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PAM cells

After complete degradation ol PAM. cells can integrate (he parenchyma... [Pg.17]

PAM Cells Characteristics containing 0.3 % Hg 2.5.1. Voltage and Discharge Performance... [Pg.171]

The best developed types of RAM cells are cylindrical cells using sleeve electrode construction, which are simply discribed as cylindrical cells. They are produced in AA, C and D size types with a typical trend to small sizes. In the Figures 15 and 16 of chapter 3.1. the design changes of the different cell sizes are shown. The principal construction of the cylindrical RAM cell is identical with the equivalent PAM cell design consisting of the same cell components. Differencies between these systems exist mainly in the capacity limitation of the anode to approximatly 1/3 of the cathode capacity, the application of improved separators and better anode and cathode formulations as already mentioned in the above citied chapter. A lot of experimental data exist for low-mercury (0.025 wt % Hg) as well as for mercury-free (0 % Hg) RAM cells. They are summarized in Chapter 3.6.. [Pg.177]

At the moment there are no accepted standards available for RAM cells. They have to be subjected to standard tests for primary alkaline manganese dioxide zinc (PAM) cells. Table 7... [Pg.184]

Note The capacity of the first cycle of a RAM cell is approximately 75-85 % of the capacity of a PAM cell. [Pg.184]

LM RAM cells surpass these requirements by over 25 %. The table also indicates that LM RAM cells are capable of providing approximately 80 % of the service life of North American premium primary cells. In summary, one can say that RAM cells provide a similar service life on their initial use cycle compared to the performance of PAM cells. [Pg.185]

The LM and MF RAM cells improve their performance on the 3.9 Q and 10 Q load test when the operating temperature is increased to as high as 65 °C without leakage or bulging. They show excellent discharge performance compared with commercial PAM cells. In... [Pg.186]

The charge retention of a new RAM cell is quite similar to the one of a PAM cell as demonstrated in Figure 33. It has been shown in accelerated tests that RAM cells retain approximately 80 % of the charge for a period of five years from the date of manufacture. Table 9 shows a comparison between LM and MF RAM cells regarding charge retention in an accelerated test. It can be seen that MF RAM cells are capable of excellent charge retention. [Pg.187]

Table 10 shows a comparison of RAM cell performance with other commercially available dry cells [56]. RAM cells have an excellent shelf life comparable with PAM cells and a good cycle life depending on depth of discharge (50-500 cycles), nearly in the range of Ni-Cd cells. The average discharge capacity even exceeds the values for Ni-Cd cells, only PAM cells are better. But one of the most important advantage of RAM cells is the low toxicity (0.025 % Hg... [Pg.187]

Primary alkaline manganese dioxide - zinc batteries (PAM cells)... [Pg.740]

B. Ortel, A. Tenew, H. Honigsmann (1993). Lethal photosensitization by endogenous porphyrins of PAM cells - modification by desferrioxamine. J. Photochem. Photobiol. B Biol, 17, 273-278. [Pg.103]

The problem of low specific surface (which, however, has a beneficial effect on the corrosion rate) cannot be solved so easily. This was one important reason for the development of the alkaline Mn02 / zinc cell known as "alkaline" or "PAM" (primary alkaline manganese dioxide). [Pg.200]

Verma, R.P., Hansch, C. and Selassie, C.D. (2007) Comparative QSAR studies on PAM PA/modified PAM PA for high throughput profiling of drug absorption potential with respect to Caco-2 cells and human intestinal absorption. Journal of... [Pg.143]

The studies reported above implicated calcium movement in the mechanism.It was postulated that 2-PAM may Increase the rate of calcium movement either by interfering with calcium binding to its binding site or by directly stimulating the release of bound calcium.21 It was suggested that 2-PAM may not have increased cell permeability or affected the rate of re-entry of calcium into the cell, or 2-PAM may have increased calcium distribution in the vicinity of myofilaments. [Pg.27]

Studies of the efflux of Ca by stimulated rabbit atria have characterized three calcium pools. Phase I may represent extracellular washout of the Ca that binds to the surface of muscle membrane and is characterized by a high rate constant. Phase II may represent loosely bound calcium present in cell membrane and calcium released at the sarcoplasmic reticulum. Calcium in this pool is directly related to contractility.65,84,93 phase III may represent the tightly bound calcium that exchanges very slotrly and does not play a role in maintaining calcium concentrations. Recent study has shown that the storage or release of calcium at the sarcoplasmic reticulum and other loosely bound calcium sites (cell membrane) that are involved in muscle contractility can be directly affected by 2-PAM.21 These results Indicate that 2-PAM increases the rate of release of Phase II calcium. [Pg.27]

The only indicator that suggested an effect on the composition of the blood of the dogs was the white-cell count after 8 wk of injection of 2-PAM I. This increased by a mean of 27.6%, whereas it decreased by 5.5% in the control group during the same period. If the plasma concentration of an oxime 5 min after intravenous Injection was taken as the Initial value, at 30 minutes it had fallen to 21.8% (2-PAM I) or 28.3% (III) and at 60 min it had fallen further to 10.7% (2-PAM I) or 14.4% (III). It is apparent, therefore, that III is removed initially from the plasma somewhat more slowly than 2-PAM I, but that the difference is not great and that there may be an Increase in the rate of removal of III somewhere between 30 and 60 min after the initial value. The percentages of the initial concentrations of 2-PAM I and III remaining in the plasma at 155 min after estimation of the initial values differed by only about 0.1%... [Pg.277]

Fleisher reported that both sarin and VX increased the sensitivity of the isolated frog s rectus abdominis to external application of acetylcholine and at the same time decreased the activity of cholinesterase in the external surfaces of the muscle cells. Sarin at 5 x 10-7 M reduced the threshold concentration of acetylcholine for inducing contraction of the muscle to 8% of that required before application of sarin. The same concentration of VX reduced the threshold concentration of acetylcholine to 6.7% of that needed previously. Contemporaneously, the activity of cholinesterase in the external surfaces of the muscle cells was reduced to 8.1% and 0% of that before application of sarin and VX, respectively. Addition of 2-PAM I at 5 x 10 M to the baths in which the muscles were suspended had little effect on the activity of the enzyme in homogenates of the muscles, but restored 75% and 91%, respectively, of the activity of cholinesterase in the external surfaces of the muscles exposed to sarin and VX. At the same time, the concentration of acetylcholine required to induce contraction of the muscles was raised to 53.3% and 58.3% of the original threshold concentrations, respectively, for the muscles exposed to sarin and to VX. [Pg.282]

The only undesirable effects observed during these studies were signs and complaints of lodlnlsm by the subjects given 2-PAM 1 and decreases in red-cell and plasma cholinesterase activities of about 20% in the subjects given 111. Less of 111 was excreted in the urine (3% during 24 h) than of the monoquaternary compounds (27% in 14 h). [Pg.306]

Similarly, Chien et al. used a poly(acrylic acid)/poly(acrylamide) (PAA/PAM) multilayer system in which PAA was replaced by PAA conjugated with photoreactive 4-azidoaniline (AZ) after several bilayers [110]. As a result, the polyelectrolyte multilayer could be covalently crosslinked by UV irradiation through a mask. For an enhanced cell repellence, poly(allylamine) was conjugated with polyethylene glycol methyl ether) and incorporated into the top layers of the film. [Pg.53]

Absorption rate coefficients and permeability values obtained through different systems, i.e. in vitro or in situ, finally are determined with the objective in mind of predicting the fraction of a dose that will be absorbed through the intestine when the drug is orally administered. In order to use the data obtained in those systems it is essential to validate them properly. The present section reviews the capability of the parameters representatives of the absorption determining with different techniques to predict in vivo drug absorption in absence of any limited step (as dissolution or solubility) by means of the previously described model and Eq. (16). In particular, the absorption rate constant obtained with an in situ close loop assay, permeability through Caco-2 cell lines, and PAM PA models have been examined. [Pg.101]

Fig. 2. RP-HPLC chromatograms of human B cell chemoattractant-1 (BCA-1) (11), an 87 residue chemokine that is the ligand for CXCR5, which is the human homolog of the mouse receptor BLR-1. Its sequence is VLEVYYTSLRCRCVQESSVFIPRR FIDRIQILPRGNGCPRKEIIVWKKNKSIVCVDPQAEWIQRMMEVLR KRSSSTLPVPVFK (11). The BCA-1 polypeptide was synthesized starting with Lys-Pam resin and adding the appropriate protected amino acids until the N-terminal valine was added. The profile of the crude product (A) reveals a major broad peak that consists of the correct polypeptide and numerous closely related and closely eluting... Fig. 2. RP-HPLC chromatograms of human B cell chemoattractant-1 (BCA-1) (11), an 87 residue chemokine that is the ligand for CXCR5, which is the human homolog of the mouse receptor BLR-1. Its sequence is VLEVYYTSLRCRCVQESSVFIPRR FIDRIQILPRGNGCPRKEIIVWKKNKSIVCVDPQAEWIQRMMEVLR KRSSSTLPVPVFK (11). The BCA-1 polypeptide was synthesized starting with Lys-Pam resin and adding the appropriate protected amino acids until the N-terminal valine was added. The profile of the crude product (A) reveals a major broad peak that consists of the correct polypeptide and numerous closely related and closely eluting...
As early as 1983, de Gennes and Hervet [85] proposed a simple equation derived from fundamental principles, to predict the Starburst limited or dense-packed generation mt for PAM AM dendrimers. Based on ideal dendrimer growth, with tertiary amine branch junctures connected by linear, flexible branch cell segments P, this equation relates m, to the branch cell segment length 1 or P ... [Pg.281]

Kusic et al. (1991) have tested the oxime HI-6 in OP pesticide poisoning in 60 patients. HI-6 was administered four times a day as a single i.m. injection of 500 mg with atropine and diazepam treatment. Oxime therapy was started on admission and continued for 2 to 7 days. Most patients were treated with HI-6 and nine patients severely poisoned with quinalphos were treated 2-PAM Cl (1,000 mg four times per day). HI-6 rapidly reactivated human red blood cell AChE inhibited by diethoxy OPs (phorate, pyr-idaphenthion, quinalphos) as well as that inhibited by dichlorvos (a dimethoxy OP). AChE inhibited with other dimethoxy OPs (dimethoate and phosphamidon) was reported to be resistant to HI-6 treatment, whereas reactivation with malathion was slow (reactivation half-time 10 h). Both HI-6 and 2-PAM successfully reactivated AChE in quinalphos-poisoned patients, with HI-6 acting as a faster AChE reactivator than 2-PAM. [Pg.992]


See other pages where PAM cells is mentioned: [Pg.165]    [Pg.170]    [Pg.185]    [Pg.188]    [Pg.192]    [Pg.613]    [Pg.165]    [Pg.170]    [Pg.185]    [Pg.188]    [Pg.192]    [Pg.613]    [Pg.144]    [Pg.45]    [Pg.105]    [Pg.324]    [Pg.325]    [Pg.588]    [Pg.110]    [Pg.318]    [Pg.642]    [Pg.140]    [Pg.55]    [Pg.27]    [Pg.116]    [Pg.68]    [Pg.394]    [Pg.72]    [Pg.494]    [Pg.272]    [Pg.258]    [Pg.23]    [Pg.1044]   
See also in sourсe #XX -- [ Pg.165 ]




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