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Intranasal administration delivers peptoids to the rat central nervous system.

机译:鼻内给药将类肽递送至大鼠中枢神经系统。

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摘要

Intranasal administration of therapeutic agents offers a noninvasive method of drug delivery that bypasses the blood-brain barrier and directly targets the central nervous system (CNS) and lymph nodes. We examined whether intranasal peptoid CHIR5585, an antagonist of the urokinase plasminogen activator receptor (uPAR), is delivered to the CNS. Peptoids are a novel class of peptide isomers that are oligomeric N-substituted glycine peptides. Anesthetized male rats were administered peptoid CHIR5585 intranasally, and tissue distribution was evaluated quantitatively by gamma counting and qualitatively by autoradiography. Intranasal administration resulted in significant delivery throughout the CNS (olfactory bulbs, 3.9microM; cortex, 0.3microM; trigeminal nerve, 1.7microM) and deep cervical lymph nodes (4.5microM). Autoradiography demonstrated a similar delivery pattern to the CNS.
机译:鼻内给药治疗剂提供了一种无创的药物输送方法,该方法绕过了血脑屏障,直接靶向中枢神经系统(CNS)和淋巴结。我们检查了鼻内类肽CHIR5585(尿激酶纤溶酶原激活物受体(uPAR)的拮抗剂)是否被递送至中枢神经系统。类肽是一类新型的肽异构体,其是寡聚的N-取代的甘氨酸肽。给麻醉的雄性大鼠鼻内给予类肽CHIR5585,并通过γ计数定量评估组织分布,并通过放射自显影定性评估组织分布。鼻内给药导致整个中枢神经系统(嗅球,3.9microM;皮质,0.3microM;三叉神经,1.7microM)和深颈淋巴结(4.5microM)的大量递送。放射自显影显示出与中枢神经系统相似的递送模式。

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