Comparing chromium phyto-assessment in Brachiaria mutica and Leptochloa fusca growing on chromium polluted soil.

Industrial discharge of chromium (Cr) into environment puts serious threat on living beings due to its potent toxicity. Phytostabilization, a type of in-situ phytoremediation is aimed to immobilize and stabilize the toxic elements in soil using root system of metal resistant potential plants. To evaluate the phytostabilization potential of two grass species Brachiaria mutica and Leptochloa fusca, a pot study was conducted using soil spiked with different concentrations of Cr (control, 25, 50 and 100 mg kg-1). Three plants were sown in each pot with three replications and arranged following completely randomized design. After three months of growth, the plants were harvested and above and below ground plant's parts were analyzed for various growth and physiological parameters. Data revealed that plant biomass, chlorophylls and carotenoids reduced substantially with increasing Cr concentration. Antioxidant enzymatic activity increased significantly in L. fusca as compared to B. mutica with increasing Cr levels (up to 50 mg kg-1), then reduced at maximum Cr level (100 mg kg-1) in both grasses. Leptochloa fusca performed better with maximum root Cr accumulation 93.7 µg plant-1, shoot Cr accumulation 24.7 µg plant-1, root bioconcentration factor (BCF) 2.0, shoot BCF 0.08, shoot TF 0.06 and MTI 87%. While B. mutica showed maximum root Cr accumulation 18.4 µg plant-1, shoot Cr accumulation 7.6 µg plant-1, shoot BCF 0.03, root BCF 1.28, shoot TF 0.04, and MTI 56%. These results showed that L. fusca possessed good potential with better Cr bioaccumulation, MTI, BCF and antioxidant activities compared to B. mutica. Hence L. fusca can be used as good phytostabilizing agent for the soils contaminated with lower to moderate levels of Cr.

Cost analysis of registered brands of oral antidepressant drugs in Pakistan: a descriptive analysis.

Background and objective: Depression is a global public health threat, and its treatment constitutes drugs in psychopharmacology, a domain that is rapidly growing with the addition of newer agents in market that are of high cost. Therefore, the present study aims to investigate the number of registered brands and price variation of oral antidepressants in Pakistan. Methods: A descriptive observational study was carried out to analyze the cost of oral antidepressants in Pakistan. Pharma guide 2019 was used to derive the cost of antidepressants marketed in Pakistan. The details about the number of registered brands and maximum and minimum prices of antidepressant drugs were calculated. Results: Sixteen drugs in 38 formulations were registered in 607 brands in Pakistan. Variations among 38 different formulations range from 0% to 746.39%. Out of these 38 formulations, 31 had variations below 200%, while 7 formulations had price variation above 200%. The highest price (746.39%) variation was observed for citalopram 20 mg (price per tablet PKR 6.79 to PKR 57.47) and no (0%) price variation was for bupropion 75 mg (price per tablet PKR 10). Conclusion: The study revealed wide variations in the number of registered brands and prices of oral tablets of antidepressants in Pakistan. The government needs to devise effective strategies to implement established policies to ensure uniformity in price, quality, and effectiveness with the ultimate goal to reduce treatment cost. Also, measures should be taken to inform prescribers about cost variation of drugs as prerequisite for cost-effective treatments to ultimately reduce treatment cost and financial burden and improve patient's adherence to therapy.

Microfluidic-based, live-cell analysis allows assessment of NK-cell migration in response to crosstalk with dendritic cells.

Migration and localization of NK cells into peripheral tissues are tightly regulated under normal and pathological conditions. The physiological importance of NK cell-DC crosstalk has been well documented. However, the ways in which DCs regulate the migratory properties of NK cells (such as chemotaxis, chemokinesis, chemo-repulsion) are not fully defined in vitro. Here, we employed a microfluidic platform to examine, at the single-cell level, C57BL/6 NK-cell migrations in a stable chemical gradient. We observed that soluble factors released by the immature and LPS-activated mature DCs induced a high level of chemotactic movement of IL-2-activated NK cells in vitro. We confirmed these findings in a standard trans-well migration assay, and identified CXCR3 as a key receptor on the NK cells that mediated the migration. More interestingly, we revealed a novel function of granulocyte macrophage colony-stimulating factor in repulsing NK-cell migrations. The future uses of such microfluidic device in the systematic evaluations of NK-cell migratory responses in NK cell-DC crosstalk will provide new insights into the development of DC-based NK-cell therapies against tumor and infections.