Intracellular pH plays a vital role in cell biology, including signal transduction, ion transport and homeostasis. Herein, a ratiometric fluorescent silica probe was developed to detect intracellular pH values. The pH sensitive dye fluorescein isothiocyanate isomer I (FITC), emitting green fluorescence, was hybridized with reference dye rhodamine B (RB), emitting red fluorescence, as a dual-emission fluorophore, in which RB was embedded in a silica core of ∼40 nm diameter. Moreover, to prevent fluorescence resonance energy transfer between FITC and RB, FITC was grafted onto the surface of core-shell silica colloidal particles with a shell thickness of 10-12 nm. The nanoprobe exhibited dual emission bands centered at 517 and 570 nm, under single wavelength excitation of 488 nm. RB encapsulated in silica was inert to pH change and only served as reference signals for providing built-in correction to avoid environmental effects. Moreover, FITC (λem = 517 nm) showed high selectivity toward H(+) against metal ions and amino acids, leading to fluorescence variation upon pH change. Consequently, variations of the two fluorescence intensities (Fgreen/Fred) resulted in a ratiometric pH fluorescent sensor. The specific nanoprobe showed good linearity with pH variation in the range of 6.0-7.8. It can be noted that the fluorescent silica probe demonstrated good water dispersibility, high stability and low cytotoxicity. Accordingly, imaging and biosensing of pH variation was successfully achieved in HeLa cells.

A fluorescence spectroscopic assay using Newton black film (NBF) for sensitive and selective detection of gaseous formaldehyde at room temperature is reported. The method relies on the Hantzsch reaction of formaldehyde with ammonium citrate and acetylacetone, plus a combination of the large surface area-to-volume ratio (5 × 10 m) and efficient uptake of gas by the nanometer-thick aqueous core of NBF. The assay has a limit of detection (LOD) of 4 ppb, a linear signal-to-concentration correlation up to 300 ppb of HCHO gas in the air, and a nonlinear monotonic increasing correlation in the range of 300 ppb to 1.2 ppm. It is unaffected by relevant analytes such as acetaldehyde, benzaldehyde, acetone, and propionaldehyde. We also demonstrate the sensing of formaldehyde outgassing from a plywood sample using this method and the results agree with the factory specifications.

Relying on the nanometer-thick water core and large surface area-to-volume ratio (∼2 × 10 m) of common black film (CBF), we are able to use a pH-sensitive dye (carboxy-seminaphthorhodafluor-1, SNARF-1) to detect ammonia and acetic acid gas adsorption into the CBF, with the limit of detection reaching 0.8 ppm for NH gas and 3 ppb for CHCOOH gas in the air. Data analysis reveals that fluorescence signal change is linearly proportional to the gas concentration up to 15 ppm and 65 ppb for NH and CHCOOH, respectively.

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