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This study investigated the impact of high-pressure processing (HPP) treatment on the structure and physicochemical properties of pectin (PEC)/carboxymethyl cellulose (CMC) composite films, along with the development of new active films incorporating emodin as an antibacterial agent. The results showed that 500 MPa/20 min HPP treatment significantly improved the tensile strength (from 45.91 ± 4.63 MPa to 52.24 ± 4.87 MPa) and elongation at the break (from 5.00 ± 1.44 % to 11.72 ± 2.97 %) of the films. It also improved the film's thermal stability and had no significant effect on its thermal degradability. Moreover, emodin was incorporated into the PEC/CMC film-forming solution and subjected to 500 MPa/20 min HPP treatment to investigate the structure, functional properties, optical properties, and antibacterial activity of the film. The emodin caused the film structural alteration, but significantly improved the water vapor barrier properties. It also reduced the film brightness and light transmission. The antibacterial assessment demonstrated that the film's antibacterial activity was correlated positively with increasing emodin content, and the number of viable cells of Staphylococcus aureus decreased by 1.29 log CFU/mL, 1.70 log CFU/mL, and 1.80 log CFU/mL with different levels of EM antimicrobial films after 12 h.
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http://dx.doi.org/10.1016/j.ijbiomac.2024.136462 | DOI Listing |
Bone Rep
September 2025
Department of Clinical Chemistry, and Department of Biomedical and Clinical Sciences, Linköping University, SE-58185 Linköping, Sweden.
Hypophosphatasia (HPP) is a rare inborn-error-of-metabolism caused by mutations in the gene, resulting in deficient activity of tissue-nonspecific alkaline phosphatase and impaired skeletal mineralization. Affected individuals have a higher prevalence of chronic kidney disease (CKD) than the general population. We report a woman who underwent craniosynostosis surgery in infancy and lost her deciduous teeth prematurely.
View Article and Find Full Text PDFClin Med Insights Case Rep
August 2025
SR Sanjeevani Hospital, Kalyanpur, Siraha, Nepal.
Introduction: Hypokalemic periodic paralysis (HPP) is a severe yet reversible neuromuscular condition precipitated by profound hypokalemia. Autoimmune disorders can exacerbate renal potassium loss resulting in abrupt muscle weakness. Primary Sjögren's syndrome (pSS), an autoimmune disease characterized by exocrine gland insufficiency, can lead to renal tubular dysfunction and episodes of HPP when distal acidification is compromised.
View Article and Find Full Text PDFInorg Chem
September 2025
Department of Chemistry, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong, China.
Reactions of a cerium(III) o-,-dimethylaminobenzyl (DMAB) complex with oxidizing agents, dichalcogenides, and a thiophosphinic amide have been studied. Treatment of the reported homoleptic DMAB complex [Ce(DMAB)] () with Ag(OTs) (OTs = tosylate) and Ag(OTf) (OTf = triflate) in tetrahydrofuran (thf) afforded [Ce(DMAB)(μ-OTs)(thf)] () and [Ce(DMAB)(OTf)(thf)] (), respectively. Reactions of with CuI and CuCl led to isolation of [Ce(DMAB)I] () and [Cu(DMAB)], respectively.
View Article and Find Full Text PDFAppl Environ Microbiol
August 2025
Laboratory of Microbial Processes in Foods, Department of Food Engineering, Technology Center, Federal University of Paraíba, João Pessoa, Paraíba, Brazil.
Contamination of food and water by viruses is a major public health issue worldwide. Several viruses are associated with foodborne outbreaks, with norovirus and hepatitis A virus being the primary causes of foodborne outbreaks, followed by hepatitis E virus and rotavirus. These viruses are responsible for the majority of outbreaks reported globally, representing a significant challenge to food safety; therefore, effective viral inactivation processes are needed.
View Article and Find Full Text PDFFront Oral Health
July 2025
Department of Stomatology, Shenzhen Maternity and Child Healthcare Hospital, Southern Medical University, Shenzhen, Guangdong, China.
Hypophosphatasia (HPP) is a rare metabolic bone disorder caused by functional mutations in the gene Alkaline Phosphatase, Liver/Bone/Kidney (), resulting in impaired mineralization of bones and teeth. We report a female patient who experienced adolescent teeth loss and underwent dental rehabilitation, yet remained undiagnosed until her son developed similar symptoms before age two. Genetic testing confirmed HPP in both cases, more than a decade after her initial symptoms appeared.
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