scholarly journals Well-defined poly(ethylene glycol) polymers as non-conventional reactive tracers of colloidal transport in porous media

2021 ◽  
Vol 584 ◽  
pp. 592-601
Author(s):  
Thomas Ritschel ◽  
Katharina Lehmann ◽  
Michaela Brunzel ◽  
Jürgen Vitz ◽  
Ivo Nischang ◽  
...  
2021 ◽  
Author(s):  
Thomas Ritschel ◽  
Katharina Lehmann ◽  
Michaela Brunzel ◽  
Jürgen Vitz ◽  
Ivo Nischang ◽  
...  

<p>A large fraction of organic matter in natural aqueous soil solutions is given by molecules in sizes above one nanometer, which classifies them as colloids according to the IUPAC definition. Such colloids feature discernable mobility in soils and their transport is decisive for the cycling of carbon as well as the migration of nutrients or contaminants. Yet, their size-dependent hydrodynamics and functional diversity result in transport phenomena that are specific to colloids and, thus, largely differ from those observed for smaller substances. Still, tracers that appropriately represent small organic colloids are not available and the investigation of their transport in laboratory column experiments, in dependence of size and chemistry, remains difficult. To overcome this limitation, we tested if well-defined synthetic polymers in the colloidal size range are suitable as non-conventional tracers of colloidal transport. As polymer backbone, we selected poly(ethylene glycol) (PEG) due to its high water-solubility and established pathway of synthesis that permits tailoring of functional moieties to the fullest extent. An easy and sensitive detection in the aqueous phase became possible by using a fluorophore as starting group. After full characterization, we studied PEG adsorption to quartz, illite, goethite, and their mixtures in batch and column transport experiments. In numerical simulations, we successfully reconstructed and predicted PEG transport based on its physicochemical as well as hydrodynamic properties and, thus, show that PEG transport can be comprehensively and quantitatively studied. Considering also its low adverse effect on the environment, functional PEG therefore presents as promising candidate to be used as organic tracer, designable in the size range of natural organic (macro-)molecules (Ritschel et al., 2021).</p><p>References</p><p>Ritschel, T., Lehmann, K., Brunzel, M., Vitz, J., Nischang, I., Schubert, U., Totsche, K. U. (2021) <strong>Well-defined poly(ethylene glycol) polymers as non-conventional reactive tracers of colloidal transport in porous media</strong>.<em> J. Colloid Interface Sci.</em> 548, 592-601, doi: 10.1016/j.jcis.2020.09.056.</p>


2019 ◽  
Vol 10 (10) ◽  
Author(s):  
Anton Bonartsev ◽  
Vera Voinova ◽  
Elizaveta Akoulina ◽  
Andrey Dudun ◽  
Irina Zharkova ◽  
...  

2007 ◽  
Vol 32 (5) ◽  
pp. 431-446 ◽  
Author(s):  
Tahar Bartil ◽  
Mahmoud Bounekhel ◽  
Cedric Calberg ◽  
Robert Jerome

2019 ◽  
Author(s):  
Alex Khang ◽  
Andrea Gonzalez Rodriguez ◽  
Megan E. Schroeder ◽  
Jacob Sansom ◽  
Emma Lejeune ◽  
...  

2019 ◽  
Vol 14 (3) ◽  
pp. 280-291 ◽  
Author(s):  
Jaleh Varshosaz ◽  
Farshid Hassanzadeh ◽  
Batool Hashemi-Beni ◽  
Mohsen Minaiyan ◽  
Saeedeh Enteshari

Background: Due to the low water solubility of Docetaxel (DTX), it is formulated with ethanol and Tween 80 with lots of side effects. For this reason, special attention has been paid to formulate it in new drug nano-carriers. Objective: The goal of this study was to evaluate the safety, antitumor activity and tissue distribution of the novel synthesized Raloxifene (RA) targeted polymeric micelles. Methods: DTX-loaded RA-targeted polymeric micelles composed of poly(styrene-maleic acid)- poly(amide-ether-ester-imide)-poly(ethylene glycol) (SMA-PAEE-PEG) were prepared and their antitumor activity was studied in MC4-L2 tumor-bearing mice compared with non-targeted micelles and free DTX. Safety of the micelles was studied by Hematoxylin and Eosin (H&E) staining of tumors and major organs of the mice. The drug accumulation in the tumor and major organs was measured by HPLC method. Results: The results showed better tumor growth inhibition and increased survival of mice treated with DTX-loaded in targeted micelles compared to the non-targeted micelles and free DTX. Histopathological studies, H&E staining of tumors and immunohistochemical examination showed the potential of DTX-loaded RA-targeted micelles to inhibit tumor cells proliferation. The higher accumulation of the DTX in the tumor tissue after injection of the micelles compared to the free DTX may indicate the higher uptake of the targeted micelles by the G-Protein-Coupled Estrogen Receptors (GPER). Conclusion: The results indicate that RA-conjugated polymeric micelles may be a strong and effective drug delivery system for DTX therapy and uptake of the drug into tumor cells, and overcome the disadvantages and side effects of conventional DTX.


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