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The current study highlights a new polyvalent inhibitor approach based on Vancomycin conjugated with graphene oxide (Van@GO) against a Vancomycin-resistant

The advances in the arena of biomedical engineering enable us to fabricate novel biomaterials that provide a suitable platform for rapid bone regeneration. Herein, we have investigated the in vitro and in vivo osteogenic differentiation, proliferation, and bone regeneration capability of molybdenum disulfide nanosheets (MoS2NSs) reinforced HAP nanocomposite scaffolds. The MG-63 cells were incubated with HAP and HAP/MoS2NSs nanocomposite and followed for various cellular activities. The cells incubated with HAP@2 shows higher cell adhesion, cell proliferation, and alkaline phosphatase activity (ALP) in contrast to HAP. The in vivo and in vitro results of the increased ALP level confirm that HAP@2 promotes osteogenic differentiation. This improved osteogenesis was validated with upregulation of osteogenic marker viz. transcription factor, RUNX-2 (∼34 fold), collagen-1 (∼15 fold), osteopontin (∼11 fold), osteocalcin (∼20 fold), and bone morphogenetic protein-2 (∼12 fold) after 12 week postimplantation in comparison to drilled. The X-ray imaging demonstrates that HAP@2 implants promote rapid osteogenesis and bioresorbability than HAP and drilled. The outcomes of the present study provide a promising tool for the regeneration of bone deformities, without using any external growth factor.

The current study highlights a new polyvalent inhibitor approach based on Vancomycin conjugated with graphene oxide (Van@GO) against a Vancomycin-resistant Staphylococcus aureus (VRSA) strain. Phys...

Carbon quantum dots (CQDs) and their derivatives have potential applications in the field of biomedical imaging. Toxicity is one of the critical parameters that can hamper their success in biological applications. In this context, our goal was to systematically investigate both in vivo and in vitro toxicity of nitrogen doped carbon quantum dots (NCQDs). In vivo toxic effects were evaluated for 30 days in Swiss albino mice at two different concentrations (5.0 mg per kg body weight (BW) and 10.0 mg per kg BW) of NCQDs. Results of haematological, serum biochemical, antioxidant and histopathological parameters showed no noteworthy defects at both of these concentrations. An in vitro assessment was performed against the human cervical cancer cell line (HeLa cells) at the concentration of 0-400 μg ml-1. The LDH profile, DNA fragmentation, apoptosis, and growth cycle of cells showed no apparent toxicity of NCQDs. The overall study offers highly biocompatible N-doped carbon quantum dots, which may be considered as an attractive material for future biomedical applications.

Quinolinic acid (QA) is a metabolite of tryptophan degradation obtained through kynurenine pathway, produced naturally in the mammalian brain as well as in the human cerebrospinal fluid. The presence of QA ~10-40µM is a clear indicator of many neurological disorders as well as deficiency of vitamin B6 in human being. In the present work; rapid, sensitive and cost-effective bio-electrodes were prepared to detect the trace amount of endogenous neurotoxin (QA). Cyclic voltammetry (CV) and differential pulse voltammetry (DPV) studies were carried out to measure the electrochemical response of the fabricated bio-electrodes as a function of QA concentrations. These devices were found to exhibit desirable sensitivity of ~7.86mAμM-1cm-2 in wide concentration range (6.5μM-65mM). The lower detection limit of this device is as low as 6.5μM and it has excellent storage stability of ~30 days. The capability of the proposed electrochemical bio-sensor was also checked to detect QA in the real samples (human serum). These results reveal that the use of this electrochemical bio-sensor may provide a potential platform for the detection of QA in the real samples for the prior detection of many diseases.

Carbon quantum dots (CQDs) and their derivatives have potential applications in the field of biomedical imaging. Toxicity is one of the critical parameters that can hamper their success in biological applications. In this context, our goal was to systematically investigate both in vivo and in vitro toxicity of nitrogen doped carbon quantum dots (NCQDs). In vivo toxic effects were evaluated for 30 days in Swiss albino mice at two different concentrations (5.0 mg per kg body weight (BW) and 10.0 mg per kg BW) of NCQDs. Results of haematological, serum biochemical, antioxidant and histopathological parameters showed no noteworthy defects at both of these concentrations. An in vitro assessment was performed against the human cervical cancer cell line (HeLa cells) at the concentration of 0–400 μg ml(–1). The LDH profile, DNA fragmentation, apoptosis, and growth cycle of cells showed no apparent toxicity of NCQDs. The overall study offers highly biocompatible N-doped carbon quantum dots, which may be considered as an attractive material for future biomedical applications.

The present work introduces partially reduced graphene oxide (pRGO)-silica (SiO2) particles hybrid system (pRGOSHs) for sensitive and cost effective free cholesterol detection. Fabricated out of thin layers of pRGOSHs, these proposed ChOx/pRGOSHs/ITO based biosensors have a detection range of 2.6–15.5 mM with an appreciable detection limit of 1.3 mM and sensitivity of 11.1 μA/mM/cm2. Low Michaelis–Menten constant (Km) (4.9 × 10− 4 mM) and high diffusivity constant (D) (3.2 × 10− 10 cm2/s) values clearly indicate enhanced immobilization of enzyme over the substrate. Additionally, electrochemical impedance studies indicate that the synergistic combination of SiO2 and pRGO also results in much lower impedance values (40% and 18% decrease in comparison to SiO2 and pRGO respectively) for an overall enhanced sensing performance. These results are further corroborated by the density functional theory based theoretical simulations indicating enhanced electron density (theoretically) in case of the proposed hybrid system. Finally, the present work also highlights the importance of Si–OH bonds formation in the proposed pRGOSHs composite system for attaining such enhanced biosensing ability.