2022
DOI: 10.1016/j.actbio.2022.02.043
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Design and development of Branched Poly(ß-aminoester) nanoparticles for Interleukin-10 gene delivery in a mouse model of atherosclerosis

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Cited by 10 publications
(3 citation statements)
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“…modified the VHPK peptide on the surface of poly(β‐aminoester) to construct VHPK NPs that specifically targeted the aortic ECs of mice. [ 178 ] Furthermore, intravenous injections of VHPK NPs in an AS mouse model showed a significant accumulation of the plasmid DNA carried by the NPs within the atherosclerotic plaque sites.…”
Section: Therapeutic Strategies For Asmentioning
confidence: 99%
“…modified the VHPK peptide on the surface of poly(β‐aminoester) to construct VHPK NPs that specifically targeted the aortic ECs of mice. [ 178 ] Furthermore, intravenous injections of VHPK NPs in an AS mouse model showed a significant accumulation of the plasmid DNA carried by the NPs within the atherosclerotic plaque sites.…”
Section: Therapeutic Strategies For Asmentioning
confidence: 99%
“…More targeted approaches involve protein corona modulation 22,23 and antibody or peptidemediated targeting. 24,25 Surface engineering with antibodies and peptides increases the complexity of the delivery system, limiting clinical translation. [26][27][28] Hence, there is a need for rational functional design of these polymers emerging from the biological identity of the target cell.…”
Section: Introductionmentioning
confidence: 99%
“…[ 24 ] Regarding adverse reactions associated with drugs or surgery, nanomaterials achieve higher drug utilization rates or further enrich the range of surgical options (such as nanodrug‐coated balloons or stents) through elaborated design. [ 25 ] Importantly, nanomaterials provide the ability to integrate diagnosis and treatment for atherosclerosis. In the past, diagnosis and treatment were two separate fields.…”
Section: Introductionmentioning
confidence: 99%