Heparin, a highly sulfated glycosaminoglycan, is a naturally occurring anticoagulant that plays a vital role in various physiological processes. The remarkable structural complexity of heparin, consisting of repeating disaccharide units, makes it a crucial molecule for the development of commercial drugs in the pharmaceutical industry. Over the past few decades, significant progress has been made in the development of cost-effective adsorbents specifically designed for the adsorption of heparin from porcine intestinal mucosa. This advancement has been driven by the need for efficient and scalable methods to extract heparin from natural sources. In this study, we investigated the use of cationic ammonium-functionalized diatomaceous earth, featuring enhanced porosity, larger surface area, and higher thermal stability, to maximize the isolated heparin recovery. Our results showed that the higher cationic density and less bulky quaternary modified diatomaceous earth (QDADE) could adsorb up to 16.3 mg·g−1 (31%) of heparin from the real mucosa samples. Additionally, we explored the conditions of the adsorbent surface for recovery of the heparin molecule and optimized various factors, such as temperature and pH, to optimize the heparin uptake. This is the introductory account of the implementation of modified diatomaceous earth with quaternary amines for heparin capture.

Heparin, usually isolated from porcine intestinal mucosa, is an active pharmaceutical ingredient of great material value. Traditionally, diverse types of commercial resins were employed as an adsorbent for heparin retrieval from biological samples. However, more recent years have encouraged the advent of new cost-effective adsorbents to achieve enhanced heparin retrieval. Inexpensive cationic ammonium-functionalized silica gels, monodispersed with larger surface area, porosity, and higher thermal stability, were chosen to evaluate the heparin recovery yield from porcine intestinal mucosa. We demonstrated that higher positively charged and less bulky quaternary modified silica gel (e.g., QDASi) could adsorb ~28% (14.7 mg g−1) heparin from the real samples. In addition, we also determined suitable surface conditions for the heparin molecule adsorption by mechanistic studies and optimized different variables, such as pH, temperature, etc., to improve the heparin adsorption. This is going to be the first reported study on the usage of quaternary amine-functionalized silica gel for HEP uptake.

Heparin is one of the most valuable active pharmaceutical ingredients, and it is generally isolated from porcine intestinal mucosa. Traditionally, different types of commercial resins are employed as an adsorbent for heparin uptake; however, using new, less expensive adsorbents has attracted more interest in the past few years to enhance the heparin recovery. Zeolite imidazolate framework-8 (ZIF-8), as a metal–organic framework (MOF) with a high surface area, porosity, and good stability at high temperatures, was selected to examine the heparin recovery. In this research, we demonstrate that ZIF-8 can recover up to ~70% (37 mg g−1) of heparin from porcine intestinal mucosa. A mechanistic study through kinetic and thermodynamic models on the adsorption revealed appropriate surface conditions for the adsorption of heparin molecules. The effect of different variables such as pH and temperature on heparin adsorption was also studied to optimize the recovery. This study is the first to investigate the usage of MOFs for heparin uptake.

Organic semiconductors (OSCs) are promising advanced materials, due to various advantages including their lightweight, flexibility and processability. As a result, applications for their use in organic photovoltaics, organic light-emitting diodes, and organic field-effect transistors have been identified. However, up to this point, most of the feedstock from which OSCs are synthesized comes from nonrenewable resources, such as petroleum and coal. It is imperative to switch to renewable feedstocks to ensure a sustainable future; therefore there has been considerable effort to synthesize OSCs from sustainable feedstocks. There are many compounds present in nature, which could be used as OSCs as found in their natural forms. Similarly, there are also many natural moieties that could be modified, oligomerized, or polymerized to synthesize OSCs. In this chapter, we cover a wide range of examples of such research occurring in the last few decades.

ABSTRACTSubbituminous coal from the powder river basin was extracted with N,N‐dimethylformamide at atmospheric pressure to yield a solid extract that provided phenolic and carboxylic acid groups. The coal extract was employed as polyol in polyurethane (PU) synthesis. A solvent‐free synthesis using 2,4‐toluene diisocyanate (TDI) resulted in a porous PU solid. Reaction with TDI in solution resulted in a soluble PU that could be applied as adhesive or coating. Coatings were also prepared from coal extract solutions and commercial, polymeric isocyanates, providing excellent adhesion to aluminum. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020, 137, 48776.

An efficient copper-catalyzed direct arylation reaction for the regioselective functionalization of benzodithiophene-S,S-tetraoxide has been developed. The method demonstrates a broad scope with isolated yields ranging from good to excellent. Furthermore, the reaction specificity for aryl iodides over the unreactive aryl bromides provide a opportunity to generate a new donor-acceptor-donor triad.

An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.