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99mTc-prulifloxacin in artificially infected animals. Radiosynthesis and biological evaluation.

机译:人工感染动物中的99mTc-普鲁沙星。放射合成和生物学评估。

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Aim: The radiosynthesis of 99mTc-Prulifloxacin (99mTc-PRN) was assessed in terms of stability, binding with Staphylococcus aureus (S. aureus), biodistribution in rats (RT) and scintigraphic profile in rabbits (RB). Animals, material, methods: 99mTc-PRN was synthesized by mixing 25 microg of stannous fluoride (SnF2) with 18.5 MBq of sodium pertechnetate. Thereafter, 0.5 mg of the prufloxacin (PRN) was added to the reaction mixture and the pH was set at 5.1 with 0.01 mol/l HCl. The reaction mixture was incubated at room temperature. The same process was repeated by increasing the concentration of the stannous fluoride from 25 to 250 microg, sodium pertechnetate from 18,5 to 185 MBq and the PRN from 0.5 to 5 mg. The radiochemical stability of the 99mTc-PRN was investigated in higher concentration of the cystein. In-vitro binding investigation was performed using living and heat killed S. aureus to verify specificity of the 99mTc-PRN. Biodistribution was evaluated in artificially infected rats and scintigraphic precision in rabbits at different interval. Results: The 99mTc-RPN prepared by mixing 2 mg of PRN, 74 MBq sodium pertechnetate, 100 microg stannous fluoride at pH 5.4, appeared to be more than 90% stable with a maximum radiochemical yield of 98.15 +/- 0.25% at 30 min. The 99mTc-PRN showed higher stability in serum and satisfactory in-vitro binding to living as compared to heat killed S. aureus. 14.25 +/- 0.15% of the injected dose was accumulated in the infected muscle of the model RT. Infected to normal muscle ratio was 5.12 and inflamed to normal muscle was 1.2. The biodistribution was validated by the scintigraphic localization of infection in rabbits. Conclusion: This investigation of 99mTc-PRN confirmed its momentous radiochemical immovability in saline, serum, preferential in-vitro binding to living bacteria, higher uptake in the infected muscle of model RT and precise localization in the infected muscle of model RB.
机译:目的:从稳定性,与金黄色葡萄球菌(金黄色葡萄球菌)的结合,大鼠体内的生物分布(RT)和兔的闪烁显像特征(RB)方面评估99mTc-普鲁利沙星(99mTc-PRN)的放射合成。动物,材料,方法:通过将25微克氟化亚锡(SnF2)与18.5 MBq高tech酸钠混合来合成99mTc-PRN。此后,将0.5mg普鲁沙星(PRN)加入反应混合物中,并用0.01mol / l HCl将pH设置为5.1。将反应混合物在室温下孵育。通过将氟化亚锡的浓度从25微克增加到250微克,高tech酸钠从18,5 MB增加到185 MBq,将PRN从0.5毫克增加到5毫克来重复相同的过程。在高浓度的半胱氨酸中研究了99mTc-PRN的放射化学稳定性。使用活的和热杀死的金黄色葡萄球菌进行体外结合研究,以验证99mTc-PRN的特异性。在不同的时间间隔评估人工感染大鼠的生物分布和兔的闪烁显像精度。结果:在pH 5.4下,将2 mg PRN,74 MBq高per酸钠,100 microg氟化亚锡混合制备的99mTc-RPN表现出超过90%的稳定性,在30分钟时的最大放射化学产率为98.15 +/- 0.25%。 。与热灭活的金黄色葡萄球菌相比,99mTc-PRN在血清中显示出更高的稳定性,并具有令人满意的体外结合生活能力。在RT模型的感染肌肉中累积了14.25 +/- 0.15%的注射剂量。感染与正常肌肉的比率为5.12,发炎至正常肌肉的比率为1.2。通过对兔子的感染进行闪烁显像定位来验证生物分布。结论:对99mTc-PRN的这项研究证实了其在盐水,血清中的瞬时放射化学不可移动性,与活菌的优先体外结合,RT模型感染肌肉的更高摄取以及RB模型感染肌肉的精确定位。

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