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Beilstein J. Nanotechnol. 2025, 16, 11–24, doi:10.3762/bjnano.16.2
Scheme 1: Synthesis of Atr@p(Hist-CA) and Atr release following ACh hydrolysis.
Figure 1: Data for p(Hist-CA): (a, b) TEM images, (c) distribution diagram of the hydrodynamic diameter, C = ...
Figure 2: IR spectra of (a) BA, (b) p(Hist-CA), (c) Hist-RA and (d) CA-RA in KBr.
Figure 3: Agglutination assay. Blood samples were observed in the plate wells following the addition of dilut...
Figure 4: Bright-field microscopy (Nikon Eclipse Ci, 400× magnification). K(−) for intact cells; K(+) for the...
Figure 5: The concentration-dependent conductivity of (a) CA-RA, Hist-RA, and the mixture CA-RA + Hist-RA in H...
Figure 6: (a) UV and fluorescence spectra of Fl (red dotted line) and Fl@p(Hist-CA) (blue line), (b) fluoresc...
Figure 7: 1H NMR spectra for Atr@p(Hist-CA): (a) dialysate after synthesis of Atr@p(Hist-CA), (b) dialysate a...
Figure 8: Time-dependent Atr release from Atr@p(Hist-CA) without ACh and after addition of ACh 0.04, 4 and 40...
Scheme 2: Synthesis of Hist-RA.
Scheme 3: Synthesis of CA-RA.
Beilstein J. Nanotechnol. 2018, 9, 1594–1601, doi:10.3762/bjnano.9.151
Scheme 1: Synthesis of SRA.
Scheme 2: Synthesis of p(SRA-B).
Figure 1: AFM images of p(SRA-B).
Figure 2: UV–vis and fluorescence spectra of (A) Fl, (B) Py and (C) PTS in aqueous media (black dashed line) ...
Scheme 3: Dye release from p(SRA-B) under the action of pH value or glucose.
Figure 3: Fluorescence spectra of free D (dashed lines) and D@p(SRA-B) (0.27 mg/mL) (solid lines) at pH 3–9 w...
Figure 4: (A) Fl@p(SRA-B) spectra after addition of glucose (0.4 mM); D release from D@p(SRA-B), where D = Fl...