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Recent gene delivery patents for treatment of atherosclerosis

机译:最近的基因递送专利用于治疗动脉粥样硬化

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摘要

Around the world, cardiovascular disorders are increasing in prevalence. Atherosclerosis acts as a silent disease, involving the build-up of a plaque in the arteries, restricting blood flow and leading organ failure, such as a heart attack or stroke [1]. Current therapeutic approaches to the disease involve lipid-lowering pharmaceutical, in combination with anti-inflammatory medication. In extreme cases, the plaque can be surgically removed. Statins, fibrates, bile acid binding resins and antihypertensive drugs can all be used to lower lipid levels, but often come with adverse side effects and high-risk profiles, for example statins can cause muscle aches and tenderness [2]. More recent novel treatment strategies, such as HDL mimetics, stearoyl-CoA desaturase regulators and purinergic receptor modulators, have not achieved clinical success, so there is still a need for an alternative way to effectively treat atherosclerosis without side effects. Gene therapy may have the potential to fill this gap by correcting the underlying cause of disease. The field has recently attracted wide interest from the researchers, as a potential source of therapies for cancer, cardiovascular, neurological, infectious and other diseases [3].
机译:在世界各地,心血管障碍患病率增加。动脉粥样硬化是一种沉默疾病,涉及动脉中斑块的积聚,限制血液流动和前导器失效,例如心脏病发作或中风[1]。目前对疾病的治疗方法涉及降脂药物,与抗炎药组合。在极端情况下,可以手术地移除牙菌斑。他汀类药物,纤维剂,胆汁酸结合树脂和抗高血压药物都可以用于降低脂质水平,但通常具有不利的副作用和高风险谱,例如他汀类药物会导致肌肉酸痛和柔软[2]。更新的新型治疗策略,如HDL模拟物,硬脂酰基去脱硫酶调节剂和嘌呤能受体调节剂,仍未实现临床成功,因此仍然需要一种有效治疗动脉粥样硬化而无需副作用的替代方法。基因治疗可以通过校正疾病的潜在原因来填补这种差距。该领域最近吸引了研究人员的广泛兴趣,作为癌症,心血管,神经学,传染病和其他疾病的潜在疗法来源[3]。

著录项

  • 来源
    《Pharmaceutical patent analyst》 |2018年第3期|共3页
  • 作者

    Ambikanan Misra;

  • 作者单位

    Faculty of Pharmacy The Maharaja Sayajirao University of Baroda Kalabhavan Campus Vadodara;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 药学;
  • 关键词

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