Literature DB >> 28713881

Drug Delivery and Nanoformulations for the Cardiovascular System.

W J Geldenhuys1, M T Khayat1,2, J Yun3, M A Nayeem1.   

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 A2A 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.

Entities:  

Keywords:  Cardiac death; Drug delivery; Exosomes; Formulation; Myocardial infarction; Nanoparticles; Targeting; Vascular tone; atherosclerosis

Year:  2017        PMID: 28713881      PMCID: PMC5507069     

Source DB:  PubMed          Journal:  Res Rev Drug Deliv


  74 in total

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Journal:  J Pharmacol Exp Ther       Date:  1999-11       Impact factor: 4.030

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6.  High-salt diet enhances mouse aortic relaxation through adenosine A2A receptor via CYP epoxygenases.

Authors:  Mohammed A Nayeem; Dovenia S Ponnoth; Matthew A Boegehold; Darryl C Zeldin; John R Falck; S Jamal Mustafa
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2008-12-24       Impact factor: 3.619

Review 7.  Preclinical pharmacokinetics: an approach towards safer and efficacious drugs.

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Journal:  Curr Drug Metab       Date:  2006-02       Impact factor: 3.731

8.  Basics and recent advances in peptide and protein drug delivery.

Authors:  Benjamin J Bruno; Geoffrey D Miller; Carol S Lim
Journal:  Ther Deliv       Date:  2013-11

9.  Pioglitazone-Incorporated Nanoparticles Prevent Plaque Destabilization and Rupture by Regulating Monocyte/Macrophage Differentiation in ApoE-/- Mice.

Authors:  Soichi Nakashiro; Tetsuya Matoba; Ryuta Umezu; Jun-Ichiro Koga; Masaki Tokutome; Shunsuke Katsuki; Kaku Nakano; Kenji Sunagawa; Kensuke Egashira
Journal:  Arterioscler Thromb Vasc Biol       Date:  2016-01-28       Impact factor: 8.311

10.  Therapeutic siRNA silencing in inflammatory monocytes in mice.

Authors:  Florian Leuschner; Partha Dutta; Rostic Gorbatov; Tatiana I Novobrantseva; Jessica S Donahoe; Gabriel Courties; Kang Mi Lee; James I Kim; James F Markmann; Brett Marinelli; Peter Panizzi; Won Woo Lee; Yoshiko Iwamoto; Stuart Milstein; Hila Epstein-Barash; William Cantley; Jamie Wong; Virna Cortez-Retamozo; Andita Newton; Kevin Love; Peter Libby; Mikael J Pittet; Filip K Swirski; Victor Koteliansky; Robert Langer; Ralph Weissleder; Daniel G Anderson; Matthias Nahrendorf
Journal:  Nat Biotechnol       Date:  2011-10-09       Impact factor: 54.908

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  2 in total

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2.  PPARα ligand, AVE8134, and cyclooxygenase inhibitor therapy synergistically suppress lung cancer growth and metastasis.

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Journal:  BMC Cancer       Date:  2019-12-02       Impact factor: 4.430

  2 in total

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