Liposome-Supported Peritoneal Dialysis for the Treatment of Hyperammonemia-Associated Encephalopathy

被引:26
作者
Agostoni, Valentina [1 ]
Lee, Soo Hyeon [1 ]
Forster, Vincent [2 ]
Kabbaj, Meriam [2 ]
Bosoi, Cristina R. [3 ]
Tremblay, Melanie [3 ]
Zadory, Matthias [1 ]
Rose, Christopher F. [3 ]
Leroux, Jean-Christophe [1 ]
机构
[1] Swiss Fed Inst Technol, Inst Pharmaceut Sci, Dept Chem & Appl Biosci, Vladimir Prelog Weg 1-5-10, CH-8093 Zurich, Switzerland
[2] Versantis AG, Otto Stern Weg 7, CH-8093 Zurich, Switzerland
[3] Univ Montreal, Hepatoneuro Lab, Ctr Hosp Univ Montreal, 900 St Denis, Montreal, PQ H2X0A9, Canada
关键词
INBORN-ERRORS; HEPATIC-ENCEPHALOPATHY; INFUSION REACTIONS; PORCINE MODEL; LIVER-FAILURE; AMMONIA; METABOLISM; BRAIN; HEMODIALYSIS; DOXORUBICIN;
D O I
10.1002/adfm.201603519
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Hyperammonemia can lead to cerebral dysfunction, encephalopathy, coma, and death if not treated adequately. The poor prognosis associated with this condition reflects the unmet medical need for effective ammonia-lowering treatments. Here, the translational potential of liposome-supported peritoneal dialysis (LSPD), a recently-developed detoxification strategy for the removal of small ionizable molecules like ammonia, is described. Dialysis fluids supplemented with micrometer-sized, transmembrane pH-gradient liposomes are prepared via an innovative, osmotic shock-based method overcoming sterilization and long-term stability issues. LSPD is able to sequester ammonia in healthy rats in relation to the injected dose, buffering capacity of the liposomal core, and membrane composition. In a rat model of cirrhosis, LSPD outperforms conventional peritoneal dialysis in lowering plasmatic ammonia levels and attenuating brain edema. LSPD does not trigger any hypersensitive reaction in pigs, a side effect commonly observed upon the injection of colloids in this animal model and in humans. These findings support the development of LSPD for the treatment of hyperammonemia-induced encephalopathy.
引用
收藏
页码:8382 / 8389
页数:8
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