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A simple and cost‐effective approach was used to synthesize different morphologies of Linde Type L (LTL) nanozeolite. The resulting products were characterized by techniques such as X‐ray diffraction, Fourier transform infrared spectroscopy, scanning electronic microscopy, and Brunauer‐Emmett‐Teller measurements. The results showed that LTL nanozeolite was successfully synthesized, and different morphologies, including spherical‐like and disk‐shaped nanoparticles, were obtained. Then, the effect of size and morphology on the antibacterial activity of the obtained products was studied. Spherical‐like LTL nanoparticles showed higher antibacterial activity due to their larger pore volume and surface area and higher loading of biocidal zinc cations. [ABSTRACT FROM AUTHOR]

Most of the previously reported fluorescent organic probes for cancer cell and tumor imaging have significant limitations including chemical toxicity, structural instability, low Stokes shift value, and the inability for selective accumulations in tumors during in vivo imaging. To overcome the mentioned challenges, we synthesized the fluorescent probes with protected polar functional groups to enhance the non‐toxicity nature and increase the selectivity toward tumors. In addition, the structural rigidity of the fluorescent probes was increased by embedding aromatic rings in the probe structure. This issue enables us to obtain ultrabright cell images due to enhanced fluorescence quantum yield (ΦFL) values. After synthesis and spectral characterizations, the applicability of two furan‐based and imidazole‐based fluorescent probes ( abbreviated as DCPEF and DBPPI, respectively) was investigated for ultrabright in vitro and in vivo imaging of cancer cells. The probe DCPEF shows the ΦFL value of 0.946 and the Stocks shift of 86 nm. In addition, probe DBPPI offers the ΦFL value of 0.400 and a Stocks shift of 150 nm. The MTT colorimetric cytotoxicity assay showed that probe DCPEF has minimal effects against HT‐29 (cancer) and Vero (normal) cells. The probe DCPEF produced ultrabright fluorescence images from HT‐29 cells. In addition, in vivo imaging of cancer cells showed that probe DCPEF selectively accumulates in the 4T1 tumor in mice. The spectral and chemical stability, minimal cytotoxicity, significant Stokes shift, and high degree of selectivity for tumor cells during in vivo imaging make DCPEF an appropriate candidate to be used as a standard probe for cancer cell imaging. [ABSTRACT FROM AUTHOR]