The Schwartz technique is a simple method for labeling McAb directly with  ̄(99m)Tc and can he utilized to design a one-step radiopharmacelltical kit.In this study,it was applied to label anti-human gastric cancer McA...The Schwartz technique is a simple method for labeling McAb directly with  ̄(99m)Tc and can he utilized to design a one-step radiopharmacelltical kit.In this study,it was applied to label anti-human gastric cancer McAb 3H11. The antibody was reduced at room temperature for 30 min with a 1000-fold molar ratio excess of 2mercaptoethanol. The mean labeling efficiency of  ̄(99m)Tc3H11 was more than 95%. The immunoreactivity of  ̄(99m)Tc-3H11 was more than 80% by ELISA's method. Competition results in vitro showed that  ̄(99m)Tc was combined with the high affinity sites of antibody by HPLC. The biodistribution in nude mice bearing 823 gastric cancer xenographts showed that the radioactivity of tumor uptake at 24 h post-injection was the highest except for kidney.The tumor uptake was 8.98±2.42% i.d/g.The count ratio of tumor to blood was over 1.5 and that tumor to liver was more than 2.5 at 24 h post-injection.And the tumor was clearly imaged at 22 h post-injection. The initial clinical results showed that ̄(99m)Tc-3H11 was stable in vivo and well good located at the lesion sites.展开更多
Objective: To explore the law and role of apoptosis inducing effect of allicin on human acute T-lymphocyte leukemia cell line (6T-CEM).Methods: Terminal deoxylnucleotide transferase directed X-UTP nick and end labelin...Objective: To explore the law and role of apoptosis inducing effect of allicin on human acute T-lymphocyte leukemia cell line (6T-CEM).Methods: Terminal deoxylnucleotide transferase directed X-UTP nick and end labeling (TUNEL) assay, DNA gel electrophoresis, light microscopy and revers transcription-polymerase chair reaction (RT-PCR) were used to observe apoptosis of cells.Results: Allicin showed significant inducing effect on apoptosis of 6T-CEM cell when the concentration was 0.1 μg/ml, reaching its peak effect when the concentration was 50 μg/ml, with the apoptosis rate as 36.4%. Allicin (15 μg/ml) acted on 6T-CEM for 2 h and induced obvious cell apoptosis, the highest effect reached after 24 h of action, with the apoptosis rate as 56.9%. Actidione or actinomycin D could induce apoptosis of 6T-CEM, the allicin could not enhance their apoptosis inducing effect. Allicin could cause significant reduction of bcl-2 and bax gene expression of 6T-CEM, especially the bcl-2.Conclusion: Allicin could induce cell apoptosis of 6T-CEM with significant time and dose effect. Mechanism of the effect is through inhibiting the bcl-2 gene expression to reduce bcl-2/bax ratio.展开更多
文摘The Schwartz technique is a simple method for labeling McAb directly with  ̄(99m)Tc and can he utilized to design a one-step radiopharmacelltical kit.In this study,it was applied to label anti-human gastric cancer McAb 3H11. The antibody was reduced at room temperature for 30 min with a 1000-fold molar ratio excess of 2mercaptoethanol. The mean labeling efficiency of  ̄(99m)Tc3H11 was more than 95%. The immunoreactivity of  ̄(99m)Tc-3H11 was more than 80% by ELISA's method. Competition results in vitro showed that  ̄(99m)Tc was combined with the high affinity sites of antibody by HPLC. The biodistribution in nude mice bearing 823 gastric cancer xenographts showed that the radioactivity of tumor uptake at 24 h post-injection was the highest except for kidney.The tumor uptake was 8.98±2.42% i.d/g.The count ratio of tumor to blood was over 1.5 and that tumor to liver was more than 2.5 at 24 h post-injection.And the tumor was clearly imaged at 22 h post-injection. The initial clinical results showed that ̄(99m)Tc-3H11 was stable in vivo and well good located at the lesion sites.
文摘Objective: To explore the law and role of apoptosis inducing effect of allicin on human acute T-lymphocyte leukemia cell line (6T-CEM).Methods: Terminal deoxylnucleotide transferase directed X-UTP nick and end labeling (TUNEL) assay, DNA gel electrophoresis, light microscopy and revers transcription-polymerase chair reaction (RT-PCR) were used to observe apoptosis of cells.Results: Allicin showed significant inducing effect on apoptosis of 6T-CEM cell when the concentration was 0.1 μg/ml, reaching its peak effect when the concentration was 50 μg/ml, with the apoptosis rate as 36.4%. Allicin (15 μg/ml) acted on 6T-CEM for 2 h and induced obvious cell apoptosis, the highest effect reached after 24 h of action, with the apoptosis rate as 56.9%. Actidione or actinomycin D could induce apoptosis of 6T-CEM, the allicin could not enhance their apoptosis inducing effect. Allicin could cause significant reduction of bcl-2 and bax gene expression of 6T-CEM, especially the bcl-2.Conclusion: Allicin could induce cell apoptosis of 6T-CEM with significant time and dose effect. Mechanism of the effect is through inhibiting the bcl-2 gene expression to reduce bcl-2/bax ratio.