Polymer conjugates as anticancer nanomedicines
By R. Duncan. Nature Reviews. Cancer, 2006
1,862 citations recorded by the source corpus.
Subfields: Biomaterials, Biomedical Engineering, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/6b138de1384692fe30afacacafc42de3e5389918
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Citations in the corpus
- PLGA-lecithin-PEG core-shell nanoparticles for controlled drug delivery. (2009, background): “Among these products, liposomal drugs [4] and polymer– drug conjugates [5] are two dominant classes, accounting for the majority of clinically approved products.”
- Cancer nanotechnology: the impact of passive and active targeting in the era of modern cancer biology. (2014, background): “Although this product failed in phase II due to lack of efficacy [306], it was observed in humans that the ligand conferred some level of liver targeting to this polymer-drug conjugate [305].”
- Nanocarriers as an emerging platform for cancer therapy. (2007, background): “Recent reviews provide perspective on the use of nanotechnology as a fundamental tool in cancer research and nanomedicin”
- The journey of a drug-carrier in the body: an anatomo-physiological perspective. (2012, background): “conjugates [16], dendrimers [17] or other macromolecules [18]), which are in a dissolved state.”
- Nanomedicine in cancer therapy (2023, background): “283,284 The mannose receptor is a C-type lectin mainly present on the surface of macrophages, immature dendritic cells (iDCs), liver sinusoidal endothelial cells (LSECs), and tumor cells.”
- Strategies in the design of nanoparticles for therapeutic applications (2010, background): “Polymer–drug conjugates have also been extensively investigated, and several have received regulatory approva”
- Advanced Materials and Processing for Drug Delivery: The Past and the Future (2012, background): “However, subsequent analysis did show that Xyotax could improve survival rate in women although not in men [54, 64].”