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针对意外的化学、生物、放射和核暴露的医学应对措施:第二部分 放射和核威胁以及近期应对措施专利综述

Medical countermeasures for unwanted CBRN exposures: part II radiological and nuclear threats with review of recent countermeasure patents.

作者信息

Singh Vijay K, Romaine Patricia L P, Newman Victoria L, Seed Thomas M

机构信息

a Department of Pharmacology and Molecular Therapeutics , F. Edward Hébert School of Medicine, Uniformed Services University of the Health Sciences , Bethesda , MD , USA.

b Armed Forces Radiobiology Research Institute , Uniformed Services University of the Health Sciences , Bethesda , MD , USA.

出版信息

Expert Opin Ther Pat. 2016 Dec;26(12):1399-1408. doi: 10.1080/13543776.2016.1231805. Epub 2016 Sep 9.

Abstract

The global threat of a chemical, biological, radiological, or nuclear (CBRN) disaster is an important priority for all government agencies involved in domestic security and public health preparedness. Radiological/nuclear (RN) attacks or accidents have become a larger focus of the United States Food and Drug administration (US FDA) over time because of their increased likeliness. Clinical signs and symptoms of a developing acute radiation syndrome (ARS) are grouped into three sub-syndromes named for the dominant organ system affected, namely the hematopoietic (H-ARS), gastrointestinal (GI-ARS), and neurovascular systems. The availability of safe and effective countermeasures against radiological/nuclear threats currently represents a significant unmet medical need. Areas covered: This article reviews the development of RN threat medical countermeasures and highlights those specific countermeasures that have been recently patented and approved following the FDA Animal Rule. Patents for such agents from 2015 have been presented. Expert opinion: Two granulocyte colony-stimulating factor (G-CSF)-based radiation countermeasures (Neupogen® (Amgen, Thousand Oaks, CA) and Neulasta® (Amgen, Thousand Oaks, CA)) have recently been approved by the FDA for treatment of H-ARS and both these agents are radiomitigators, used after radiation exposure. To date, there are no FDA-approved radioprotectors for ARS.

摘要

化学、生物、放射或核(CBRN)灾难的全球威胁是所有参与国内安全和公共卫生防范的政府机构的一项重要优先事项。随着时间的推移,放射/核(RN)袭击或事故因其可能性增加而成为美国食品药品监督管理局(US FDA)更为关注的焦点。正在发展的急性放射综合征(ARS)的临床体征和症状分为三个子综合征,根据受影响的主要器官系统命名,即造血系统(H-ARS)、胃肠道系统(GI-ARS)和神经血管系统。目前,针对放射/核威胁的安全有效对策的可用性代表了一项重大未满足的医疗需求。涵盖领域:本文回顾了RN威胁医疗对策的发展,并重点介绍了那些最近根据FDA动物规则获得专利并获批的具体对策。列出了2015年以来此类药剂的专利。专家意见:两种基于粒细胞集落刺激因子(G-CSF)的辐射对策(Neupogen®(安进公司,加利福尼亚州千橡市)和Neulasta®(安进公司,加利福尼亚州千橡市))最近已获FDA批准用于治疗H-ARS,这两种药剂都是辐射缓解剂,在辐射暴露后使用。迄今为止,尚无FDA批准的用于ARS的辐射防护剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c34/5152556/a6f5b53226d5/ietp_a_1231805_f0001_b.jpg

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