Development of an assay for colorimetric and fluorometric detection of HS.

Hydrogen sulfide is a highly toxic gas that can produce extremely rapid CNS and respiratory depression and sometimes becomes fatal at high concentrations. There is no proven antidote for hydrogen sulfide poisoning. Hence, it is important to reduce the production of HS in several industries, such as oil and gas refining and mining industries.

Differential detection of aspartic acid in MCF-7 breast cancer cells.

Aspartic acid is a non-essential amino acid obtained in the neuroendocrine tissues of vertebrates and invertebrates. Aspartic acid, a major excitatory neurotransmitter in the mammalian central nervous system, plays a key role in memory and acts in many other normal and abnormal physiological processes. In this work, we have developed an efficient chemosensor (PCF) based on the pyridine-carbazole moiety for the differential detection of aspartic acid in biological systems.

In vivo 'turn on' fluorescence detection of free cysteine in zebrafish kidney and liver.

Cysteine is directly associated with a wide range of biological processes. Besides its essential role in protein synthesis, cysteine undergoes a variety of post-translational modifications which modulate several physiological processes. Dysregulated cysteine metabolism is associated with several neurodegenerative disorders.

Involvement of a unique chemodosimeter in the selective estimation of noxious cyanide in common water hyacinth (): an environmental refinement.

A naphthaldehyde-pyridoxal conjugated chemodosimeter (NPLC) was developed and employed for the sensitive and selective detection and estimation of cyanide in common water hyacinth (), a free floating macrophyte used in the phytoremediation process since ancient times. The non-fluorescent nature of the probe NPLC, directed by the possibility of excited state intramolecular proton transfer process (ESIPT), was promptly changed due to CN induced di-deprotonation of the probe. The naked eye color change and turn on vivid fluorescent color of NPLC was attributed to the inhibition of the ESIPT mechanism in the deprotonated NPLC (NPLC-D).