Institute of Pharmaceutical Sciences, Department of Chemistry and Applied Biosciences, ETH Zurich, 8093 Zurich, Switzerland.
Soft Matter. 2020 Mar 18;16(11):2725-2735. doi: 10.1039/d0sm00183j.
Transmembrane pH gradient poly(isoprene)-block-poly(ethylene glycol) (PI-b-PEG) polymersomes were investigated for their potential use in the detoxification of ammonia, a metabolite that is excessively present in patients suffering from urea cycle disorders and advanced liver diseases, and which causes neurotoxic effects (e.g., hepatic encephalopathy). Polymers varying in PI and PEG block length were synthesized via nitroxide-mediated polymerization and screened for their ability to self-assemble into polymersomes in aqueous media. Ammonia sequestration by the polymersomes was investigated in vitro. While most vesicular systems were able to capture ammonia in simulated intestinal fluids, uptake was lost in partially dehydrated medium mimicking conditions in the colon. Polymeric crosslinking of residual olefinic bonds in the PI block increased polymersome stability, partially preserving the ammonia capture capacity in the simulated colon environment. These more stable vesicular systems hold promise for the chronic oral treatment of hyperammonemia.
研究了跨膜 pH 梯度聚异戊二烯嵌段聚乙二醇(PI-b-PEG)聚合物囊泡在解毒氨方面的潜在应用,氨是尿素循环紊乱和晚期肝病患者中过度存在的代谢物,会引起神经毒性作用(例如肝性脑病)。通过氮氧自由基介导的聚合合成了具有不同 PI 和 PEG 嵌段长度的聚合物,并筛选其在水介质中自组装成聚合物囊泡的能力。在体外研究了聚合物囊泡对氨的螯合作用。虽然大多数囊泡系统能够在模拟肠液中捕获氨,但在部分脱水介质中,模拟结肠条件下,摄取会丢失。PI 嵌段中残留的烯键的聚合交联增加了聚合物囊泡的稳定性,部分保留了在模拟结肠环境中的氨捕获能力。这些更稳定的囊泡系统有望用于慢性口服高氨血症的治疗。