system had great potential for targeted tumor therapy.…”
Section: Specificity and Infection Properties Mimic Designs For Tarmentioning
confidence: 99%