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载磺胺嘧啶聚乙二醇前药的制备及抗菌性能研究

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以不同分子量的聚乙二醇(PEG)与一氯乙酸为原料,通过酯化反应合成氯乙酰聚乙二醇酯,将它与抗菌剂磺胺嘧啶(SD)结合制备了不同分子量的PEG-SD前药,并进行了红外、核磁和紫外的表征.结果表明,磺胺嘧啶成功接载到聚乙二醇链末端.随着聚乙烯醇的分子量降低,其酯化程度增加,接负SD的比例增加.水解实验表明,PEG-SD前药具有长效缓释抗菌的功能.随着分子量的降低,抑菌效果越好.PEG600-SD对大肠杆菌和金黄色葡萄球菌的最小抑菌浓度分别为31.25 μg·mL-1和15.62 μg·mL-1,具有最好的抑菌效果.
Preparation and Antibacterial Properties of Sulfadiazine Loaded Polyethylene Glycol Prodrugs
Using polyethylene glycol(PEG)with different molecular weights and monochloroacetic acid as raw materials,chloroacetyl polyethylene glycol ester was synthesized by esterification,and PEG-SD prodrugs with different molecular weights were prepared by combining it with sulfadiazine(SD),and were characterized by IR,NMR and UV.The results showed that sulfamethoxazole was successfully loaded onto the end of the polyethylene glycol chain.As the molecular weight of polyvinyl alcohol decreased,its esterification degree increased and the proportion of negative SD increased.Hydrolysis experiments showed that PEG-SD prodrug had a long-lasting sustained-release antibacterial function.As the molecular weight decreased,the antibacterial effect became better.The minimum inhibitory concentrations of PEG600-SD against Escherichia coli and Staphylococcus aureus were 31.25 μg·mL-1 and 15.62 μg·mL-1,respectively,it had the best antibacterial effect.

Polyethylene glycolSulfadiazineEsterificationPolymeric prodrug

常军、曹晓蝶、刘岩、靳梦月、谭忠阳

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沈阳理工大学材料科学与工程学院,辽宁 沈阳 110159

聚乙二醇 磺胺嘧啶 酯化反应 高分子前药

国家自然科学基金项目

52203063

2024

辽宁化工
辽宁省化工学会

辽宁化工

影响因子:0.234
ISSN:1004-0935
年,卷(期):2024.53(8)