scholarly journals Residue and dissipation dynamic of spinetoram insecticide in pear fruits

2021 ◽  
Vol 57 (No. 4) ◽  
pp. 236-332
Author(s):  
Dragana Sunjka ◽  
Sanja D. Lazić ◽  
Slavica M. Vuković ◽  
Aleksandra S. Alavanja ◽  
Đura J. Nađ ◽  
...  

Cacopsylla pyri (Linnaeus, 1758) is the most significant and widespread pear pest. It attacks the pear only, causing direct and indirect damages. This study was conducted in order to evaluate the efficacy of insecticide spinetoram in the control of C. pyri. The experiment was set up according to EPPO methods, at the locality Kula (Republic of Serbia) in a pear orchard (Williams variety). Spinetoram (250 g/kg a.i., WG) was foliar applied in the amount of 0.3 kg/ha, during overlapping pest generations, when pear was on BBCH 75 scale. The efficacy was evaluated through the number of larvae aged L<sub>1</sub>–L<sub>3</sub> and L<sub>4</sub>–L<sub>5</sub>. Spinetoram has shown satisfying efficacy, especially in the control of L<sub>1</sub>–L<sub>3</sub> larvae (81.6%). In a dissipation study, spinetoram residues in pear fruits were determined using QuEChERS method followed by HPLC-DAD. The method was validated to fulfill SANTE/12682/2019 criteria. Three days after the application, spinetoram residues in pear fruits were below the MRL (0.2 mg/kg). The results have shown that spinetoram dissipation pattern followed the first-order kinetics (R<sup>2 </sup>= 0.979) with a half-life of 2.17 days, in pear fruits. This study suggests that spinetoram could be safely used in pear, and it could take an important place in insecticide resistance management.

2020 ◽  
Vol 16 ◽  
Author(s):  
M. Alarjah

Background: Prodrugs principle is widely used to improve the pharmacological and pharmacokinetic properties of some active drugs. Much effort was made to develop metronidazole prodrugs to enhance antibacterial activity and or to improve pharmacokinetic properties of the molecule or to lower the adverse effects of metronidazole. Objective: In this work, the pharmacokinetic properties of some of monoterpenes and eugenol pro metronidazole molecules that were developed earlier were evaluated in-vitro. The kinetic hydrolysis rate constants and half-life time estimation of the new metronidazole derivatives were calculated using the validated RP-HPLC method. Method: Chromatographic analysis was done using Zorbbax Eclipse eXtra Dense Bonding (XDB)-C18 column of dimensions (250 mm, 4.6 mm, 5 μm), at ambient column temperature. The mobile phase was a mixture of sodium dihydrogen phosphate buffer of pH 4.5 and methanol in gradient elution, at 1ml/min flow rate. The method was fully validated according to the International Council for Harmonization (ICH) guidelines. The hydrolysis process carried out in an acidic buffer pH 1.2 and in an alkaline buffer pH 7.4 in a thermostatic bath at 37ºC. Results: The results followed pseudo-first-order kinetics. All metronidazole prodrugs were stable in the acidic pH, while they were hydrolysed in the alkaline buffer within a few hours (6-8 hr). The rate constant and half-life values were calculated, and their values were found to be 0.082- 0.117 hr-1 and 5.9- 8.5 hr., respectively. Conclusion: The developed method was accurate, sensitive, and selective for the prodrugs. For most of the prodrugs, the hydrolysis followed pseudo-first-order kinetics; the method might be utilised to conduct an in-vivo study for the metronidazole derivatives with monoterpenes and eugenol.


1989 ◽  
Vol 35 (8) ◽  
pp. 1774-1776 ◽  
Author(s):  
D A Smith ◽  
G C Moses ◽  
A R Henderson

Abstract We examined the stability of human lactate dehydrogenase (EC 1.1.1.27) isoenzyme 5--purified to a specific activity of about 400 kU/g--when lyophilized in a buffered, stabilized matrix of bovine albumin. This isoenzyme was prepared with a final activity of about 500 U/L and stored at -20, 4, 20, 37, and 56 degrees C for as long as six months. This isoenzyme decayed with approximate first-order kinetics, with an estimated half-life at -20 degrees C of about 475 years. Stability of reconstituted samples stored at 20 or 4 degrees C was poor, suggesting that the reconstituted material should be used without delay; material stored at -20 degrees C showed excellent stability for 15 days. We propose that such preparations might be further investigated as standards for use in electrophoresis of lactate dehydrogenase isoenzymes.


1983 ◽  
Vol 96 (2) ◽  
pp. 347-353 ◽  
Author(s):  
PJM Van Haaster ◽  
PR Van Der Heijden

Extracellular cAMP induces chemotaxis and cell aggregation in dictyostelium discoideum cells. cAMP added to a cell suspension is rapidly hydrolyzed (half-life of 10 s) and induces a rapid increase of intracellular cGMP levels, which reach a peak at 10 s and recover prestimulated levels at about 30 s. This recovery is not due to removal of the stimulus because the nonhydrolyzable analogue adenosine 3',5'-monophosphorothioate-Sp- stereoisomer (cAMPS) induced a comparable cGMP response, which peaked at 10 s, even at subsaturating cAMPS concentrations. When cells were stimulated twice with the same cAMP concentration at a 30-s interval, only the first stimulus produced a cGMP response. Cells did respond to the second stimulus when the concentration of the second stimulus was higher than that of the first stimulus. By increasing the interval between two identical stimuli, the response to the second stimulus gradually increased. Recovery from the first stimulus showed first-order kinetics with a half-life of 1-2 min. The stimulation period was shortened by adding phosphodieterase to the cell suspension. The cGMP response was unaltered if the half-life of cAMP was reduced to 2 S. The peak of the transient cGMP accumulation still appeared at 10 s even when the half- life of cAMP was 0.4 s; however, the height of the cGMP peak was reduced. The cGMP response at 10 s after stimulation was diminished by 50 percent when the half-life of 10(-7) M cAMP was 0.5 s or when the half-life of 10(-8) M cAMP was 3.0 s. These results show that the cAMP signal is transduced to two opposing processes: excitation and adaptation. Within 10 s after addition of cAMP to a cell suspension the level of adaptation reaches the level of excitation, which causes the extinction of the transduction of the signal. Deadaptation starts as soon as the signal is removed, and it has first-order kinetics with a half-life of 1-2 min.


Author(s):  
Md. Mifta Faizullah ◽  
T. Ramprakash ◽  
T. Anjaiah ◽  
M. Madhavi

Persistence of diuron applied to cotton as preemergence spray at varied rates of application (0.5, 0.75, 1.0 kg ha-1) was studied in field experiments conducted simultaneously in red and black soils at Professor Jayashankar Telangana State Agricultural University, Rajendranagar during kharif, 2018. In both red and black soils, persistence of diuron was observed beyond 120 days after application and the concentration of diuron in the top soil (0-15 cm) was higher in black soils compared to red soils from 0 Days to 120 Days. Higher dose of diuron showed greater soil persistence in both red and black soil. Diuron dissipation in soil followed first order kinetics in both the soils. Field half life of diuron was higher in black soil was 53.3-77.0 days at different rates of application than in red soil (53.3-69.3 days).


2013 ◽  
Vol 25 (2) ◽  
pp. 200-203 ◽  
Author(s):  
Nilfur Nahar ◽  
Mohammad Shoeb ◽  
M Iqbal Rouf Mamun ◽  
Sultan Ahmed ◽  
Mir Mahadi Hasan ◽  
...  

Dissipation pattern of cypermethrin (Ripcord 10EC) on tomato plants sprayed at recommended and double the recommended doses followed first order kinetics. In both the doses residues were found below the maximum residue level (0.5 ppm) after one day of application. Recoveries were found to be 80.88% &77.09% spiked at 0.2 & 0.5 ppm, respectively. LOD and LOQ were found to be 0.01 and 0.06 ppm, respectively. Journal of Bangladesh Chemical Society, Vol. 25(2), 200-203, 2012 DOI: http://dx.doi.org/10.3329/jbcs.v25i2.15087


1969 ◽  
Vol 21 (03) ◽  
pp. 580-593
Author(s):  
L. A Pálos ◽  
G Sas ◽  
A Csurgay

SummaryThe reaction kinetics of the second phase of blood clotting (conversion of fibrinogen to fibrin) has been studied in euglobulin and thrombin-antithrombin systems. It was intended to set up relationships that would make mathematical expression of the processes possible and which would, moreover, help in detecting dynamic and functional relationships characteristic of the mechanism involved in coagulation.The experiments have yielded the following results:1. In the euglobulin solution containing no antithrombin the fibrinogen-thrombin reaction can be characterized with a constant deviation from the first order kinetics.2. The process of thrombin inactivation is a reaction of first order in the initial phase.3. The two basic processes (clotting by thrombin in euglobulin solution, inactivation of thrombin in defibrinated plasma) make it possible to predetermine the thrombin time of citrated plasma. Theoretical and actual clotting times were in good agreement.4. The thrombin time of plasma can be computed even if thrombin is not introduced to the system at one stride but gradually, a manner of administration which is a better imitation of what happening in vivo. 5. In connection with the computation of the “thrombin time” of citrated blood, we determined experimentally (and expressed by means of a function) the modification produced by the corpuscular elements of the blood in the reaction between fibrinogen and thrombin under atraumatic conditions.


1985 ◽  
Vol 53 (02) ◽  
pp. 208-211 ◽  
Author(s):  
G Bratt ◽  
E Törnebohm ◽  
D Lockner ◽  
G Bergströ

SummaryThe pharmacokinetics of a heparin fragment of low molecular weight (LMWH) of 4000-5000 D and unfractioned standard heparin (UFH) have been studied after i. v. injections of different doses and infusions in 8 humans.The heparin activity was significantly higher and the effect on APTT lower after LMWH fragment as compared to UFH in the same doses.The half-life of heparin activity was about 1 hr for UFH and about 2 hr for LMWH. LMWH was found to be eliminated according to first order kinetics and there were no signs of dose dependency.


Weed Science ◽  
1976 ◽  
Vol 24 (5) ◽  
pp. 508-511 ◽  
Author(s):  
James S. Ladlie ◽  
William F. Meggitt ◽  
Donald Penner

Metribuzin [4-amino-6-tert-butyl-3-(methylthio)-as-triazine-5(4H)one] residue analysis of soil samples showed greater amounts of residue extractable at soil pH 6.7 than 4.6. Metribuzin leaching increased with increasing soil pH. Metribuzin disappearance from soil followed pseudo first-order kinetics. The half-life of metribuzin decreased as soil pH increased and increased at all soil pH levels as depth of sampling increased. The decreased activity and decreased rate of metribuzin dissipation at lower soil pH is apparently due to protonation and increased adsorption.


1986 ◽  
Vol 233 (3) ◽  
pp. 905-908
Author(s):  
K C Kleene

The equations that have been used previously to analyse the rate of decay of hnRNA implicitly assume that nascent hnRNAs are degraded stochastically. This assumption is inconsistent with electron-microscopic studies of transcription cited here, which show that nascent hnRNAs are not degraded during transcription, implying that hnRNA degradation occurs only after termination of transcription and release of the hnRNA from chromatin. Equations are derived describing the accumulation of radioactivity hnRNA during continuous labelling assuming that nascent hnRNAs are stable and that hnRNAs decay with first-order kinetics only after completion of transcription. The effects of the transient stability of nascent hnRNAs on the kinetics of hnRNA turnover can become important when the half-life of the hnRNA is shorter than the time to transcribe an hnRNA from the point of initiation to the point of termination. These equations should prove useful in studies of hnRNA turnover that require a precise description of the labelling kinetics of nascent and completed subpopulations of hnRNA.


2014 ◽  
Vol 7 ◽  
pp. ASWR.S14847 ◽  
Author(s):  
Ankita Verma ◽  
Anjana Srivastava ◽  
Shailendra Singh Chauhan ◽  
Prakash Chandra Srivastava

In a laboratory investigation, the effect of natural sunlight and UV light exposure on dissipation of fipronil insecticide from two soils (clay loam and sandy clay loam) and the effect of pH on the persistence of fipronil in aqueous medium were studied. Dissipation of fipronil insecticide under sunlight followed biphasic first order kinetics in both soils. The half-life of the insecticide in sandy clay loam type soil was found to be 5.71 days for the first faster phase and 23.88 days for the second slower phase, whereas, in clay loam soil, the corresponding half-lives were 4.02 and 8.38 days, respectively. Under the UV light exposure, the dissipation of fipronil followed a single phase first order kinetics in both the soils with a half-life of 3.77 days in clay loam and 5.37 days in sandy clay loam, respectively. Residues of fipronil dissipated faster in clay loam than in sandy clay loam under both sunlight and UV lamp light. As compared to sunlight, dissipation was found to be faster under UV lamp light. Persistence of fipronil in aqueous medium under different pH conditions revealed that fipronil residues were below the limit of detection (LOD), <0.05 μg g−1, after 40 days of sampling at all the three pH. The dissipation of fipronil from aqueous medium increased with increasing pH from 5.0 to 9.0; the corresponding half-lives were 14.12, 9.83, and 6.76 days at pH 5.0, 7.0, and 9.0, respectively.


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