Patent Application
20060116349
Restless Legs Syndrome
Victims seriously afflicted with Restless Leg Syndrome (RLS; also known as Ekbom's syndrome), are virtually unable to remain seated or even to stand still. Activities that require maintaining motor rest and limited cognitive stimulation, such as transportation (car, plane, train, etc.) or attending longer meetings, lectures, movies or other performances, become difficult if not impossible. Tortured by these sensations which become more severe at night, RLS patients find sleep to be virtually impossible, adding to the diminishing quality of their lives. The urge to move, which increases over periods of rest, can be completely dissipated by movement, such as walking. However, once movement ceases, symptoms return with increased intensity. If an RLS patient is forced to lie still, symptoms will continue to build like a loaded spring and, eventually, the legs will involuntary move, relieving symptoms immediately. Rhythmic or semi-rhythmic movements of the legs are observed if the patient attempts to remain laying down (Pollmacher and Schulz 1993). These movements are referred to as dyskinesias-while-awake (DWA) (Hening et al. 1986) or more commonly, periodic limb movements while awake (PLMW).
Clinically, RLS is indicated when four diagnostic criteria are met: (1) a sensation of an urge to move the limbs (usually the legs); (2) motor restlessness to reduce sensations; (3) when at rest, symptoms return or worsen; and (4) marked circadian variation in occurrence or severity of RLS symptoms; that is, symptoms worsen in the evening and at night (Allen and Earley 2001a). First recognized by Willis in 1685, RLS has been misunderstood and confused with periodic limb movements in sleep (PLMS; which may be a part of RLS, but does not define RLS), periodic limb movement disorder (PLMD; a sleep disorder) and nocturnal (or sleep) myoclonus (Allen and Earley 2001a).
Iron and Dopamine Concentrations are Intertwined Factors in RLS.
Lack of iron and reduced dopamine synthesis in the brain are important factors in RLS (Ekbom 1960, Nordlander 1953). Dopamine is a neural transmitter synthesized in the brain that is essential for proper central nervous system (CNS) function. In the synthesis of dopamine, iron is a cofactor for the enzyme tyrosine hydroxylase, which is the rate-limiting step in dopamine metabolism (Cooper et al. 1991). Iron in the dopaminergic system appears to be an important component in RLS pathophysiology (Chesson A L et al. 1999, Ekbom 1960, Hening et al., 1999, Montplaisir et al. 1991).
Because iron is a co-factor for tyrosine hydroxylase in dopamine synthesis, dopamine is reduced. When chelators (substances that make iron physiologically unavailable) are administered to rats having excessive brain iron, they were effective in reducing dopamine and dopamine turnover (Ward et al. 1995). Studies in iron-deficient animals have also demonstrated decreases in dopamine receptors (Ben-Shachar et al. 1985, Ward et al. 1995), dopamine transporter function and density, and an elevation in extracellular dopamine (Erikson et al. 2000, Nelson et al. 1997). These observations in rats are also observed in RLS patients. For example, a decrease in dopamine receptors has been observed in basal ganglia (Staedt et al. 1995, Turjanski et al. 1999). RLS patients have 65% less cerebral spinal fluid (CFS) ferritin (an important iron storage protein) and three-fold more CSF transferrin (iron transport blood protein), despite normal serum levels of ferritin and transferrin in both RLS and controls (Earley et al. 2000). Iron concentrations vary throughout the brain, the site of dopamine synthesis; RLS patients have less iron in the substantia nigra and in the putamen parts of the brain (Allen et al. 2001). In general, decreased ferritin levels are indicative of RLS severity (O'Keeffe et al. 1994, Sun et al. 1998). These observations indicate that the ability of the brain to transport or store iron is abnormal in idiopathic RLS (RLS having no apparent cause).
1Table derived from (Chesson AL et al. 1999), except for intravenous iron dextran.
2Studies were performed on patients suffering from the indicated disease, not RLS, with the indicated drug.
3As reported in the studies referenced within (Chesson AL et al. 1999). See Chesson et al. 1999 for more information. The percent (&) range is derived from the reported percentages for each side effect; thus in the first example, 12-17% suffered from dyskinesia, 6% from nausea and 4% from hallucinations; the reported range is 4-17%.
Treating RLS
Current treatments for RLS are varied and plagued with undesirable side effects (see Table 1). Therapies have included the administration of dopamine agonists (substances that prod the production of dopamine), other dopaminergic agents, benzodiazepines, opiates and anti-convulsants. In cases where RLS results from a secondary condition, such as pregnancy, end-stage renal disease, erythropoietin (EPO) treatment and iron deficiency, removing the condition, such as giving birth or treating with traditional iron supplementation, can reduce or eliminate symptoms in at least some cases (Allen and Earley 2001a). However, RLS resulting from non-secondary conditions (“idiopathic” RLS), presents a greater treatment challenge.
Dopaminergic agents such as levodopa generally provide effective initial treatment, but with continued use, tolerance and symptom augmentation occur in about 80% of RLS patients (Allen and Earley 1996); this complication is also common for dopamine agonists (Earley and Allen 1996, Silber et al. 1997). The other alternatives, benzodiazepines, opiates and anti-convulsants are not as uniformly effective as the dopamine agents (Chesson A L et al. 1999, Hening et al. 1999). Despite changes in their treatment regimes, 15-20% of patients find that all medications are inadequate because of adverse effects and limited treatment benefit (Earley and Allen 1996).
Because of the link between iron and dopamine synthesis, iron administration would appear to be a simple and safe treatment to increase body iron stores. An obvious choice is oral administration of iron since such administration is simple and inexpensive. In fact, RLS patients with serum iron deficiency respond dramatically to oral iron supplements (Ekbom 1960, O'Keeffe et al. 1994). However, in RLS patients with normal_serum ferritin levels, the benefits of oral iron therapy decrease inversely to baseline serum ferritin levels: the higher the ferritin at the time of initiating therapy, the less pronounced the benefits (O'Keeffe et al. 1994). This approach to raise body stores of iron is ineffective because the gut controls iron absorption, responding not to dopamine synthesis cues, but to serum iron levels (Conrad et al. 1999). To increase body stores of iron when serum ferritin levels are normal, unacceptably high oral doses for months would need to be administered, or methods that bypass gut regulation would need to be used.
Intravenous administration of iron circumvents the problems and ineffectiveness of orally-administered iron for those RLS patients with normal serum ferritin levels. In fact, intravenous administration of iron dextrose solutions, such as INFeD® (Watson Pharma, Inc.; Corona, Calif. (having an average apparent molecular weight of 165,000 g/mole with a range of approximately ±10%), and Dexferrum® (American Regent Laboratories, Inc.; Shirley, N.Y.) and those outlined in (Andreasen and Christensen 2001); referred to collectively as “IDI”) successfully treats RLS. However, the dosage is high—1000 mg/administration; or about two- to ten-fold more than the usual dose when used to treat other conditions. While IDI offers hope to some RLS patients, it also suffers from significant disadvantages: not only is the dosage high, but also dextran causes anaphylaxis in about 1.7% of the population (Fishbane et al. 1996), a life threatening condition; just less than 50% of those suffering anaphylaxis die.
Among the various aspects of the present invention is the provision of a method of treating Restless Leg Syndrome (RLS). Briefly, therefore, the present invention is directed to treating RLS with an iron carbohydrate complex of particular iron release rate and/or iron core size. Thus, the methods described herein provide for the safe and efficicacious delivery of iron to subjects in need thereof as well as allowing thorough tissue distribution, faster labile iron release, and increased in vitro donation of iron to transferrin.
The present teachings include methods for treating Restless Leg Syndrome that involve the administration of an iron complex to a patient suffering from RLS. The iron complex can be selected from an iron carbohydrate, an iron aminoglycan, or an iron polymer. The iron release rate of the iron complex used in this aspect of the invention is at least 115 μg/dl at a concentration of at least 2,000 μg/dl.
In accordance with a further aspect, RLS is treated by administering an iron complex of particular iron core size to a patient suffering from RLS. The iron complex can be selected from an iron carbohydrate, an iron aminoglycan, or an iron polymer. The iron core size of the iron complex used in this aspect is no greater than 9 nm.
Yet another aspect provides kits, comprising an iron complex having an iron core size no greater than 9 nm (in solution or lyophilized), a syringe, and a syringe needle. The kit may also include instructions for use.
Other objects and features will be in part apparent and in part pointed out hereinafter.
Those of skill in the art will understand that the drawings, described below, are for illustrative purposes only. The drawings are not intended to limit the scope of the present teachings in any way.
The present invention makes use of the discovery that an iron complex, having a higher release rate of iron than IDI, has the same effect for the treatment of RLS, but at a lower dosage. These iron complexes avoid the risks of anaphylactic shock associated with IDI when administered intravenously and, because of the higher release rate, dosage can be lowered.
An example of such an iron complex is Venofer®, an iron sucrose complex that has an incidence of anaphylactoid reactions of 0.0046% (that is, 1 out of 20,000 people; IDI has a rate of anaphylaxis of 1.7%, or almost 2 out of 100 people). However, any iron complex that has a release rate greater than that of IDI is an effective RLS therapeutic.
Iron Compositions for the Treatment of RLS
Iron complexes are compounds which contain iron in (II) or (III) oxidation state, complexed with an organic compound. These include iron polymer complexes, iron carbohydrate complexes, and iron aminoglycosan complexes. These complexes are commercially available, or have well known syntheses (see, for example, (Andreasen and Christensen 2001, Andreasen and Christensen 2001, Geisser et al. 1992, Groman and Josephson 1990, Groman et al. 1989)).
Examples of iron carbohydrate complexes include iron simple saccharide complexes, iron oligosaccharide complexes, and iron polysaccharide complexes, such as: iron carboxymaltose, iron sucrose, iron polyisomaltose (iron dextran), iron polymaltose (iron dextrin), iron gluconate, iron sorbital, iron hydrogenated dextran, which may be further complexed with other compounds, such as sorbital, citric acid and gluconic acid (for example iron dextrin-sorbitol-citric acid complex and iron sucrose-gluconic acid complex), and mixtures thereof.
Examples of iron aminoglycosan complexes include iron chondroitin sulfate, iron dermatin sulfate, iron keratan sulfate, which may be further complexed with other compounds and mixtures thereof.
Examples of iron polymer complexes include iron hyluronic acid complex, iron protein complexes, and mixtures thereof. Iron protein complexes include ferritin, transferritin, as well as ferritin or transferritin with amino acid substitutions, and mixtures thereof. Preferably, the iron complexes have a molecular mass of at least 30,000, more preferably of 30,000 to 100,000 as determined by HPLC/CPG (as described in Geisser et al. 1992). Preferably, the iron complexes have a size of at most 0.1 micrometer, more preferably 0.035 to 0.1 micrometer, as determined by filtration.
One preferred iron complex is iron sucrose (Venofer®). This composition also avoids toxicity issues that are associated with smaller sugars, especially gluconates, which have high iron release rates. Iron sucrose compositions balance these toxicity issues with optimal iron release rates.
Determining Iron Complex Iron Release Rates (Esposito, 2002)
The methods of the invention take advantage of the discovery that iron complexes having higher release rates of iron than IDI can be effectively administered at lower doses. IDI has an iron release rate of 69.5-113.5 μg/dl. In the present invention, the iron complex must have a release rate of at least 115 μg/dl at a concentration of at least 2000 μg/dl; including 2000, 3000, 3500, 5000, and 10,000 μg/dl. Preferably, at least 120 μg/dl, more preferably, at least 140 μg/dl. Two tests can be implemented to determine iron release rates, that by Esposito et al. (2000) and by Jacobs et al. (1990).
“Chelator Test” (Esposito et al. 2000)
The release rate of a candidate iron complex is the ability of the candidate complex to donate iron to apotransferrin or to an iron chelator, such as desferrioxamine. To detect such transfer, the probes fluorescein-transferrin (FI-Tf) and fluorescein-desferrioxamine (FI-DFO) can be used, which undergo quenching upon binding to iron (Breuer and Cabantchik 2001). In short, the method involves mobilization of iron from serum with 10 mM oxalate and its transfer to the metallosensor fluoresceinated apotransferrin (FI-aTf). Gallium is present in the assay to prevent the binding of labile plasma iron to the unlabelled apotransferrin in the sample. Labile plasma iron values are derived from the magnitude of quenching of the fluorescence signal of fluoresceinated apotransferrin. Fluorescence may be measured using, for example, 96-well plates and a plate reader operating at 485/538 nm excitation/emission filter pair (gain=25).
“Alumina Column Test” (Jacobs et al. 1990)
In this test, samples (serum and candidate iron composition) are passed over an alumina column to absorb organic and drug-bound iron, the elutants are then collected and reconstituted to a pre-selected volume (e.g., 1.5 ml), and the final iron concentration determined using a chemistry analyzer, such as a Hitachi 717 chemistry analyzer. Ferrozine reagents are used, which included detergent, buffers of citric acid and thiourea, ascorbate, and ferrozine. This test is a non-proteinizing method in which detergent clarifies lipemic samples, buffers lower the pH to <2.0 to free iron as Fe3+ from transferrin, ascorbate reduces Fe3+ to Fe2+, and ferrozine reacts with Fe2+ to form a colored complex measured spectophotometrically at 560 nm. From this result the value of a control (blank) sample is subtracted from the experimental sample readings, and the result are recorded as the Δ Tf-bound iron (μg/dl).
Pharmaceutical Compositions
In many cases, the iron complex may be delivered as a simple composition comprising the iron complex and the buffer in which it is dissolved. However, other products may be added, if desired, to maximize iron delivery, preservation, or to optimize a particular method of delivery.
A “pharmaceutically acceptable carrier” includes any and all solvents, dispersion media, coatings, antibacterial and anti-fungal agents, isotonic and absorption delaying agents, and the like, compatible with pharmaceutical administration (Gennaro 2000). Preferred examples of such carriers or diluents include, but are not limited to, water, saline, Finger's solutions and dextrose solution. Supplementary active compounds can also be incorporated into the compositions. For intravenous administration, Venofer® is preferably diluted in normal saline to approximately 2-5 mg/ml. The volume of the pharmaceutical solution is based on the safe volume for the individual patient, as determined by a medical professional
General Considerations
An iron complex composition of the invention for administration is formulated to be compatible with the intended route of administration, such as intravenous injection. Solutions and suspensions used for parenteral, intradermal or subcutaneous application can include a sterile diluent, such as water for injection, saline solution, polyethylene glycols, glycerine, propylene glycol or other synthetic solvents; antibacterial agents such as benzyl alcohol or methyl parabens; antioxidants such as ascorbic acid or sodium bisulfite; buffers such as acetates, citrates or phosphates, and agents for the adjustment of tonicity such as sodium chloride or dextrose. The pH can be adjusted with acids or bases, such as hydrochloric acid or sodium hydroxide. Preparations can be enclosed in ampules, disposable syringes or multiple dose vials made of glass or plastic.
Pharmaceutical compositions suitable for injection include sterile aqueous solutions or dispersions for the extemporaneous preparation of sterile injectable solutions or dispersion. For intravenous administration, suitable carriers include physiological saline, bacteriostatic water, CREMOPHOR EL™ (BASF; Parsippany, N.J.) or phosphate buffered saline (PBS). The composition must be sterile and should be fluid so as to be administered using a syringe. Such compositions should be stable during manufacture and storage and must be preserved against contamination from microorganisms, such as bacteria and fungi. The carrier can be a dispersion medium containing, for example, water, polyolo (such as glycerol, propylene glycol, and liquid polyethylene glycol), and other compatible, suitable mixtures. Various antibacterial and anti-fungal agents, for example, parabens, chlorobutanol, phenol, ascorbic acid, and thimerosal, can contain microorganism contamination. Isotonic agents such as sugars, polyalcohols, such as manitol, sorbitol, and sodium chloride can be included in the composition. Compositions that can delay absorption include agents such as aluminum monostearate and gelatin.
Sterile injectable solutions can be prepared by incorporating an iron complex in the required amount in an appropriate solvent with a single or combination of ingredients as required, followed by sterilization. Methods of preparation of sterile solids for the preparation of sterile injectable solutions include vacuum drying and freeze-drying to yield a solid containing the iron complex and any other desired ingredient.
Systemic Administration
Systemic administration can be transmucosal or transdermal. For transmucosal or transdermal administration, penetrants that can permeate the target barrier(s) are selected. Transmucosal penetrants include, detergents, bile salts, and fusidic acid derivatives. Nasal sprays or suppositories can be used for transmucosal administration. For transdermal administration, the active compounds are formulated into ointments, salves, gels, or creams.
Carriers
Active compounds may be prepared with carriers that protect the compound against rapid elimination from the body, such as a controlled release formulation, including implants and microencapsulated delivery systems. Biodegradable or biocompatible polymers can be used, such as ethylene vinyl acetate, polyanhydrides, polyglycolic acid, collagen, polyorthoesters, and polylactic acid. Such materials can be obtained commercially from ALZA Corporation (Mountain View, Calif.) and NOVA Pharmaceuticals, Inc. (Lake Elsinore, Calif.), or prepared by one of skill in the art.
Kits for Pharmaceutical Compositions
Iron complex compositions can be included in a kit, container, pack or dispenser, together with instructions for administration. When the invention is supplied as a kit, the different components of the composition may be packaged in separate containers, such as ampules or vials, and admixed immediately before use. Such packaging of the components separately may permit long-term storage without losing the activity of the components.
Kits may also include reagents in separate containers that facilitate the execution of a specific test, such as diagnostic tests.
Containers or Vessels
The reagents included in kits can be supplied in containers of any sort such that the life of the different components are preserved and are not adsorbed or altered by the materials of the container. For example, sealed glass ampules or vials may contain lyophilized iron complex or buffer that have been packaged under a neutral non-reacting gas, such as nitrogen. Ampules may consist of any suitable material, such as glass, organic polymers, such as polycarbonate, polystyrene, etc., ceramic, metal or any other material typically employed to hold reagents. Other examples of suitable containers include bottles that are fabricated from similar substances as ampules, and envelopes that consist of foil-lined interiors, such as aluminum or an alloy. Other containers include test tubes, vials, flasks, bottles, syringes, etc. Containers may have a sterile access port, such as a bottle having a stopper that can be pierced by a hypodermic injection needle. Other containers may have two compartments that are separated by a readily removable membrane that, upon removal, permits the components to mix. Removable membranes may be glass, plastic, rubber, etc.
Instructional Materials
Kits may also be supplied with instructional materials. Instructions may be printed on paper or other substrate, and/or may be supplied on an electronic-readable medium, such as a floppy disc, CD-ROM, DVD-ROM, mini-disc, SACD, Zip disc, videotape, audio tape, etc. Detailed instructions may not be physically associated with the kit; instead, a user may be directed to an internet web site specified by the manufacturer or distributor of the kit, or supplied as electronic mail.
Methods for the Treatment of RLS with Iron Complex Compositions
Methods of treatment of RLS with iron complex compositions having greater iron release rates than 115 μg/dl and/or core size no greater than 9 nm comprise the administration of the complex, either as doses administered over pre-determined time intervals or in response to the appearance and reappearance of RLS symptoms. In general, dosage depends on the route of administration. The preferred route of administration is intravenous infusion; however, certain iron compounds may be administered intramuscularly such as iron dextran. However, any route is acceptable as long as iron from the iron complex is quickly released (more quickly than IDI administered intravenously) such that RLS symptoms are treated.
An appropriate dosage level will generally be about 0.1 mg to 1000 mg of elemental iron per dose, which can be administered in single or multiple doses, particularly at least 1.0, 5.0, 10.0, 15.0, 20.0, 25.0, 50.0, 75.0, 100.0, 150.0, 200.0, 250.0, 300.0, 400.0, 500.0, 600.0, 750.0, 800.0, 900.0, 1000.0, 1100.0, 1200.0, 1300.0, 1400.0, 1500.0, 1600.0, 1700.0, 1800.0, 1900.0, 2000.0, 2100.0, 2200.0, 2300.0, 2400.0 or 2500.0 milligrams of elemental iron to the maximal tolerated dose (MTD) per administration. For example, the dosage level can be about 0.1 to about 1000 mg per dose; or about 100 mg to about 500 mg per dose. Alternatively, the dosage level can be, for example, about 1800 mg to about 1900 mg. The compounds may be administered on various regimes (see Example 3).
For example, a 1000 mg of elemental iron of an injectable intravenous iron sucrose complex (Venofer®) is given as a single dose (as a 1.5-5 mg iron/ml in normal saline) to RLS patients. A single intravenous treatment will provide relief of symptoms for an extended period of time, approximately two to twelve months (Nordlander 1953), although relief may be granted for shorter or longer periods. If desired, post-infusion changes in CNS iron status can be monitored using measurements of CSF ferritin (and other iron-related proteins) and of brain iron stores using MRI. Post-infusion changes in RLS are assessed using standard subjective (e.g., patient diary, rating scale) and objective (e.g., P50, SIT, Leg Activity Meters) measures of clinical status. If desired, to better evaluate RLS symptom amelioration, CSF and serum iron values, MRI measures of brain iron and full clinical evaluations with sleep and immobilization tests are obtained prior to treatment, approximately two weeks after treatment, and again twelve months later or when symptoms return. Clinical ratings, Leg Activity Meter recordings and serum ferritin are obtained monthly after treatment. CSF ferritin changes can also be used to assess symptom dissipation. More details are provided in Example 2 and the references cited therein.
The frequency of dosing depends on the response of each individual patient and the administered amount of elemental iron. An appropriate regime of dosing will be once every week to once every eighteen months, more preferably once every two to twelve months, or any interval between, such as once every two months and one day, three, four, five, six, seven, eight, nine, ten and eleven months. Alternatively, the iron complexes may be administered ad hoc, that is, as symptoms reappear, as long as safety precautions are regarded as practiced by medical professionals.
It will be understood, however, that the specific dose and frequency of administration for any particular patient may be varied and depends upon a variety of factors, including the activity of the employed iron complex, the metabolic stability and length of action of that complex, the age, body weight, general health, sex, diet, mode and time of administration, rate of excretion, drug combination, the severity of the particular condition, and the host undergoing therapy.
Core Size
Intravenous iron agents are generally spheroidal iron-carbohydrate nanoparticles. See
One of the primary determinants of iron bioactivity is the size of the core and the surface area to volume ratio. Generally, the rate of labile iron release in each agent is inversely related to the size of its iron core. Van Wyck et al. (2004). Furthermore, in vitro iron donation to transferrin is inversely related to core size. Core size can depend upon the number of iron atoms contained within. For example, the number of iron atoms contained within a 1 nm core is calculated to be 13, while a 10 nm core is calculated to contain 12770 iron atoms. Where agents share the same core chemistry, the rate of iron release per unit surface area is likely similar, differing perhaps by the strength of the carbohydrate ligand-core iron bound. But for the same total amount of core iron, surface area available for iron release increases dramatically as core radius decreases. That is to say, for equal amounts of iron, the smaller the core, the greater the surface area available for iron release. Of course, the explanation for this non-linear trend is the fact that volume is radius cubed. In short, a collection of many small spheres exposes a greater total surface area than does a collection of an equal mass of fewer, larger spheres. Van Wyck (2004).
A smaller iron core size of an iron complex administered for the treatment of RLS allows wider distribution through tissues, a greater rate of labile iron release, and increased in vitro iron donation to transferrin. Furthermore, the iron complex is more evenly distributed and metabolizes faster due to the smaller core size. But if the core size is too small, the iron complex can move into cells unable to metabolize iron. In one embodiment, an iron complex with a mean iron core size of no greater than 9 nm is administered to a subject for the treatment of Restless Leg Syndrome. In various embodiments, mean iron core size is less than 9 nm but greater than 1 nm, 2 nm, 3 nm, 4 nm, 5 nm, 6 nm, 7 nm, or 8 nm. Mean iron core size can be, for example, between 1 nm and 9 nm; between 3 nm and 7 nm; or between 4 nm and 5 nm. The iron carbohydrate complex with core size less than 9 nm can be, for example, an iron carbohydrate, an iron aminoglycan, or an iron polymer. In one embodiment, the iron complex is not an iron sucrose.
Furthermore, the combination of a small iron core size along with faster iron release rates is more efficacious for the treatment of RLS as compared to iron complexes with larger iron core size and slower iron release rates. In various embodiments, an iron complex with an iron release rate of at least 115 μg/dl at a concentration of at least 2,000 μg/dl and a mean iron core size of no greater than 9 nm is administered to a subject for the treatment of Restless Leg Syndrome. The iron complex can be, for example, an iron carbohydrate other than iron sucrose, an iron aminoglycan, or an iron polymer. In various embodiments, mean iron core size of an iron complex with an iron release rate of at least 115 μg/dl at a concentration of at least 2,000 μg/dl is less than 9 nm but greater than 1 nm, 2 nm, 3 nm, 4 nm, 5 nm, 6 nm, 7 nm, or 8 nm. The mean iron core size can be, for example, at least 1 nm but no greater than 9 nm. As another example, the mean iron core size can be at least 3 nm but no greater than 7 nm. As a further example, the mean iron core size can be at least 4 nm but not greater than 5 nm.
The molecular weight (i.e., the whole molecular weight of the agent) is considered a primary determinant in the pharmacokinetics, or in other words, how quickly it is cleared from the blood stream. The amount of labile iron is inversely correlated with the molecular weight of the iron-carbohydrate complex. Van Wyck (2004) J. Am. Soc. Nephrology 15, S107-S111, S109. That is to say, the magnitude of labile iron effect is greatest in iron-carbohydrate compounds of lowest molecular weight and least in those of the highest molecular weight. Generally, there is a direct relationship between the molecular weight of the agent and the mean diameter of the entire particle (i.e., the iron core along with the carbohydrate shell). In various embodiments, the mean diameter size of a particle of the iron carbohydrate complex is no greater than 25 nm. For example, the particle mean size can be no greater than 20 nm. As another example, the particle mean size can be no greater than 15 nm. As a further example, the particle mean size can be no greater than 10 nm.
Having described the invention in detail, it will be apparent that modifications, variations, and equivalent embodiments are possible without departing the scope of the invention defined in the appended claims. Furthermore, it should be appreciated that all examples in the present disclosure are provided as non-limiting examples.
The following non-limiting examples are provided to further illustrate the present invention. It should be appreciated by those of skill in the art that the techniques disclosed in the examples that follow represent approaches the inventors have found function well in the practice of the invention, and thus can be considered to constitute examples of modes for its practice. However, those of skill in the art should, in light of the present disclosure, appreciate that many changes can be made in the specific embodiments that are disclosed and still obtain a like or similar result without departing from the spirit and scope of the invention.
Intravenous iron agents donate iron to transferrin indirectly through prior intracellular uptake, processing and controlled release. However, evidence that many adverse reactions to intravenous iron agents are dose-related, dose-limiting and vary by class of agent support the hypothesis that direct donation may also occur. Intravenous iron administration at sufficient doses may transiently over-saturate iron binding capacity, and that agents may vary in their potential to donate iron directly.
The ability of candidate iron complexes (intravenous injection preparations for ferric gluconate (also known as sodium ferric gluconate in sucrose, Ferrlecit®)), iron sucrose (iron sucrose for injection, Venofer®) and both available formulations of iron dextran (INFeD® and Dexferrum®) to donate iron to transferrin in serum in vitro was assayed. A series of dilutions of the iron agents were added to fresh serum, passed over an alumina column to remove iron-sugar complexes, and the resulting elutant assayed for transferrin-bound iron.
This assay reliably excludes both iron agent and inorganic iron from interfering with the calorimetric assay of transferrin-bound iron in serum (Jacobs and Alexander 1990).
Parenteral Iron Formulations
Ferric gluconate Ferrlecit®,12.5 mg/ml in 5 ml ampules (Watson Pharmaceuticals, Inc, Corona, Calif.), iron sucrose (iron sucrose for injection, Venofer®, 20 mg/ml in 5 ml vials; American Regent Laboratories, Inc., Shirley, N.Y.) and two formulations of iron dextran (INFeD®; Watson Pharmaceuticals, Inc, Corona, Calif.; and Dexferrum®; American Regent Laboratories, Inc, Shirley, N.Y.; both 100 mg/ml in 2 ml vials)] were used.
For each experiment, all agents at all experimental concentrations were examined on the same day. For each concentration of iron agent, an equimolar stock solution was prepared on the day of use, using successive dilutions (≦1:10) in 0.9% NaCl.
Experimental Iron Concentrations
We examined concentrations of iron formulations over a range expected to include the maximum plasma concentration of agent after intravenous push injection (Cmax) of 125 mg ferric gluconate (1900 μg/dl; (anonymous 2001)), 100 mg iron sucrose (3,000 μg/dl (Danielson et al. 1996)) or 100 mg iron dextran (3,080 to 3,396 μg/dl, data on file, American Regent Laboratories, Shirley, N.Y.).
Determination of Transferrin Bound Iron
The method of Jacobs et al., was used to determine the amount or iron serum transferrin bound (Jacobs and Alexander 1990). 0.1 ml of stock iron formulation solutions were added to 1.5 ml of fresh pooled serum and incubated for 5 minutes. The samples were passed over a 2.0 g alumina column to absorb organic and drug-bound iron, the elutants collected and reconstituted to a total volume of 1.5 ml, and the final iron concentration was determined using a Hitachi 717 chemistry analyzer (Boehringer Mannheim Corporation; Indianapolis, Ind.). Hitachi-specified ferrozine reagents (Boehringer) were used, which included detergent, buffers of citric acid and thiourea, ascorbate, and ferrozine. Briefly, this is a non-proteinizing method in which detergent clarifies lipemic samples, buffers lower pH to <2.0 to free iron as Fe3+ from transferrin, ascorbate reduces Fe3+ to Fe2+ and ferrozine reacts with Fe2+ to form a colored complex measured spectophotometrically at 56 0 nm. From this result the value of a control (blank) sample (0.1 ml 0.9% NaCl plus 1.5 ml serum, no added iron agent) was subtracted from the experimental sample readings, and the result were recorded as the Δ Tf-bound iron (μg/dl).
The following results were observed, and are represented below in Table 2 and graphically in
(3) Δ iron response differed in a dose-related manner among the four agents.
The following tests are provided to aid in the evaluation of RLS diagnosis and treatment. Medical practitioners will select those tests that are appropriate for each particular patient. In many cases, monitoring for the diagnostic criteria for RLS will be sufficient to assess treatment efficacy.
Diagnostic factors RLS is indicated when four diagnostic criteria are met: (1) a sensation of an urge to move the limbs (usually the legs); (2) motor restlessness to reduce sensations; (3) when at rest, symptoms return or worsen; and (4) marked circadian variation in occurrence or severity of RLS symptoms; that is, symptoms worsen in the evening and night (Allen and Earley 2001a).
The Johns Hopkins RLS Severity Scale (JHRLSS) (Allen and Earley 2001b) This four point scale (0-3, corresponding to no symptom s to severe) is based on the time of day that RLS symptoms usually occur. Severity based on this scale can be derived from structured diagnostic clinical interviews (see below); this scale is most often used for characterization, not as a measure of treatment outcome.
Structured diagnostic clinical interviews and diagnostic questionnaires. These are administered by trained personnel. The forms and questions that may be asked of a potential RLS patient can be those presented in, for example, U.S. Pat. No. 6,960,571 (from U.S. application Ser. No. 10/389,228) (incorporated herein by reference).
Sleep-RLS Log (Earley et al. 1998) This log is kept by RLS patients and record when RLS symptoms and sleep occur during the time periods requested by the clinician.
CNS and blood iron status sampling (lumbar puncture and blood sample methods) Lumbar puncture is done between L4/L5 or L5 μl lumbar interspace using sterile technique. Ten mls of CSF are collected in 1 ml aliquots. From these samples, iron, ferritin ceruloplasm and transferrin concentrations are determined using standard techniques.
At the time of lumbar puncture, 10 mls of blood are also taken. The serum is then used to determine iron, ferritin, total iron binding capacity (TIBC), percentage iron saturation (% Sat) and transferrin receptor concentration. These variables are the most accurate blood indices for determining total body iron stores.
For many patients, blood sampling may be sufficient for monitoring treatment success and is desirable, given the risks that are involved in lumbar punctures.
Polysomnogram (PSG) Night PSGs provide a direct measurement of sleep efficiency and the number of PLMS per hour of NREM sleep. Both of these measurements can be used to as primary dependent measures of severity. Sleep can also be scored visually according to the Rechtschaffen and Kales criteria (Rechtschaffen and Kales 1968), and PLMS can be scored using accepted standards (Force 1993).
Full standard clinical polysomnograms are obtained for two consecutive nights following methods well known in the art (Montplaisir et al. 1998). Hours that are usually monitored are 23:00 to 07:00.
Suggested Immobilization Test (SIT) (Montplaisir et al. 1986, Pelletier et al. 1992, Montplaisir et al. 1998)
The subject lies with the legs out and the upper body at a 60° incline. Subjects are monitored by EEG to prevent them from falling asleep, and EMG over the anterior tibial muscle to record leg movements. Subjects are requested not to move for one hour. During this period, movement will occur, and the number of movements correlate to RLS severity. Hours that are usually monitored are 08:00-09:00, 16:00-17:00 and 22:00-23:00.
Leg Activity Meters/Monitors (LAM) Ambulatory recordings of leg activity can be obtained with the LAM. The LAM determines PLMS/hr with an error of ±5% compared to PSGs for patients with insomnia or PLMS (Gorny et al. 1986). The LAMs are habitually worn for at least 3 consecutive nights for each arbitrary period that the clinician would like to evaluate.
MRI measurements of brain iron (Allen et al. 2001) Briefly, multi-slice measurements of the relaxation rates R2* and R2 are obtained from a single scan using the gradient-echo sampling of FID and echo (GESFIDE) sequence on a GE 1.5T Signa System (General Electric, Milwaukee, Wis.), following known procedures (Gelman et al. 1999).
R2* and R2 images are reconstructed as a single, multi-slice “stack” in NIH Image 1.61, public domain NIH Image program (developed at the U.S. National Institutes of Health and available from the Institute). The slices showing the iron-containing structures on the R2* images are displayed. The structures are then manually traced independently by two trained investigators, using standard anatomic guidelines for the slice with the best presentation of the area. Relaxation rates are averaged for both left and right hemispheres. R2′ is then calculated from the difference of R2* and R2.
Dosage of Venofer® may be adjusted by a medical professional according to body weight, disease severity, and each patients' individual response to the medication. Intravenous administration of Venofer® or other iron complexes are given as in Table 3.
For example, a 1000 mg of Venofer® is given as a single intravenous dose to RLS patients. A single intravenous treatment will provide relief from RLS symptoms for an extended period of time, approximately 2-12 months, although relief may be granted for shorter or longer periods. If desired, post-infusion changes in CNS iron status can be monitored using CNS and blood iron tests (see Example 2). Post-infusion changes in RLS are assessed using standard subjective (patient diary, rating scale) as well as objective (P50, SIT, Leg Activity Meters, see Example 2) measures of clinical status. If desired, to better evaluate RLS symptom amelioration, CSF and serum iron values are determined, as well as those for brain iron, and full clinical evaluations with sleep and immobilization tests are obtained prior to treatment, approximately two weeks after treatment, and again 12 months later or when symptoms return.
Prior to administration, Venofer® [supplied as 100 mg elemental iron in 5 ml (20 mg/ml] is diluted in normal saline to 2-5 mg/ml. The solution is then administered through a free-flowing peripheral or central intravenous infusion. The volume of the pharmaceutical solution is based on the safe volume for the individual patient, as determined by a medical professional.
For direct injection, 100 mg may be administered over 2 minutes and 200 mg over 5 minutes. The injection is repeated a week later, or as necessary upon the recurrence of RLS symptoms.
Core size and particle size were determined for three iron carobhydrate complexes. These complexes include an iron dextran (Dexferrum), an iron carboxymaltose (Vit−45), and an iron sucrose (Venofer). See Table 4. Size data was taken from electron micrograph images of iron carbohydrate complex particles. See e.g.,
This is a continuation-in-part of co-pending U.S. patent application Ser. No. 10/389,228, filed Mar. 14, 2003. The above reference is incorporated herein by reference in its entirety.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 10389228 | Mar 2003 | US |
| Child | 11263510 | Oct 2005 | US |
