Recent Advances of Cell Membrane Coated Nanoparticles in Treating Cardiovascular Disorders
Cardiovascular diseases (CVDs) are the leading cause of death worldwide, causing approximately 17.9 million deaths annually, an estimated 31% of all deaths, according to the WHO. CVDs are essentially rooted in atherosclerosis and are clinically classified into coronary heart disease, stroke and peri...
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Published in | Molecules (Basel, Switzerland) Vol. 26; no. 11; p. 3428 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
MDPI AG
05.06.2021
MDPI |
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Online Access | Get full text |
ISSN | 1420-3049 1420-3049 |
DOI | 10.3390/molecules26113428 |
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Abstract | Cardiovascular diseases (CVDs) are the leading cause of death worldwide, causing approximately 17.9 million deaths annually, an estimated 31% of all deaths, according to the WHO. CVDs are essentially rooted in atherosclerosis and are clinically classified into coronary heart disease, stroke and peripheral vascular disorders. Current clinical interventions include early diagnosis, the insertion of stents, and long-term preventive therapy. However, clinical diagnostic and therapeutic tools are subject to a number of limitations including, but not limited to, potential toxicity induced by contrast agents and unexpected bleeding caused by anti-platelet drugs. Nanomedicine has achieved great advancements in biomedical area. Among them, cell membrane coated nanoparticles, denoted as CMCNPs, have acquired enormous expectations due to their biomimetic properties. Such membrane coating technology not only helps avoid immune clearance, but also endows nanoparticles with diverse cellular and functional mimicry. In this review, we will describe the superiorities of CMCNPs in treating cardiovascular diseases and their potentials in optimizing current clinical managements. |
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AbstractList | Cardiovascular diseases (CVDs) are the leading cause of death worldwide, causing approximately 17.9 million deaths annually, an estimated 31% of all deaths, according to the WHO. CVDs are essentially rooted in atherosclerosis and are clinically classified into coronary heart disease, stroke and peripheral vascular disorders. Current clinical interventions include early diagnosis, the insertion of stents, and long-term preventive therapy. However, clinical diagnostic and therapeutic tools are subject to a number of limitations including, but not limited to, potential toxicity induced by contrast agents and unexpected bleeding caused by anti-platelet drugs. Nanomedicine has achieved great advancements in biomedical area. Among them, cell membrane coated nanoparticles, denoted as CMCNPs, have acquired enormous expectations due to their biomimetic properties. Such membrane coating technology not only helps avoid immune clearance, but also endows nanoparticles with diverse cellular and functional mimicry. In this review, we will describe the superiorities of CMCNPs in treating cardiovascular diseases and their potentials in optimizing current clinical managements. Cardiovascular diseases (CVDs) are the leading cause of death worldwide, causing approximately 17.9 million deaths annually, an estimated 31% of all deaths, according to the WHO. CVDs are essentially rooted in atherosclerosis and are clinically classified into coronary heart disease, stroke and peripheral vascular disorders. Current clinical interventions include early diagnosis, the insertion of stents, and long-term preventive therapy. However, clinical diagnostic and therapeutic tools are subject to a number of limitations including, but not limited to, potential toxicity induced by contrast agents and unexpected bleeding caused by anti-platelet drugs. Nanomedicine has achieved great advancements in biomedical area. Among them, cell membrane coated nanoparticles, denoted as CMCNPs, have acquired enormous expectations due to their biomimetic properties. Such membrane coating technology not only helps avoid immune clearance, but also endows nanoparticles with diverse cellular and functional mimicry. In this review, we will describe the superiorities of CMCNPs in treating cardiovascular diseases and their potentials in optimizing current clinical managements.Cardiovascular diseases (CVDs) are the leading cause of death worldwide, causing approximately 17.9 million deaths annually, an estimated 31% of all deaths, according to the WHO. CVDs are essentially rooted in atherosclerosis and are clinically classified into coronary heart disease, stroke and peripheral vascular disorders. Current clinical interventions include early diagnosis, the insertion of stents, and long-term preventive therapy. However, clinical diagnostic and therapeutic tools are subject to a number of limitations including, but not limited to, potential toxicity induced by contrast agents and unexpected bleeding caused by anti-platelet drugs. Nanomedicine has achieved great advancements in biomedical area. Among them, cell membrane coated nanoparticles, denoted as CMCNPs, have acquired enormous expectations due to their biomimetic properties. Such membrane coating technology not only helps avoid immune clearance, but also endows nanoparticles with diverse cellular and functional mimicry. In this review, we will describe the superiorities of CMCNPs in treating cardiovascular diseases and their potentials in optimizing current clinical managements. |
Author | Wang, Qiwen Zhu, Chaojie Ma, Junkai Ji, Zhiheng Shen, Jie |
AuthorAffiliation | 2 Chu Kochen Honors College, Zhejiang University, Hangzhou 310058, China; 3180101531@zju.edu.cn (J.M.); 3180103158@zju.edu.cn (Z.J.) 1 Department of Cardiology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China; 3180101530@zju.edu.cn 3 Institute of Pharmaceutics, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, China 4 Department of Pharmacy, School of Medicine, Zhejiang University City College, Hangzhou 310015, China |
AuthorAffiliation_xml | – name: 1 Department of Cardiology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China; 3180101530@zju.edu.cn – name: 2 Chu Kochen Honors College, Zhejiang University, Hangzhou 310058, China; 3180101531@zju.edu.cn (J.M.); 3180103158@zju.edu.cn (Z.J.) – name: 3 Institute of Pharmaceutics, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, China – name: 4 Department of Pharmacy, School of Medicine, Zhejiang University City College, Hangzhou 310015, China |
Author_xml | – sequence: 1 givenname: Chaojie orcidid: 0000-0002-9375-6725 surname: Zhu fullname: Zhu, Chaojie – sequence: 2 givenname: Junkai surname: Ma fullname: Ma, Junkai – sequence: 3 givenname: Zhiheng surname: Ji fullname: Ji, Zhiheng – sequence: 4 givenname: Jie surname: Shen fullname: Shen, Jie – sequence: 5 givenname: Qiwen orcidid: 0000-0002-4255-3960 surname: Wang fullname: Wang, Qiwen |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/34198794$$D View this record in MEDLINE/PubMed |
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SubjectTerms | Anticoagulants Atherosclerosis Biomimetic Materials - chemical synthesis Biomimetic Materials - chemistry Biomimetic Materials - therapeutic use Blood clots Cardiovascular disease Cardiovascular Diseases - drug therapy Cell Membrane - chemistry cell membrane coated nanoparticle diagnosis and therapy Drug Delivery Systems Embolisms Heart attacks Humans Hypertension Inflammation Intermittent claudication Ischemia Lipoproteins Magnetic resonance imaging Medical imaging Nanomaterials Nanoparticles Neutrophils Prevention Proteins Review Stroke Thrombosis |
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