scholarly journals Antibody glycation during a CHO fed-batch process is following a constrained second order reaction

2021 ◽  
Author(s):  
Magdalena Pappenreiter ◽  
Gabriele Lhota ◽  
Karola Vorauer-Uhl ◽  
Bernhard Sissolak
Keyword(s):  
Cell Culture ◽  
Kinetic Studies ◽  
Batch Process ◽  
Reaction Rate Constant ◽  
Order Reaction ◽  
Second Order ◽  
In Vivo Model ◽  
Second Order Reaction ◽  
Fed Batch

Glycation on lysine side chains of recombinant monoclonal antibodies (mAb) is a well known phenomenon in manufacturing processes of biopharmaceuticals that potentially alter the efficacy of the therapeutic protein. Previously, we reported a method to quantify the level of glycation formation directly from cell culture supernatants using boronate affinity chromatography (BAC). In this study, we report kinetic studies of glycation formation of the model protein Adalimumab, related to glucose and non-glycated protein in six CHO fed batch cultivations. An in-vivo model was demonstrated from glycation kinetic studies that is capable of estimating the reaction rate constant in static and dynamic bioprocesses, respectively. As anticipated, pseudo first order reactions with respect to present glucose concentration or non-glycated mAb were not sufficient to describe the glycation formation during the bioprocesses. However, second order reactions did not reveal linear relationship of glycated mAb to the product of glucose and non-glycated mAb, suggesting a reconsideration of kinetic equation. With the introduction of a constraint using only the newly formed product, i.e., the nascent protein, the second-order reaction was successfully implemented. These results show that the process knowledge derived from dynamic can be transferred to static experiments and vice versa. Hence, intensified DoE can be an applicable and useful tool in product quality studies in cell culture processes.

scholarly journals Kinetic Studies of the Glycerolysis of Urea to Glycerol Carbonate in the Presence of Amberlyst-15 as Catalyst

2021 ◽  
Vol 16 (1) ◽  
pp. 52-62
Author(s):  
Hary Sulistyo ◽  
Wahyudi Budi Sediawan ◽  
Reviana Inda Dwi Suyatno ◽  
Indah Hartati
Keyword(s):  
Kinetic Model ◽  
Active Sites ◽  
Outer Part ◽  
Kinetic Studies ◽  
Order Reaction ◽  
Second Order ◽  
Glycerol Carbonate ◽  
Glycerol Concentration ◽  
Second Order Reaction ◽  
Amberlyst 15

Amberlyst-15, a strong acidic ion-exchange resin, has showed as a potential and an effective catalyst for the glycerolysis process of urea to glycerol carbonate. In this work, the kinetic model of the urea glycerolysis over Amberlyst-15 catalyst was investigated. The kinetic model was developed by considering simultaneous steps of urea dissolution in glycerol, mass transfer of urea and glycerol from the bulk of the liquid into the outer part of the catalyst, diffusion of urea and glycerol into the inner part of the particle through the catalyst pores, and irreversible second order reaction of urea and glycerol on the active sites. The irreversibility of second order reaction of urea glycerolysis was validated and proven. The proposed kinetic model was simulated and validated with the experimental data. The kinetic studies show that mechanism proposed works well. Furthermore, the activation energy was found to be 145.58 kJ.mol−1 and the collision factor was in 8.00×1010 (m3)2.kg−1.mol−1.s−1. The simulation result shows that the predicted liquid temperatures were close to the experimental temperature data. It also gave glycerol concentration profile inside the catalyst particle as a function of glycerolysis time and position. Copyright © 2021 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0). 

Stability of radical anions derived from substituted 5-nitrofurans investigated by ESR spectroscopy

1985 ◽  
Vol 50 (7) ◽  
pp. 1594-1601 ◽  
Author(s):  
Jiří Klíma ◽  
Larisa Baumane ◽  
Janis Stradinš ◽  
Jiří Volke ◽  
Romualds Gavars
Keyword(s):  
Radical Anion ◽  
High Stability ◽  
Esr Spectroscopy ◽  
Reaction Path ◽  
Order Reaction ◽  
Second Order ◽  
Radical Anions ◽  
Second Order Reaction ◽  
Unpaired Electron Density ◽  
The Stability

It has been found that the decay in dimethylformamide and dimethylformamide-water mixtures of radical anions in five of the investigated 5-nitrofurans is governed by a second-order reaction. Only the decay of the radical anion generated from 5-nitro-2-furfural III may be described by an equation including parallel first- and second-order reactions; this behaviour is evidently caused by the relatively high stability of the corresponding dianion, this being an intermediate in the reaction path. The presence of a larger conjugated system in the substituent in position 2 results in a decrease of the unpaired electron density in the nitro group and, consequently, an increase in the stability of the corresponding radical anions.

Kinetics of the reaction between hexamethylenediisocyanate and 1-pentanol

1983 ◽  
Vol 48 (11) ◽  
pp. 3279-3286
Author(s):  
Slavko Hudeček ◽  
Miloslav Bohdanecký ◽  
Ivana Hudečková ◽  
Pavel Špaček ◽  
Pavel Čefelín
Keyword(s):  
Liquid Chromatography ◽  
Rate Constants ◽  
Reversed Phase ◽  
Order Reaction ◽  
Second Order ◽  
Second Order Reaction ◽  
Reversed Phase Liquid Chromatography ◽  
Consecutive Reactions ◽  
Phase Liquid ◽  
Kinetics Of

The reaction between hexamethylenediisocyanate and 1-pentanol in toluene was studied by means of reversed-phase liquid chromatography. By employing this method, it was possible to determine all components of the reaction mixture including both products, i.e. N-(6-isocyanate hexyl)pentylcarbamate and N,N'-bis(pentyloxycarbonyl)hexamethylenediamine. Relations for the calculation of kinetic constants were derived assuming a competitive consecutive second-order reaction. It was demonstrated that the reaction involved in this case is indeed a second-order reaction, and the rate constants of the first and second consecutive reactions were determined.

Photocatalytic Degradation of Methyl Orange by TiO2/Schorl Photocatalyst: Kinetics and Thermodynamics

2015 ◽  
Vol 713-715 ◽  
pp. 2789-2792
Author(s):  
Huan Yan Xu ◽  
Xue Li ◽  
Yan Li ◽  
Ping Li ◽  
Wei Chao Liu
Keyword(s):  
Methyl Orange ◽  
Reaction Rate ◽  
Reaction Kinetic ◽  
Kinetic Studies ◽  
Reaction Rate Constant ◽  
Order Reaction ◽  
Solution Ph ◽  
Kinetics And Thermodynamics ◽  
Hoff Equation ◽  
Degradation Of Methyl Orange

An active dye, Methyl Orange (MO) was employed as the target pollutant to evaluate the photocatalytic activity of TiO2/schorl composite and the kinetics and thermodynamics of this process was emphasized in this work. Langmuir–Hinshelwood kinetic model was employed for the kinetic studies and the results revealed that the process of MO photocatalytic discoloration by TiO2/schorl composite followed one order reaction kinetic equation under different conditions. The reaction rate constant (k) increased with initial MO concentration decreasing. When the catalyst dosage or solution pH increased,kvalues increased and then decreased. The possible reasons for these phenomena were discussed. Finally, the thermodynamic parameters ΔG, ΔH, ΔSwere obtained by the classical Van't Hoff equation.

Analytical resolution of a parallel second-order reaction mechanism

2003 ◽  
Vol 35 (6) ◽  
pp. 246-251
Author(s):  
A. E. Croce ◽  
L. V. Mogni ◽  
C. Vicente Irrazábal
Keyword(s):  
Reaction Mechanism ◽  
Order Reaction ◽  
Second Order ◽  
Second Order Reaction ◽  
Analytical Resolution

scholarly journals Ribonucleic acid–deoxyribonucleic acid hybridization as a second-order reaction

1973 ◽  
Vol 135 (3) ◽  
pp. 573-576 ◽  
Author(s):  
Bryan D. Young ◽  
John Paul
Keyword(s):  
Dna Hybridization ◽  
Ribonucleic Acid ◽  
Deoxyribonucleic Acid ◽  
Order Reaction ◽  
Second Order ◽  
Second Order Reaction ◽  
Reaction Theory

Certain features of RNA–DNA hybridization can be accounted for in terms of second-order-reaction theory. These include the use of annealing kinetics to estimate RNA complexity and the occurrence of approximately linear double-reciprocal plots.

scholarly journals Water defluoridation by alumina modified Turkey clinoptilolite: equilibrium, kinetic models and experimental design approaches

2017 ◽  
Vol 18 (1) ◽  
pp. 14-22 ◽  
Author(s):  
Selim Selimoglu ◽  
Esra Bilgin Simsek ◽  
Ulker Beker
Keyword(s):  
Natural Zeolite ◽  
Kinetic Studies ◽  
Order Reaction ◽  
Operating Conditions ◽  
Second Order Reaction ◽  
Freundlich Model ◽  
Box Behnken Design ◽  
Fluoride Adsorption ◽  
Exothermic Process ◽  
Pseudo Second Order

Abstract In the current work, alumina modified natural zeolite (Z-Al) was used for fluoride adsorption in aqueous solution. Effects of process parameters such as pH, temperature, initial concentration and contact time were investigated. Box–Behnken design was found effective in defining the operating conditions for fluoride sorption onto Z-Al. Confirmatory experiments were conducted to examine the reliability of the regression equation. The predicted (2.261 mg g−1) and experimental (2.289 mg g−1) capacities were found to be similar, demonstrating the accuracy of the model. The fluoride adsorption onto Z-Al was well described by the Freundlich model. Kinetic studies revealed that the adsorption followed a pseudo-second-order reaction. Thermodynamic parameters depicted that the fluoride adsorption on the alumina modified zeolite was a spontaneous and exothermic process. The co-existing ions affected the defluoridation performance significantly. Regeneration of exhausted Z-Al was achieved with H2SO4.

scholarly journals The alcoholysis of 1,2,2-trimethylpropyl-methylfluorophosphonate

2000 ◽  
Vol 65 (12) ◽  
pp. 857-866
Author(s):  
Mladjen Micevic ◽  
Slobodan Petrovic
Keyword(s):  
Kinetic Data ◽  
Reaction Rate ◽  
Frequency Factor ◽  
Reaction Rate Constant ◽  
Order Reaction ◽  
Activation Entropy ◽  
Second Order Reaction ◽  
Third Order ◽  
First Order ◽  
Kinetics Of

The alcoholysis of 1,2,2-trimethylpropyl-methylfluorophosphonate (soman) was examined with a series of alkoxides and in corresponding alcohols: methanol, ethanol, 1-propanol, 2-propanol, 2-methoxyethanol and 2-ethoxyethanol. Soman reacts with the used alkoxides in a second order reaction, first order in each reactant. The kinetics of the reaction between 1,2,2-trimethylpropyl-methylfluorophosphonate and ethanol in the presence of diethylenetriamine was also examined. A third order reaction rate constant was calculated, first order in each reactant. The activation energy, frequency factor and activation entropy were determined on the basis of the kinetic data.

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