Carbon-based nanomaterials are contemporary and are outpacing the technology platform. Graphene quantum dots (GQDs) had a significant impact on the subject of bioengineering, pharmaceuticals, biomedicine, biosensors, fuel, energy, etc. Depending on how quickly this field is developing, it is important to recognize the new difficulties that GQDs have to overcome. This is incredibly significant because many novel applications and innovations that have made GQD synthesis easier recently have not been systematically evaluated in prior studies. Their ability to combine the benefits of quantum dots, sp2 carbon materials (large specific surface area), and have rich functional groups at the edge makes them special. The naturally occurring inert carbon helps to stabilize chemical and physical characteristics and makes significant advancements in the creation of benchmark photocatalysts. Moreover, current challenges and potential of these rapidly developing GQDs are emphasized. The future of GQD research is limitless, according to the assessment in this review, notably if future research focuses on simplicity of purification and ecofriendly synthesis. This feature article offers a realistic summary on recent developments in the synthesis, characteristics, and uses of GQDs. Frequent review articles focusing on the progress of GQDs for specific applications are published but a thorough review article on GQDs for their numerous uses has not yet been published. The recent trends of scientific research based on new optical biosensing applications, including the comprehensive applications of different zero-dimensional nanomaterials, specially GQDs are discussed in this study.

Urease is an enzyme that plays a significant role in the hydrolysis of urea into carbonic acid and ammonia via the carbamic acid formation. The resultant increase in pH leads to the onset of various pathologies such as gastric cancer, urolithiasis, hepatic coma, hepatic encephalopathy, duodenal ulcers and peptic ulcers. Urease inhibitors can reduce the urea hydrolysis rate and development of various diseases. The Cinnamomum genus is used in a large number of traditional medicines. It is well established that stem bark of Cinnamomum cassia exhibits antiulcerogenic potential. The present study evaluated the inhibitory effect of seven extracts of Cinnamomum camphora, Cinnamomum verum and two pure compounds Camphene and Cuminaldehyde on urease enzyme. Kinetic studies of potential inhibitors were carried out. Methanol extract (IC50 980 µg/mL) of C. camphora and a monoterpene Camphene (IC50 0.147 µg/mL) possess significant inhibitory activity. The Lineweaver Burk plot analysis suggested the competitive inhibition by methanol extract, hexane fraction and Camphene. The Gas Chromatography-Mass Spectroscopy (GC–MS) analysis of hexane fraction revealed the contribution of various terpenes. The present study targets terpenes as a new class of inhibitors that have potential therapeutic value for further development as novel drugs.

Cancer a death havoc is increasing at an alarming pace globally. There is a need to explore novel chemicals having anticancerous potential for its treatment with minimal side effects. Natural compounds obtained from plants have less toxic properties and can be proved as a better medication against this lethal disease. Thus, the secondary metabolites having anticancer properties found in plants, fruits, and vegetables are being persistently evaluated for research in cancer treatment like anticancer drugs- vinblastine, vincristine and taxol which are derived from plants. This review summarizes the anticancer properties of chemical repertoires of plants inhabiting the hot arid regions present in India against various cancer cell lines like HepG2, MCF7, PC3, HT116 etc. The mechanism of action of flavonoids in the induction of apoptosis through suppression/promotion of various factors including Ras-ERK and PI3K-Akt signaling pathways and genes mainly such as Bax, Bcl-2, p53 involved in the proliferation of cancer cells play emphatically in combating the extent of the disease by promoting apoptosis in cancer cells. The insight about the reported mechanisms will open further avenues of the anticancer potential of novel secondary metabolites.