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Hydroxyapatite (HAp) and β-tricalcium phosphate (β-TCP) are widely used in bone graft materials, because they have excellent biocompatibility. However, the degradation rates of HAp and β-TCP do not match the rate of osteogenesis, which limits their clinical applications. Therefore, forming biphasic calcium phosphate (BCP) is a promising method to control the biodegradation rate of the material. In addition, strontium (Sr) is an important element that promotes osteogenesis and inhibits bone absorption. Therefore, this study focused on the effects of Sr in the as-synthesized BCP with varied Sr concentrations of 1, 5, and 15 mol%, which are synthesized by chemical precipitation and a high-temperature calcination method. In this study, we assume that Sr is doped into Ca(5) of β-TCP and Ca(1) & Ca(2) of HAp during the Rietveld refinement. On the basis of the Rietveld refinement results obtained from X-ray diffraction (XRD) patterns, with increasing Sr concentration, the mass percentage of HAp decreases first, which is due to the distortion of the HAp structure, resulting in a decrease in HAp stability and phase variation from HAp to β-TCP. However, when the concentration of Sr reaches 15 mol%, the mass percentage of HAp increases, which may be because of the phase transformation from β-TCP to calcium-deficient apatite by the diffusion of Ca. In addition, the increase in the lattice constants and volumes indicates that Sr has been successfully doped into the crystal lattices of both β-TCP and HAp, since the ion radius of Sr2+ (0.113 nm) is larger than the ion radius of Ca2+ (0.099 nm). As shown in the X-ray photoelectron spectroscopy (XPS) results, the intensities of Sr3d and Sr3p increase with increasing Sr concentrations, which indicates that Sr is not only on the surface of the sample but also in the crystalline structures of both β-TCP and HAp. [ABSTRACT FROM AUTHOR]

The contamination of freshwater by nanoplastics (NPs) poses a significant threat to various organisms. However, the influence of food factors on the NPs toxicity and the associated risks to water safety remains poorly understood. In this study, we employed highly fluorescent NPs incorporating aggregation-induced emission fluorogens to quantify and visualize the interactions of NPs with freshwater phytoplanktonic alga Chlamydomonas reinhardtii and zooplankton Daphnia magna , including the uptake of NPs by algae and daphnids, as well as gut environment responses through both waterborne and foodborne routes. NPs at environmentally relevant concentrations were capable of aggregating and internalizing in planktonic algae, thus permeating the food chain and potentially causing ecological risks. Notably, positively charged NPs exhibited greater infiltration than the negatively charged NPs. Our findings indicated that NPs had a greater tendency to accumulate in Daphnia via the food chain rather than through direct exposure to water. This was attributed to the loss of selectivity, suggesting a potential mechanism for NP accumulation in aquatic food chains. However, daphnids exposed to NPs through waterborne route exhibited more gut pH acidification, esterase activity, and gut inflammation compared to those exposed via the foodborne route. Moreover, chronic exposure to NPs through waterborne routes significantly disrupted the growth, molting, and reproduction of Daphnia compared to the foodborne group. These findings provided valuable insights into the complexities of plastic pollution on primary trophic levels in aquatic environments. [Display omitted] • Nanoplastics were capable of aggregating and internalizing in planktonic algae. • Positively charged NPs exhibited greater infiltration to algae. • NPs tended to accumulate more in Daphnia by dietborne than waterborne exposure. • Waterborne produced more gut pH shift and inflammation than dietborne exposure. • Waterborne had higher disruption of daphnid physiological responses than dietborne exposure. [ABSTRACT FROM AUTHOR]

The sight into photoconversion of toluene, a ubiquitous typical pollutant, attentively by the involvement of PM2.5 in the real air environment is crucial for controlling haze pollution. Compared with the large-size PM2.5 on normal day (PM2.5-ND), the PM2.5 on haze day (PM2.5-HD) formed of small particle agglomerates featured greater oxidation capability, evidenced by the valence distribution of sulfur species. Notably, PM2.5-HD had abundant O 2 −• and •OH and participated in the photochemical reaction of toluene, giving it a greater toluene conversion with a first-order kinetic rate constant of 0.4 d−1 on haze day than on normal day (0.2 d−1). During the toluene photoconversion, isotopic labelling traced small molecules including benzene and newfound pentane, ethylbenzene, 1,3,8-p-menthatriene and 4-methyl-1-pentanone benzene that could be formed by methyl breakage, ring opening, fragmentation reforming and addition reaction of toluene. Given ADMET properties, 1,3,8-p-menthatriene was assigned high priority since it had poor metabolism, low excretion and severe toxicity, while benzene and 4-methyl-1-pentanone benzene should also be noticeable. FT-ICR MS results indicated that toluene could create multiple macromolecular products that are more sensitive to SOA generation in haze air matrix with broader carbon number and O/C, more oxygenated substitution with CHO/CHON occupying by 81.4%, lower DBE average at 4.66 and higher O S C ‾ at −1.60 than normal air matrix. Accordingly, a photochemical reaction mechanism for toluene in real air atmosphere was proposed. The stronger oxidation property of PM2.5 not only facilitated toluene to generate small molecules but also boosted the conversion of intermediates to oxygenated macromolecular products, contributing to the formation of SOA. [Display omitted] • PM2.5 on haze day had higher oxidation capability with more O 2 −.• and •OH. • PM2.5- mediated reactive oxygen radical boosted photoconversion of toluene. • Isotopic labelling traced four newfound products mostly with more toxicity. • More macromolecular products were formed in haze air matrix by FT-ICR MS. • They featured more oxygenated substitution, low DBE average , and higher O S C ‾. [ABSTRACT FROM AUTHOR]

The Chinese Government has established stringent policies since 2005 to control SO 2 , particulate matter, and NO x emissions from sintering plants with the aim of tackling severe air pollution in China. Notably, sintering is also important sources of polychlorinated naphthalenes (PCNs), but it is not clear whether the air pollution control policies have led to decreased PCN emissions. In this study, the PCN concentrations in 144 stack gas, 87 discarded fly ash, and 24 desulfurization by-product samples from 24 Chinese sintering plants were determined. This study revealed that desulfurization processes decreased PCN emissions by 47.2%–72.2%. However, these PCNs were not completely eliminated, and transformed to desulfurization by-product. PCN emission in such previously ignored solid residues, including of desulfurization by-product and fine particles, produced in the process of cutting down air pollutants emissions from Chinese sintering plants between 2005 and 2015 was found contained 324 kg, and these residues therefore need to be managed better than currently. Furthermore, PCN concentrations were higher from produced in old plants than produced in new plants, so it is necessary to increase the rate at which out-of-date sintering plants are eliminated. Phasing out old sintering processes decreased total PCN emissions in China by 1549 kg between 2005 and 2015. Image 1 • Controlling air pollutant emissions during sintering can decrease PCN emissions. • PCNs in discarded fly ash and desulfurization by-products cannot be ignored. • Decreases in PCN emissions achieved by closing old sintering plants were estimated. Controlling SO 2 , particulate matter, and NOx emissions during sintering could synergistically control PCN emissions. [ABSTRACT FROM AUTHOR]

The human gut microbiome (GM) in healthy people is chronically exposed to tetracycline (TET) via environmental exposure and dietary uptake. However, limited information is available on its effect on the GM metabolome and effect on the host, especially at the dietary exposure level. Here, we investigated how TET at both sub-pharmaceutical and dietary exposure levels affects the metabolome and the secretome-induced host immune response by studying several representative gut bacteria. Interestingly, the metabolome showed a highly species-specific pattern with a distinct dose-response relationship. B. fragilis was highly sensitive to TET and vitamin, nucleotide, and amino acid metabolism pathways were the most vulnerable metabolic pathways at dietary exposure level. For key metabolite short chain fatty acids, TET significantly induced the synthesis of butyrate in B. fragilis , rather than C. sporogenes and E. coli. Furthermore, TET induced the release of lipopolysaccharides (LPS) in E. coli and enhanced the immune response; however, there was no obvious effect on B. fragilis. Interestingly, the overall immune response modulation with TET exposure relied on the ratio between E. coli and B. fragilis , possibly due to the neutralization of active LPS from E. coli by the LPS from B. fragilis. Overall, our results showed that the effect of TET from environmental exposure on the host health would be highly dependent on the GM composition, especially for the gut bacterial metabolome and secretome induced immune response. Unlabelled Image • The gut bacterial metabolome showed a species-specific, dose dependent response towards tetracycline (TET). • Vitamin, nucleotide, and amino acid metabolism pathways were highly affected at dietary exposure level. • TET significantly induced the synthesis of butyrate in B. fragilis. • The overall immune response modulation with TET exposure relied on the ratio between E. coli and B. fragilis. [ABSTRACT FROM AUTHOR]

Graphical abstract Abstract To overstep the dilemma of chemical drug degradation within powerful lysosomes of tumor associated macrophages (TAMs), a sialic acid-polyethylenimine-cholesterol (SA-PEI-CH) modified liposomal doxorubicin (DOX-SPCL) was designed with both TAMs targeting and smart lysosomal trafficking. The modified liposome DOX-SPCL performed particle size as 103.2 ± 3.1 nm and zeta potential as −4.5 ± 0.9 mV with encapsulation efficiency as 95.8 ± 0.5%. In in vitro cell experiments, compared with conventional liposomal doxorubicin (DOX-CL) and PEGylated liposomal doxorubicin (DOX-PL), DOX-SPCL showed a selective binding on TAMs and a mere lysosomal concentration. In pharmacokinetic study, DOX-SPCL effectively impeded/delayed the disposition of mononuclear phagocyte system (MPS) with a value of AUC 0-t as 796.03 ± 66.93 mg L−1 h. In S180 sarcomas bearing mice, DOX-SPCL showed the greatest tumor inhibition rate (92.7% ± 3.6%) compared with DOX-CL (46.4% ± 2.0%) or DOX-PL (58.8% ± 7.6%). The <0.5% positive region of TAMs in tumor section indicated a super TAMs exhaustion for DOX-SPCL treatment. Conclusively, DOX-SPCL was supposed as a safe and effective liposomal preparation for clinical sarcoma treatment via TAMs targeting/deletion delivery strategy. [ABSTRACT FROM AUTHOR]

• The body weight of juvenile zebrafish was increased upon tetracycline (TET) exposure. • Lipid vacuoles were generated in the zebrafish livers after TET exposure. • Hepatic triglyceride (TAG) levels were upregulated after TET exposure. • Hepatic metabolism was altered upon TET exposure. • Zebrafish gut microbial community diversity was increased after TET exposure. The application of tetracycline (TET) is very common in medical treatment, fisheries, and animal husbandry, resulting in its frequent detection with abundant concentrations in the aquatic environment. Though the effects of TET on zebrafish (Danio rerio) at embryonic and larval stages have been reported, there is very limited information on the possible long-term effect on aquatic fishes at the juvenile stage, especially at environmentally relevant levels. In this study, we have exposed juvenile zebrafish to two levels of TET at 1 and 100 µg/L for one month until their adulthood. The result showed that both levels of TET can significantly increase the body weight of the zebrafish, while there is no change in the body length. TET exposure also affected the liver microstructure by lipid vacuoles generation and global lipidomics analysis revealed a significant upregulation in hepatic triglyceride (TAG) levels. The metabolomics analysis showed great dysregulations in hepatic metabolic pathways including linoleic acid metabolism, tyrosine metabolism, and methionine metabolism, which are known to be linked with increased body weight gain through hepatic lipid accumulation. The hepatic gene expression involved in lipid transport (e.g., apoa4 and fabp11) and lipogenic factors (e.g., ppar) have been significantly upregulated in the livers of TET exposed zebrafish. Interestingly, the 16 rRNA gene sequence-based zebrafish gut microbial community analysis revealed an enhanced community diversity and altered microbial community composition upon TET exposure. To our knowledge, this is the first study showing that TET exposure can increase the body weight in juvenile zebrafish and the study on the ecotoxicity of antibiotic occurrences in the aquatic system can be further warranted. [ABSTRACT FROM AUTHOR]

[Display omitted] • Microplastics distribution in QTP region was fully explored with mainly PP and PET. • Human activities and exogenous tributaries primarily contributed to MPs in QTP. • The contribution of the unique prayer flag culture to MPs in QTP was nonnegligible. • PERI model can evaluate the risk of MPs more objectively and comprehensively. • Qinghai Lake featured the highest ecosystem risk due to more PVC. Microplastics (MPs) as emerging contaminants have become a major global concern, however, the distribution and origin of MPs in Qinghai-Tibet Plateau (QTP) and their impacts on ecosystem are poorly known. Hence, we systematically evaluated the profile of MPs on the representative metropolitan locations of Lhasa and Huangshui Rivers and the scenic sites of Namco and Qinghai Lake. The average abundance of MPs in the water samples was 7020 items/m3, which was 34 and 52 times higher than those for the sediment (206.7 items/m3) and soil samples (134.7 items/m3), respectively. Huangshui River had the highest levels, followed by Qinghai Lake, Lhasa River and Namco. Human activities rather than altitude and salinity impacted the distribution of MPs in those areas. Besides the consumption of plastic products by locals and tourists, laundry wastewater and exogenous tributary inputs, the unique prayer flag culture also contributed to the MPs emission in QTP. Notably, the stability and fragment of MPs were crucial for their fate. Multiple assessment models were employed to evaluate the risk of MPs. PERI model took MP concentration, background value and toxicity into account, comprehensively describing the risk differences of each site. The large PVC proportion in Qinghai Lake posed the highest risk. Furthermore, concerns should be raised about PVC, PE and PET in Lhasa and Huangshui Rivers, and PC in Namco Lake. Risk quotient suggested that aged MPs in sediments slowly released biotoxic DEHP and should be cleaned up promptly. The findings offer baseline data of MPs in QTP and ecological risks, providing important support for the prioritization of future control measures. [ABSTRACT FROM AUTHOR]

Human exposure to harmful phthalates has raised global health concerns. According to cellular and molecular investigations, phthalates and their metabolites can promote prostate cancer (PCa). Despite being a prevalent cancer afflicting the global male population, the epidemiological association between phthalates and prostate cancer remains understudied. This work aims to investigate whether phthalate metabolites are related to prostate cancer. Moreover, we sought to understand whether their elevated concentrations are associated with increased serum concentrations of prostate-specific antigen (PSA), among non-prostate cancer interviewees. According to National Health and Nutrition Examination Survey (NHANES) data from 2003 to 2010, we screened eligible men aged 20 years or older. Then, crude and multivariate regression models were constructed to assess the relationship. The phthalates significantly related to PCa were analyzed based on variables associated with PCa status and PSA. The molar sum ∑di-2-ethylhexyl phthalate (∑DEHP) was simultaneously associated with increased risk of PCa and increasing PSA concentrations. Among PCa-related phthalates, high molecular weight phthalate metabolites included mono-benzyl phthalate (MBzP) and three metabolites of DEHP. In summary, phthalates are potentially associated with prostate tumorigenesis in the US population. However, additional in-depth prospective studies in different ethnic groups are required to validate the causality between both. • Phthalate metabolites demonstrate clear relationships with the prostate cancer. • Phthalate metabolites are positively correlated with prostate-specific antigen. • There are associations between the molar sum ∑DEHP and the prostate cancer. • MEHHP, MEOHP, MECPP and MBzP are associated with the risk of prostate cancer. • Prostate cancer-related phthalates are all high molecular weight phthalates. [ABSTRACT FROM AUTHOR]

Long-range atmospheric transportation (LRAT) of persistent organic pollutants followed by their deposition in cold, arid regions is of wide concern. This problem occurs at Qinghai Lake in the northeastern Tibetan Plateau, a sparsely populated area with extreme weather conditions and little current or historical anthropogenic pollution. The concentrations and distribution patterns of the mono-to octa-chlorinated dibenzo- p -dioxin and dibenzofuran (PCDD/F) congeners in surface soil samples collected from around Qinghai Lake were quantified. Concentration differences between low-(mono-to tri-) chlorinated PCDD/Fs and high-(tetra-to octa-) chlorinated PCDD/Fs were measured. High PCDD/F levels were detected, with total concentrations of 15,108 ± 6323 pg/g for the 27 PCDD/F congeners and 15,104 ± 6324 pg/g for the low-chlorinated PCDD/Fs. The concentrations of 17 2,3,7,8-substituted PCDD/Fs were only 3.1 ± 4.4 pg/g and the corresponding international toxicity equivalency (I-TEQ) was 0.11 ± 0.22 pg I-TEQ/g. Given their higher vapor pressures and lower boiling points, low-chlorinated PCDD/Fs, were predominantly gaseous, whereas high-chlorinated PCDD/Fs were predominantly solid, indicating that there is a higher potential for long-range transport of low-chlorinated PCDD/Fs. Overall, because of their high LRAT potential, low-chlorinated PCDD/Fs may pose a greater risk to local ecosystems in cold, remote areas than high-chlorinated PCDD/Fs. [ABSTRACT FROM AUTHOR]

Large amounts of heavy metals discharged by industrial cities that are located along the middle reach of Yellow River, China have detrimental impacts on both the ecological environment and human health. In this study, fourteen surface sediment samples were taken in the middle reach of the Yellow River. Contents of Zn, Pb, Ni, Cu, Cr, Cd, As were measured, and the pollution status was assessed using three widely used pollution assessment methods, including the single factor index method, Nemerow pollution index method and potential ecological risk index. The concentrations of the studied heavy metals followed the order: Zn > Cr > Cu > Ni > Pb > As > Cd. Nearly 50% of sites had Cu and Cr accumulation. The concentration of Cu at the Yiluo River exceeded the secondary standard value of the Environmental quality standard for soils. Comparison of heavy metal concentrations between this study and other selected rivers indicated that Cu and Cr may be the major pollutants in our case. The single factor index indicated that many samples were at high levels of pollution for Cu and Cd; the Nemerow pollution index indicated that the Yihe River, Luohe River, Yiluo River and Huayuankou were polluted. According to the results of potential ecological risk assessment, Cd in the tributaries of Luo River, Yihe River, and Yiluo River showed high risk toward the ecosystem and human health, Cd in Huanyuankou and Cu in Yiluo River showed a middle level of risk and other samples were at a low level of risk. [ABSTRACT FROM AUTHOR]