Xylenol orange-modified CdTe quantum dots as a fluorescent/colorimetric dual-modal probe for anthrax biomarker based on competitive coordination.

Bacillus anthracis spores can make humans infected with vicious anthrax, so it is significant to detect their biomarker 2,6-pyridinedicarboxylic acid (DPA). The development of dual-modal methods for DPA detection that are more flexible in practical applications remains a challenge. Herein, colorimetric xylenol orange (XO) was modified on fluorescent CdTe quantum dots (QDs) for dual-modal detection of DPA through competitive coordination. After the binding of XO on CdTe QDs via coordination with Cd2+, CdTe QDs displayed quenched red fluorescence and the bound XO was presented as red color. The competitive coordination of DPA with Cd2+ made XO released from CdTe QDs, causing the enhanced red fluorescence of CdTe QDs and the yellow color of free XO. On this basis, DPA was rapidly (1 min) quantified through fluorescent and colorimetric modes within the ranges of 0.1-5 µM and 0.5-40 µM, respectively. The detection limits for DPA were calculated as low as 42 nM and 240 nM, respectively assigned to fluorescent and colorimetric modes. The level of urinary DPA was further measured. Satisfactory relative standard deviations (fluorescent mode: 0.1%-10.2%, colorimetric mode: 0.8%-1.8%) and spiked recoveries (fluorescent mode: 100.0%-115.0%, colorimetric mode: 86.0%-96.6%) were obtained.

Bifunctional ratiometric fluorescent probe for sensing anthrax spore biomarker and tetracycline at different excitation channels.

Multifunctional fluorescent probes have received increasing attention for the sake of atom economy and high-density integration. Herein, CdTe quantum dots (QDs) modified with Eu3+ were synthesized as the bifunctional ratiometric fluorescent probe for sensing two hazardous substances tetracycline (TC) and anthrax spore biomarker 2,6-dipicolinic acid (DPA) at different excitation channels, based on the discrepant excitation wavelengths of Eu3+ and the fluorescence quenching of CdTe QDs after interaction with them. Both DPA and TC enhanced the red emission of Eu3+ via antenna effect but caused the green emission of CdTe QDs to quench. Interestingly, the excitation wavelengths of Eu3+ after coordinating with DPA and TC were 275 and 386 nm, respectively. On this basis, CdTe QDs-Eu3+ achieved the bifunctional ratiometric detection of DPA (λex = 275 nm) and TC (λex = 386 nm) with different excitation channels. Both DPA and TC were selectively detected by CdTe QDs-Eu3+ with rapid response (DPA-1 min, TC-1 min) and high sensitivity (DPA-LOD 0.3 µM, TC-LOD 2.2 nM). CdTe QDs-Eu3+ were applied to analyzing DPA and TC in food, biological and environmental samples. Satisfactory spiked recoveries (80.0-119.0 %) and relative standard deviations (0.5-8.4 %) were obtained for measuring DPA and TC in these samples.

A ratiometric fluorescence-scattering sensor for rapid, sensitive and selective detection of doxycycline in animal foodstuffs.

The residue problem of tetracycline antibiotics, especially doxycycline (DC), in animal foodstuffs has attracted much attention. This paper reported ZIF-8 and bovine serum albumin (BSA) as a ratiometric fluorescence-scattering sensor for DC. The mechanism relied on the disassembly of ZIF-8 caused by DC, bringing weakened second-order scattering, and the double fluorescence amplification of DC under ZIF-8 with BSA, inducing enhanced fluorescence. The response of the sensor was completed within 1 min, and the detection limit for DC (3.4 nM) was 1-2 orders of magnitude lower than the reported ones. The distinguishment of DC from other tetracycline antibiotics was also achieved by the sensor. The sensor was applied to detecting DC in animal foodstuffs with satisfactory recoveries (80.0-104.0%). Hence, this work develops a rapid, sensitive and selective ratiometric sensor to monitor the DC residue in animal foodstuffs, also opens the window to construct ratiometric DC sensors with the fluorescence-scattering strategy.