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Design Strategies and Applications of Circulating Cell-Mediated Drug Delivery Systems

期刊

ACS BIOMATERIALS SCIENCE & ENGINEERING
卷 1, 期 4, 页码 201-217

出版社

AMER CHEMICAL SOC
DOI: 10.1021/ab500179h

关键词

drug delivery; nanoparticles; immune cells; circulating cells; stem cells; targeting

资金

  1. National Institutes of Health (NIH) [NIBIB EB012575, NCI CA182670, NHLBI HL118498]
  2. National Science Foundation (NSF) [DMR 1313553, CMMI 1266116, CBET-BME 1330663]
  3. Direct For Mathematical & Physical Scien
  4. Division Of Materials Research [1313553] Funding Source: National Science Foundation
  5. Div Of Civil, Mechanical, & Manufact Inn
  6. Directorate For Engineering [1266116] Funding Source: National Science Foundation

向作者/读者索取更多资源

Drug delivery systems, particularly nanomaterial-based drug delivery systems, possess a tremendous amount of potential to improve the diagnostic and therapeutic effects of drugs. Controlled drug delivery targeted to a specific disease is designed to significantly improve the pharmaceutical effects of drugs and reduce their side effects. Unfortunately, only a few targeted drug delivery systems can achieve high targeting efficiency after intravenous injection, even with the development of numerous surface markers and targeting modalities. Thus, alternative drug and nanomedicine targeting approaches are desired. Circulating cells, such as erythrocytes, leukocytes, and stem cells, present innate disease sensing and homing properties. Hence, using living cells as drug delivery carriers has gained increasing interest in recent years. This review highlights the recent advances in the design of cell-mediated drug delivery systems and targeting mechanisms. The approaches of drug encapsulation/conjugation to cell carriers, cell-mediated targeting mechanisms, and the methods of controlled drug release are elaborated here. Cell-based live targeting and delivery could be used to facilitate a more specific, robust, and smart payload distribution for the next-generation drug delivery systems.

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