Modulation of chemical carcinogenesis in rats by alkyl lysophospholipids

The influence of 1-O-octadecyl-2-O-methyl-rac-glycero-3-phosphocholine (ET-18-OCH₃) and 1-hexadecylmercapto-2-methoxymethyl-rac-propyl-3-phosphocholine (TLP, BM41.440) on methylnitrosourea (MNU)-induced rat mammary carcinomas and of ET-18-OCH₃ on 7,12-dimethylbenzanthracene (DMBA)-induced leukemias was investigated. Both agents effectively delayed MNU-induced mammary tumor formation at high, cytotoxic dosages but TLP had no influence at low “immunomodulatory” doses. ET-18-OCH₃ also significantly protected against leukemia development in DMBA-treated Long-Evans rats.     

Kinetic analysis of plasma VLDL-TG and VLDL-remnant-TG turnover in anesthetized rats

We have estimated the turnover and relative pool sizes of nascent-VLDL-TG and VLDL-remnants-TG in anesthetized rats. [1-¹⁴C]Palmitoyl- and [2-³H]glyceryl-labeled “VLDL”-TG (including nascent VLDL-TG and VLDL-remnants-TG) were prepared by injecting labeled palmitate and glycerol into donor rats. Labeled serum from these rats was then injected intravenously into nembutalized male rats and serial blood samples taken for 30 min. Special care was taken to define any early components in the labeled “VLDL”-TG disappearance curves. In other experiments, the donors were rendered functionally hepatectomized 30 min after injection of³H-glycerol and the endogenous labeled VLDL-TG was allowed to circulate 30–60 min before collection of the TG-labeled VLDL-remnants-containing serum. The latter was injected into 4 recipient nembutalized rats and the remnant-TG-turnover measured by serial sampling as above. In two cases,¹⁴C-“VLDL” and³H-VLDL-remnants were injected as a single bolus into ether-anesthetized rats. Despite its complex composition, “VLDL”-TG in most cases disappeared in a single exponential fashion for 30 min with an average half-life of 5.9 min in nembutalized and 2.8 in ether-anesthetized rats. VLDL-remnants-TG showed a more complex behavior, but contained a major rapid component with a mean t_1/2 of ca. 1.5 min in both groups. The data, analyzed by multicompartmental analysis, were fitted to a simple model in which turnover of a larger nascent VLDL-TG pool with formation of a more rapidly turning over smaller pool of VLDL-remnant-TG is the rate-limiting step in overall TG removal from the d<1.006 fraction of rat serum. The data are consistent with our theoretical prediction that under these conditions the kinetics of the VLDL-remnants cannot be resolved from analysis of the total composite “VLDL” (nascent plus remnant) pool.     

Structure-cytotoxicity studies on alkyl lysophospholipids and some analogs in leukemic blasts of human origin in vitro

Eleven lipids have been tested for cytotoxic (trypan blue dye exclusion) activity in cells from eight freshly explanted human leukemias in vitro. 4-Aminomethyl-1-[2,3-(di-N-decyloxy)N-propyl]-4-phenylpiperidine (CP-46,665), 1-mercapto-hexadecyl-2-methoxymethyl-rac-glycero-3-phosphocholine (BM 41.440), the 2-acetamide analog of platelet-activating factor (PAF) and 1-O-octadecyl-2-O-methyl-rac-glycero-3-phosphocholine (ET-18-OCH₃) were found among the most active compounds. 2-Lysophosphatidylcholine (2-LPC) showed the lowest activity. However, in addition there was variation among the results regarding the activity of the 1-octadecyl-rac-glycero-3-phosphocholine (ET-18-OH) and its D- and L-forms, but a significantly higher cytotoxic activity of D-ET-18-OH compared with L-ET-18-OH on the basis of 2-LPC as control after an incubation time of 48 hr. We conclude that with the limited number of structures available, this type of study is not sufficient to yield further information about the mode of the accumulation and toxicity of this type of lipids.     

Determination of TBA number by high performance liquid chromatography

A high performance liquid chromatographic (HPLC) method for the quantitation of malonaldehyde in aqueous distillates was developed. Compared with the standard TBA test, the HPLC method was faster, and less affected by side feactions. A total of 5 min was necessary to assay each distillate and only malonaldehyde was detected. The standard curves were reproducible and standards were stable for up to 6 days. The HPLC method could detect malonaldehyde levels ranging from 1×10⁻¹¹ to 4×10⁻¹¹ mol/10μL and either peak height or peak area could be used to quantitate the malonaldehyde concentration. The coefficient of determination between absorbance values determined by the TBA test and peak heights determined by HPLC was 0.946. Twenty-one freeze-dried chicken samples with TBA numbers ranging from 3.93 to 16.6 were used for this correlation.     

Synthesis of EPDM-g-MAN by suspension graft copolymerization and its toughening effect on SAN resin

Suspension graft copolymerization of methyl methacrylate and acrylonitrile onto ethylene–propylene–diene terpolymer (EPDM) was carried out under different reaction conditions. A series of graft products of EPDM-graft-methyl methacrylate and acrylonitrile (EPDM-g-MAN), characterized by Fourier-transform infrared spectroscopy, was blended separately with styrene–acrylonitrile (SAN) resin to investigate their toughening effect on SAN matrix. The relationship between the polarity of EPDM-g-MAN and toughness of EPDM-g-MAN/SAN resin blends (AEMS) was evaluated. The compatibility and morphologies of AEMS were probed by dynamic mechanical analysis, transmission electron microscopy, and scanning electron microscopy to determine the toughing mechanism of the blends. Thermogravimetry results showed that the thermal stability of AEMS was enhanced with the incorporation of EPDM-g-MAN graft copolymer.     

Antineoplastic activity of the thioether lysophospholipid derivative BM 41.440 in vitro

Thioether lysophospholipid derivatives (TLP) inhibited the in vitro uptake of [³H]thymidine into blasts of eight leukemias and cells of 12 different solid tumors of human origin. This effect correlated with trypan blue dye exclusion, which was used to assess cell damage. Cytostatic and cytotoxic effects of TLP were dependent on dosage and incubation time. Destruction of leukemic blasts was completed with >5 μg/ml after an incubation of >48 hr, but 10 to 20 μg/ml were necessary in solid tumors. Ester-linked 2-lysophosphatidylcholine was ineffective in the same dose range, which points to the requirement of the alkyl moiety insn-1 and a stablesn-2 substitution of the molecule for the antineoplastic effect. To assess putative antileukemic selectivity, the cytotoxicity (trypan blue dye exclusion) of TLP was compared in human cell samples of 19 non-neoplastic bone marrows and 9 leukemias. Results revealed a significantly higher activity of the TLP BM 41.440 in leukemic blasts.     

Automated AOM test for fat stability

A home-built version of the automated AOM test was used with Canola, corn, sunflower, olive and Crisco? oils, shortening and lard. The endpoint was found by measuring the conductivity of a solution of the exit gas from the reaction tube. Coefficients of variability of the samples ranged from 1.1% to 8.3%. The endpoint of the test was ca. 100 PV for Canola oil, ca. 200 PV for corn oil and 35 PV for lard. The aqueous solutions of the volatiles of three oils were used to determine the TBA value. Canola, sunflower and olive oil had TBA values ranging from 6–60 μg malonaldehyde/g at the end point. No apparent relationship was found between the TBA values of the volatiles’ solutions and the PV’s of the oils. Presented at the 73rd AOCS Annual Meeting, Toronto, 1982.     

Cytotoxic activity of the thioether phospholipid analogue BM 41.440 in primary human tumor cultures

The inhibitory effect of the new thioether alkyl lysophospholipid analogue 1-hexadecylmercapto-2-methoxymethyl-rac-glycero-3-phosphocholine (BM 41.440, Ilmofosine) on colony formation of different spontaneous human tumors was studied in vitro using a methyl cellulose monolayer assay. The most sensitive tumors were lung (small cell, squamous cell and adenocarcinomas), gastrointestinal and ovarian cancers and hyernephromas. On the basis of the current difinition of sensitivity by the National Cancer Institute, Bethesda, MD, i.e. more than 70% inhibition of colony formation at an arbitrary concentration of 10 μg/ml, 34 out of 64 malignancies tested were susceptible to BM 41.440.     

Electrospinning of chitosan/poly(lactic acid-co-glycolic acid)/hydroxyapatite composite nanofibrous mats for tissue engineering applications

Electrospinning, which is a fiber fabrication technique using electrical forces to produce fibers with diameters ranging from nanometers to several micrometers, can be used to prepare materials mimicking the extracellular matrix proteins for potential use as tissue engineering scaffolds. In this study, nanofibrous mats of chitosan (CH) and poly(lactic acid-co-glycolic acid) (PLGA) having fiber diameters between 167 to 525 nm, and containing hydroxyapatite (HAp), were prepared by electrospinning technique. Morphological, chemical, thermal and degradation tests and cell affinity tests were carried out. Chitosan mats were stable in aqueous media and showed degradability in the presence of lysozyme. In PBS solution, PLGA mats disintegrated completely in 2 weeks. Meanwhile, CH-PLGA mats containing equal amounts of both CH and PLGA fibers and CH-PLGA-HAp samples containing 20 % HAp lost 50 and 40 % of their initial weight in 4 weeks, respectively. Cell culture tests showed that all electrospun fibrous mats promoted SaOs-2 cell attachment and proliferation. However, cell proliferation on CH-PLGA-HAp fibrous mats was higher compared to the others after 7 days demonstrating the positive effect of HAp on cell affinity properties compared to pristine CH or PLGA fibrous scaffolds.     

Receptors of sex pheromones and abstinons inMusca domestica andGlossina morsitans

Receptors arranged in two pairs on the inner and outer sides of the proximal end of the tibia of legs ofMusca domestica L. andGlossina morsitans morsitans Westwood are described here for the first time. In the male fly, these receptors function in perception of sex pheromones, as demonstrated in experiments in which the sense organs were coated with paraffin. Similar techniques showed that sense organs for abstinon are located on the tarsi. Scanning electron microscopy and light microscopy show that the tibial sense organs ofMusca may be sensilla of the coeloconic type.     

Effect of nafion membrane thickness on performance of vanadium redox flow battery

The performance of vanadium redox ow batteries (VRFBs) using different membrane thicknesses was evaluated and compared. The associated experiments were conducted with Nafion® 117 and 212 membranes that have 175 and 50 μm of thickness, respectively. The charge efficiency (CE) and energy efficiency (EE) of VRFB using Nafion® 117 were higher than those of VRFB using Nafion® 212, while power efficiency was vice versa. In terms of amounts of charge and discharge that are measured in different charging current densities, the amounts in VRFB using Nafion® 212 are more than that in VRFB using Nafion® 117. To further characterize the effect of membrane thickness on VRFB performance, electrochemical impedance spectroscopy (EIS) and UV-vis. spectrophotometer (UV-vis) were used. In EIS measurements, VRFB using Nafion® 117 was more stable than that using Nafion® 212, while in UV-vis measurements, vanadium crossover rate of VRFB usingNafion® 212 (0.0125M/hr) was higher than that of VRFB using Nafion® 117 (0.0054 M/hr). These results are attributed to high crossover rate of vanadium ion in VRFB using Nafion® 212. With these results, vanadium crossover plays more dominant role than electrochemical reaction resistance in deciding performance of VRFB in condition of different membranes.     

Reversible addition-fragmentation chain transfer polymerization of vinyl acetate and vinyl pivalate in supercritical carbon dioxide

Two highly supercritical CO₂-soluble, poly(vinyl acetate) (PVAc)-based macro-reversible addition-fragmentation chain transfer (RAFT) agents were synthesized. The RAFT agents were used for the first time in RAFT/macromolecular design via the interchange of xanthates (MADIX) and polymerization of vinyl acetate (VAc) and vinyl pivalate (VPi) in supercritical carbon dioxide (scCO₂). A homopolymer PVAc and a block copolymer PVAc-b-PVPi made by RAFT/MADIX polymerization were characterized, and the effects of time and RAFT agents on polymerization were examined. For the 8.4 wt% RAFT agent in VAc, the molecular mass (M _n ) of homopolymer PVAc was 26,000 g mol^?1 and PDI was 1.35. For the copolymerization of VPi using 9.8 wt% PVAc-RAFT agent in VPi for 24 h, the M _n and PDI of PVAc-b-PVPi reached 32,400 g mol^?1 and 1.42, respectively. These results suggest that the polydispersity can be controlled during the clean production of PVAc and PVPi by RAFT/MADIX polymerization in scCO₂.     

Nutritional aspects in textured soy proteins

Textured soy protein products have found extensive use in pet foods and many human foods. They extend and complement meats in formulated foods. Numerous feeding tests with people and experimental animals show that biological values are high and protein efficiency ratios compare favorably with pure meat products. By careful processing of the textured soy products, high quality, safe, low cost protein food can be prepared. Textured soy proteins are an excellent example of man’s creative ability to engineer a supplementary food that is nutritious, palatable, and economical.     

Selected factors influencing neurohormonal regulation of sex pheromone production inHeliothis species

Sex pheromone production and release in females ofHeliothis species exhibit a diel periodicity. Phermone production is controlled by a hormone, the pheromone biosynthesis activating neuropeptide (PBAN). Release of PBAN to activate pheromone production follows a circadian rhythm. InH. zea females, mating terminates pheromone production. An unidentified hemolymph-borne factor is transferred from the male to the female during mating. It is speculated that this factor interacts with the release mechanism of PBAN to prevent further production of the pheromone following mating. Wild females ofH. phloxiphaga (reared from larvae collected in the field) did not produce or release the sex pheromone unless kept in association with the host plant. Pheromone production could be induced in these females by the injection of PBAN. It is suggested that a signal from the host plant is essential to trigger the release of PBAN to induce pheromone production.     

The synthesis and biological activity of thiolcarnitine and its thiolesters

Acetyl-D,L-thiolcarnitine was synthesized by the acid-catalyzed addition of thiolacetic acid to 4-trimethylammonio-2-butenoic acid. Acetyl-D,L-thiolcarnitine was the precursor of D,L-thilcarnitine, which was prepared by base hydrolysis. Thiolcarnitine significantly enriched in the L-isomer was prepared from acetyl-D,L-thiolcarnitine using carnitine acetyltransferase as the resolving agent. The C₂, C₈ and C₁₆ carnitine thiolesters were obtained by acylating thiolcarnitine with the corresponding N-hydroxysuccinimide esters. As a substrate for carnitine acetyltransferase, acetylthiolcarnitine gave the same kinetic constants as did acetylcarnitine; on the other hand, thiolcarnitine and carnitine gave the same K_m but the V_max with thiolcarnitine was less than 5% of the value obtained with carnitine. With thiolcarnitine and acetylthiolcarnitine as reactants, the measured K_eq, at 30 C and pH 7.0, for the reaction catalyzed by carnitine acetyltransferase (see below) was 4.6±.1. acetylthiolcarnitine+CoA—acetyl-CoA+thiolcarnitine     

Rheological behavior of a LDPE/PS/SBS blending melt

The dynamic rheological behaviors are measured by small amplitude oscillatory shear on a rotational rheometer for a low-density polyethylene (LDPE)/polystyrene (PS)/styrene–butadiene–styrene (SBS) block copolymer blend with the tool of cole–cole plot. The morphology of the blend is measured by scanning electron microscope (SEM) micrograph, the storage moduli–angular frequency (G′–ω) data are fit by the Palierne model, and the relaxation time spectrum is investigated. The storage modulus and loss modulus of the LDPE/PS/SBS blend at low frequency increase when the weight ratio LDPE/PS increases from 10/90, reaches a maximum of 30/70, and drops thereafter. The cole–cole plots of some blends (10/90/3, 70/30/3, 90/10/3 and 100/0/3) have only one main arc due to compatibilizing effect of the SBS, and those of other blends (0/100/3, 30/70/3 and 50/50/3) have a second arc or a long tail besides the main arc probably due to phase separation. The SEM micrographs of the LDPE/PS/SBS = 10/90/3, 30/70/3, 50/50/3 show sea-island, semi-co-continuous and co-continuous structure, respectively. G′–ω curve of two LDPE/PS/SBS = 30/70/3 and 50/50/3 blends shows a power law, and the power index is much lower than one (0.748 and 0.817), respectively, showing a co-continuous morphology also verified by the SEM micrographs. The experimental data of G′–ω curve of the LDPE/PS/SBS blends are fit by Palierne model, the deviation between the fit line and the experimental data increases gradually as the LDPE/PS weight ratio decreases from 90/10 to 10/90. For the LDPE/PS/SBS blends, the weighted relaxation spectra τH (τ)–τ show a main as well as a second arc or tail; the former corresponding to the relaxation of PS phase and the latter corresponding to that of LDPE phase. Due to the compatibilizing effect of SBS the relaxation time and spectrum strength of LDPE/PS = 50/50 (wt) blends are both increased.     

The analysis of glycerol by gas chromatography

Commencai glycerol and its organic impurities can be measured accurately by a single gas Chromatographic GC analysis utilizing Tenax-GC® and flame detection.     

Quantitation of a bioactive metabolite in undisturbed rhizosphere—Benzyl isothiocyanate fromCarica papaya L.

A “continuous root exudate trapping system” was recently developed in this laboratory by which the allelopathic metabolites from the undisturbed rhizosphere ofHemarthria altissima (Poir.) Stapf. et Hubb. were collected. Twelve phenolic compounds were identified by capillary GC-MS (Tang and Young, 1982). In this report, we further describe its use for the quantitation of benzyl isothiocyanate (BITC), a highly bioactive volatile compound, in the rhizosphere of growing papaya plants. Samples were collected from 64 individual papaya (Carica papaya L.) trees of Waimanalo and Higgins cultivars. Hydrophobie compounds collected on XAD-4 columns were eluted with acetone and the levels of BITC were determined by a gas Chromatograph equipped with a sulfur-specific flame photometric detector. For 2-month-old trees, the rate of BITC released from the root system of Waimanalo was 2.03 ± 0.85μg/tree/day. From Higgins, it was 2.36 ± 1.06 μg/tree/day. It has been reported that Waimanalo is resistant whereas Higgins is susceptible toPhytophthora palmivora Butl., the major root rot fungal pathogen of papaya trees in Hawaii. Our results lead us to conclude that the rate of BITC released alone cannot account for differences in the resistance of these two cultivars to the pathogen.     

Ionic conductivity of oxides based on Li4SiO4

Lithium orthosilicate, Li₄SiO₄, and its solid solutions are a new group of solids of high ionic conductivity. Either Li or Si may be at least partially replaced by several other di-, tri- or tetra-valent cations. Highest conductivities were found for solid solutions with Si partially replaced by Ti; typical values were 10^?3 to 10^?4 Ω^?1 cm^?1 at 300°C rising toc. l Ω^?1 cm^?1 by 700°C. The solid solutions are easy to prepare and are stable in air. Conductivities were measured on pressed cubes of powdered material using variable frequency a.c. methods. The conductivities of these Li₄SiO₄ solid solutions are compared with those of other known Li-conducting solids; Li₄SiO₄ solid solutions are probably the best all-round, polycrystalline Li-electrolytes yet found for temperatures abovec. 200°C.     

Rapid analysis of dimer acid by HPLC/FID

A method was developed for the rapid analysis of polymerized fatty acids (dimer acid) using normal phase HPLC with a flame ionization detector (FID). The use of analytical scale HPLC with the FID is a significant limprovement over existing methodology for dimer analysis. The HPLC analysis takes only 25 min per sample, with no derivatization required. The FID response is linear for dimer samples from 10% to 90% monomer content. Absolute measurement precision is typically less than 0.5 area percent. Recovery of synthetic dimer blends averaged 102%. Results for the analysis of commercial dimer acid are comparable to those obtained using an HPLC/gravimetric method. The HPLC/FID method is applicable to the analysis of crude dimer as well as the finished dimer product.