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Development of a Procedure for Preparing ~(103)Pd-Microspheres of Human Blood Albumin, a Potential Radiopharmaceutical for Treatment of Malignant Tumors

机译:人血白蛋白〜(103)Pd微球的制备方法的开发,这是一种潜在的放射性药物,可治疗恶性肿瘤

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Sorption of Pd by albumin microspheres (AMSs) largely depends on the HCl concentration, reaching a maximum at an HCl concentration of 0.08 M. Sorption of Pd grows with an increase in its equilibrium concentration in 0.08 M HCl. The optimal amount of inactive palladium chloride as ~(103)Pd carrier is 0.6 mg. Under these conditions, sorption of Pd by the protein matrix of albumin microspheres occurs with 70-80percent efficiency. The reduction of the sorbed Pd in albumin microspheres leads to its considerable retention by the protein matrix of the microspheres. This was confirmed by biological studies on laboratory animals. The radionuclide clearance from the muscle tissue after local administration of ~(103)Pd-AMSs with the reduced Pd is considerably slower compared to the unreduced Pd. The results obtained form a basis for the development of a novel radiopharmaceutical for intratissue radionuclide therapy of tumor diseases.
机译:白蛋白微球(AMS)对Pd的吸附在很大程度上取决于HCl的浓度,在0.08 M的HCl浓度下达到最大值。在0.08 M的HCl中,Pd的吸附随着平衡浓度的增加而增长。作为〜(103)Pd载体的惰性氯化钯的最佳量为0.6 mg。在这些条件下,白蛋白微球蛋白基质对Pd的吸附效率为70-80%。白蛋白微球中吸附的Pd的减少导致其被微球的蛋白质基质大量保留。实验动物的生物学研究证实了这一点。与未还原的Pd相比,局部施用〜(103)Pd-AMSs后的Pd降低了从肌肉组织中清除核素的速度。获得的结果为开发用于组织内放射性核素治疗肿瘤疾病的新型放射性药物奠定了基础。

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