Antioxidant activity of various teas against free radicals and LDL oxidation

Tea is a widely consumed beverage throughout the world. We assessed the antioxidant activity of six teas, including the aqueous extracts of green tea and oolong tea (Camellia sinensis), tochu (Eucommia ulmoides), Gymnema sylvestre, Japanese mugwort (Artemisia princeps), and barley (Hordeum vulgare), against 1,1-diphenyl-2-picrylhydrazyl (DPPH) radicals and LDL oxidation, and examined the association of LDL oxidizability with the plasma catechin levels in 10 healthy volunteers with a single dose of 5 g green tea powder. In vitro, the inhibitory effects of DPPH radicals and LDL oxidation were found to be strongest in the extract of green tea and weakest in that of barley. After the ingestion of green tea powder, the lag time increased from basal 52.2±4.1 to 60.3±4.2 min at 1 h and 59.5±4.1 min at 2 h, and then returned to the baseline lag time (51.9±1.4 at 4 h and 52.1±4.7 min at 6 h). Regarding the plasma catechin levels, epigallocatechingallate and epicatechingallate significantly increased from basal 3.7±1.3 and 0.8±0.8 ng/mL to 65.7±11.6 and 54.6±12.6 ng/mL at 1 h, and 74.4±18.6 and 49.4±7.1 ng/mL at 2 h, respectively. Green tea therefore showed the strongest antioxidant activity among the six different teas, and the inhibitory effects of green tea on LDL oxidation depended on the plasma catechin levels.     

Deposition of Inhaled Ultrafine Aerosols in Replicas of Nasal Airways of Infants

Experimentally measured deposition of ultrafine particles, ranging from 13–100 nm in diameter, in nasal airway replicas of ten infants aged 3–18 months is presented. The replicas included the face, nostrils, and nasal airways including the upper trachea. A differential mobility analyzer (DMA) and a condensation particle counter (CPC) were used to quantify the nasal deposition by comparing the number of polydisperse sodium chloride particles, generated by evaporation from a Collison atomizer, at the inlet and outlet of the replicas. Particles were individually classified in size by DMA and subsequently were counted one size bin at a time by CPC upstream and downstream of each replica. Since in vivo data is not available for infants to compare to, we validated our experimental procedure instead by comparing deposition in nasal airway replicas of six adults with in vivo measurements reported in literature. In the infant replicas, tidal inhalation was simulated at two physiologically compatible flow rates and the effect of flow rate on deposition was found to be small. Deposition obtained at constant flow rates is lower than with tidal breathing, indicating the importance of unsteadiness, in contrast to similar data in adults where unsteadiness is known to be unimportant. An empirical equation, containing geometrical features of the nasal airways in the form of related non-dimensional dynamical parameters (Reynolds, Schmidt, and Womersley numbers), was best fitted to the infant data. This equation may be useful for a priori prediction of nasal deposition and intersubject variability during exposure of infants to ultrafine aerosols.     

Intravenous injection of tridihomo-γ-linolenoyl-glycerol into mice and its effects on delayed-type hypersensitivity

Highly purified tridihomo-γ-linolenoyl-glycerol (DGLA-TG) was emulsified with egg yolk lecithin as a 10% (wt/vol) DGLA-TG emulsion. We injected 0.05 or 0.5 mL of the emulsion into mice through the tail vein and investigated its effects on the fatty acid composition of spleen cells and on delayed-type hypersensitivity (DTH) response. At 1 h after the injection, dihomo-γ-linolenic acid (DGLA) concentrations were increased significantly in the total phospholipid fraction of spleen cells from 1.21±0.13 mol% to 2.09 ±0.74 mol% (P<0.02) and 7.95±1.25 mol% (P<0.001) in the 0.05-mL and 0.05-mL groups respectively. Mice, which had already been immunized with sheep red blood cells (SRBC), were challenged by the injection of SRBC into the right-hind footpad. Intravenous injection into mice with 0.5 mL of the emulsion immediately before the challenge almost completely suppressed DTH response measured by the swelling of the right-hind footpads 24 h thereafter. This inhibitory effect on the DTH response was significant with as little as 0.05 mL of the emulsion, whereas a soybean oil emulsion was not effective at all. In conclusion, intravenous injection of a DGLA emulsion increased DGLA concentrations in immune cells within 1 h and suppressed the DTH reaction.     

Preparation of goat milk powder with Lactobacillus casei L61 and antioxidant peptides: optimization of the composite thermal protectants and evaluation of storage stability

Abstract

The Lactobacillus casei L61 has great ability for producing antioxidant peptides. For reducing the mortality of L. casei L61 in spray drying process, the Box-Behnken design (BBD) was adopted to optimize the composite thermal protective agent formula. The results exhibited that the composite thermal protective agent formula of L. casei L61 contained glucose at 6.03% (w/v), skim milk at 18.98?g/L, and glycerol at 12.50?mL/L. Under the optimal conditions, the average survival of L. casei L61 in the fermented goat milk reached 14.58?±?0.72% after heat treatment at 75?°C for 10?min, which was higher than the control (13.14%). The average hydroxyl free radical scavenging activity of L. casei L61 reached 85.09?±?0.98%, which was not significantly different from the predicted value (86.83%). Therefore, the BBD is feasible for optimizing the composite thermal protective agent formula of L. casei L61. Under the optimal conditions with the inlet air temperature of 130?°C and feed rate of 4.5?mL/min, the maximum viable counts and survival rate of L. casei L61 were 7.46?×?10⁸ cfu/g and 23.41?±?1.28%, respectively. More importantly, the storage stability of antioxidative probiotic goat milk powder was predicted by temperature acceleration test. The shelf life of antioxidative probiotic goat milk powder was estimated to be 352?days at 4?°C and 117?days at 25?°C, embodying the great long-term stability. This study provides a technical reference for industrialized production of probiotic goat milk powder.     

Development and characterization of an oro-nasal inhalation plethysmography mask exposure system

An oro-nasal inhalation plethysmography mask exposure system (ONIPMES) was developed to challenge nonhuman primates and rabbits with biological agents while determining real-time respiratory parameters. The system included novel challenge plethysmography and sample collection masks that delivered aerosol directly to the breathing zone of the animals and to the sample collection probes. Challenge plethysmography masks were fitted with a differential pressure transducer that interfaced with a signal amplifier and computer software to quantify respiratory tidal volume, frequency, and minute volume. Challenge plethysmography masks were calibrated and verified with certified registered gas-tight syringes. Accuracy was determined from simultaneous comparison tests between the challenge plethysmography mask and head-out plethysmographs using live animals. For cynomolgus macaques, the mean differences in tidal volume, frequency, and minute volume were 4.20 ± 0.872 mL, 3.50 ± 3.15 breaths per minute (bpm), and 99.3 ± 91.7 mL/min. For New Zealand white rabbits, the mean differences in tidal volume, frequency, and minute volume were 1.13 ± 0.551 mL, 1.07 ± 0.404 bpm, and 209.3 ± 97.37 mL/min. Standardized tests were used to characterize the inhalation exposure system. The fractional leak rate was 4.17 × 10^?5 min^?1. The theoretical T₉₉ was 1.694 min and the observed T₉₉ was 0.588 min. Mask to mask spatial variation was 0.9%. The particle size distribution (PSD), mass median aerodynamic diameter (MMAD), and geometric standard deviation (GSD) of a 25 mg/mL saline solution was 1.2 ± 0.01 µm and 1.9 ± 0.20. The ONIPMES minimizes dermal and ocular contamination and multiple species may be used.     

Production of bulk SiC parts by electrophoretic deposition from concentrated aqueous suspension

Abstract

This paper reports on electrophoretic deposition of SiC bulk parts from highly loaded aqueous suspensions of submicron and nanosized powders. The effects of suspensions parameters (ζ-potential, conductivity, solids content) and deposition parameters (voltage, current density, time) on quality of deposits were examined. It is presented that by using well defined suspension parameters high process stability is assured. For submicron powder, relatively high density was achieved, i.e. 60% TD (±2%), while for the nanosized SiC, the highest density was 42% TD (±2%). Mixing of powders did not result in density increase. Bulk >4 cm thick deposits were proved to have homogeneous density distribution, which is one of the advantages of electrophoretic deposition (EPD) process in comparison to other ceramic shape forming processes.     

Continuous Measurements of Ambient Particle Deposition in Human Subjects

The total deposition fraction (TDF) of fine and ultrafine aerosols was measured in a group of six healthy adults exposed to polydisperse ambient aerosols in Boston. Fifteen repeated inhalation-exhalation cycles were conducted during a given exposure session. Deposition efficiency for particles with aerodynamic diameter ranging from 63.5 to 2045 nm was determined using the average concentration of inhaled and exhaled particles measured during these cycles. Deposition efficiencies ranged from 7.3±18.7%(240-275 nm) to 98.6±28.1%(1545-2045 nm). Subjects exhibited similar deposition patterns with minimum efficiencies between 200-400 nm. Results from ANOVA and mixed-model regression analyses showed significant differences (p < 0.05) in particle deposition efficiency by particle size as well as among the subjects. Deposition efficiencies varied most among the subjects for particles between 100 and 1000 nm in size. A comparison with the ICRP model showed good agreement, with best agreement for male subjects and particle sizes <400 nm.     

Sonication Assisted Three Phase Partitioning for the Extraction of Palmitic Acid and Elaidic Acid from Cassia sophera Linn.

Ultrasound assisted three phase partitioning (UATPP) has been explored for the extraction of palmitic acid (PA) and elaidic acid (EA) from Cassia sophera Linn. seed powder, and the process were optimized. Ultrasound was applied with TPP to improve the yield with operating frequencies of 25 and 40 kHz and at a power 200 W. The yield of PA and EA was 0.25 ± 0.005% and 0.26 ± 0.006%, respectively, with TPP. The yield was found 0.31 ± 0.002% and 0.32 ± 0.016%, with UATPP at 40 kHz and 180 W power. UATPP was found to be an effective technique.     

Comparison of methanol/hydrochloric,ferric chloride acid versus tribochemical silica coating for adhesion of resin cement to zirconium dioxide

This study compared air-abrasion and etching regimens on adhesion of resin luting agent to zirconium dioxide. Ceramic specimens (LAVA, 3 M ESPE) (N = 16) were embedded in acrylic resin and exposed surfaces were polished. The specimens were randomly assigned into four groups (n = 12, 3 specimens for each disc): SC: Air-borne particle abrasion (30 μm aluminum oxide particles coated with silica, CoJet, 3 M ESPE); MH: Heated chemical solution (Methanol-800 mL; 37% Hydrochloric Acid-200 mL; Ferric Chloride-2 g) at 100 °C for 30 min, MHP: Primer (Metal/Zirconia Primer, Ivoclar Vivadent) + MH, P: Primer only (Metal/Zirconia Primer). Cylindrical molds (internal diameter: 0.7 mm; height: 1.5 mm) were placed on each conditioned specimen, filled with resin cement (Multilink Automix) and photo-polymerized for 60 s. After 24 h, the molds were removed and the specimens were stored in distilled water at 37 °C for six months). Microshear test was performed in a Universal Testing Machine (1 mm/min). Failures types were classified as adhesive, mixed, or cohesive. In another set of specimens (n = 2 per group) contact angle measurements were recorded. Data were analyzed statistically using Kruskal–Wallis and Dunn’s tests (α = 0.05). The surface conditioning method significantly affected the mean bond strength (MPa) (p < 0.0001): SC(18.3 ± 0.3)^a < P(5.00 ± 0.07)^b < MHP(4.7 ± 0.08)^c < MH(0.84 ± 0.01)^c. While Group SC showed mainly adhesive (58%) and mixed (41.7%) failure types, groups MH, MHP, and P presented exclusively adhesive failures. SC, MHP, and P (29–32°) showed lower contact angle than MH (78.9°). Volume loss was the highest with MHP (9.92 μl) followed by SC (9.67 μl).     

Improved mechanical strength of p(AAm) interpenetrating hydrogel network due to microgranular cellulose embedding

Here, polyacrylamide [p(AAm)]‐based hydrogels were synthesized via redox polymerization technique in the presence of various amounts of microgranular cellulose (MGCell) such as 0, 10, 25, 50, 100, and 150 mg MGCell/g. The synthesized p(AAm)‐MGCell interpenetrating hydrogels were characterized spectroscopically by FTIR, thermally by TGA analysis, and mechanically via dynamic mechanical measurements. Furthermore, the effect of the amount of MGCell in p(AAm) hydrogels on swelling% (S%) degree and mechanical strength was investigated. It was found that the S% was decreased from 727 ± 9 to 667 ± 6, 642 ± 8 and 619 ± 10, 568 ± 6 for p(AAm)‐MGCell interpenetrating network hydrogels containing 10, 50, 100, and 150 mg MGCell, respectively. On the other hand, the Young modulus of p(AAm)‐based hydrogels increased from 2.8 ± 0.2 kPa to 3.1 ± 0.03, 3.4 ± 0.1, 3.6 ± 0.3 and 4.3 ± 0.3 kPa with the incorporation of 10, 50, 100, and 150 mg MGCell into p(AAm) hydrogels. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44854.     

Characteristics and gel properties of gelatin from goat skin as affected by spray drying

Gelatin powder from goat skin prepared by spray drying at various inlet temperatures (160–200°C) was characterized. Predominant particle sizes were in the range of 4.65–5.14?µm. Gelatin powder was mostly concave in shape with varying sizes, depending on inlet temperatures used. All gelatin powders were creamy whitish. Powder generally became more yellowish as the inlet temperature of spray drying increased (p?p?p?p?>?0.05). Goat skin gelatin spray dried with inlet temperatures of 160 or 180°C had higher gel strength than commercial bovine gelatin (p?相似文献   

Novel non-bouncing PM2.5 impactor modified from well impactor ninety-six

The impaction well containing an oil-soaked glass fiber (GF) filter of the well impactor ninety-six (WINS) needs to be replaced every five sampling days to avoid particle overloading which affects the cutoff diameter (d_pa50) and the sampling accuracy. This study developed a novel modified WINS (M-WINS) which uses water to wash the wetted GF filter substrate clean continuously to eliminate the particle overloading effect and extend the service life of the impactor without the need of impaction well cleaning and replacement of the oil-soaked GF filter. The laboratory test showed that d_pa50 of the M-WINS only varied slightly from 2.44 to 2.49 µm while d_pa50 of the WINS decreased from 2.44 to 2.05 µm when the loaded particle mass increased from 0–6 mg. The field test showed that d_pa50 and the sampling bias of the novel M-WINS met the USEPA requirements (d_pa50 = 2.5 ± 0.2 µm and sampling bias <±5%) while the WINS without regular replacement of the well showed the decrease in d_pa50 down to 2.12 µm and the increase in the negative sampling bias to ?20% after 17 continuous sampling days. Therefore, the current M-WINS can be used as the PM_2.5 inlet for unattended, continuous sampling for a long time with a very good sampling accuracy.

Copyright © 2017 American Association for Aerosol Research     

Electrochemical Separation of Alanine,Cysteine, and Glycine Using a Digital Thruster

The present work deals with the use of a digital thruster for the electrochemical separation of amino acids. A digital thruster (DT) is a micro controller based digital electronic switching system (DT-MCDESS). Mixtures of amino acids were injected into the free electrolytic diffusion apparatus (FEDA). Micro cathodes surrounding a central anode were covered with agarose coated filter paper strips and programmed with DT-MCDESS. The charge was distributed over micro cathodes at time intervals of 100 and 200 µs, which result in deposition and separation of alanine, cysteine, and glycine filter paper strips. For identification of each amino acid, ninhydrin was sprayed to develop separate colors for deposited amino acids on filter paper strips. Alanine displayed as purple, cysteine as red, and glycine as yellow. The separation of alanine, cysteine, and glycine was performed at two frequencies, 312.5 Hertz and 625 Hertz.     

Characterization and Benzo[a]pyrene Content Analysis of Camellia Seed Oil Extracted by a Novel Subcritical Fluid Extraction

A novel continuous subcritical n‐butane extraction technique for Camellia seed oil was explored. The fatty acid composition, physicochemical properties, and benzo[a]pyrene content of Camellia seed oil extracted using this subcritical technique were analyzed. Orthogonal experiment design (L₉(3⁴)) was adopted to optimize extraction conditions. At a temperature of 45 °C, a pressure of 0.5 MPa, a time of 50 min and a bulk density of 0.7 kg/L, an extraction yield of 99.12 ± 0.20 % was obtained. The major components of Camellia seed oil are oleic acid (73.12 ± 0.40 %), palmitic acid (10.38 ± 0.05 %), and linoleic acid (9.15 ± 0.03 %). Unsaturated fatty acids represent 83.78 ± 0.03 % of the total fatty acids present. Eight physicochemical indexes were assayed, namely, iodine value (83.00 ± 0.21 g I/100 g), saponification value (154.81 ± 2.00 mg KOH/g), freezing‐point (?8.00 ± 0.10 °C), unsaponifiable matter (5.00 ± 0.40 g/kg), smoke point (215.00 ± 1.00 °C), acid value (1.24 ± 0.03 mg KOH/g), refrigeration test (transparent, at 0 °C for 5.5 h), and refractive index (1.46 ± 0.06, at 25 °C). Benzo[a]pyrene was not detected in Camellia seed oil extracted by continuous subcritical n‐butane extraction. In comparison, the benzo[a]pyrene levels of crude Camellia seed oil extracted by hot press extraction and refined Camellia seed oil were measured at 26.55 ± 0.70 and 5.69 ± 0.04 μg/kg respectively.     

Optimizing Filtration Experiments for Length and Fractal Dimension Characterization of Non-Spherical Particles

By combination of a differential mobility analyzer (DMA) with a filter with uniform pores, namely a filter sensor, a new method for differentiating nanoparticles with various mass-mobility fractal dimensions, D_fm, was developed and validated experimentally and theoretically. The sensor is also able to measure the effective length (or maximum projected length) of nanoparticles with different shapes, which is an important parameter responsible for the lung deposition due to interception. At the same mobility diameter, it was observed that the compact NaCl had the highest penetration followed by partially sintered silver (Ag) aggregates and then the loose Ag and soot agglomerates. The result indicates that the stronger interception by the filter is correlated to the more elongated shape of the particles. A modified capillary tube model for predicting the penetration of Ag nanoparticles with different mass-mobility fractal dimensions was validated by experimental data. By using the validated model, this study found that the sensor could have a further enhanced sensitivity if the porosity and thickness of the filter were adjusted to 0.01 and 5 µm, respectively. The penetration differences obtained from the model are as high as 7–18%, 14–35%, and 24–40% between spheres and loose agglomerates (D_fm = 2.1) for 50–100, 100–300, and 300–1000 nm particles as the filter pore sizes are 0.4, 1, and 3 µm, respectively. This new filter sensor can measure the effective length and mass-mobility fractal dimension in nearly real-time and may be applied in nanotoxicity studies and quality control of nanomaterial productions (e.g., by flame reactors).

Copyright 2015 American Association for Aerosol Research     

Studies on processing of layered oxide-bonded porous sic ceramic filter materials

Oxide-bonded porous SiC ceramic filter supports were prepared using SiC powder (d₅₀ = 212 µm), Al₂O₃, and clay as bond forming additives and graphite as pore former following reaction bonding of powder compacts at 1400°C in air. Reaction bonding characteristics, phase composition, porosity, pore size, mechanical strength, and microstructure of porous SiC ceramic supports were investigated. Mullite bond phase formation kinetics was studied following the Johnson–Mehl–Avrami–Kolmogorov (JMAK) model using non-isothermal differential thermal analysis (DTA) data. Compared to porous SiC ceramic filter supports having no needle-like mullite bond phase, materials processed by the mullite bonding technique exhibited higher average strength (22.1%) and elastic modulus (5.4%) at a similar porosity level of ~38%, with upper and lower bounds of their strength, modulus, and porosity being 39.1 MPa, 40.2 GPa, and 36.3% and 34.2 MPa, 31.3 GPa, and 33.0%, respectively. Spray coating method was applied for preparation of oxidation-bonded SiC filtration layer having thickness of ~150 µm and pore size of ~5–20 µm over the porous SiC support compacts using aqueous slurry made of fine SiC powder (d₅₀ = 15 µm) followed by sintering. The layered ceramics thus prepared are potential materials for gas filter applications.     

Dietary linoleic acid-induced hypercholesterolemia and accumulation of very light HDL in steers

This experiment was designed to study the effects in fattening steers of n−6 PUFA supplementation on the plasma distribution and chemical composition of major lipoproteins (TG-rich lipoproteins: d<1.006 g/mL; intermediate density lipoproteins + LDL: 1.019<d<1.060 g/mL; light HDL: 1.060<d<1.091 g/mL; and heavy HDL: 1.091<d<1.180 g/mL). For a period of 70 d, animals [454±20 d; 528±36 kg (mean±SD)] were given a control diet (diet C, n=6) consisting of hay and concentrate mixture (54 and 46% of diet dry matter, respectively) or the same diet supplemented with sunflower oil (4% of dry matter), given either as crushed seeds (diet S, n=6) or as free oil continuously infused into the duodenum through a chronic canula to avoid ruminal PUFA hydrogenation (diet O, n=6). Plasma lipids increased in steers given diet S (×1.4, P<0.05) and diet O (×2.3, P<0.05), leading to hyperphospholipemia and hypercholesterolemia. With diet S, hypercholesterolemia was associated with higher levels of light (×1.4, P<0.05) and heavy HDL (×1.3, NS). With diet O, it was linked to higher levels of light HDL (×1.8, P<0.005) and to very light HDL accumulation within density limits of 1.019 to 1.060 g/mL, as demonstrated by the apolipoprotein A-I profile. Diet O favored incorporation of 18∶2n−6 into polar (×2.2, P<0.05) and neutral lipids (×1.5 to ×8, P<0.05) at the expense of SFA, MUFA, and n−3 PUFA. Thus, protection of dietary PUFA against ruminal hydrogenation allowed them to accumulate in plasma lipoproteins, but the effects of hypercholesterolemia on animal health linked to very light HDL accumulation remain to be elucidated.     

EPA,but not DHA,decreases mean platelet volume in normal subjects

The first indication of platelet activation is an increase in mean platelet volume (MPV). n−3 FA are known to inhibit platelet function and to reduce the risk for coronary heart disease. The purpose of this study was to determine the effects of FPA and DHA on MPV. Healthy subjects received olive oil placebo for 4 wk and then were randomly assigned to receive 4g of ethyl esters of either safflower oil (n=11), EPA (n=10), or DHA (n=12) for 4 wk. At the end of placebo run-in and treatment periods, MPV (fL; mean±SEM) and platelet count (PLT-CT; 10³/μL blood) were measured in the basal state and after ex vivo stimulation with collagen (10 μg/mL), cold (4°C), and heat (37°C). Unlike DHA, EPA lowered MPV as compared with safflower oil (7.2±0.1 vs. 7.5±0.1 fL; P<0.05) and raised PLT-CT (211±18 vs. 192±18 10³/μL; P<0.05) in the fasting state. Collagen and cold significantly increased MPV whereas heat lowered MPV regardless of treatment. All stimuli decreased PLT-CT. EPA significantly increased platelet EPA (0.2±0.1 vs. 3.3±0.4%) and docosapentaenoic acid (DPA; 2.2±0.3 vs. 2.9±0.3%) concentrations, but not DHA. DHA treatment significantly increased DHA (1.4±0.2 vs. 4.1±0.5%) and DPA (2.0±0.4 vs. 3.0±0.4%) concentrations, but not EPA. In conclusion, EPA, but not DHA, reduces platelet activation, an early step in platelet aggregation.     

Human platelets release a paf-acether: Acetylhydrolase similar to that in plasma

Intact washed human platelets aggregated in response to paf-acether (paf) and did not metabolize [³H]paf at concentrations up to 10 nM. However, when platelets were lysed by exposure to pH 9.5, resulting in 37.5±2.5% (mean ±SD, n=3) lactic dehydrogenase (LDH) release, 20.5±5.7% of the radioactivity was detected as labeled lyso paf and 5.7±3.1% as labeled alkylacylglycerophosphocholine. When platelets were aggregated with 0.5 IU/mL thrombin or high concentrations of paf (100 nM), they released a part of their acetylhydrolase without releasing LDH. In supernatants obtained from aggregated platelets, 21±2% or 10±2% (n=3), respectively, of the total platelet acetylhydrolase activity was detectedvs. none in supernatants of resting cells. The release of acetylhydrolase was concentration-and time-dependent and paralleled the release of PF 4, a marker for α-granules. The acetylhydrolase affinity for paf (K_m) measured in sonicates of resting and thrombin-activated platelets was 8.3±1.5 μMvs. 10.6±1.5 μM, n=5, n.s. in a “Mann Whitney” test. The latter K_m was slightly but significantly different (P<0.05, n=5) from that of the thrombin-released acetylhydrolase (7.9 ±1.5 μM) and that of the latter was itself different from plasma acetylhydrolase (5.3±0.5,P<0.05, n=5). Addition of plasma (acid-treated to inactivate acetylhydrolase) decreased the K_m value of supernatant acetylhydrolase to 6.1±1.4 μM. All preparations of acetylhydrolase exhibited similar pH requirements and sensitvity to various inhibitors. Thus paf and thrombin cause release of acetylhydrolase from platelets in parallel with release of the α-granule marker PF4. This phenomenon might represent a protective mechanism against paf-mediated effects in thrombotic and cardiovascular diseases. This study has been presented in part as a preliminary report at the 72nd Annual Meeting of the Federation of American Societies for Experimental Biology, Las Vegas, NV, May 1988 (1).     

Separation,Identification, Antioxidant,and Anti-Tumor Activities of Hibiscus sabdariffa L. Extracts

Roselle (Hibiscus sabdariffa L.) belongs to the malvaceae family. Its calyx is used for making jellies, jams, and beverages. Despite it usefulness, there are few or no studies on the purification and structural identification of HAs and Roselle extracts. This paper therefore seeks to investigate the purification and structural identification of Hibiscus sabdariffa L. extracts, and to evaluate their antioxidant activities on DPPH and ABTS and anti-tumor activities on human cervical cancer HeLa cells of purified fractions. Two fractions (fraction 1 and fraction 2) from Roselle (Hibiscus sabdariffa L.) extracts were purified with C-18 Sep-Pak cartridge, followed by Sephadex LH-20 column and characterized by HPLC-ESI-MS/MS. The contents of the anthocyanins in fraction 1 and fraction 2 were 863.41 mg/g and 617.35 mg/g, respectively. Nine compounds were identified with HPLC-ESI-MS/MS, seven of which have not been reported before in Roselle. Two fractions and HAs-rich extracts purified with C-18 Sep-Pak cartridge showed high capacity on radicals scavenging and HeLa cells inhibition in a dose-dependent manner. The orders of both activities were: fraction 1 > fraction 2 > HAs-rich extracts. IC₅₀ values of fraction 1 on DPPH and ABTS radicals were 17.14 ± 2.24 μg/mL and 85.91 ± 6.72 μg/mL, respectively. The cell inhibition ratio of fraction 1 against HeLa cells reached 83.67 ± 3.07% at the concentration of 200 μg/mL. Two fractions and HAs-rich extracts could be a good supplements for natural antioxidant and anti-tumor activities.