Targeted cancer therapy: conferring specificity to cytotoxic drugs.
By R. Chari. Accounts of Chemical Research, 2008
781 citations recorded by the source corpus.
Subfields: Organic Chemistry, Radiology, Nuclear Medicine and Imaging
View Paper: https://www.semanticscholar.org/paper/e2652ccce683be6194269d775f85df984a7d2845
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In Organic Chemistry
In Radiology, Nuclear Medicine and Imaging
Citations in the corpus
- Site-specific antibody drug conjugates for cancer therapy (2013, methodology): “An immune response mounted against an ADC, such as human anti-mouse antibodies (HAMA) against a murine ADC, can prevent repeat cycles of therapy.(23) It is also important to select an antibody with optimal PK properties (longer half-life with slower clearance in plasma).”
- Antibody Drug Conjugates for Cancer Therapy (2016, background): “the hydrophobic nature of maytansinoids and auristatins can drive antibody aggregation and negatively impact pharmacokinetics (Hamblett et al., 2004; Chari, 2008).”
- Conjugation site modulates the in vivo stability and therapeutic activity of antibody-drug conjugates (2012, background): “and by selecting the appropriate antibody and payloa”