An overview of technology transfer in industry

The objective of this review article is to study how technology is transferred in the pharmaceutical industry. This review article is to discuss the procedure for technology transfer process in pharmaceutical industry, importance of technology transfer, reasons for using technology transfer, methods of technology transfer, facets of technology transfer, list of institutes in Indian assisting in technology transfer, organization of technology transfer, function of technology transfer, steps involved in technology transfer, few case of involved in the technology transfer in the pharmaceutical industry and understand the aspects related with technology transfer

Design and Development of Mechanical Solar Tracking System

In recent years, the growing global interest in the conservation of environment has provided a fresh motivation for research in the area of solar energy utilization. Already, installation of solar energy extraction devices such as solar panels, solar water heaters, solar cookers etc. is becoming popular in urban buildings. Most of these devices consist of a solar receptor that is kept facing the sun during the day, but the sun moves from east to west and the efficiency of the panel decreases. If one could trap this extra energy source then the efficiency of the solar panel would be increased. A tracking mechanism following the sun would achieve this aim. An attempt has been made to develop a simple yet efficient sun tracking mechanism using a motor, a speed reduction mechanism and real timer. The mechanism has been designed such that the sunrays falling on the panel are always perpendicular to the panel resulting in increase in efficiency of the electricity generation. This report presents, in detail, the design and construction adopted to develop the functional model that was fabricated and tested for performance which yielded the efficiency increase of 28.41% as compared to the conventional stationary panel position

Peptidomimetic and Non- Peptidomimetic Derivatives as Possible SARS-CoV-2 Main Protease (Mpro) Inhibitors

To design novel inhibitors of the SARS-CoV-2 main protease (Mpro), we investigated the binding mode of the recently reported α-ketoamide inhibitors of this enzyme. Following, we utilized in-silico screening to identify 168 peptidomimetic and non-peptidomimetic compounds that are high probability Mpro binding candidates. The compounds were synthesized in 5 to 10 mg for initial screening for their potential inhibition of Mpro using Fluorescence Resonance Energy Transfer (FRET) assay. The study was conducted using the main protease, MBP-tagged (SARS-CoV-2) Assay Kit (BPS Bioscience, #79955-2), and the fluorescence due to enzymatic cleavage of substrate measured using BMG LABTECH CLARIOstar™, a fluorescent microplate reader, with an excited/emission wavelength of 360 nm/460 nm, respectively. The FRET assay showed 29 compounds to exhibit lower fluorescence compared to the positive control, indicating inhibitory activity, with three of the compounds exhibiting over 50% enzymatic inhibition. The assay average scores were plotted as dose inhibition curves using variable parameter nonlinear regression to calculate the IC50 values. To design more potent inhibitors, an in-silico molecular docking simulation using the SARS-CoV-2 Mpro crystal structure was conducted to investigate on a molecular level the key binding residues at the active site, as well as the possible binding modes and affinity of the lead inhibitors. Additionally, an in-silico study of the compounds\u27 molecular properties and physicochemical profiles was performed to predict their pharmacokinetic properties and assess their suitability as potential orally active drug candidates.https://scholarscompass.vcu.edu/gradposters/1139/thumbnail.jp

The progestational and androgenic properties of medroxyprogesterone acetate: gene regulatory overlap with dihydrotestosterone in breast cancer cells

INTRODUCTION: Medroxyprogesterone acetate (MPA), the major progestin used for oral contraception and hormone replacement therapy, has been implicated in increased breast cancer risk. Is this risk due to its progestational or androgenic properties? To address this, we assessed the transcriptional effects of MPA as compared with those of progesterone and dihydrotestosterone (DHT) in human breast cancer cells. METHOD: A new progesterone receptor-negative, androgen receptor-positive human breast cancer cell line, designated Y-AR, was engineered and characterized. Transcription assays using a synthetic promoter/reporter construct, as well as endogenous gene expression profiling comparing progesterone, MPA and DHT, were performed in cells either lacking or containing progesterone receptor and/or androgen receptor. RESULTS: In progesterone receptor-positive cells, MPA was found to be an effective progestin through both progesterone receptor isoforms in transient transcription assays. Interestingly, DHT signaled through progesterone receptor type B. Expression profiling of endogenous progesterone receptor-regulated genes comparing progesterone and MPA suggested that although MPA may be a somewhat more potent progestin than progesterone, it is qualitatively similar to progesterone. To address effects of MPA through androgen receptor, expression profiling was performed comparing progesterone, MPA and DHT using Y-AR cells. These studies showed extensive gene regulatory overlap between DHT and MPA through androgen receptor and none with progesterone. Interestingly, there was no difference between pharmacological MPA and physiological MPA, suggesting that high-dose therapeutic MPA may be superfluous. CONCLUSION: Our comparison of the gene regulatory profiles of MPA and progesterone suggests that, for physiologic hormone replacement therapy, the actions of MPA do not mimic those of endogenous progesterone alone. Clinically, the complex pharmacology of MPA not only influences its side-effect profile; but it is also possible that the increased breast cancer risk and/or the therapeutic efficacy of MPA in cancer treatment is in part mediated by androgen receptor

Bacterial laccases: some recent advances and applications

Laccases belong to the large family of multi-copper oxidases (MCOs) that couple the one-electron oxidation of substrates with the four-electron reduction of molecular oxygen to water. Because of their high relative non-specific oxidation capacity particularly on phenols and aromatic amines as well as the lack of requirement for expensive organic cofactors, they have found application in a large number of biotechnological fields. The vast majority of studies and applications were performed using fungal laccases, but bacterial laccases show interesting properties such as optimal temperature above 50 °C, optimal pH at the neutral to alkaline range, thermal and chemical stability and increased salt tolerance. Additionally, bacterial systems benefit from a wide range of molecular biology tools that facilitates their engineering and achievement of high yields of protein production and set-up of cost-effective bioprocesses. In this review we will provide up-to-date information on the distribution and putative physiological role of bacterial laccases and highlight their distinctive structural and biochemical properties, discuss the key role of copper in the biochemical properties, discuss thermostability determinants and, finally, review biotechnological applications with a focus on catalytic mechanisms on phenolics and aromatic amines.info:eu-repo/semantics/publishedVersio

Inheritance and relationships of flowering time and seed size in kabuli chickpea

Flowering time and seed size are the important traits for adaptation in chickpea. Early phenology (time of flowering, podding and maturity) enhance chickpea adaptation to short season environments. Along with a trait of consumer preference, seed size has also been considered as an important factor for subsequent plant growth parameters including germination, seedling vigour and seedling mass. Small seeded kabuli genotype ICC 16644 was crossed with four genotypes (JGK 2, KAK 2, KRIPA and ICC 17109) to study inheritance of flowering time and seed size. The relationships of phenology with seed size, grain yield and its component traits were studied. The study included parents, F1, F2 and F3 of four crosses. The segregation data of F2 indicated flowering time in chickpea was governed by two genes with duplicate recessive epistasis and lateness was dominant to earliness. Two genes were controlling 100-seed weight where small seed size was dominant over large seed size. Early phenology had significant negative or no association (ICC 16644 × ICC 17109) with 100-seed weight. Yield per plant had significant positive association with number of seeds per plant, number of pods per plant, biological yield per plant, 100-seed weight, harvest index and plant height and hence could be considered as factors for seed yield improvement. Phenology had no correlation with yield per se (seed yield per plant) in any of the crosses studied. Thus, present study shows that in certain genetic background it might be possible to breed early flowering genotypes with large seed size in chickpea and selection of early flowering genotypes may not essentially have a yield penalty

Use of aromatic polyamide membranes in desalination

173-177Piperazine containing polymers, having no 'H' atom at amide nitrogen have been prepared from diaminobenzanilides and diacid chlorides by low temperature polycondensation method. These polymers have been characterised by inherent viscosity, percent moisture regain, solubility, IR and thermal analysis. Amount of chlorine absorbed by the polyamides has been calculated by titrating polymer suspension with sodium thiosulphate. Membranes were cast from the polymer solution in dimethyl acetamide containing lithium chloride as an additive. These membranes' were studied for reverse osmosis (RO) performance in salt water with and without chlorine containing medium.</span

Terpenoids-LXVI: ring enlargement produced by the alkaline fusion of ω-bromolongifolene

By analogy with ω-bromocamphene, ω-bromolongifolene on fusion with alkali, but at a comparatively higher temperature, gives several monomeric and dimeric products as a result of ring enlargement. The monomeric products have been characterized as longihomocamphenilone (VIII) and longi-isohomocamphenilone (IX). The dimeric products are composed of a mixture of longifolenyl ethers and the kinetic dimers. lead tetraacetate oxidation of longifolene, according to the method of Ourisson, has been found to yield, not only longihomocamphenilone and longidione, but also a crystalline alcohol, identified as isolongifolol (XI)