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The odds of unresolved symptoms after 28 days were associated with age for RSV only. Illness deterioration was associated with age for RSV, with patients 75+ at increased risk, but not for influenza. CONCLUSION In adults presenting to primary care with acute cough, the diagnostic features of RSV or influenza infection are not associated with age. For RSV both the prevalence and illness course are significantly worse at higher age, for influenza only the illness course is. Since the novel coronavirus disease (COVID-19) emerged in December 2019 in China, it has rapidly spread around the world, leading to one of the most significant pandemic events of recent history. Deriving reliable estimates of the COVID-19 epidemic growth rate is quite important to guide the timing and intensity of intervention strategies. Indeed, many studies have quantified the epidemic growth rate using time-series of reported cases during the early phase of the outbreak to estimate the basic reproduction number, R0. Using daily time series of COVID-19 incidence, we illustrate how epidemic curves of reported cases may not always reflect the true epidemic growth rate due to changes in testing rates, which could be influenced by limited diagnostic testing capacity during the early epidemic phase. Tissue engineering approach offers alternative strategies to develop multi-layered/multi-component osteochondral mimetic constructs to meet the requirements of the heterogeneous and layered structure of native osteochondral tissue. Herein, an iterative overlaying process to fabricate a multi-layered scaffold with a gradient composition and layer specific structure have been developed by combining the natural extracellular matrix (ECM) components-chitosan, type I collagen, type II collagen, nanohydroxyapatite- of the osteochondral tissue in biomimetic compositions. Subchondral bone layer was prepared by using freeze-drying method to obtain 3D porous scaffolds. The calcified cartilage and cartilage layers were prepared by thermal gelation method in the hydrogel form. Osteochondral scaffolds fabricated by iterative overlaying of each distinct layer exhibited a porous, continuous gradient structure and supported cell proliferation in a co-culture of MC3T3-E1 preosteoblasts and ATDC5 chondrocytes. Histology and biochemical analysis showed enhanced extracellular matrix production and demonstrated collagen and glycosaminoglycan deposition. Expression of genes specific for bone, calcified cartilage and cartilage were improved in the osteochondral scaffold. Overall, these findings suggest that iterative overlaying of freeze-dried scaffolds and hydrogel matrices prepared by using ECM components in biomimetic ratios to fabricate gradient, multi-layered structures can be a promising strategy without the need for growth factors. V.Herein, we have reported a cost-effective method of synthesizing highly efficient silica nanomaterial from rice husks for its application as a chemotherapeutic agent. Silica particle with two different sizes ~20 nm and ~40 nm were achieved from silica precursor obtained from rice husk. 5-Fluorouracil was functionalized onto the surface of silica nanoparticles by direct conjugation and chitosan mediated conjugation. Particle size analysis, zeta potential and functional analyzes were performed in systematic methodology to confirm chitosan coating and 5-Fluorouracil conjugation on silica nanoparticles. The drug loading percentage with respect to the particle size shows that ~20 nm particles have higher loading capacity. The chitosan mediated conjugation of drug shows sustained release in acidic pH and hence suitable for cancer cell-targeted delivery. The in vitro cell culture studies performed on MC3T3 fibroblast cell lines, MCF-7 and A549 cancer cell lines depicts that, compared to direct conjugation of 5-Fluorouracil, chitosan mediated drug conjugation on the surface of silica nanoparticles shows lesser toxic to fibroblast cell lines and higher toxicity towards cancer cell lines. The results of this toxicity were also confirmed from the nucleic acid spectral signature of Raman spectra treated with drug conjugated silica nanoparticles. V.To improve ocular bioavailability of baicalein (BAI), trimethyl chitosan coated lipid nanoparticles of baicalein (TMC-BAI-LNPs) were prepared, optimized and characterized. The properties of TMC-BAI-LNPs such as morphology, particle size, zeta potential and fourier transform infrared spectroscopy were investigated. Additionally, molecular dynamics simulation was applied as a new method to evaluate drug-biological membrane interactions. Transmission electron microscopy showed that the LNPs were approximately spherical in shape with a smooth surface. TMC-BAI-LNPs had a particle size of 162.8 nm, a positive surface charge with a zeta potential of 26.6 mV. Infigratinib The entrapment efficiency and drug loading values of BAI in the formulation were 90.65% and 2.04%, respectively. Moreover, in vitro drug release revealed that TMC-BAI-LNPs had a sustained release effect. In vivo studies indicated TMC-BAI-LNPs had no ocular irritation and the AUC of TMC-BAI-LNPs was 3.17-fold than that of the control (p  less then  0.01). Molecular dynamics simulation data showed that BAI had a poor membrane permeability, which limited the ocular bioavailability. The results indicated that TMC-BAI-LNPs might open up a new avenue for ocular administration. Furthermore, molecular dynamics simulation could predict permeability of drugs. V.The main objective of this study was to evaluate the most suitable conditions to prepare 5-fluorouracil (5-FU) loaded chitosan nanoparticles (CSNPs). 5-FU loaded CSNPs were prepared employing the ionic gelation technique using three different molecular weights of CS with the polyanion sodium tripolyphosphate (STPP) as cross-linking agent. The preparation was based on the ionic interaction of positively charged CS and negatively charged STPP. The entrapment efficiency (EE%) of CSNPs was in the range of 3.86-21.82% EE% exhibited a clear increase with increasing CS concentration. The averge particles size was in the nanosize range and monodisperse in nature whereas transmission electron microscope micrographs showed that the prepared nanoparticles have a spherical shape. Fourier transform infrared (FTIR), X- ray differaction (XRD) and differential scanning calorimetry (DSC) confirmed successful incorporation of 5-FU in prepared CSNPs. In vitro release of 5-FU from selected formulations exhibited sustained release from the nanoparticles where slower release was observed when higher molecular weight CS was used.