Targeting ischemic penumbra Part II: selective drug delivery using liposome technologies.

Shimin Liu, Steven R Levine, H Richard Winn
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引用次数: 19

Abstract

In the present review (part II), we discuss the challenges and promises of selective drug delivery to ischemic brain tissue by liposome technologies. In part I of this serial review, we proposed "selective drug delivery to ischemic brain tissue" as a technique for neuroprotective treatment of acute ischemic stroke. To be effective, drugs must pass a series of barriers to arrive at ischemic brain. Brain ischemia results in metabolic and structural changes in the ischemic region, which cause additional obstacles for drug delivery. Liposome drug delivery system can pass these barriers and selectively target ischemic tissue by utilizing ischemia-induced changes in metabolism and molecular structure.

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靶向缺血半暗区第二部分:脂质体技术的选择性给药。
在目前的回顾(第二部分)中,我们讨论了脂质体技术选择性给药缺血性脑组织的挑战和前景。在本系列综述的第一部分中,我们提出了“选择性给药缺血性脑组织”作为急性缺血性卒中神经保护治疗的一种技术。为了有效,药物必须通过一系列障碍才能到达缺血的大脑。脑缺血导致缺血区域的代谢和结构变化,这对药物递送造成了额外的障碍。脂质体给药系统可以通过这些屏障,利用缺血引起的代谢和分子结构的变化,选择性地靶向缺血组织。
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Chemokine receptor-like 2 is involved in ischemic brain injury. Chemokine receptor-like 2 is involved in ischemic brain injury. Acute bioenergetic intervention or pharmacological preconditioning protects neuron against ischemic injury. Acute bioenergetic intervention or pharmacological preconditioning protects neuron against ischemic injury. Strategies for therapeutic hypometabothermia.
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