Transoral removal of a hilo-parenchymal submandibular sialolith.

In sialolithiasis, the lithiasis is often large and located at the junction of the middle and posterior third of the duct, in the hilum region. In such cases, transoral approach for submandibular lithiases (TASL) is a useful treatment of choice in patients with large submandibular stones that can be palpated bimanually.

Evaluation and development of a novel pre-treatment method for mulberry leaves to enhance their bioactivity via enzymatic degradation of GAL-DNJ to DNJ.

Mulberry leaves are rich in 1-deoxynojirimycin (DNJ) and 2-O-α-D-galactopyranosyl-deoxynojirimycin (GAL-DNJ). Compared to DNJ, the bioactive potency of GAL-DNJ is low. We proposed that the conversion of GAL-DNJ into DNJ may improve its bioavailability. We evaluated this hypothesis and constructed a novel enzymatic-based method to induce the hydrolysis of GAL-DNJ to DNJ in order to improve the therapeutic potency of mulberry leaves.

Intestinal Absorption and Tissue Distribution of Aza-Sugars from Mulberry Leaves and Evaluation of Their Transport by Sugar Transporters.

Mulberry leaves are rich in aza-sugars, particularly 1-deoxynojirimycin (DNJ), fagomine, and 2-O-α-d-galactopyranosyl-1-deoxynojirimycin (GAL-DNJ), which have antidiabetes and antiobesity properties. To help us understand the mechanisms of action of aza-sugars, pharmacokinetic studies are necessary. Therefore, in this study, we evaluated and compared the absorption and organ distribution of these aza-sugars in rats. Following oral intake, DNJ exhibited the highest plasma concentration followed by fagomine and GAL-DNJ. Meanwhile, similar amounts of DNJ and fagomine were present in organs, while GAL-DNJ was hardly detected, suggesting the diversity in absorption and distribution characteristics of these aza-sugars. We then investigated the role of the sodium-glucose cotransporter and the glucose transporter (GLUT) in the transport of aza-sugars and found that both are involved in DNJ transport, while transport of fagomine is solely facilitated by the GLUT. These findings provide insight into the bioavailability and bioactive mechanisms of these aza-sugars.

Degradation of cellulose in NaOH and NaOH/urea aqueous solutions by ultrasonic irradiation.

Ultrasonic degradation of cellulose with low molecular weight in NaOH and NaOH/urea solutions was investigated at 20 and 500 kHz frequencies by measuring the solution viscosity. The viscosity decreased with sonication time. A small difference in viscosity ratio which is defined as the ratio of specific viscosity of solution after and before sonication was observed for the longer sonication. The degrees of the polymerization were reduced from 230 to 150 for 30 min sonication at 20 kHz and for 120 min sonication at 500 kHz. From XRD measurement, it was estimated that the crystallinity after sonication was the same as that before sonication. The crystallinity structure after sonication corresponded to Cellulose II. The yield of water-soluble components after ultrasonic irradiation was 20 wt% at 20 kHz in NaOH solutions and 30 wt% for 720 min at 500 kHz in NaOH/urea solution. Oligosaccharides and their derivative were detected by the SEC analysis of water-soluble components after sonication.

Clinical Usefulness of Immunohistochemical Staining of p57 kip2 for the Differential Diagnosis of Complete Mole.

OBJECTIVE: Can polymer-based immunohistochemical staining of p57(kip2) replace DNA analysis as an inexpensive means of differentiating complete mole from partial mole or hydropic abortion? METHODS AND MATERIALS: Original paraffin-embedded tissue blocks from 14 equivocal cases were turned over to our laboratory and examined by immunohistochemical staining of p57(kip2). RESULTS: Four of the 14 cases showed clearly negative nuclear staining in cytotrophoblasts and villous stromal cells: these results were fully concordant with the control staining. The remaining 10 cases showed apparently positive staining in cytotrophoblasts and villous stromal cells. Without DNA analysis we are able to clearly differentiate the 4 cases of complete mole among the 14 equivocal cases. During follow-up, secondary low-risk gestational trophoblastic neoplasia (GTN) developed in 1 of the 4 cases of complete mole: the GTN was treated by single-agent chemotherapy. No subsequent changes were observed during follow-up in the other cases. CONCLUSION: Polymer-based immunohistochemical staining of p57(kip2) (paternally imprinted gene, expressed from maternal allele) is a very effective method that can be used to differentiate androgenetic complete mole from partial mole and hydropic abortion. We might be able to avoid the cost of DNA analysis.

Physical and chemical characteristics of ultrasonically-prepared water-in-diesel fuel: effects of ultrasonic horn position and water content.

An ultrasonic technique was applied to preparation of two-phase water-in-oil (W/O) emulsified fuel of water/diesel oil/surfactant. In this study, an ultrasonic apparatus with a 28 kHz rod horn was used. The influence of the horn tip position during ultrasonic treatment, sonication time and water content (5 or 10 vol%) on the emulsion stability, viscosity, water droplet size and water surface area of emulsion fuels prepared by ultrasonication was investigated. The emulsion stability of ultrasonically-prepared fuel significantly depended on the horn tip position during ultrasonic irradiation. It was found that the change in the stability with the horn tip position was partly related to that in the ultrasonic power estimated by calorimetry. Emulsion stability, viscosity and sum of water droplets surface area increased and water droplet size decreased with an increase in sonication time, and they approached each limiting value in the longer time. The maximum values of the viscosity and water surface area increased with water content, while the limiting values of the emulsion stability and water droplet size were almost independent of water content. During ultrasonication of water/diesel oil mixture, the hydrogen and methane were identified and the cracking of hydrocarbon components in the diesel oil occurred. The combustion characteristics of ultrasonically-prepared emulsion fuel were studied and compared with those of diesel oil. The soot and NOx emissions during combustion of the emulsified fuel with higher water contents were significantly reduced compared with those during combustion of diesel oil.

Effect of mulberry leaf extract with enriched 1-deoxynojirimycin content on postprandial glycemic control in subjects with impaired glucose metabolism.

UNLABELLED: Aims/Introduction: The glucose analogue, 1-deoxynojirimycin (DNJ), found in mulberry (Morus alba) leaves, is a promising α-glucosidase inhibitor. We evaluated the effect of the ingestion of mulberry leaf extract with enriched DNJ content on postprandial hyperglycemia in subjects with impaired glucose metabolism. MATERIALS AND METHODS: In study 1, we carried out a randomized, double-blind, crossover trial to assess the effects of single ingestion of mulberry leaf extract (3, 6 or 9 mg DNJ) or placebo on blood glucose and insulin concentrations during 2 h after a carbohydrate (200 g boiled white rice) challenge in 12 subjects with fasting plasma glucose (FPG) in the range of 100-140 mg/dL. Study 2 was a randomized, double-blind, placebo-controlled trial to assess the efficacy of 12-week extract supplementation (6 mg DNJ, t.i.d.) for long-term glycemic control in 76 subjects with FPG in the range of 110-140 mg/dL. RESULTS: In study 1, ingestion of the mulberry leaf extract led to attenuated postchallenge acute glycemia in a dose-dependent manner (P = 0.006, group × time interaction, two-way anova). In study 2, the serum 1,5-anhydroglucitol concentration, a sensitive indicator of postprandial glycemic control, in the extract group increased and was higher than that in the placebo group over the 12-week treatment period (P < 0.001, group × time interaction, two-way anova); no differences in FPG, glycated hemoglobin and glycated albumin concentrations were observed between the groups. CONCLUSIONS: Long-term ingestion of mulberry leaf extract with enriched DNJ content could result in improved postprandial glycemic control in individuals with impaired glucose metabolism. These trials were registered with UMIN (no. UMIN000003154 and UMIN000003155). (J Diabetes Invest, doi: 10.1111/j.2040-1124.2011.00101.x, 2011).

Effects of mulberry leaf extract rich in 1-deoxynojirimycin on blood lipid profiles in humans.

Mulberry leaves are rich in 1-deoxynojirimycin (DNJ), an inhibitor of α-glucosidase. We previously showed that DNJ-rich mulberry leaf extract suppressed elevation of postprandial blood glucose in humans. The objective of this study was to evaluate the effects of DNJ-rich mulberry leaf extract on plasma lipid profiles in humans. An open-label, single-group study was conducted in 10 subjects with initial serum triglyceride (TG) level ≥200 mg/dl. Subjects ingested capsules containing DNJ-rich mulberry leaf extract at 12 mg three times daily before meals for 12 weeks. Our findings showed a modest decrease in serum TG level and beneficial changes in the lipoprotein profile following 12-week administration of DNJ-rich mulberry leaf extract. No significant changes in hematological or biochemical parameters were observed during the study period; no adverse events associated with DNJ-rich mulberry leaf extract occurred.

The effects of acoustic flow and mechanical flow on the sonochemical efficiency in a rectangular sonochemical reactor.

Visualization of cavitation behavior in a rectangular sonochemical reactor at 490 kHz was carried out by a laser sheet technique and the distribution of liquid flow was measured by a laser Doppler velocimeter. The pattern of liquid flow and distribution of acoustic pressure of the rectangular sonochemical reactor were investigated as a function of the input power from 10 to 50 W. The liquid moved upward above the transducer at every power. As increasing the input power, the random flow out side the cylindrical part above the transducer changed into the convective one and the region of the visualized standing wave which was formed in the cylindrical part changed with the input power. The position showing the sonochemical luminescence exists inside or near the region where the standing wave was visualized. Introduction of a stirrer resulted in disturbance of liquid flow and expanded the position showing the sonochemical luminescence, but the luminescence intensity was weakened. The sonochemical efficiency was enhanced by about twice by introduction of the stirrer. From these results, we discussed the effects of liquid flow on sonochemical efficiency with and without a stirrer.

Stabilization of long-lived metastable state in long alkylated spin-crossover cobalt(II) compound.

The A mixed crystal compound [Co(0.8)Fe(0.2)(C16-terpy)(2)](BF(4))(2) (2) (C16-terpy is 4'-hexadecyloxy-2,2':6',2''-terpyridine) with long alkyl chains was prepared by mixing [Co(C16-terpy)(2)](BF(4))(2) (1), which exhibits unique magnetic behavior, and the diamagnetic iron(II) compound [Fe(C16-terpy)(2)](BF(4))(2) (3). The long-lived metastable state in the frozen-in effect was observed for the first time in the spin-crossover cobalt(II) compound 2. Furthermore, relaxation from metastable to stable states was very slow because of a large structural transition resulting from the long alkyl chains.

Bis[2-(8-quinolylimino-meth-yl)phenolato-κN,N',O]iron(III) azide.

The title compound, [Fe(C(16)H(11)N(2)O)(2)]N(3), consists of a [Fe(qsal)(2)](+) cation [Hqsal = N-(8-quinol-yl)salicylaldimine] and an azide anion. The Fe(III) ion, lying on a twofold rotation axis, is coordinated by four N atoms and two O atoms from two tridentate qsal ligands in an octa-hedral geometry. The mol-ecules are connected into a three-dimensional network by inter-molecular C-H⋯N and C-H⋯O inter-actions. π-π inter-actions [inter-planar distance = 3.58 (1) Å] between the quinoline rings of adjacent mol-ecules further stabilize the crystal structure.

Bis(1H-imidazole-κN){2,2'-[propane-1,2-diylbis(nitrilo-methyl-idyne)]diphenolato-κO,N,N',O'}iron(III) perchlorate.

The title compound, [Fe(C(17)H(16)N(2)O(2))(C(3)H(4)N(2))(2)]ClO(4), consists of monomeric [Fe(salmen)(HIm)(2)](+) cations {salmen is the 2,2'-[propane-1,2-diylbis(nitrilo-methyl-idyne)]diphen-olate dianion and HIm is 1H-imiazole} and perchlorate anions. In the cation, the Fe(3+) ion is octahedrally coordinated by two N atoms and two O atoms from a tetra-dentate salmen anion and two N atoms from two Him mol-ecules. These ligands are coordinated to the iron ion in a direction perpendicular to the [Fe(salmen)](+) coordination plane. The benzene ring planes in the salmen ligands are oriented nearly parallel to one another inter-molecularly [dihedral angle = 6.36 (3)°]. The dihedral angle between the mean planes through the imidazole rings in the cation is 76.9 (2)°. In the crystal, N-H⋯O inter-actions link the mol-ecules into a one-dimensional double chain running along [101] and C-H⋯O inter-actions link the double chains into a two-dimensional network, running parallel to the ac plane.

Dynamic structural conversion in a spin-crossover cobalt(ii) compound with long alkyl chains.

A cobalt(ii) compound [Co(C14-terpy)(2)](BF(4))(2).MeOH (1) with long alkyl chains was prepared, and exhibited unique SCO at T(1) = 50 K and spin transition at T(2) upward arrow = 206 K and T(2) downward arrow = 184 K with hysteresis (DeltaT = 22 K) accompanying the motion of the long alkyl chains.

Food-grade mulberry powder enriched with 1-deoxynojirimycin suppresses the elevation of postprandial blood glucose in humans.

Mulberry 1-deoxynojirimycin (DNJ), a potent glucosidase inhibitor, has been hypothesized to be beneficial for the suppression of abnormally high blood glucose levels and thereby prevention of diabetes mellitus. However, DNJ contents in commercial mulberry products were as low as about 0.1% (100 mg/100 g of dry product), implying that the bioavailability of DNJ might not be expected. We carried out studies in two directions: (1) production of food-grade mulberry powder containing a maximally high DNJ content; (2) determination of the optimal dose of the DNJ-enriched powder for the suppression of the postprandial blood glucose through clinical trials. The following method was used: (1) DNJ concentrations in mulberry leaves from different cultivars, harvest seasons, and leaf locations were determined using hydrophilic interaction chromatography with evaporative light scattering detection. (2) Healthy volunteers received 0, 0.4, 0.8, and 1.2 g of DNJ-enriched powder (corresponding to 0, 6, 12, and 18 mg of DNJ, respectively), followed by 50 g of sucrose. Before and 30-180 min after the DNJ/sucrose administration, plasma glucose and insulin were determined. The following results were obtained: (1) Young mulberry leaves taken from the top part of the branches in summer contained the highest amount of DNJ. After optimization of the harvesting and drying processes for young mulberry leaves (Morus alba L. var. Shin ichinose), DNJ-enriched powder (1.5%) was produced. (2) A human study indicated that the single oral administration of 0.8 and 1.2 g of DNJ-enriched powder significantly suppressed the elevation of postprandial blood glucose and secretion of insulin, revealing the physiological impact of mulberry DNJ (effective dose and efficacy in humans). This study suggests that the newly developed DNJ-enriched powder can be used as a dietary supplement for preventing diabetes mellitus.

Enhancement of saccharin removal from aqueous solution by activated carbon adsorption with ultrasonic treatment.

This study investigates the use of ultrasonication as a pretreatment process and its effect on the adsorption characteristics of saccharin onto activated carbon (AC). Ultrasonic decomposition of saccharin was performed at a frequency of 500 kHz under argon and O2/N2 (20/80 vol%) atmospheres. Adsorption was carried out using a commercial activated carbon. The behavior of total organic carbon (TOC) during ultrasonication was investigated. Saccharin removal after 180 min of ultrasonication under Ar and O2/N2 atmospheres are 38% and 26%, respectively, while the amount of saccharin removed by activated carbon adsorption without US pretreatment is 40% after 16 h. After 16 h of AC adsorption with 180 min of ultrasonic pretreatment under Ar and O2/N2 atmospheres, both removal ratios increased to 75%. These results indicated that the pretreatment of sonication under O2/N2 leads to the increase in the amount of saccharin adsorbed on AC. On the other hand, the TOC removal by decomposition by ultrasound is not more than 5% in both Ar and O2/N2 atmospheres after 180 min ultrasonication. However, the TOC removal increased to 54% and 69% after 16 h of adsorption of saccharin pretreated by ultrasonication for 180 min under Ar and O2/N2 atmospheres, respectively. About 13% and 16% TOC removal in Ar and in O2/N2, respectively, were achieved due to adsorption of the by-products. It is considered that the improvement in TOC removal is also brought about by the formation of the by-products that were adsorbed onto AC.

Effects of dissolved gas species on ultrasonic degradation of (4-chloro-2-methylphenoxy) acetic acid (MCPA) in aqueous solution.

Sonochemical degradation of MCPA ((4-chloro-2-methylphenoxy) acetic acid) in dilute aqueous solutions was studied using ultrasound with a frequency of 500 kHz. The effect of gas atmosphere on MCPA degradation was investigated in nitrogen (N(2)), air (O(2)/N(2)), oxygen (O(2)), argon (Ar) and Ar/O(2) (60/40% v/v) atmospheres. For sonochemical degradation of MCPA in N(2), air (O(2)/N(2)), O(2) and Ar atmospheres, the rate enhancement of MCPA decomposition by sonolysis was found to be more effective in an O(2)-enriched atmosphere compared to Ar atmosphere. It was considered that a higher amount of oxidants was formed in a higher O(2) partial pressure, which accelerated MCPA decomposition in a radical reaction system. On the other hand, both dechlorination and total organic carbon (TOC) removal rates were higher in Ar atmosphere, compared to those in O(2)/N(2) atmosphere. It was found that, MCPA was most effectively decomposed by sonication in Ar/O(2) (60/40% v/v) atmosphere, with higher rates of decomposition, dechlorination and TOC removal.

Catalytic wet oxidation of o-chlorophenol at mild temperatures under alkaline conditions.

Wet oxidation of a 100 ppm aqueous solution of o-chlorophenol (o-CP) was performed in a lab-scale batch reactor using 3% Ru/TiO(2) catalyst at 373 and 413 K, and a partial oxygen pressure of 0.1 MPa. The experiments were conducted by varying the initial pH values of o-CP solution from pH 6.3 to 9.8 and 11.8. From the results, it was revealed that the catalytic decomposition of o-CP occurred most effectively at 413 K and at the initial pH of 9.8. Complete decomposition and dechlorination of o-CP were almost achieved within 1h, and about 85% of TOC was removed in 3.0 h. On the other hand, the catalytic wet oxidation of o-CP at a higher pH value of 11.8 was not effective in the removal of TOC. The incomplete removal of TOC at the initial pH of 11.8 is likely attributed to a low pK(a) of carboxylic acids formed during the wet oxidation of o-CP.

Adsorption equilibrium modeling and solution chemistry dependence of fluoride removal from water by trivalent-cation-exchanged zeolite F-9.

Fluoride in drinking water above permissible levels is responsible for human dental and skeletal fluorosis. In this study, therefore, the large internal surface area of zeolite was utilized to create active sites for fluoride sorption by exchanging Na+-bound zeolite with Al3+ or La3+ ions. Fluoride removal from water using Al3+- and La3+-exchanged zeolite F-9 particles was subsequently investigated to evaluate the fluoride sorption characteristics of the sorbents. Equilibrium isotherms such as the two-site Langmuir (L), Freundlich (F), Langmuir-Freundlich (LF), Redlich-Peterson (RP), Toth (T), and Dubinin-Radushkevitch (DR) were successfully used to model the experimental data. Modeling results showed that the isotherm parameters weakly depended on the solution temperature. From the DR isotherm parameters, it was considered that the uptake of fluoride by Al3+-exchanged zeolite proceeded by an ion-exchange mechanism (E = 11.32-12.13 kJ/mol), while fluoride-La3+-exchanged zeolite interaction proceeded by physical adsorption (E = 7.41-7.72 kJ/mol). Factors from the solution chemistry that affected fluoride removal from water were the solution pH and bicarbonate content. The latter factor buffered the system pH at higher values and thus diminished the affinity of the active sites for fluoride. Natural groundwater samples from two Kenyan tube wells were tested and results are discussed in relation to solution chemistry. In overall, Al3+-exchanged zeolite was found to be superior to La3+-exchanged zeolite in fluoride uptake within the tested concentration range.