Azzopardi Ernest A, Ferguson Elaine L, Thomas David W
Advanced Therapies Group, School of Dentistry, Cardiff University, Heath Park, Cardiff, United Kingdom The Welsh Centre for Burns and Plastic Surgery, Morriston Hospital, Swansea, United Kingdom
Advanced Therapies Group, School of Dentistry, Cardiff University, Heath Park, Cardiff, United Kingdom.
Antimicrob Agents Chemother. 2015 Apr;59(4):1837-43. doi: 10.1128/AAC.03708-14. Epub 2014 Dec 15.
This study describes the use of a novel, two-compartment, static dialysis bag model to study the release, diffusion, and antibacterial activity of a novel, bioresponsive dextrin-colistin polymer conjugate against multidrug resistant (MDR) wild-type Acinetobacter baumannii. In this model, colistin sulfate, at its MIC, produced a rapid and extensive drop in viable bacterial counts (<2 log10 CFU/ml at 4 h); however, a marked recovery was observed thereafter, with regrowth equivalent to that of control by 48 h. In contrast, dextrin-colistin conjugate, at its MIC, suppressed bacterial growth for up to 48 h, with 3 log10 CFU/ml lower bacterial counts after 48 h than those of controls. Doubling the concentration of dextrin-colistin conjugate (to 2× MIC) led to an initial bacterial killing of 3 log10 CFU/ml at 8 h, with a similar regrowth profile to 1× MIC treatment thereafter. The addition of colistin sulfate (1× MIC) to dextrin-colistin conjugate (1× MIC) resulted in undetectable bacterial counts after 4 h, followed by suppressed bacterial growth (3.5 log10 CFU/ml lower than that of control at 48 h). Incubation of dextrin-colistin conjugates with infected wound exudate from a series of burn patients (n = 6) revealed an increasing concentration of unmasked colistin in the outer compartment (OC) over time (up to 86.3% of the initial dose at 48 h), confirming that colistin would be liberated from the conjugate by endogenous α-amylase within the wound environment. These studies confirm the utility of this model system to simulate the pharmacokinetics of colistin formation in humans administered dextrin-colistin conjugates and further supports the development of antibiotic polymer conjugates in the treatment of MDR infections.
本研究描述了一种新型的双室静态透析袋模型的应用,该模型用于研究一种新型生物响应性糊精 - 黏菌素聚合物共轭物对多重耐药(MDR)野生型鲍曼不动杆菌的释放、扩散及抗菌活性。在该模型中,硫酸黏菌素在其最低抑菌浓度(MIC)下,可使活菌数迅速大幅下降(4小时时<2 log10 CFU/ml);然而,此后观察到明显的恢复,到48小时时细菌再生长情况与对照组相当。相比之下,糊精 - 黏菌素共轭物在其MIC下可抑制细菌生长长达48小时,48小时后细菌数比对照组低3 log10 CFU/ml。将糊精 - 黏菌素共轭物浓度加倍(至2×MIC),在8小时时可使细菌初始杀灭量达到3 log10 CFU/ml,此后其再生长情况与1×MIC处理相似。向糊精 - 黏菌素共轭物(1×MIC)中添加硫酸黏菌素(1×MIC),4小时后细菌数降至检测不到,随后细菌生长受到抑制(48小时时比对照组低3.5 log10 CFU/ml)。用一系列烧伤患者(n = 6)的感染伤口渗出液孵育糊精 - 黏菌素共轭物,结果显示随着时间推移,外室(OC)中未被掩盖的黏菌素浓度增加(48小时时高达初始剂量的86.3%),证实伤口环境中的内源性α - 淀粉酶可使黏菌素从共轭物中释放出来。这些研究证实了该模型系统在模拟给予糊精 - 黏菌素共轭物的人体中黏菌素形成的药代动力学方面的实用性,并进一步支持了抗生素聚合物共轭物在治疗MDR感染方面的开发。