For an enzymatic assay, tumour cells are incubated at different concentrations in individual vials (Table 1). Please note that the final reaction volume differs between the three setups. Vial No. A (ml) В (ml) C (ml) H20 1 5 Tris/HCl buffer pH7|1 1 1 Tumour cells (5% 1 4 (w/v)) in buffer Glucose [25mM] 0.5 0.75 1 Table 1. a) Calculate the weight (in gram/ml) of tumour cells in each vial. Show your workings. b) Calculate the glucose concentration in each vial (in mol/ml). Show your workings. Based on Table 1, calculate the glucose concentration / 1 gram tumour cells in conditions A, B and C. Show your workings. 3.

For an enzymatic assay, tumour cells are incubated at different concentrations in individual vials (Table 1). Please note that the final reaction volume differs between the three setups. Vial No. A (ml) В (ml) C (ml) H20 1 5 Tris/HCl buffer pH7|1 1 1 Tumour cells (5% 1 4 (w/v)) in buffer Glucose [25mM] 0.5 0.75 1 Table 1. a) Calculate the weight (in gram/ml) of tumour cells in each vial. Show your workings. b) Calculate the glucose concentration in each vial (in mol/ml). Show your workings. Based on Table 1, calculate the glucose concentration / 1 gram tumour cells in conditions A, B and C. Show your workings. 3.

Appl Of Ms Excel In Analytical Chemistry

2nd Edition

ISBN:9781285686691

Author:Crouch

Publisher:Crouch

Chapter12: Spectrochemical Methods

Section: Chapter Questions

Problem 7P

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A 5.00-mL sample of blood was treated with trichloroacetic acid to precipitate proteins. After centrifugation, the resulting solution was brought to pH 3 and extracted with two 5-mL portions of methyl isobutyl ketone containing the lead-complexing agent APCD. The extract was aspirated directly into an air/acetylene flame and yielded an absorbance of 0.569 at 283.3 nm. Five-milliliter aliquots of standard solutions containing 0.400 and 0.600 ppm of lead were treated in the same way and yielded absorbances of 0.396 and 0.599. Please calculate the concentration of lead in the sample in ppm.
In order to improve the peptide separation by using a HPLC system, trifluoroacetic acid acts as mobile-phase modifier was added during the preparation of mobile phase. The preparation was performed by a postgraduate student as following:“2.851 g trifluoroacetic acid (MW: 114.02 g/mol) was made up to 500 cm3 in a graduated flask. To this solution, 50 cm3 of ethanol was added, and after mixing the mobile phase was placed in the solvent reservoir and pumping was commenced at 1.5 cm3 min-1.”Based on the given preparation procedure, identify THREE mistakes that were made.
A 5.00-mL sample of blood was treated with trichloroacetic acid to precipitate proteins. After centrifugation, the resulting solution was brought to pH 3 and extracted with two 5-mL portions of methyl isobutyl ketone containing the lead-complexing agent APCD. The extract was aspirated directly into an air/acetylene flame and yielded an absorbance of 0.527 at 283.3 nm. Five-milliliter aliquots of standard solutions containing 0.400 and 0.600 ppm of lead were treated in the same way and yielded absorbances of 0.396 and 0.599. Find the concentration of lead in the sample in ppm assuming that Beer’s law is followed.
A 0.0200 gram blood sample was decomposed by a microwave digestion technique followed by dilution to 100.0 mL in a volumetric flask. Aliquots of the sample solution were treated with a lead complexing reagent and water as follows: Solution 1: 10.0 ml blood sample + 20.0 mL complexing agent + 30.0 mL H20. Solution 2: 10.0 ml blood sample + 20.0 mL complexing agent + 26.0 mL H20 + 4.00 mL of 78 ppb Pb2+ standard. The resulting solutions were analyzed by UV/Vis at 375 nm. Absorbance for solution 1 = 0.155 and for solution 2 = 0.216. Calculate the concentration of lead (ppb) in the original sample.
what weight of betazole phosphotungstate might be expected in the assay of 0.1550 g sample of betazole hydrochloride containing 98% C5H9N3.2HC? Gravimetric factor = 0.0909
The concentration of purified OXA-M290 is tested with a BCA assay. Serial dilutions of a bovine serum albumin (BSA) stock solution are prepared, then pipetted into a 96-well plate; each dilution of the BSA standard is tested in triplicate. Then, bicinchoninic acid and Cu2+ ions are added to all of the wells of the plate. After incubating the plate for 1 hour, a microplate reader is used to measure the absorbance of all of the wells in the plate at 560 nm. This generates the following data: BSA conc. (μg/mL), Replicate 1 Absorbance, Replicate 2 Absorbance, Replicate 3 Absorbance 40, 1.360, 1.403, 1.481 20, 0.750, 0.745, 0.810 10, 0.380, 0.344, 0.398 5, 0.198, 0.160, 0.183 2.5, 0.090, 0.100, 0.085 1.25, 0.038, 0.043, 0.051 0.625, 0.024, 0.028, 0.019 Prepare a calibration curve using these data. You can use Excel, R, SPSS or an equivalent graphing software. In this graph, plot absorbance (y-axis) against the concentration of the protein standard (x-axis). Calculate and plot…
In a similar experiment, the mass of 3 PB tablets was measured to be 3.1823 g. The tablets were crushed, and 2.9801 g of the powder was transferred to a beaker and reacted with HCl. After filtration, the filtrate was transferred to a 50-mL volumetric flask and diluted with water. 10.00 mL of this stock solution was combined with 0.2 M Na3PO4. The resulting precipitate weighed 0.2425 g after drying. What is the mass of BSS per tablet in mg?Round your answer to 1 decimal place.
From a kinetics experiment, the Vmax was determined to be 325µM*min^-1. for the kinetic assay, 0.1mL of a 0.25mg/mL solution of enzyme was used, and the enzyme has a molecular weight of 75,000 g/mole. Assume a reaction volume of 700µL. Calculate the kcat (in sec^-1) for the enzyme
A 100 ml bottle of metronidazole 100 mg/ml suspension is available in your pharmacy. Calculate the volume of this suspension needed to be diluted with cherry syrup to prepare 60 ml of a 4% metronidazole suspension. 1 ml of a 1:1000 epinephrine injection was mixed with 20 ml of 1% lidocaine injection. Calculate the new ratio strength of epinephrine in the admixture. (IGNORE ANY VOLUME CHANGES AFTER ADMIXTURE) Instead of preparing 4 grams of tetracaine hydrochloride 4% gel an 8% gel was compounded by mistake. How many grams of the 8% gel and gel base must be mixed to get 4 grams of a 4% gel? How many milliliters of 70% ethanol and 20% ethanol must be mixed to prepare 500 ml of 30% ethanol? A diphenhydramine elixir contains 12.5 mg drug in one teaspoon. The volume of oral vehicle that is to be added to 100 ml of this elixir to reduce its strength by one half its original strength is; 6. 90 capsules of Liothyronine (T3) 15 micrograms are to be prepared. The formula calls for a 1:10000…
3. Assume that in extraction from water into toulene, analyte A has distribution ratio of 10. A 20 mL portion of an aqueous solution of A is extracted with toulene. Which of thw following procedures will result in most efficient removal of A from the aqueous phase into toulene? (Please show the solution of the correct answer) A. 1 extraction with 20 mL of touleneB. 1 extraction with 40 mL of touleneC. 2 extractions with 20 mL of toulene eachD. 4 extractions with 10 mL of toulene each
20 tablets containing the dibasic drug ethambutol hydrochloride (MW 277.2 g/mol) were powdered. 0.3354 g of tablet powder was dissolved in 10 mL of 2 M sodium hydroxide and was extracted with 5 x 25 mL quantities of chloroform. The combined extracts were evaporated and the residue was dissolved in 100 mL of anhydrous acetic acid. Non-aqueous titration was carried out using 1-naphtholbenzein solution as indicator and 0.1014 M acetous perchloric acid. Volume of acetous perchloric acid required = 14.2 mL, weight of 20 tablets = 3.367 g, state content of ethambutol hydrochloride per tablet = 100 mg. Calculate the % of stated content in the tablets.
Two analysts each made six determinations of the paracetamol content of the same batch of tablets. The results are shown below:Analyst Paracetamol content % (m/m)A 84.32 84.51 84.63 84.61 84.64 84.51B 84.24 84.25 84.41 84.13 84.00 84.30 How many moles of the analyte P is gravimetrically equivalent to P2O5?A) 1B) 2C) 3D) 4E) 5