An alternative model for the selection of therapeutic chelating agents

An alternative model is presented for the selection of therapeutic chelating agents to enhance the mobilization and excretion of a toxic metal. The model is based on the in vivo patterns of absorption, distribution, reaction and excretion of the chelating agent, a typical toxic metal ion and complexes of the two. The model emphasizes the kinetic aspects of the processes involved and indicates how other processes may be incorporated such as redox reactions involving the chelating agent or metal. The identification of rate determining steps and methods for their manipulation are assumed to be of importance. The application of this model to specific metals is outlined.     

The effect of some chelating agents on the biliary and urinary excretion of manganese in rats

The biliary excretion of manganese, in rats which have been loaded with manganese via their drinking water, can be significantly enhanced by the administration of the chelating agents: desferrioxamine (DSF), sodium bis(hydroxyethyl) dithiocarbamate (DEDTC), and sodium isonipecotamidedithiocarbamate (INADTC). The effect of these chelating agents on the urinary excretion of manganese was more complex and was found to be dependent upon the level of loading of manganese as well as the individual chelating agent. For animals with drinking water containing 400 mg/liter of manganese, the administration of the chelating agents led to a decrease in the sum of the biliary plus urinary manganese excretion. The results are of special interest in that they show that under some conditions the administration of chelating agents can lead to changes other than those expected.     

Chelate-Enhanced Phytoremediation of Soils Polluted with Heavy Metals

In general, hyperaccumulators are low biomass, slow-growing plants. High biomass non-hyperaccumulator plants by themselves are not a valid alternative for phytoextraction as they also have many limitations, such as small root uptake and little root-to-shoot translocation. In this context, chemically-induced phytoextraction (based on the fact that the application of certain chemicals, mostly chelating agents, to the soil significantly enhances metal accumulation by plants) has been proposed as an alternative for the cleaning up of metal polluted soils. But chelate-induced phytoextraction increases the risk of adverse environmental effects due to metal mobilization during extended periods of time. In order to minimize the phytotoxicity and environmental problems associated with the use of chelating agents, nowadays, research is being carried out on the gradual application of small doses of the chelating agent during the growth period. However, EDTA utilization in the future will most likely be limited to ex situconditions where control of the leachates can be achieved. There are other mobilizing agents which are much less harmful to the environment such as citric acid, NTA, and particularly EDDS. Research should also be aimed towards more innovative agronomic practices. Environmentally safe methods of chelate-induced phytoextraction must be developed before steps towards further development and commercialization of this remediation technology are taken. Most importantly, more applied projects in this field are needed to clarify the real potential and risks of this technology.     

Sensitivity of bacterial coaggregation to chelating agents

Coaggregation between pairs of microorganisms was found to be inhibited by chelating agents, such as acetylacetone, citrate, EDTA and carboxymethylcellulose. Assays were conducted on eight pairs of periodontopathogens and one pair consisting of Escherichia coli and Saccharomyces cerevisiae. The inhibitory effects of the chelating agents were reversible except for Actinomyces naeslundii 12104, the adhesin of which was irreversibly inactivated. Even though the bacteria possessed different kinds of adhesins, their sensitivity to chelating agents appears to be a common property. Non-toxic chelating agents, such as carboxymethylcellulose and citrate, may prove to be useful anti-adhesins.     

The Effect of Chelating Agents on Soil Sodicity

Results of laboratory and field tests suggest that chelating agents could be used to alleviate adverse soil properties caused by excess sodium, such as low permeability. Adding multi-dentate carboxylic acid chelating agents to sodic soil, or to mixtures of soil with sodium-contaminated waste, significantly reduced sodium adsorption ratio (SAR) values. Judging from cation concentrations in saturated paste (sat. paste) filtrates, chelating agents act to ameliorate soil sodicity by releasing Ca and to a lesser extent Mg from undissolved compounds. After adding chelating agents to moist soils that contained free lime, measured weight losses were consistent with CO ₂ evolution due to CaCO ₃ decomposition. The electrical conductivity (EC) of the sat. paste filtrate of materials treated with chelating agents increased less than when equivalent Ca or Mg was supplied in conventional, soluble form. Bigger sat. paste vacuum filtration volumes, improved soil permeability and faster field infiltration rates were observed after treatment with chelating agents. The Ca- and Mg-complexes of agents such as citric and malic acid degrade in moist soil; such agents could perhaps be used in a series of applications to improve ease of cultivation and permeability of cropped land. The agent ethylenediamine tetraacetic acid (EDTA) forms stable complexes, and could therefore be used as a one-time treatment for sodic materials that are to be disposed of by burial, following guidelines for soil SAR and EC.     

Effect of divalent cations and chelators on metaphase to telophase progression and nuclear envelope formation in Chinese hamster cells

Chinese hamster DON cells in log phase were treated with Colcemid in the G₂ period with or without divalent cation chelating agents. The metaphase cells were isolated and incubated in two ways: 1) without Colcemid but with chelating agents or La³⁺ and observed for metaphase to telophase progression, and 2) with Colcemid, with or without chelating agents and the rate of micronuclei formation in the absence of anaphase monitored. The effect of the chelating agents on cellular ⁴⁵Ca²⁺ during metaphase to telophase progression was also studied.The results indicate that Ca²⁺ and possibly Mg²⁺ ions are involved in the regulation of certain segments of mitosis. The reduction of environmental and plasma membrane associated Ca²⁺ with the chelators and La³⁺ promoted the metaphase to telophase progression as well as nuclear envelope and micronuclei formation.     

Effect of Chelating Agents and Metal Ions on Gametangial Formation in the Moss Bryum argenteum Hedw

Chelating agents such as EDTA and EDDHA markedly stimulate theformation of gametangia in the dioecious moss Bryum argenteum,and the effect is more pronounced on male than on female clones.EDTA-stimulated gametangial formation is associated with significantincreases in endogenous iron and copper. Ferric citrate alsoenhances gametangial formation, but copper sulphate is inhibitory.The present findings are discussed in the context of earlierinvestigations on other plants in an attempt to explain thepossible involvement of chelating agents and metal ions in stimulatingthe onset of the reproductive phase in this moss. Bryum argenteum, gametangial formation, chelating agents, metal ions     

Combined chelation of bi-functional bis-hydroxypiridinone and mono-hydroxypiridinone: Synthesis, solution and in vivo evaluation

3-Hydroxy-4-pyridinones (3,4-HP) are well known iron-chelators with applications in medicinal chemistry, mainly associated with their high affinity towards trivalent hard metal ions (e.g. M³⁺, M = Fe, Al, Ga) and use as decorporating agents in situations of metal accumulation. The polydenticity and the extra-functionality of 3,4-HP derivatives have been explored, aimed at improving the chelating efficacy and the selectivity of the interaction with specific biological receptors. However, the ideal conjugation of both features in one molecular unity usually leads to high molecular weight compounds which can have crossing-membrane limitations.Herein, a different approach is used combining a arylpiperazine-containing bis-hydroxypyridone (H₂L¹) with a biomimetic mono-hydroxypyridinone, ornithine-derivative (HL²), to assess the potential coadjuvating effect that could result from the administration of both compounds for the decorporation of hard metal ions. This work reports the results of solution and in vivo studies on their chelating efficacy either as a simple binary or a ternary system (H₂L¹:HL²:M³⁺), using potentiometric and spectrophotometric methods. The solution complexation studies with Fe(III) indicate that the solubility of the complexes is considerably increased in the ternary system, an important feature for the metal complex excretion, upon the metal sequestration. The results of the in vivo studies with ⁶⁷Ga-injected mice show differences on the biodistribution profiles of the radiotracer, upon the administration of each chelating agent, that are mainly ascribed to the differences of their extra-functional groups and lipo/hydrophilic character. However, administration of both chelating agents leads to a more steady metal mobilization, which may be attributed to an improved access to different cellular compartments.     

Coordination chemical studies on metalloenzymes. II. Kinetic behavior of various types of chelating agents towards bovine carbonic anhydrase.

In order to investigate the kinetics and mechanism of the removal of zinc ions from bovine carbonic anhydrase [EC 4.2.1.1] (BCA), several chelating agents with various stability constants were used to remove zinc from BCA. The second-order rate constants (kaap) of zinc removal from BCA were found to be in the following order; 2,6-pyridinedicarboxylic acid greater than 2-pyridinecarboxylic acid greater than 2,4-pyridinedicarboxylic acid greater than 2,3-pyridinedicarboxylic acid greater than or approximately 1,10-phenanthroline greater than or approximately 5-methyl-1,10-phenanthroline greater than 2,2'-bipyridine. With similar chelating agents the greater the stability constant, the faster was the rate of removal of zinc ions from BCA. With EDTA, trans-1,2-cyclohexanediaminetetraacetic acid, and nitrilotriacetic acid, the rate of zinc ion removal from the native enzyme was governed by the rate of spontaneous dissociation of zinc enzyme. The rate constants for the removal of zinc ions from BCA were governed by the affinity of the chelating agents for the metal ion and the conformation of the chelating agents. Based on these findings, reaction pathways for various chelating agents are proposed.     

N-terminal modification of immunoglobulin polypeptide chains tagged with isothiocyanato chelates

Conjugates of monoclonal antibodies with drugs, toxins, radionuclides, and other agents are in widespread use in therapeutic trials and as clinical research tools. The characterization of these immunoconjugates generally does not include determining the individual sites at which such agents are attached. We have begun to explore the attachment of the bifunctional chelating agent isothiocyanatobenzyl-EDTA (CITC1) to the N-termini of the light chains of the Lym-1 monoclonal antibody. The similarity between this bifunctional chelating agent and Edman's reagent, phenyl isothiocyanate, led us to develop methods to distinguish between chelate-conjugated alpha-amino groups and epsilon-amino groups by Edman degradation. Practically all the N-terminal Asp alpha-NH2 groups of Lym-1 can be modified at neutral pH, while attachment at lysine side chains predominates at pH 9. Comparison of the immunoreactivities of Lym-1-CITC conjugates with and without N-terminal conjugation shows that both are almost fully active. This implies that modification of light-chain N-termini has little or no effect on immunoreactivity, despite the fact that these residues lie near the antigen-binding sites.     

Contribution of blue-green pigments to hemolytic activity of Pseudomonas aeruginosa cultural fluid

AIM: To assess the contribution of blue-green pigments of Pseudomonas aeruginosa to hemolytic activity of its cultural fluid. MATERIALS AND METHODS. Eight hospital strains and reference strain ATCC 15442 were used. Growth dynamics of strains as well as features of accumulation of hemolytic and phospholipase activity were studied. Purified samples of pyoverdin and pyocyanin were extracted by gel-chromatography and chloroform extraction methods. Hemolytic and lecitinase activities of the samples as well as effect of active oxygen scavengers and chelating agents on these activities were studied. RESULTS: Dynamics of accumulation of hemolytic activity significantly differed from that of phospholipase activity when strains were grown in liquid medium. Chromatographic separation of the pigments from cultural fluid supernatants sharply reduced its hemolytic activity. Purified samples of pyoverdin and pyocyanin were capable to lyse erythrocytes and chicken egg lecitin. These characteristics of the pigments were inhibited by nitroblue tetrazolium and sensitive to chelating agents. Conclusion. Pyoverdin and pyocyanin of pathogenic strains of P. aeruginosa are capable to lyse erythrocytes and suspension of purified chicken egg lecitin, they contribute to total hemolytic activity of pathogenic strains of Pseudomonas, which is not determined only by phospholipase C produced by microorganism. Lytic activity of the pigments is blocked by nitroblue tetrazolium and susceptible to some chelating agents. Apparently, this activity is mediated by superoxide radical and determined by presence of metals with transient valence in pigments' molecules.     

Chelating agents and rat liver mitochondria

The chelating agents (EGTA and EDTA) and inorganic phosphate (Pi) are the most variable components of experiments involving isolated liver mitochondria. In the absence of EGTA or EDTA, swelling induced by Pi leads to rapid loss of endogenous adenine nucleotides to adenosine. Chelating agents prevent swelling and loss of adenine nucleotides. Concentrations below about 0.1 mM are ineffective. The protective effects depend on the continuous presence of the chelating agent; they are lost on washing EGTA-containing suspensions with chelating-agent-free medium. We question the accepted view that chelating agents stabilize mitochondria by binding Ca2+ to prevent activation of phospholipase.     

Recommendations for testing new chelating agents for removal of incorporated actinides from the body

Summary The body content of certain radionuclides and the consequences of accidental incorporation may be reduced by treatment with chelating agents. Such agents have been widely studied and have proved to be useful in man. Chelation therapy may also be advantageous in certain cases of heavy metal poisoning. There is still a need to develop new, more efficient and less toxic agents and better therapeutic schedules for using the existing agents. So far as possible the testing of potential new compounds should be carried out using standardized methods.Supported by the Radiation Protection Programme of the Commission of the European Communities-publication no 1889     

Chelation in Auxin Action: I. A STUDY OF THE INTERACTIONS OF 3-INDOLYLACETIC ACID AND SYNTHETIC CHELATING AGENTS AS AFFECTING THE GROWTH OF WHEAT ROOTS AND COLEOPTILE SECTIONS

Factorial experiments have been carried out on the effects,upon growth of roots of intact wheat seedlings and growth ofwheat coleoptile sections, of different concentrations of 3-indolylaceticacid (IAA) and various known chelating agents. These have demonstrateda similar mutual antagonism between pairs of agents whetherthese are IAA and a single known chelating agent or two knownchelating agents. This interaction takes the form that eitheragent alone in ‘high’ concentration severely inhibitsgrowth but this inhibitory effect is almost or entirely removedby the presence of one-millionth the concentration of the otheragent; when both agents are present in ‘high’ concentrationthe inhibition is again severe. The substitution of a non-chelatinganalogue for one of the agents either destroys the mutual characterof the antagonism or entirely prevents either agent at low concentrationfrom reducing measurably the inhibition caused by high concentrationof the other. The fact that IAA interacts with known chelatingagents, in controlling the growth both of roots and coleoptilesections, in the same unexpected and symmetrical way that theseinteract with each other, is held strongly to support the hypothesisthat it is here itself acting as a chelating or complexing agent;the absence of such interactions with a non-chelating analoguemakes this the more convincing. These results are concernedwith the removal of growth inhibition, due to supra-optimalconcentrations of one agent, by minute proportions of another;it cannot be regarded as proven that the promotion of growthby IAA in the absence of another agent is also due to chelationor complex formation. This seems probable, however, when thefindings here presented are taken in conjunction with the accumulatingevidence that IAA and other auxins can form complexes or chelateswith metals in vitro, and with the finding already publishedin detail that the eight chelating agents tried promoted growthin the wheat coleoptile test. The main criticisms to which this hypothesis has been subjectedhave been concerned with the relative magnitudes of effectsof IAA and chelating agents upon growth, with the low stabilityconstants of metal complexes with IAA and other auxins, withthe lack of parallelism between stability constants and growth-promotingactivity, and with the fact that one chelating agent (ethylenediamine-tetraaceticacid; EDTA) has been found inactive in certain growth tests.A series of factorial experiments comparing the authors' techniques(which are here described in detail), chemicals, and strainof wheat with those used by Fawcett et al. (1956) demonstratethat the discrepancies found, both as regards magnitudes ofeffects of IAA and EDTA and optimal concentrations, were partlydue to differences in strain but mainly to differences of technique.It is considered that ‘foreign’ molecules such asEDTA are likely to have side effects, which may well differin different strains or tests; competition with internal chelators(Burstrom and Tullin, 1957) is also likely to differ; differencesin rate of penetration and steric hindrance may also be involved.For these reasons effective chelating activity in vivo may bevery different from that in vitro and in the first instancethe magnitudes of growth-promoting effects of chelating agents(which may indeed be the net result of stimulatory and inhibitoryprocesses) seem less important than the fact that they are foundin so many instances. Possible ways in which IAA and other growth substances may regulategrowth by chelation or complex-formation are discussed.     

Optimization of the cell envelope disruption of extremely halophilic bacteria

This paper describes an examination of the cell envelope stability opposite to disruption by chemical and physical methods of extremely halophilic bacteria. The following methods of cell treatment were studied: solvent and chelating agents; pressure shearing at several pressures; ultrasonic disintegration for various times; ballistic disintegration; grinding with cold alumina; lysozyme digestion; osmotic shock; and freezing and thawing. The procedure is based on the determination of three cytoplasmic enzymes released by the cell treatment. Menadione reductase was also used as convenient marker enzyme for damage to the permeability barrier. Of all the methods, only pressure shearing and ultrasonic disintegration yielded a crude extract with high halophilic enzyme activities. These procedures are suitable in designing a cell fractionation scheme for halophilic enzyme purifications.     

Stimulation of prolyl hydroxylase activity by chelating agents.

The activity of purified prolyl hydroxylase was enhanced several fold by addition of some chelating agents to the assay medium. Chelating agents could be classified into three groups. The chelating agents of Group I such as α, α′-dipyridyl were inactive until they reached equimolar concentration with ferrous ion in the assay mixture. The Group II agents, EDTA, diethylenetriaminepentaacetic acid, etc., stimulated the enzymatic activity 1.5- to 3-fold at equimolar concentration with ferrous ion. But the agents of both groups precipitously inhibited the enzymatic activity at concentrations greater than ferrous ion. On the other hand, Group III chelating agents, such as nitrilotriacetic acid, enhanced the enzymatic activity 5- to 10-fold at concentrations greater than ferrous ion. Nucleoside triphosphates, which also stimulate the enzymatic activity several fold and whose optimal concentrations are 1–3 × 10^?m, may be analogous to nitrilotriacetic acid of Group III.     

Chelating Agents as Histological and Histochemical Decalcifiers

The alterations caused by chelating agents (disodium ethylenediaminetetraacetate) used as decalcifying solutions at pH 7.0, in histological and histochemical technics have been studied comparatively. They have been controlled by the staining with hematoxylin and eosin, Gomori's aldehyde fuchsin, periodic acid-Schiff, metachromasia, and alkaline phosphatase. Their effect on the tissues was similar to that of buffered acid decalcifying solutions, such as that of Greep, Fischer and Morse (equal parts of 2% formic acid and 20% sodium citrate).

The use of 1% sodium diethylbarbiturate for 24 hr as a reactivating agent for alkaline phosphatase in the specimens treated with chelating agents is recommended.     

Effect of Chelate-Assisted Hexavalent Chromium on Physiological Changes,Biochemical Alterations,and Chromium Bioavailability in Crop Plants—An In Vitro Phytoremediation Approach

This study revealed heavy metal–induced physiological and biochemical alterations in crop seedlings by supplementing chelating agents in the nutrient solution. Hexavalent chromium (Cr⁺⁶) induces several toxic effects in hydroponically grown rice, wheat, and green gram seedlings. A noticeable decrease was observed in root length, shoot length, biomass content, and chlorophyll biosynthesis of the seedlings grown in the nutrient solutions supplemented with Cr⁺⁶ at 100 μM. The seedling growth was stimulated with supplement of chelating agents such as EDTA, DTPA, and EDDHA. An increase in proline content was noticed with the application of Cr⁺⁶ (100 μM) in nutrient solutions. Stimulated activities of antioxidant enzymes such as catalase and peroxidase were noticed with increasing concentrations of chromium. Cr bioaccumulation was significantly high in roots of seedlings treated with Cr⁺⁶ at 100 μM in nutrient solution. Shoot translocation of Cr as depicted by transportation index (Ti) values for different crops were enhanced with the application of chelating agents. The total accumulation rate (TAR) for Cr was enhanced with the supplementation of DTPA in rice and wheat, whereas the application of EDDHA was found effective for increasing the accumulation rate of Cr in green gram seedlings. This study demonstates the role of chelating agents in lessening the toxic effects of Cr⁺⁶. The chelating agents supplemented with Cr⁺⁶ in the culture medium enhanced the Cr bioavailability in plants.     

The action of chelating agents on human liver aldehyde dehydrogenase.

Human liver aldehyde dehydrogenase was inhibited by aromatic chelating agents. However, structurally related compounds with much lower metal-complexing ability displayed affinities for enzyme essentially equal to those of their respective chelating analogues. Inhibition was competitive with respect to the coenzyme. It is suggested that hydrophobic interactions between the inhibitors and the coenzyme-binding site of the enzyme are responsible for the observed effects on activity.     

Effects of chelating agents on crossing-over inNeurospora crassa

Screening methods were adapted to find out effective concentrations of the chelating agents, ethylenediamine tetraacetic acid and 8-hydroxy quinoline which produced modifications in the cross-over frequencies. Final crosses were designed to study the close and distantly placed regions on either side of the centromeres. Eleven regions were studied using tetrads, and eight regions using randomly selected ascospores.The magnitude and intensity of modification in the cross-over values vary from region to region, but an overall increase in the cross-over frequency was observed.Significant departures in cross-over values were found between the various treated crosses with respect to a number of regions.The mode of action of the chelating agents was not easy to formulate, but implications attached to it have been discussed.