The effects of penicillin potassium salt （PenK） on the solubility, Krafft temperature TK, critical micelle concentration CMC of SDS micelle and the phase behavior of SDS/n-C5H11OH/H2O system were studied. The partia...The effects of penicillin potassium salt （PenK） on the solubility, Krafft temperature TK, critical micelle concentration CMC of SDS micelle and the phase behavior of SDS/n-C5H11OH/H2O system were studied. The partial phase diagrams of SDS/PenK/H2O system at different temperatures were determined. The release amounts of PenK in SDS/n-C5H11OH/H2O system and the distribution coefficient of PenK between micelle and water were measured by UV-Vis spectroscopy. The results show that in the presence of PenK, the CMC of SDS was decreased while the TK of SDS was increased and the solubility of SDS in both water and SDS/n-C5H11OH/H2O oil in water （O/W） microemulsion was decreased, but increased in water in oil （W/O） microemulsion. SDS micelles and SDS/n- C5H11OH/H20 O/W microemulsion could accelerate the release rate of PenK. The addition of SDS and water could both increase the release rate of PenK, whereas the presence of n-C5H11OH reduced the release rate of PenK. The above results were related to the electrostatic repulsion between PenK and SDS.展开更多
为确定青霉素G钾(penicillin G potassium,PG)在土壤中的半衰期和降解动力学,选择灭菌与未灭菌、施肥与未施肥蔬菜地土壤作为基质,研究了PG在不同基质中的降解曲线,并拟合了降解动力学方程。结果表明,PG在蔬菜地土壤中的半衰期为1.61~1....为确定青霉素G钾(penicillin G potassium,PG)在土壤中的半衰期和降解动力学,选择灭菌与未灭菌、施肥与未施肥蔬菜地土壤作为基质,研究了PG在不同基质中的降解曲线,并拟合了降解动力学方程。结果表明,PG在蔬菜地土壤中的半衰期为1.61~1.67 d,最终降解率均达到99.7%以上,但PG不会完全降解,仍会以较低的水平(21~73μg·kg^-1)在土壤中长期存在。降解动力学方程拟合结果表明,PG的初始浓度会对降解速率产生影响,初始浓度越高,降解速率越快。在灭菌与未灭菌土壤中降解曲线显示其降解过程受生物和非生物作用共同影响,但添加有机肥的降解过程和未添加组没有显著差异。由于PG在土壤中不能被完全降解,从而增加了诱导抗性基因产生及转移的风险。展开更多
Injury to peripheral nerves during injections of therapeutic agents such as penicillin G potas-sium is common in developing countries. It has been shown that cyclosporin A, a powerful immunosuppressive agent, can reta...Injury to peripheral nerves during injections of therapeutic agents such as penicillin G potas-sium is common in developing countries. It has been shown that cyclosporin A, a powerful immunosuppressive agent, can retard Wallerian degeneration after peripheral nerve crush injury. However, few studies are reported on the effects of cyclosporin A on peripheral nerve drug in-jection injury. This study aimed to assess the time-dependent efifcacy of cyclosporine-A as an immunosuppressant therapy in an experimental rat nerve injection injury model established by penicillin G potassium injection. The rats were randomly divided into three groups based on the length of time after nerve injury induced by cyclosporine-A administration （30 minutes, 8 or 24 hours）. The compound muscle action potentials were recorded pre-injury, early post-injury （within 1 hour） and 4 weeks after injury and compared statistically. Tissue samples were taken from each animal for histological analysis. Compared to the control group, a significant im-provement of the compound muscle action potential amplitude value was observed only when cyclosporine-A was administered within 30 minutes of the injection injury （P 〈 0.05）; at 8 or 24 hours after cyclosporine-A administration, compound muscle action potential amplitude was not changed compared with the control group. Thus, early immunosuppressant drug therapy may be a good alternative neuroprotective therapy option in experimental nerve injection injury induced by penicillin G potassium injection.展开更多
基金ProJect supported by the National Natural Science Foundation of China （No. 20233010）.
文摘The effects of penicillin potassium salt （PenK） on the solubility, Krafft temperature TK, critical micelle concentration CMC of SDS micelle and the phase behavior of SDS/n-C5H11OH/H2O system were studied. The partial phase diagrams of SDS/PenK/H2O system at different temperatures were determined. The release amounts of PenK in SDS/n-C5H11OH/H2O system and the distribution coefficient of PenK between micelle and water were measured by UV-Vis spectroscopy. The results show that in the presence of PenK, the CMC of SDS was decreased while the TK of SDS was increased and the solubility of SDS in both water and SDS/n-C5H11OH/H2O oil in water （O/W） microemulsion was decreased, but increased in water in oil （W/O） microemulsion. SDS micelles and SDS/n- C5H11OH/H20 O/W microemulsion could accelerate the release rate of PenK. The addition of SDS and water could both increase the release rate of PenK, whereas the presence of n-C5H11OH reduced the release rate of PenK. The above results were related to the electrostatic repulsion between PenK and SDS.
文摘为确定青霉素G钾(penicillin G potassium,PG)在土壤中的半衰期和降解动力学,选择灭菌与未灭菌、施肥与未施肥蔬菜地土壤作为基质,研究了PG在不同基质中的降解曲线,并拟合了降解动力学方程。结果表明,PG在蔬菜地土壤中的半衰期为1.61~1.67 d,最终降解率均达到99.7%以上,但PG不会完全降解,仍会以较低的水平(21~73μg·kg^-1)在土壤中长期存在。降解动力学方程拟合结果表明,PG的初始浓度会对降解速率产生影响,初始浓度越高,降解速率越快。在灭菌与未灭菌土壤中降解曲线显示其降解过程受生物和非生物作用共同影响,但添加有机肥的降解过程和未添加组没有显著差异。由于PG在土壤中不能被完全降解,从而增加了诱导抗性基因产生及转移的风险。
文摘Injury to peripheral nerves during injections of therapeutic agents such as penicillin G potas-sium is common in developing countries. It has been shown that cyclosporin A, a powerful immunosuppressive agent, can retard Wallerian degeneration after peripheral nerve crush injury. However, few studies are reported on the effects of cyclosporin A on peripheral nerve drug in-jection injury. This study aimed to assess the time-dependent efifcacy of cyclosporine-A as an immunosuppressant therapy in an experimental rat nerve injection injury model established by penicillin G potassium injection. The rats were randomly divided into three groups based on the length of time after nerve injury induced by cyclosporine-A administration （30 minutes, 8 or 24 hours）. The compound muscle action potentials were recorded pre-injury, early post-injury （within 1 hour） and 4 weeks after injury and compared statistically. Tissue samples were taken from each animal for histological analysis. Compared to the control group, a significant im-provement of the compound muscle action potential amplitude value was observed only when cyclosporine-A was administered within 30 minutes of the injection injury （P 〈 0.05）; at 8 or 24 hours after cyclosporine-A administration, compound muscle action potential amplitude was not changed compared with the control group. Thus, early immunosuppressant drug therapy may be a good alternative neuroprotective therapy option in experimental nerve injection injury induced by penicillin G potassium injection.
