Kinetic modeling and experiments on removal of COD/nutrients from dairy effluent using chlorella and co-culture.

A sustainable and cost-effective approach of waste water management is biological treatment for reducing organic carbon, nitrate, and phosphate content. Co-culturing of algae with bacteria in wastewater leads to higher biomass yield and improvement in COD/nutrients removal compared to the single strain counterparts. In this study, a mathematical modeling framework is proposed to predict the dynamic behavior of microbial co-culture in dairy waste water.

Mixotrophic cultivation of microalgae using industrial flue gases for biodiesel production.

In the present study, an attempt has been made to grow microalgae Scenedesmus quadricauda, Chlorella vulgaris and Botryococcus braunii in mixotropic cultivation mode using two different substrates, i.e. sewage and glucose as organic carbon sources along with flue gas inputs as inorganic carbon source.

Frog intestinal perfusion to evaluate drug permeability: application to p-gp and cyp3a4 substrates.

To evaluate the reliability of using in situ frog intestinal perfusion technique for permeability assessment of carrier transported drugs which are also substrates for CYP enzymes. Single Pass Intestinal Perfusion (SPIP) studies were performed in frogs of the species Rana tigrina using established method for rats with some modifications after inducing anesthesia. Effective permeability coefficient (P eff) of losartan and midazolam was calculated in the presence and absence of inhibitors using the parallel-tube model.

LC-MS/MS method for the determination of pitolisant: application to rat pharmacokinetic and brain penetration studies.

A simple and sensitive LC-MS/MS method was developed and validated for the quantitation of pitolisant, an H3 receptor antagonist/inverse agonist. Acetonitrile protein precipitation technique was used to prepare rat blood and brain tissue homogenate samples by using aripiprazole as internal standard (IS). Chromatographic separation was performed by using Xbridge column (2.

LC-MS/MS method for the quantification of almotriptan in dialysates: application to rat brain and blood microdialysis study.

A sensitive LC-MS/MS method was developed and validated for the quantification of almotriptan in rat brain and blood dialysates. Almotriptan is a 5HT1B/1D receptor agonist used for the treatment of migraine pain. Method consists of rapid gradient elution program with 10mM ammonium formate (pH 3) and acetonitrile on a Xbridge column.

Dried blood spot analysis of an iron chelator--deferasirox and its potential application to therapeutic drug monitoring.

Deferasirox is an iron chelating agent for the treatment of transfusional iron over load in patients with chronic anemia. These anemic patients require close monitoring of the deferasirox exposures for ensuring its therapeutic efficacy. Dried blood spot (DBS) sampling methodology has the advantages of low volume of blood withdrawal and ease of transportation and storage over liquid blood methods.

A rapid and highly sensitive UPLC-MS-MS method for the quantification of zolpidem tartrate in human EDTA plasma and its application to pharmacokinetic study.

A rapid and high sensitive liquid chromatography-tandem mass spectrometry (LC-MS-MS) method was developed and validated for the quantification of zolpidem in human EDTA plasma using ondansetron (IS) as an internal standard. The analyte and IS were extracted from human plasma using ethyl acetate and separated on a C18 column (Inertsil-ODS, 5 µm, 4.6 × 50 mm) interfaced with a triple quadrupole tandem mass spectrometer.

Multi wall carbon nanotubes induce oxidative stress and cytotoxicity in human embryonic kidney (HEK293) cells.

The present study was aimed at evaluating the potential toxicity and the general mechanism involved in multi wall carbon nanotubes (MWCNT)-induced cytotoxicity using human embryonic kidney cell line (HEK293) cells. Two multi wall carbon nanotubes (coded as MWCNT1, size: 90-150nm and MWCNT2, size: 60-80nm) used in this study are MWCNT1 (produced by the electric arc method and size of the nanotubes was 90-150nm) and MWCNT2 (produced by the chemical vapor deposition method with size of 60-80nm). To elucidate the possible mechanisms of MWCNT induced cytotoxicity, cell viability, mitochondrial function (MTT assay), cell membrane damage (LDH assay), reduced glutathione (GSH), interleukin-8 (IL-8) and lipid peroxidation levels were quantitatively assessed under carbon nanotubes exposed (48h) conditions.