Opsonization, biodistribution, and pharmacokinetics of polymeric nanoparticles.
By Donald E. Owens, Nicholas A. Peppas. International journal of pharmaceutics, 2006
3,500 citations recorded by the source corpus.
Subfields: Biomaterials, Physiology, Pulmonary and Respiratory Medicine
View Paper: https://www.semanticscholar.org/paper/9b2dc26d5f74751ce05806a8f3ae8697f87b4f0d
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Biomaterials
In Physiology
- S. Mitragotri
- O. Farokhzad
- N. Bertrand
- Phatsapong Yingchoncharoen
- D. Richardson
- D. Kalinowski
- A. Swami
In Pulmonary and Respiratory Medicine
Citations in the corpus
- Nanoparticle PEGylation for imaging and therapy (2011, background): “are also more vulnerable to the RES and hydrophilic PEG reduces these complications [22].”
- Understanding biophysicochemical interactions at the nano-bio interface. (2009, background): “Complement and immunoglobulin binding leads to particle opsonization: that is, it promotes receptor-mediated phagocytosi”
- Insight into nanoparticle cellular uptake and intracellular targeting (2014, neutral): “The soluble factors involved in the opsonization process include proteins of the complement system, antibodies, acetylcholine, laminin, fibronectin, C-reactive protein, and type-I collagen [29].”