In recent years ever-increasing amounts of pharmaceuticals are being detected in the aquatic environment and in some cases, they have even been discovered in drinking water. Their presence is attributed mainly to the inability of sewage treatment plants to adequately remove these compounds from the sewage influent. The aim of this study was to investigate the feasibility, kinetics and efficiency of using liquid-core microcapsules as a novel methodology, termed capsular perstraction, to remove seven pharmaceuticals commonly found in the environment, from water. The process involves the envelopment of pre-selected organic solvents within a porous hydrogel membrane to form liquid-core microcapsules, which can be used to extract a large range of compounds. Results indicate that this novel approach is capable of extracting the seven chosen compounds rapidly and with a variable efficiency. The simultaneous use of both dibutyl sebacate and oleic acid liquid-core microcapsules at a liquid volume ratio of only 4% (v/v) resulted in the following extractions within 50min of capsule addition to contaminated water: furosemide 15%; clofibric acid 19%; sulfamethoxazole 22%; carbamazepine 54%; warfarin 80%; metoprolol 90% and diclofenac 100%. The effects of different agitation rates, microcapsule size and membrane thickness on the rate of mass transfer of warfarin into the liquid-core (dibutyl sebacate) of microcapsules was also examined. Results showed that the main rate-limiting step to mass transfer was due to the stagnant organic film (microcapsule size) within the core of the microcapsules. A volumetric mass transfer coefficient of 2.28x10(-6)m/s was obtained for the smallest microcapsules, which was nearly 4-fold higher compared to the value (0.6x10(-6)m/s) obtained for the largest microcapsules used in this study. Even with this resistance liquid-core microcapsules are still capable of the rapid extraction of the tested compounds and may provide a platform for the safe disposal of the pharmaceuticals after removal.
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http://dx.doi.org/10.1016/j.watres.2009.12.036 | DOI Listing |
Open Res Eur
October 2024
The BioRobotics Institute, Sant'Anna School of Advanced Studies, Pisa, Tuscany, 56025, Italy.
ACS Appl Mater Interfaces
May 2024
Institute of Biomaterials, University of Erlangen-Nuremberg, Cauerstrasse 6, Erlangen 91058, Germany.
Aqueous core-shell structures can serve as an efficient approach that allows cells to generate 3D spheroids with -like cell-to-cell contacts. Here, a novel strategy for fabricating liquid-core-shell capsules is proposed by inverse gelation of alginate (ALG) and layer-by-layer (LbL) coating. We hypothesized that the unique properties of polyethylenimine (PEI) could be utilized to overcome the low structural stability and the limited cell recognition motifs of ALG.
View Article and Find Full Text PDFSmall
August 2024
School of Materials Science and Engineering, China University of Petroleum (East China), Qingdao, 266580, China.
Compartmentalization is a powerful concept to integrate multiscale components with diverse functionalities into miniature architectures. Inspired by evolution-optimized cell compartments, synthetic core-shell capsules enable storage of actives and on-demand delivery of programmed functions, driving scientific progress across various fields including adaptive materials, sustainable electronics, soft robotics, and precision medicine. To simultaneously maximize structural stability and environmental sensitivity, which are the two most critical characteristics dictating performance, diverse nanoparticles are incorporated into microcapsules with a dense shell and a liquid core.
View Article and Find Full Text PDFPharmaceutics
October 2023
Department of Bioengineering, Erik Johnson School of Engineering, The University of Texas at Dallas, Richardson, TX 75080, USA.
The use of drug-loaded microbubbles for targeted drug delivery, particularly in cancer treatment, has been extensively studied in recent years. However, the loading capacity of microbubbles has been limited due to their surface area. Typically, drug molecules are loaded on or within the shell, or drug-loaded nanoparticles are coated on the surfaces of microbubbles.
View Article and Find Full Text PDFACS Appl Mater Interfaces
June 2023
Faculty of Civil and Environmental Engineering, Technion─Israel Institute of Technology, Technion City, Haifa 3200003, Israel.
Nano- and micron-sized catalysts are continuously being discovered as efficient tools for pollutant oxidation. Their small size motivates their entrapment in beads or capsules for easier handling, but this is normally followed by reduced reaction kinetics due to slower mass transfer within the encapsulation matrix. In this study, liquid-core encapsulation was explored as a way to overcome this limitation.
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