Bioconjugate Chemistry · 2002 · 546 citations · 6 references
PharmacyPharmaceuticsPharmacologyCancer PharmacologyChemotherapyDrug DeliveryAntibody CharacterizationAntibody ConjugatesAntibody-drug ConjugatesCancer ImmunotherapyDrug DispositionPharmacokinetics Of Monoclonal AntibodiesAnthracycline-based ChemotherapyAntibody-drug Conjugate LinkersCathepsin ActivityCathepsin-cleavable ProdrugsLysosomal ProteolysisMonoclonal Antibody InteractionsTumor-associated Antigen RecognitionTumor-associated Antigen Targeting
The anticancer drug doxorubicin (DOX) has been linked to chimeric BR96, an internalizing monoclonal antibody that binds to a Lewis(y)-related, tumor-associated antigen, through two lysosomally cleavable dipeptides, Phe-Lys and Val-Cit, giving immunoconjugates 72 and 73. A self-immolative p-aminobenzyloxycarbonyl (PABC) spacer between the dipeptides and the DOX was required for rapid and quantitative generation of free drug. DOX release from model substrate Z-Phe-Lys-PABC-DOX 49 was 30-fold faster than from Z-Val-Cit-PABC-DOX 42 with the cysteine protease cathepsin B alone, but rates were identical in a rat liver lysosomal preparation suggesting the participation of more than one enzyme. Conjugates 72 and 73 showed rapid and near quantitative drug release with cathepsin B and in a lysosomal preparation, while demonstrating excellent stability in human plasma. Against tumor cell lines with varying levels of BR96 expression, both conjugates showed potent, antigen-specific cytotoxic activity, suggesting that they will be effective in delivering DOX selectively to antigen-expressing carcinomas.
6
A. John Barrett, A A Kembhavi, M A Brown et al. · Biochemical Journal · 1982 · 1K citations · Full text
Olivier Dangles, F. GUIBE, G.G.A. Balavoine et al. · The Journal of Organic Chemistry · 1987 · 259 citations