Biomimetic Nanotherapies: Red Blood Cell Based Core–Shell Structured Nanocomplexes for Atherosclerosis Management. Issue 12 (24th April 2019)
- Record Type:
- Journal Article
- Title:
- Biomimetic Nanotherapies: Red Blood Cell Based Core–Shell Structured Nanocomplexes for Atherosclerosis Management. Issue 12 (24th April 2019)
- Main Title:
- Biomimetic Nanotherapies: Red Blood Cell Based Core–Shell Structured Nanocomplexes for Atherosclerosis Management
- Authors:
- Wang, Yi
Zhang, Kang
Qin, Xian
Li, Tianhan
Qiu, Juhui
Yin, Tieying
Huang, Junli
McGinty, Sean
Pontrelli, Giuseppe
Ren, Jun
Wang, Qiwei
Wu, Wei
Wang, Guixue - Abstract:
- Abstract: Cardiovascular disease is the leading cause of mortality worldwide. Atherosclerosis, one of the most common forms of the disease, is characterized by a gradual formation of atherosclerotic plaque, hardening, and narrowing of the arteries. Nanomaterials can serve as powerful delivery platforms for atherosclerosis treatment. However, their therapeutic efficacy is substantially limited in vivo due to nonspecific clearance by the mononuclear phagocytic system. In order to address this limitation, rapamycin (RAP)‐loaded poly(lactic‐ co ‐glycolic acid) (PLGA) nanoparticles are cloaked with the cell membrane of red blood cells (RBCs), creating superior nanocomplexes with a highly complex functionalized bio‐interface. The resulting biomimetic nanocomplexes exhibit a well‐defined "core–shell" structure with favorable hydrodynamic size and negative surface charge. More importantly, the biomimetic nature of the RBC interface results in less macrophage‐mediated phagocytosis in the blood and enhanced accumulation of nanoparticles in the established atherosclerotic plaques, thereby achieving targeted drug release. The biomimetic nanocomplexes significantly attenuate the progression of atherosclerosis. Additionally, the biomimetic nanotherapy approach also displays favorable safety properties. Overall, this study demonstrates the therapeutic advantages of biomimetic nanotherapy for atherosclerosis treatment, which holds considerable promise as a new generation of drug deliveryAbstract: Cardiovascular disease is the leading cause of mortality worldwide. Atherosclerosis, one of the most common forms of the disease, is characterized by a gradual formation of atherosclerotic plaque, hardening, and narrowing of the arteries. Nanomaterials can serve as powerful delivery platforms for atherosclerosis treatment. However, their therapeutic efficacy is substantially limited in vivo due to nonspecific clearance by the mononuclear phagocytic system. In order to address this limitation, rapamycin (RAP)‐loaded poly(lactic‐ co ‐glycolic acid) (PLGA) nanoparticles are cloaked with the cell membrane of red blood cells (RBCs), creating superior nanocomplexes with a highly complex functionalized bio‐interface. The resulting biomimetic nanocomplexes exhibit a well‐defined "core–shell" structure with favorable hydrodynamic size and negative surface charge. More importantly, the biomimetic nature of the RBC interface results in less macrophage‐mediated phagocytosis in the blood and enhanced accumulation of nanoparticles in the established atherosclerotic plaques, thereby achieving targeted drug release. The biomimetic nanocomplexes significantly attenuate the progression of atherosclerosis. Additionally, the biomimetic nanotherapy approach also displays favorable safety properties. Overall, this study demonstrates the therapeutic advantages of biomimetic nanotherapy for atherosclerosis treatment, which holds considerable promise as a new generation of drug delivery system for safe and efficient management of atherosclerosis. Abstract : Biomimetic nanocomplexes with typical "core–shell" structure consisting of a RAP‐loaded PLGA nanoparticle "core" and a RBC membrane "shell" (RBC/RAP@PLGA), exhibit the biomimetic nature of the RBC interface to enhance targeted drug delivery to atherosclerotic plaques. RBC/RAP@PLGA not only significantly attenuates the progression of atherosclerosis, but also shows a desirable safety profile without any significant long‐term side effects. … (more)
- Is Part Of:
- Advanced science. Volume 6:Issue 12(2019)
- Journal:
- Advanced science
- Issue:
- Volume 6:Issue 12(2019)
- Issue Display:
- Volume 6, Issue 12 (2019)
- Year:
- 2019
- Volume:
- 6
- Issue:
- 12
- Issue Sort Value:
- 2019-0006-0012-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2019-04-24
- Subjects:
- atherosclerosis -- biomimetic -- mathematical modeling -- nanocomplexes -- targeted delivery
Science -- Periodicals
505 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2198-3844 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/advs.201900172 ↗
- Languages:
- English
- ISSNs:
- 2198-3844
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 11254.xml