Suppr超能文献

用于心血管系统的药物递送与纳米制剂

Drug Delivery and Nanoformulations for the Cardiovascular System.

作者信息

Geldenhuys W J, Khayat M T, Yun J, Nayeem M A

机构信息

Department of Pharmaceutical Sciences, West Virginia University, School of Pharmacy, Morgantown WV 26506 USA.

Deparment of Pharmaceutical Chemistry, King Abdulaziz University, School of Pharmacy, Jeddah, Saudi Arabia.

出版信息

Res Rev Drug Deliv. 2017 Feb;1(1):32-40. Epub 2017 Mar 7.

Abstract

Therapeutic delivery to the cardiovascular system may play an important role in the successful treatment of a variety of disease state, including atherosclerosis, ischemic-reperfusion injury and other types of microvascular diseases including hypertension. In this review we evaluate the different options available for the development of suitable delivery systems that include the delivery of small organic compounds [adenosin A receptor agonist (CGS 21680), CYP-epoxygenases inhibitor (N-(methylsulfonyl)-2-(2-propynyloxy)-benzenehexanamide, trans-4-[4-(3-adamantan-1-ylureido)cyclohexyloxy] benzoic acid), soluble epoxide hydrolase inhibitor (N-methylsulfonyl-12,12-dibromododec-11-enamide), PPARγ agonist (rosiglitazone) and PPARγ antagonist (T0070907)], nanoparticles, peptides, and siRNA to the cardiovascular system. Effective formulations of nanoproducts have significant potential to overcome physiological barriers and improve therapeutic outcomes in patients. As per the literature covering targeted delivery to the cardiovascular system, we found that this area is still at infancy stage, as compare to the more mature fields of tumor cancer or brain delivery (e.g. blood-brain barrier permeability) with fewer publications focused on the targeted drug delivery technologies. Additionally, we show how pharmacology needs to be well understood when considering the cardiovascular system. Therefore, we discussed in this review various receptors agonists, antagonists, activators and inhibitors which will have effects on cardiovascular system.

摘要

向心血管系统进行治疗性给药可能在多种疾病状态的成功治疗中发挥重要作用,这些疾病包括动脉粥样硬化、缺血再灌注损伤以及其他类型的微血管疾病(包括高血压)。在本综述中,我们评估了可用于开发合适给药系统的不同选择,这些选择包括向心血管系统递送小有机化合物[腺苷A受体激动剂(CGS 21680)、CYP - 环氧酶抑制剂(N -(甲基磺酰基)- 2 -(2 - 丙炔氧基)- 苯己酰胺、反式 - 4 - [4 -(3 - 金刚烷 - 1 - 基脲基)环己氧基]苯甲酸)、可溶性环氧化物水解酶抑制剂(N - 甲基磺酰基 - 12,12 - 二溴十二碳 - 11 - 烯酰胺)、PPARγ激动剂(罗格列酮)和PPARγ拮抗剂(T0070907)]、纳米颗粒、肽和小干扰RNA。纳米产品的有效制剂具有克服生理屏障并改善患者治疗效果的巨大潜力。根据有关心血管系统靶向给药的文献,我们发现与肿瘤癌症或脑部给药等更成熟的领域(例如血脑屏障通透性)相比,该领域仍处于起步阶段,专注于靶向药物递送技术的出版物较少。此外,我们展示了在考虑心血管系统时需要如何充分理解药理学。因此,我们在本综述中讨论了各种对心血管系统有影响的受体激动剂、拮抗剂、激活剂和抑制剂。

相似文献

1
Drug Delivery and Nanoformulations for the Cardiovascular System.
Res Rev Drug Deliv. 2017 Feb;1(1):32-40. Epub 2017 Mar 7.
2
Effect of Soluble Epoxide Hydrolase on the Modulation of Coronary Reactive Hyperemia: Role of Oxylipins and PPARγ.
PLoS One. 2016 Sep 1;11(9):e0162147. doi: 10.1371/journal.pone.0162147. eCollection 2016.
3
The roles of CYP450 epoxygenases and metabolites, epoxyeicosatrienoic acids, in cardiovascular and malignant diseases.
Adv Drug Deliv Rev. 2011 Jul 18;63(8):597-609. doi: 10.1016/j.addr.2011.03.006. Epub 2011 Apr 6.
5
Recent progress of drug nanoformulations targeting to brain.
J Control Release. 2018 Dec 10;291:37-64. doi: 10.1016/j.jconrel.2018.10.004. Epub 2018 Oct 9.
6
Nanoparticle Based Treatment for Cardiovascular Diseases.
Cardiovasc Hematol Disord Drug Targets. 2019;19(1):33-44. doi: 10.2174/1871529X18666180508113253.
7
High salt diet modulates vascular response in A2AAR (+/+) and A 2AAR (-/-) mice: role of sEH, PPARγ, and K ATP channels.
Mol Cell Biochem. 2015 Jun;404(1-2):87-96. doi: 10.1007/s11010-015-2368-4. Epub 2015 Mar 5.
8
Cardiovascular therapies utilizing targeted delivery of nanomedicines and aptamers.
Int J Pharm. 2019 Mar 10;558:413-425. doi: 10.1016/j.ijpharm.2019.01.023. Epub 2019 Jan 18.
10
Nanobiotechnology-based drug delivery in brain targeting.
Curr Pharm Biotechnol. 2013;14(15):1264-74. doi: 10.2174/1389201015666140608143719.

本文引用的文献

1
In vitro 3D model and miRNA drug delivery to target calcific aortic valve disease.
Clin Sci (Lond). 2017 Feb 1;131(3):181-195. doi: 10.1042/CS20160378.
2
Nanomedicine as a strategy to fight thrombotic diseases.
Future Sci OA. 2015 Nov 1;1(4):FSO46. doi: 10.4155/fso.15.46. eCollection 2015 Nov.
3
Heart targeted nanoliposomal/nanoparticles drug delivery: An updated review.
Biomed Pharmacother. 2017 Feb;86:316-323. doi: 10.1016/j.biopha.2016.12.009. Epub 2016 Dec 21.
7
Emerging strategies of targeting lipoprotein lipase for metabolic and cardiovascular diseases.
Drug Discov Today. 2017 Feb;22(2):352-365. doi: 10.1016/j.drudis.2016.10.007. Epub 2016 Oct 19.
8
Effect of Soluble Epoxide Hydrolase on the Modulation of Coronary Reactive Hyperemia: Role of Oxylipins and PPARγ.
PLoS One. 2016 Sep 1;11(9):e0162147. doi: 10.1371/journal.pone.0162147. eCollection 2016.
9
Deletion of soluble epoxide hydrolase enhances coronary reactive hyperemia in isolated mouse heart: role of oxylipins and PPARγ.
Am J Physiol Regul Integr Comp Physiol. 2016 Oct 1;311(4):R676-R688. doi: 10.1152/ajpregu.00237.2016. Epub 2016 Aug 3.
10
Recent Trends in Cardiovascular Mortality in the United States and Public Health Goals.
JAMA Cardiol. 2016 Aug 1;1(5):594-9. doi: 10.1001/jamacardio.2016.1326.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验