Stability of Protein Pharmaceuticals: An Update
By M. Manning, Danny K. Chou, B. Murphy, Robert W. Payne, D. Katayama. 2010
1,067 citations recorded by the source corpus.
Subfields: Molecular Biology, Pharmaceutical Science, Radiology, Nuclear Medicine and Imaging
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In Molecular Biology
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Citations in the corpus
- The CamSol method of rational design of protein mutants with enhanced solubility. (2015, background): “More generally, insufficient solubility represents a major bottleneck for the development of protein-based drugs, as protein aggregates not only are non-functional but also can be toxic and may elicit an immune response in the patient [14,28].”
- Pharmacokinetic aspects of retinal drug delivery. (2017, positive): “Protein stability involves physical phenomena and conformation changes that are not relevant for small molecules (Manning et al., 2010).”