Co-delivery of drugs and DNA from cationic core–shell nanoparticles self-assembled from a biodegradable copolymer

By Yong Wang, Shujun Gao, Wen-Hui Ye, H. Yoon, Yi-Yan Yang. Nature Materials, 2006

627 citations recorded by the source corpus.

Subfields: Biomaterials, Molecular Biology

View Paper: https://www.semanticscholar.org/paper/30bf8ed41585b7051c662e25be87402b0f8f807c

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Biomaterials

1. Liangfang Zhang
2. Ying Zhang
3. K. Leong
4. Hon Fai Chan

In Molecular Biology

1. Liangfang Zhang
2. C. J. Hu
3. K. Leong
4. M. Kay

Citations in the corpus

• siRNA delivery systems for cancer treatment. (2009, background): “The co-delivery of paclitaxel and siRNA targeting Bcl-2 was shown to increase the sensitivity of MDA-MB-231 human breast cancer cells to paclitaxel [109].”
• Advanced Materials and Processing for Drug Delivery: The Past and the Future (2012, methodology): “has synthesized a cationic amphiphilic block copolymer, which comprises poly(N-methyldietheneamine sebacate) (PMDS) as the cationic block for siRNA and plasmid binding, and a cholesterol pendant group to increase the hydrophobicity of the core for efficient drug loading [47].”
• Nanoparticle-based combination therapy toward overcoming drug resistance in cancer. (2012, background): “A poly ((N-methyldietheneamine sebacate)-co-((cholesteryl oxocarbonylamido ethyl) methyl bis(ethylene) ammonium bromide) sebacate) (P(MDS-co-CES)) nanoparticle formulation was among one of the earlier efforts in demonstrating the potential of combinatorial nanoparticle co-delivering chemotherapeutic”