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Journal of Korean Medical Science ; : 128-135, 1992.
Article in English | WPRIM | ID: wpr-161616

ABSTRACT

Eight saporin peaks were obtained from the purification of seed extracts of Saponaria officinalis L. Saporin peak No. 6 (SAP-6) showed the highest activity in the inhibition of protein synthesis (98%) in an in vitro translation study. An immunotoxin (IT) was prepared from SAP-6 conjugated to a monoclonal anti-CEA antibody 26/5/1 (mab B) using N-succinimidyl pyridyl dithiopropionate (SPDP) and 2-iminothiolane as a cross linker. Under thermal stability study by a DSC (differential scanning calorimetry), the IT showed a denature temperature of 75 degrees C. In in vitro translation studies, the purified IT showed the same activity as SAP-6 at 10(-7) M and 10(-9) M protein concentration at 0, 30 and 60-min incubation effects with mab B and SAP-6 not conjugated at 24-hr incubation periods on human promyelocytic cell line HL 60 and on human colon adenocarcinoma cell lines which were SW 403, LoVo and LS 174 T. SAP-6, mab B and IT had no cytotoxic effect on HL-60. The IT showed a higher cytotoxic effect than SAP-6 in CEA-positive cell lines. The IT demonstrated the highest cytotoxic effect of 51% inhibition of control at 10(-7) M on the LS 174 T.


Subject(s)
Humans , Antibodies, Monoclonal/therapeutic use , Antineoplastic Agents, Phytogenic/administration & dosage , Carcinoembryonic Antigen/biosynthesis , Colonic Neoplasms/pathology , Hot Temperature , Immunotoxins/therapeutic use , N-Glycosyl Hydrolases , Plant Proteins/administration & dosage , Ribosome Inactivating Proteins, Type 1 , Tumor Cells, Cultured/drug effects
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