HI-6-Loaded Vehicle of Liposomes Mediated by an Amphiphilic Pillar[5]arene against Paraoxon Poisoning.
Ziliang ZhangShujie LinXiang YuJie JingYahan ZhangLongming ChenJiaqi HanZhao MengJunyi ChenQingbin MengPublished in: ACS applied materials & interfaces (2024)
Organophosphate (OP) intoxication has become a severe common health matter all over the world. For the treatment of acute OP poisoning, the effective intracerebral delivery of acetylcholinesterase reactivators is crucial. Here, an amphiphilic hydrazide-pillar[5]arene (HP5A-6C), which could be readily integrated into liposomal bilayers' zwitterionic disaturated phosphatidylcholine (DSPC), was synthesized. A T7 peptide-containing guest (G) was attached on the surface via a noncovalent interaction to make mixed liposomes a particularly appealing candidate for brain-targeting delivery. Such coassembly could remain stable at room temperature for up to 6 weeks, and safety evaluations initially verified its fine biological compatibility. The hydrophilic interiors of T7/HP5A-6C@DSPC could further load HI-6 with 89.70% encapsulation efficiency. Support for brain-targeting potency came from imaging results. Notably, intravenous injection of HI-6-loaded vesicles exhibited a remarkable therapeutic effect on paraoxon (POX)-poisoned mice, effectively alleviating seizures and brain damage and significantly increasing the improving survival rate to 60% over the course of 7 days.
Keyphrases
- drug delivery
- room temperature
- cancer therapy
- resting state
- white matter
- functional connectivity
- healthcare
- water soluble
- public health
- cerebral ischemia
- high resolution
- drug release
- liver failure
- drug induced
- air pollution
- mental health
- multiple sclerosis
- metabolic syndrome
- high dose
- intensive care unit
- health information
- wound healing
- ultrasound guided
- aortic dissection
- combination therapy
- risk assessment
- hepatitis b virus
- insulin resistance
- gestational age
- blood brain barrier
- smoking cessation