Construction and evaluation of red blood cells-based drug delivery system for chemo-photothermal therapy
[Display omitted] •An innovative drug delivery system based on red blood cells was described.•The system showed obvious controlled release of doxorubicin.•The platform exhibited great active targeting in vitro.•The system enhanced the effect of chemo-phototherapy for tumour. In this study, a novel t...
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Veröffentlicht in: | Colloids and surfaces, B, Biointerfaces B, Biointerfaces, 2021-08, Vol.204, p.111789-111789, Article 111789 |
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Format: | Artikel |
Sprache: | eng |
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•An innovative drug delivery system based on red blood cells was described.•The system showed obvious controlled release of doxorubicin.•The platform exhibited great active targeting in vitro.•The system enhanced the effect of chemo-phototherapy for tumour.
In this study, a novel tumor-targeting drug delivery system (DDS) based on red blood cells (RBCs) were fabricated for combinational chemo-phototherapy against cancer. Cyclic peptide (cRGD) and indocyanine green (ICG) were applied to the surface of RBCs to increase the targeting and photothermal effect, respectively. Doxorubicin (DOX) as a model drug was loaded into RBCs by the hypotonic dialysis method. A series of tests have been carried out to evaluate the RBCs-based DDS and these tasks include physicochemical properties, cellular uptake, targeting ability, and combination therapeutic efficiency. As a result, the DOX was successfully loaded into RBCs and the drug loading amount was 0.84 ± 0.09 mg/mL. There was no significant change of particle size after surface modification of RBCs. The RBCs-based DDS could target to the surface of cancer cells, which delivery DOX to the lesions efficiently and accurately. Meanwhile, due to the combined treatment effect, the RBCs-based DDS can effectively inhibit tumor growth. The RBCs-based DDS constructed in this research may have promising applications in cancer therapy due to their highly synergistic efficient therapy and to investigate its possibility for tumor therapy. |
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ISSN: | 0927-7765 1873-4367 |
DOI: | 10.1016/j.colsurfb.2021.111789 |