A new synthetic tripeptide-based hydrogel has been discovered at physiological pH and temperature. This hydrogel has been thoroughly characterized using different techniques including field emission scanning electron microscopic (FE-SEM) and high-resolution transmission electron microscopic (HR-TEM) imaging, small- and wide-angle X-ray diffraction analyses, FT-IR, circular dichroism, and rheometric analyses. Moreover, this gel exhibits thixotropy and injectability. This hydrogel has been used for entrapment and sustained release of an antibiotic vancomycin and vitamin B12 at physiological pH and temperature for about 2 days. Interestingly, MTT assay of these gelator molecules shows almost 100% cell viability of this peptide gelator, indicating its noncytotoxicity.

A long-chain amino acid containing dipeptide has been found to form a hydrogel in phosphate buffer whose pH ranges from 6.0 to 8.8. The hydrogel formed at pH 7.46 has been characterized by small-angle X-ray scattering (SAXS), wide-angle powder X-ray diffraction (PXRD), Fourier transform infrared (FT-IR) spectroscopy, field-emission scanning electron microscopy (FE-SEM), high-resolution transmission electron microscopy (HR-TEM) imaging and rheological analyses. The microscopic imaging studies suggest the formation of a nanofibrillar three-dimensional (3D) network for the hydrogel. As observed visually and confirmed rheologically, the hydrogel at pH 7.46 exhibits thixotropy. This thixotropic property can be exploited to inject the peptide. Furthermore, the hydrogel exhibits remarkable antibacterial activity against Gram-negative bacteria Escherichia coli and Pseudomonas aeruginosa, which are responsible for many common diseases. The hydrogel has practical applicability due to its biocompatibility with human red blood cells and human fibroblast cells. Interestingly, this hydrogel shows high resistance toward proteolytic enzymes, making it a new potential antimicrobial agent for future applications. It has also been observed that a small change in molecular structure of the gelator peptide not only turns the gelator into a nongelator molecule under similar conditions, but it also has a significant negative impact on its bactericidal character.

Synthetic tripeptide based noncytotoxic hydrogelators have been discovered for releasing an anticancer drug at physiological pH and temparature. Interestingly, gel stiffness, drug release capacity and proteolytic stability of these hydrogels have been successfully modulated by incorporating d-amino acid residues, indicating their potential use for drug delivery in the future.

An amino-acid-based (11-(4-(pyrene-1-yl)butanamido)undecanoic acid) self-repairing hydrogel is reported. The native hydrogel, as well as hybrid hydrogels, have been thoroughly characterized by using various microscopic techniques, including transmission electron microscopy (TEM), atomic force microscopy (AFM), Raman spectroscopy, fluorescence spectroscopy, FTIR spectroscopy, X-ray diffraction, and by using rheological experiments. The native hydrogel exhibited interesting fluorescence properties, as well as a self-healing property. Interestingly, the self-healing, thixotropy, and stiffness of the native hydrogel can be successfully modulated by incorporating carbon-based nanomaterials, including graphene, pristine single-walled carbon nanotubes (Pr-SWCNTs), and both graphene and Pr-SWCNTs, within the native gel system. The self-recovery time of the gel was shortened by the inclusion of reduced graphene oxide (RGO), Pr-SWCNTs, or both RGO and Pr-SWCNTs. Moreover, hybrid gels that contained RGO and/or Pr-SWCNTs exhibited interesting semiconducting behavior.

A dipeptide with a long fatty acid chain at its N-terminus gives hydrogels in phosphate buffer in the pH range 7.0-8.5. The hydrogel with a gelator concentration of 0.45% (w/v) at pH 7.46 (physiological pH) provides a very good platform to study dynamic changes within a supramolecular framework as it exhibits remarkable change in its appearance with time. Interestingly, the first formed transparent hydrogel gradually transforms into a turbid gel within 2 days. These two forms of the hydrogel have been thoroughly investigated by using small angle X-ray scattering (SAXS), powder X-ray diffraction (PXRD), field emission scanning electron microscopic (FE-SEM) and high-resolution transmission electron microscopic (HR-TEM) imaging, FT-IR and rheometric analyses. The SAXS and low angle PXRD studies substantiate different packing arrangements for the gelator molecules for these two different gel states (the freshly prepared and the aged hydrogel). Moreover, rheological studies of these two gels reveal that the aged gel is stiffer than the freshly prepared gel.

A naphthalenediimide (NDI)-based new gelator molecule has been discovered, the molecule forms interesting J/H-aggregated species depending on solvents (aliphatic/aromatic) and remarkably, the fluorescence of the gel phase materials is nicely tuned according to the electron donating capacity of the aromatic solvent.

Blue, green, orange-red, red and NIR emitting gold quantum clusters have been prepared in aqueous media by using a bioactive peptide glutathione (reduced) at physiological pH. Matrix-assisted laser desorption ionization-time-of-flight mass spectrometry (MALDI-TOF MS) analyses show that the core structure sizes of the five different gold clusters are Au7 (blue), Au16 (green), Au19 (orange-red), Au21 (red) and Au22 (NIR). The photo-stability and pH-stability of these quantum clusters have been measured, and these are photo-stable against continuous UV irradiation for a few hours. They also exhibit moderate to good pH-stability within the pH range of 5-12.5. A computational study reveals the organisation of gold atoms in the thiolate-protected blue quantum cluster and its several structural parameters, including the mode of interaction of ligand molecules with Au atoms in the Au7 cluster. Interestingly, it has been found that NIR emitting gold quantum cluster can easily be internalized into the adenocarcinomic human alveolar basal epithelial cell line (A549 cell line). Moreover, a MTT assay indicates that our NIR emitting gold quantum cluster show very low cytotoxicy to A549 cancer cells.

Blue, green, and red emitting silver quantum clusters have been prepared through green chemical approach by using a bio-active peptide glutathione (reduced) in a 50 mM phosphate buffer at pH 7.46. This study describes fluorescence emission tuning of the silver clusters by making different sized Ag clusters using slightly different reaction conditions keeping the same stabilizing ligand, reducing agent, solvent system, and silver salt precursor. The preparation procedure of these silver quantum clusters is new and highly reproducible. Each of these clusters shows very interesting fluorescence properties with large stokes shifts, and the quantum yields of blue, green, and red clusters are 2.08%, 0.125%, and 1.39%, respectively. These silver quantum clusters have been characterized by using different techniques including fluorescence spectroscopy, UV-vis spectroscopy, field-emission gun transmission electron microscopic (FEG-TEM) imaging and MALDI-TOF MS analyses. MALDI-TOF MS analyses show that the size of these blue, green and red emitting silver clusters are Ag5 (NC1, nanoclusters 1), Ag8 (NC2, nanoclusters 2) and Ag13 (NC3, nanoclusters 3), respectively, by using 2,5-dihydroxybenzoic acid as a matrix. These clusters are stable in broad ranges of pH. The NC3 (red emitting) has been successfully utilized for selective and sensitive detection of toxic Hg(II) ions in water by using even naked eyes, fluorometric, and calorimetric studies. The lower limit of detection of Hg(II) ions in water has been estimated to be 126 and 245 nM from fluorometric and UV-vis analyses, respectively. Enthalpy change (ΔH) during this Hg(II) sensing process is 2508 KJ mol(-1).