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Abstract: We have developed an analytical method for the determination of lincomycin, tylosin A and tylosin B residues in royal jelly using liquid chromatography–triple quadrupole tandem mass spectrometry analysis. For extraction and purification, we employed 1% trifluoroacetic acid and 0.1  m Na2EDTA solutions along with an Oasis HLB cartridge. The target antibiotics were well separated in a Kinetex EVO C18 reversed‐phase analytical column using a combination of 0.1% formate acid in ultrapure water (A) and acetonitrile (B) as the mobile phase. Good linearity was achieved over the tested concentration range (5–50 μg/kg) in matrix‐matched standard calibration. The coefficients of determination (R2) were 0.9933, 0.9933 and 0.996, for tylosin A, tylosin B and lincomycin, respectively. Fortified royal jelly spiked with three different concentrations of the tested antibiotics (5, 10 and 20 μg/kg) yielded recoveries in the range 80.94–109.26% with relative standard deviations ≤4%. The proposed method was applied to monitor 11 brand of royal jelly collected from domestic markets and an imported brand from New Zealand; all the samples tested negative for lincomycin, tylosin A and tylosin B residues. In conclusion, 1% trifluoroacetic acid and 0.1  m Na2EDTA aqueous solvents combined with solid‐phase extraction could effectively complete the sample preparation process for royal jelly before analysis. The developed approach can be applied for a routine analysis of lincomycin, tylosin A and tylosin B residues in royal jelly. [ABSTRACT FROM AUTHOR]

Objectives: This study aimed to elucidate the relationship between gadoxetic acid–enhanced magnetic resonance imaging (MRI) features—enhancing capsule, corona enhancement or hypointense rim—observed in hepatocellular carcinomas (HCCs). Methods: Of the HCCs surgically confirmed during a 5-year period (2013–2017), ≤ 3-cm lesions (n = 83) in 78 patients were evaluated. Presence of corona enhancement and enhancing capsule on multiphasic dynamic imaging and presence of hypointense rim on hepatobiliary phase imaging were determined retrospectively by two independent observers. The relationship among the three imaging features was statistically analysed and correlated with the presence of histologic fibrous capsules, tumour differentiation and gross morphologic type. Results: There was substantial overall interobserver agreement in determining the presence of the three imaging features. Sixty (72.3%) lesions had histologic fibrous capsule positively correlated with all three imaging features (p < 0.05). Corona enhancement was the most common (66.3%) feature followed by enhancing capsule (61.4%) and hypointense rim (33.7%), and the correspondence rate of enhancing capsule to corona enhancement was 68.6% (p = 0.004). Corona enhancement was more frequently observed in moderately differentiated HCCs than other lesions (p = 0.012) and not dependent (p = 0.465) on the tumour size, while enhancing capsule was significantly dependent on tumour size, as indicated by univariate (p < 0.001) and multivariate analyses (odds ratio, 4.241; p = 0.002). Conclusions: Among the capsular features, corona enhancement might closely relate to enhancing capsule in HCCs. Corona enhancement was not dependent on tumour size and had the highest incidence of appearance on gadoxetic acid–enhanced multiphasic dynamic MRI. Key Points: • Enhancing capsule has a limited role in the LI-RADS categorisation during gadoxetic acid–enhanced MRI. • Appearance of corona enhancement is closely related to enhancing capsule and is not dependent on size of HCCs. • Corona enhancement can substitute enhancing capsule in the diagnosis of HCCs during multiple arterial and portal venous phase gadoxetic acid–enhanced MRI. [ABSTRACT FROM AUTHOR]

Graphical abstract Highlights • A protocol was developed for detecting and quantifying scopolamine, L-hyoscyamine, and sparteine. • Target analytes were extracted from animal-based food using EN-QuEChERS and analyzed by LC-MS/MS. • EDTA solution was employed to improve recovery. • LOQ values of 1–5 µg/kg were obtained for all analytes. Abstract We developed a modified Quick, Easy, Cheap, Effective, Rugged, and Safe (CEN QuEChERS) extraction method coupled with liquid chromatography-electrospray ionization tandem mass spectrometry (LC-ESI+/MS-MS) to identify and quantify residues of three botanical alkaloids, namely, scopolamine, L-hyoscyamine, and sparteine, in animal-derived foods, including porcine muscle, egg, and milk. A combination of ethylenediaminetetraacetic acid disodium buffer and acetonitrile acidified with 0.5% trifluoroacetic acid was used as an extraction solvent, whereas QuEChERS (CEN, 15662) kits and sorbents were applied for cleanup procedures. The proposed method was validated by determining the limits of quantification (LOQs), with values of 1–5 µg/kg achieved for the target analytes in various matrices. Linearity was estimated from matrix-matched calibration curves constructed using six concentration levels ranging from 1- to 6-fold increases in the LOQs of each analyte, and the correlation coefficients (R2) were ≥0.9869. Recoveries (at three concentration levels of 1-, 2-, and 3-fold increases in the LOQ) of 73–104% were achieved with relative standard deviations (RSDs) ≤7.7% (intra-day and inter-day precision). Ten types of each matrix procured from large markets were evaluated, and all tested samples showed negative results. The current protocol is simple and versatile and can be used for routine detection of plant alkaloids in animal food products. [ABSTRACT FROM AUTHOR]

A facile, one-pot synthetic method to prepare alkoxo-functionalized homoleptic cyclometalated Ir (III) compounds with facial geometry has been developed. The reaction of Ir(COD) 2 BF 4 with two bipyridine ligands, 2′,6′-dimethoxy-4-methyl-2,3′-bipyridine and 2′,6′,4-trimethoxy-2,3′-bipyridine, afforded the homoleptic Ir (III) compounds Ir[(RO) 2 (Me)pypy] 3 ( 1 ) and Ir[(RO) 3 pypy] 3 ( 2 ) in good yields. The reaction conditions highly selectively produced the aforementioned Ir (III) compounds with facial geometry. The decomposition temperatures of 1 and 2 were 387 °C and 368 °C, respectively. Both compounds exhibited intense blue phosphorescence ( λ max = 452–458 nm) with excellent quantum efficiencies (Φ PL = 0.45–0.52). Phosphorescent organic light-emitting diodes (PHOLEDs) that used these compounds as the dopant material and 9-(3-(9H-carbazol-9-yl)phenyl)-9H-carbazol-3-yl)diphenylphosphine oxide as the host material have been fabricated. The electroluminescent device created using compound 1 at a doping level of 5 wt% exhibited the best performance, with an external quantum efficiency of 15.7–15.5% at a brightness of 10–100 cd/m 2 and color coordinates of (0.16, 0.28) at 100 cd/m 2 . [ABSTRACT FROM AUTHOR]

Graphical abstract Highlights • An analytical method was developed for detecting acetylsalicylic acid and salicylic acid. • The target analytes were extracted from six animal foods, including porcine muscle, milk, egg, shrimp, eel, and flatfish. • Acetonitrile acidified with formic acid and trifluoroacetic acid was used as the extraction solvent. • The method performance was satisfactory for both tested analytes in various matrices. • The obtained results could assist the regulatory authority in drafting the MRL for the tested analytes. Abstract This work describes a simple screening protocol for quantification of carbasalate calcium derived metabolites, acetylsalicylic acid (ASA) and salicylic acid (SA), in animal and aquatic food matrices using liquid chromatography-tandem mass spectrometry (LC-MS/MS). The analytes were extracted from porcine muscle, milk, egg, shrimp, eel, and flatfish using acetonitrile, with the addition of formic acid as well as trifluoroacetic acid, followed by liquid-liquid purification with saturated n -hexane. A reverse-phase analytical column was employed with a mobile phase comprising (A) 1 mM ammonium acetate in distilled water and (B) methanol to achieve the best chromatographic separation. Matrix-matched calibration curves (R2 ≥ 0.9817) were constructed using six concentrations of 5, 10, 20, 30, 40, and 50 µg/kg in porcine muscle, milk, egg, shrimp, eel, and flatfish matrices. The calculated limits of quantification (LOQ) were 10 and 7 µg/kg, for ASA and SA, respectively. Recoveries of 67 to 102% with relative standard deviations (RSDs) of ≤9.0% (intra-day and inter-day) were obtained for all matrices at four spiking concentrations (5, 10, 20, and 50 µg/kg). The method was feasibly applied for monitoring market samples. In conclusion, the developed method is versatile, accurate, and precise for detecting and quantifying acetylsalicylic acid and salicylic acid residues in animal-derived foods meant for human consumption. [ABSTRACT FROM AUTHOR]

A chromatographic method involving a single run was validated for the quantification of clanobutin, dichlorvos, and naftazone in products of animal origin. Pork, beef, chicken, milk, and egg samples were extracted with a solution of 0.1% formic acid in acetonitrile, defatted with n -hexane, centrifuged, and filtered prior to analysis using liquid chromatography-tandem mass spectrometry (LC-/MS/MS). The analytes were separated on a C18 column using a solution of 0.1% formic acid and 10 mM ammonium formate (A) and acetonitrile (B) as the mobile phase. A good linearity over 5–50 ng/g concentration range was obtained with coefficients of determination ( R 2 ) ≥ 0.9807. The intra- and interday accuracy (recovery %) calculated from 3 fortification levels (5, 10, and 20 ng/g) were 73.2–108.1% and 71.4–109.8%, and the precisions (expressed relative standard deviations (RSDs)) were 0.9–12.9% and 1.8–10.6%, respectively, for the 3 tested analytes in animal originated foods. The limits of quantification (LOQs) ranged between 0.1 and 1 ng/g, thus enabling the quantification of residual levels below the uniform maximum residue limit (MRL) of 0.01 mg/kg set for compounds having no MRL. The designated methodology was successfully applied to monitor various samples collected from Seoul; the tested analytes were not quantified in any of the market samples. Conclusively, the developed method is simple, sensitive, and accurate, and could be used for the detection of pharmaceuticals in various animal food matrices with variable protein and fat contents. [ABSTRACT FROM AUTHOR]

Over the past few decades, honey products have been polluted by different contaminants, such as pesticides, which are widely applied in agriculture. In this work, a modified EN – quick, easy, cheap, effective, rugged, and safe (QuEChERS) extraction method was developed for the simultaneous quantification of pesticide residues, including cymiazole, fipronil, coumaphos, fluvalinate, amitraz, and its metabolite 2,4-dimethylaniline (2,4-DMA), in four types of honey (acacia, wild, chestnut, and manuka) and royal jelly. Samples were buffered with 0.2 M dibasic sodium phosphate (pH 9), and subsequently, acetonitrile was employed as the extraction solvent. A combination of primary secondary amine (PSA) and C18 sorbents was used for purification prior to liquid chromatography-electrospray ionization tandem mass spectrometry (LC-ESI + /MS-MS) analysis. The estimated linearity measured at six concentration levels presented good correlation coefficients ( R 2 ) ≥ 0.99. The recovery, calculated from three different spiking levels, was 62.06–108.79% in honey and 67.58–106.34% in royal jelly, with an RSD < 12% for all the tested compounds. The matrix effect was also evaluated, and most of the analytes presented signal enhancement. The limits of quantification (LOQ) ranged between 0.001 and 0.005 mg/kg in various samples. These are considerably lower than the maximum residue limits (MRL) set by various regulatory authorities. A total of 43 market (domestic and imported) samples were assayed for method application. Among the tested samples, three samples were tested positive (i.e. detected and quantified) only for cymiazole residues. The residues in the rest of the samples were detected but not quantified. We concluded that the protocol developed in this work is simple and versatile for the routine quantification of cymiazole, 2,4-DMA, fipronil, coumaphos, amitraz, and fluvalinate in various types of honey and royal jelly. [ABSTRACT FROM AUTHOR]

This study was conducted to evaluate the effects of dynamic stretching combined with manual therapy on pain, range of motion, function, and quality of life in patients with adhesive capsulitis. The participants were randomly divided into two groups: the dynamic stretching combined with manual therapy (DSMT) group ( n = 17) and the static stretching combined with manual therapy (SSMT) group ( n = 17). Both groups received manual therapy for 10 min and two sessions per week for 4 weeks. The DSMT group also performed additional dynamic stretching for 20 min per session, two sessions per week for 4 weeks. The SSMT group practiced additional static stretching for 20 min per session, two sessions per week for 4 weeks. The pain, ROM, function, and quality of life were measured and evaluated before and after treatment. There were significant improvements in the outcomes of pain, flexion and abduction of shoulder ROM, Shoulder Pain and Disability Index (SPADI), and the physical component score and mental component score of the Short Form-36 (SF-36) in both groups. Additionally, the external and internal rotation of the shoulder ROM and the SF-36 general health factor increased significantly more in the A group (DSMT group) compared to the B group (SSMT). In conclusion, dynamic stretching plus manual therapy offers the same results as static stretching plus manual therapy, but with additional improvement in internal and external rotation.

This study aimed to determine the mediating effect of stress on the relationship between residential environment satisfaction and feelings of depression in the elderly. To achieve the purpose of the study, the researcher personally conducted interviews with 250 senior citizens residing in Jeollanam-do, South Korea, from October to November 2019. SPSS version 27.0 and Hayes' PROCESS ver. 4.0 were used for data analysis. As a result of testing the research hypothesis, a partial mediating effect of stress on the relationship between residential environment satisfaction and feelings of depression was confirmed. Based on these results, diverse practical and policy suggestions were recommended. First, a connection between barrier-free walking and public transportation linking elderly residences and major living facilities (transportation facilities, medical facilities, cultural facilities, social welfare facilities, parks, etc.) was suggested. Second, the application of a universal design was proposed when remodeling or building elderly residences. Third, policies promoting social participation of the elderly and providing assistance to increase the intimacy of their relationship with family members and neighbors are necessary to enable older adults to maintain their social relationships. Fourth, programs, such as educational schemes that provide older adults with a greater understating of stress, must be developed in parallel to facilitate stress self-management interventions. In future, it is necessary to include additional mediating or moderating variables to generalize these findings to the larger population., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2022 Park and Choi.)