Cellular uptake, cytotoxicity, and transport kinetics of anthracyclines in human sensitive and multidrug-resistant K562 cells

1996 ◽  
Vol 51 (10) ◽  
pp. 1341-1348 ◽  
Author(s):  
Michel Praet ◽  
Pierre Stryckmans ◽  
Jean-Marie Ruysschaert
2014 ◽  
Vol 28 (2) ◽  
pp. 187-197 ◽  
Author(s):  
Marzena Szwed ◽  
Agnieszka Matusiak ◽  
Audrey Laroche-Clary ◽  
Jacques Robert ◽  
Ilona Marszalek ◽  
...  

Cytometry ◽  
1998 ◽  
Vol 32 (4) ◽  
pp. 280-285 ◽  
Author(s):  
Loris Zamai ◽  
Adriana R. Mariani ◽  
Giorgio Zauli ◽  
Luigi Rodella ◽  
Rita Rezzani ◽  
...  

1997 ◽  
Vol 77 (2) ◽  
pp. 545-590 ◽  
Author(s):  
W. D. Stein

Most cancer deaths result from the cancer's either being intrinsically resistant to chemotherapeutic drugs or becoming resistant after being initially sensitive. Often, in cells grown in cell culture, drug resistance correlates with the presence of one or more of the so-called P-glycoproteins or multidrug resistance proteins, products of the mdr family of genes. This review is largely concerned with the transport kinetics of the P-glycoproteins. We first present a brief overview of the P-glycoproteins, their properties, and their clinical significance. Later sections of the review expand on this material with special emphasis on the substrates of P-glycoprotein and how they cross the cell membrane, on the transport kinetics of the P-glycoprotein, on reversers of its action, and on its activity as an ATPase. In a final section, we consider the mechanism of action of P-glycoprotein as an actively transporting membrane pump. The characteristic of P-glycoprotein considered the most difficult to explain is its very broad specificity (or lack of specificity), but there are precedents for this property in well-known proteins such as serum albumin, which binds a range of molecular types, including substrates and reversers of P-glycoprotein, seemingly as broad as does P-glycoprotein. Pointing out this analogy does not provide a molecular explanation for the substrate-binding properties of P-glycoprotein but does make those properties more assimilable.


2021 ◽  
Author(s):  
Yu Gao ◽  
Jun Huang ◽  
Yuwen Liu ◽  
Shengli Chen

The discrepancy between the trend in the diffusion coefficient of lithium ion (DLi+) and that in the activation energy of ion hopping signals hidden factors determining ion transport kinetics in...


2021 ◽  
Author(s):  
Gaurang Khot ◽  
Frank Platte ◽  
Neil Shirtcliffe ◽  
Tansu Celikel

AbstractCarbon nanotubes (CNTs) are suited for neurochemistry because of their biological inertness, ability to withstand biofouling, and superior electron transport kinetics. Dopamine, the canonical monoaminergic neuromodulator, contributes to reward, cognition and attention, however, its detection in real-time is challenging due to its low basal concentration in the brain (100nM L-1). In our present work, we fabricate pyrolytic carbon electrodes and perform a CNT coating to improve the electrochemical kinetics of dopamine. Upon CNTs coating, dopamine shows a sensitivity of 9±18nA/μM for a cylindrical electrode having a mean surface diameter of 8±4μm. Increasing the scan frequency from 10-100 Hz shows that dopamine electron transfer kinetics improves; wherein dopamine is oxidized at 0.35±0.09V and reduced to -0.10±0.05V for 10 Hz. Increasing the frequency results in a shift of oxidation peak towards the anodic region, wherein dopamine oxidizes at 0.08±3V and reduces at -0.1±0.05V for 100 Hz, thus showing that dopamine redox is reversible which can be attributed to the superior electron transport kinetics of CNTs. The sensor was able to distinguish dopamine signals against other neurochemicals like serotonin and foulant 3,4-Dihydroxyphenylacetic acid (DOPAC). The minimum chemical detection that can be performed using these nanopipettes is 50±18nM L-1, which is well below the physiological concentrations of dopamine in the brain.Graphical AbstractA: Pictorial view of background-subtracted voltammetry. The waveform used was -0.4V to 1.3 V and cycled back to -0.4V at 10 Hz. B: The voltammogram was converted as a 2-D representation, into current, voltage, and repetition to understand the dopamine oxidation. C: Background subtracted voltammetry for dopamine using 100 Hz waveform. D: The 2-D representation of current, voltage, and repetition.


Nanoscale ◽  
2014 ◽  
Vol 6 (13) ◽  
pp. 7325-7331 ◽  
Author(s):  
V. Hirsch ◽  
C. Kinnear ◽  
L. Rodriguez-Lorenzo ◽  
C. A. Monnier ◽  
B. Rothen-Rutishauser ◽  
...  

A well-controlled route towards biocompatible agglomerated Au-NPs is reported, which span the range from small particles with high diffusion coefficients to larger particles with lower diffusion coefficients. Difference in uptake kinetics of single NPs and agglomerates can be explained by particokinetics, without the need to consider size-mediated cellular uptake mechanisms.


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