Glycosaminoglycans (GAGs) are found covalently attached to proteins, which create conjugates known as proteoglycans. GAGs have remarkable biological activity as co-receptors for a variety of growth factors, cytokines, and chemokines. The present study identifies the key compositional differences between the GAGs isolated from whelk and mammalian GAGs. This polysaccharide represents a new, previously undescribed GAG with cytotoxic activity on cancer cells. Disaccharides were obtained by sample digestion with heparinases I, II, and III and chondroitinase ABC. The resistant oligosaccharides from whelk GAGs treated with heparinase I, II, and III and chondroitinase ABC were retained by the filter due to their larger size. Disaccharide analysis was performed using Glycan Reduction Isotope Labeling (GRIL LCQ-MS). The amounts of filter-retained fragments, as assessed by monosaccharides analysis, suggested that a proportion of the whelk GAG chains remained resistant to the enzymes used in the disaccharide analysis. Thus, the proportions of individual disaccharide produced in this analysis may not truly represent the overall proportions of disaccharide types within the intact whelk GAGs chain. However, they do serve as important descriptors for the classification and make-up of the anti-cancer GAGs chains. Furthermore, these data represent clear evidence of the compositional differences between whelk GAGs and commercial mammalian GAGs.

Kirkuk city is known for its industrial activities, especially oil and cement production, as well as its road traffic. The aim of this study was to assess potentially toxic elements (PTEs) in the soil and plants from urban areas by measuring pollution indices and estimating the effect that this pollution has on the environment. Leaf and soil samples were taken from 10 different locations in Kirkuk. These samples were pre-treated using the acid digestion method and concentrations of 12 elements were determined using inductively coupled plasma mass spectrometry (ICP-MS). The results indicate a high content of aluminum and magnesium (mg/kg) in the soil samples from all study sites. For leaf samples, the results showed a moderate to low amount of magnesium and aluminum. Based on our results, the PTE concentrations were found in the following order—Mg > Al > Ni > Cu > Cr > Pb > Co > As > Se > Cd > Hg > Ti—in leaf samples from all 10 study sites. However, in the soil samples, PTE concentrations were in the following order—Mg > Al > Cr > Ni > Cu > Pb > Co > As > Se > Ti > Cd > Hg—from all study sites. Pollution indices showed a moderate level of contamination of Pb, Cd, and Ni, and a high level of contamination of As and Hg in plant and soil samples from all study sites in Kirkuk city.

Aims Arthroplasty surgery of the knee and hip is performed in two to three million patients annually. Periprosthetic joint infections occur in 4% of these patients. Debridement, antibiotics, and implant retention (DAIR) surgery aimed at cleaning the infected prosthesis often fails, subsequently requiring invasive revision of the complete prosthetic reconstruction. Infection-specific imaging may help to guide DAIR. In this study, we evaluated a bacteria-specific hybrid tracer (99mTc-UBI29-41-Cy5) and its ability to visualize the bacterial load on femoral implants using clinical-grade image guidance methods. Methods 99mTc-UBI29-41-Cy5 specificity for Stapylococcus aureus was assessed in vitro using fluorescence confocal imaging. Topical administration was used to highlight the location of S. aureus cultured on femoral prostheses using fluorescence imaging and freehand single photon emission CT (fhSPECT) scans. Gamma counting and fhSPECT were used to quantify the bacterial load and monitor cleaning with chlorhexidine. Microbiological culturing helped to relate the imaging findings with the number of (remaining) bacteria. Results Bacteria could be effectively stained in vitro and on prostheses, irrespective of the presence of biofilm. Infected prostheses revealed bacterial presence on the transition zone between the head and neck, and in the screw hole. Qualitative 2D fluorescence images could be complemented with quantitative 3D fhSPECT scans. Despite thorough chlorhexidine treatments, 28% to 44% of the signal remained present in the locations of the infection that were identified using imaging, which included 500 to 2,000 viable bacteria. Conclusion The hybrid tracer 99mTc-UBI29-41-Cy5 allowed effective bacterial staining. Qualitative real-time fluorescence guidance could be effectively combined with nuclear imaging that enables quantitative monitoring of the effectiveness of cleaning strategies. Cite this article: Bone Joint Res 2023;12(1):72–79.

The possibility of finding anti-cancer drugs has generated interest in natural products. Several studies have in vitro observed potent anti-cancer properties of pomegranate juice against various cancers including leukemia. Although a few studies have described the bioactivities of hydrolysable tannins extracted from pomegranate juices, limited attention has been paid to other tannins extracted from different parts of a plant. Recently, polyphenols, which are found in plants, have become the most studied phytochemicals owing to their significant chemical properties and biological activities. Tannin is an astringent plant polyphenolic compound and has been observed to have anti-oxidant and anti-cancer properties. This study uses a novel approach to study variation in the structure of hydrolysable tannins from two different types of plants and their inhibition activity in leukemia K562 cells. We examined data showing anti-proliferation activity of hydrolysable tannins extracted from pomegranate peels within two concentrations of 1 mg/ml and 100 µg/ml. Hydrolysable tannin extracted from oak apple gall induces different effects than that extracted from pomegranate tannin. At the highest concentration of 100 µg/ml, the tannin from oak apple gall did not have any noticeable effects on cells, whereas at the highest concentration of 1 mg/ml, cell cycle arrest seemed to have occurred after 72 h of treatment. This most likely led to senescence caused by overstimulation of the cells by specific polyphenols compounds in oak apple gall, which affected the cells either directly or indirectly by changing the culture's environment.