New type of carriers based on grafted poly(ionic liquid)s was designed for delivery of ionically attached salicylates (Sal). Choline derived ionic liquid monomeric units were successfully introduced with various content in the side chains by the controlled radical polymerization. Properly high amounts of ionic pharmaceutics in the polymer systems were achieved by the well-fitted length and grafting degree of the side chains. In aqueous solution the graft copolymers were self-assembled into the spherical superstructures with sizes up to 73 nm. Delivery studies showed “burst” release within 4 h, after that it was slower yielding ~70% of released drug within 80 h. Proposed nanocarriers supported low toxicity against human cells (NHDF and BEAS-2B), anti-inflammation activity evaluated with the use of pro-inflammatory interleukins (IL-6 and IL-8) and antibacterial activities towards E. coli. Adjustment of ionic drug content by structural parameters of graft copolymers, including grafting degree and graft length, are advantageous to tailor nanocarriers with self-assembly properties in aqueous media. Effective release process by ionic exchange and biological activity with low toxicity are promising for further development of this type of drug delivery (DDS).

The application of polymers as a tool in the crystallization process is gaining more and more interest among the scientific community. According to Web of Science statistics the number of papers dealing with “Polymer induced crystallization” increased from 2 in 1990 to 436 in 2020, and for “Polymer controlled crystallization”—from 4 in 1990 to 344 in 2020. This is clear evidence that both topics are vivid, attractive and intensively investigated nowadays. Efficient control of crystallization and crystal properties still represents a bottleneck in the manufacturing of crystalline materials ranging from pigments, antiscalants, nanoporous materials and pharmaceuticals to semiconductor particles. However, a rapid development in precise and reliable measuring methods and techniques would enable one to better describe phenomena involved, to formulate theoretical models, and probably most importantly, to develop practical indications for how to appropriately lead many important processes in the industry. It is clearly visible at the first glance through a number of representative papers in the area, that many of them are preoccupied with the testing and production of pharmaceuticals, while the rest are addressed to new crystalline materials, renewable energy, water and wastewater technology and other branches of industry where the crystallization process takes place. In this work, authors gathered and briefly discuss over 100 papers, published in leading scientific periodicals, devoted to the influence of polymers on crystallizing solutions.

Single-walled carbon nanotubes (SWCNTs) have potential for a wide range of applications in diverse fields, but the heterogeneous properties of the synthesized mixtures of SWCNT types hinder the realization of these aspirations. Recent developments in extractive purification methods of polychiral SWCNT mixtures have somewhat gradually alleviated this problem, but either the yield or purity of the obtained fractions remains unsatisfactory. In this work, we showed the possibility of simultaneously achieving both the aforementioned goals, commonly considered mutually exclusive, via the enhancement of the capabilities of the conjugated polymer extraction (CPE) technique. We found that combining small molecular species, which alone are unwanted in the system, with a selective poly(9,9′-dioctylfluorenyl-2,7-diyl-alt-6,6′-(2,2′-bipyridine)) polymer increased the concentration of the harvested SWCNTs by an order of magnitude while maintaining near-monochiral purity of the materials. The conducted modeling revealed that the presence of these additives facilitated the folding of conjugated polymers around (6,5) SWCNTs, leading to a substantial increase in the concentration and quality of the SWCNT suspension. The obtained results lay the foundation for the widescale implementation of the CPE of usually scarcely available chirality-defined SWCNTs owing to the molecular chaperones expediting the folding of the conjugated polymers.

The inability to purify nanomaterials such as single‐walled carbon nanotubes (SWCNTs) to the desired extent hampers the progress in nanoscience. Various SWCNT types can be purified by extraction, but it is challenging to establish conditions giving rise to the isolation of high‐purity fractions. The problem stems from the fact that common organic solvents or water cannot provide an optimal environment for purification. Consequently, one must often decide between the separation yield and purity of the product. This article reports how through the self‐synthesis of poly(9,9‐dioctylfluorene‐alt‐benzothiadiazole) with tailored characteristics, in‐depth elucidation of the extraction process, and mixed‐solvent engineering, a high‐yield isolation of monochiral (7,3) SWCNTs is developed. The combination of toluene and tetralin affords a separation medium of unique properties, wherein both high yield and exceptional purity can be attained simultaneously. The reported results pave the way for further research on this rare chirality, which, as illustrated herein, is much more reactive than any of the previously separated SWCNTs.