4.6 Article

Artificial cell membrane camouflaged immunomagnetic nanoparticles for enhanced circulating tumor cell isolation

Journal

JOURNAL OF MATERIALS CHEMISTRY B
Volume 10, Issue 16, Pages 3119-3125

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1tb02676c

Keywords

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Funding

  1. National Natural Science Foundation of China (NSFC) [32071438, 31771037, U20A20394]
  2. Project in the Science and Technology Support Program of Sichuan Province [2021YFS0018]
  3. Chengdu Science and Technology Project [2021-YF05-01578-SN]

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This study proposes a method of using commercialized lipids and proteins to create artificial cell membrane camouflaged immunomagnetic nanoparticles. It overcomes the challenges of isolating circulating tumor cells and achieves high specificity capture and anti-nonspecific absorption in both mimic and clinical blood samples.
Precise and specific circulating tumor cell (CTC) isolation is heavily interfered with by blood cells and proteins. Although satisfactory results have been achieved by some cell membrane-derived platforms, the following limitations have seriously limited the commercialization potential: complex membrane composition, difficult batch difference control, inconvenient source cell expansion, etc. To overcome these limitations, artificial cell membrane camouflage made from commercialized lipids and proteins was proposed in this work. Specifically, a biotinylated phospholipid which can serve as a lipid component and provide active sites (biotin) for antibody modification, and human serum albumin (HSA), which can effectively reduce certain blood protein adsorption, were applied simultaneously to endow our immunomagnetic platform with a new biological identity. Besides, making full use of the robust lipid and protein absorption ability of graphene nanosheets (GNs), the biomimetic cell membrane can be easily integrated into the magnetic core through simple lipid and protein solution incubation. Surprisingly, the resulting artificial cell membrane camouflaged immunomagnetic nanoparticles (AIMNPs) achieved high specificity (average capture efficiency 87.0%), good sensitivity (7 model CTCs per 0.5 mL) and an enhanced anti-nonspecific absorption ability (15-105 white blood cells per 1.5 mL) in both mimic and clinical blood samples.

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