2008
DOI: 10.1016/j.jconrel.2008.07.035
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Characterization of carbosilane dendrimers as effective carriers of siRNA to HIV-infected lymphocytes

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Cited by 156 publications
(119 citation statements)
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“…MT4 lymphocytes exposed to the dendriplex retained .80% viability at a dendrimer concentration of 15 µM (equivalent to 138 µg/mL). By comparison, peripheral blood mononuclear cells and SupT1 cells exposed to a second-generation carbosilane dendrimer in a study by Weber et al 56 reached the toxicity limit of 80% at 24 µg/mL, while in another study, two second-generation dendrimers reached the toxicity limit for macrophages at 5 and 15 µM, respectively. 33 …”
Section: Notesmentioning
confidence: 96%
See 1 more Smart Citation
“…MT4 lymphocytes exposed to the dendriplex retained .80% viability at a dendrimer concentration of 15 µM (equivalent to 138 µg/mL). By comparison, peripheral blood mononuclear cells and SupT1 cells exposed to a second-generation carbosilane dendrimer in a study by Weber et al 56 reached the toxicity limit of 80% at 24 µg/mL, while in another study, two second-generation dendrimers reached the toxicity limit for macrophages at 5 and 15 µM, respectively. 33 …”
Section: Notesmentioning
confidence: 96%
“…56 The cells were harvested, washed first with PBS, then with acidglycine buffer for 30 seconds and finally again with PBS. The acid-glycine buffer (for the removal of dendriplexes bound to the surface of the cell membranes) consisted of 0.2 M glycine in PBS (adjusted to pH 3.0 by addition of hydrochloric acid).…”
Section: 55mentioning
confidence: 99%
“…Carbosilane dendrimers were also investigated in terms of other potential antiviral applications [62,63]. Knowing that dendrimers are excellent non-viral transfection agents, two polycationic G1 carbosilane dendrimers with different cores were assessed for gene therapy in order to inhibit the development of ongoing HIV infection.…”
Section: Herpes Simplex Virus (Hsv) and Human Papilloma Virus (Hpv) mentioning
confidence: 99%
“…[8][9][10] In the last few years, nanotechnology offered a huge battery of novel nanoparticles such as dendrimers and macromolecules characterized by hyperbranched, well-defined, monodisperse, three-dimensional structures that are being developed as drug delivery vehicles or as therapeutic agents. [11][12][13][14][15][16][17] The controlled synthesis of dendrimers allows the assembly of highly defined, single molecule structures that radiate out in branches from a central initiator core. The type of core and branching units can be engineered to generate a broad variety of dendrimers with different sizes, shapes, and surface chemical functionalized groups that can provide distinct biological and pharmacological properties.…”
Section: Introductionmentioning
confidence: 99%