US20110226658A1 - Packaged Iron Sucrose Products - Google Patents

Packaged Iron Sucrose Products Download PDF

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Publication number
US20110226658A1
US20110226658A1 US12/993,592 US99359209A US2011226658A1 US 20110226658 A1 US20110226658 A1 US 20110226658A1 US 99359209 A US99359209 A US 99359209A US 2011226658 A1 US2011226658 A1 US 2011226658A1
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United States
Prior art keywords
iron sucrose
glass
container
formulation
packaged
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Abandoned
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US12/993,592
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English (en)
Inventor
Seshagiri R. Tata-Venkata
Xifeng Zhang
Fay Goldblatt
Minhaj Siddiqui
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Hospira Inc
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Hospira Inc
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Priority to US12/993,592 priority Critical patent/US20110226658A1/en
Publication of US20110226658A1 publication Critical patent/US20110226658A1/en
Assigned to HOSPIRA, INC. reassignment HOSPIRA, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: SIDDIQUI, MINHAJ, TATA-VENKATA, SESHAGIRI R., GOLDBLATT, FAY, ZHANG, XIFENG
Abandoned legal-status Critical Current

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
    • A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
    • A61J1/14—Details; Accessories therefor
    • A61J1/1468—Containers characterised by specific material properties
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
    • A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65B—MACHINES, APPARATUS OR DEVICES FOR, OR METHODS OF, PACKAGING ARTICLES OR MATERIALS; UNPACKING
    • B65B3/00—Packaging plastic material, semiliquids, liquids or mixed solids and liquids, in individual containers or receptacles, e.g. bags, sacks, boxes, cartons, cans, or jars
    • B65B3/003—Filling medical containers such as ampoules, vials, syringes or the like
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D65/00—Wrappers or flexible covers; Packaging materials of special type or form
    • B65D65/38—Packaging materials of special type or form
    • B65D65/42—Applications of coated or impregnated materials

Definitions

  • the invention is generally related to pharmaceutical products.
  • the invention is more particularly related to iron sucrose products in containers having glass as a primary component.
  • Glass is currently the preferred material for packaging parenteral pharmaceutical solutions due to its chemical and physical inertness. While this presumption generally holds true, glass under certain conditions is both chemically and physically reactive. It has long been known that aqueous solutions can interact with glass leading to the formation of glass-based particulate matter. This process, known generally as glass delamination, is accelerated by solutions containing various anions, especially under alkaline conditions, or by exposure to high temperatures, such as those used during terminal sterilization.
  • Iron sucrose is an aqueous complex of polynuclear iron (III) hydroxide in sucrose for intravenous use. Following administration, iron sucrose is dissociated by the reticuloendothelial system. Iron sucrose is administered to raise the patient's hemoglobin levels, and may be used in cases of oral iron therapy intolerance or ineffectiveness. Hypersensitivity reactions are believed to be less common with iron sucrose compared to other parenteral iron products. Iron sucrose can be used for the treatment of iron deficiency anemia, for example in peritoneal dialysis and hemodialysis dependent patients receiving erythropoietin therapy and non-dialysis dependent, chronic kidney disease patients. Iron sucrose has also been suggested for use in the treatment of restless leg syndrome.
  • iron sucrose At a conventionally-packaged concentration (20 mg elemental iron/mL), iron sucrose is very dark brown in color, and is effectively opaque as packaged.
  • Certain conventional formulations of iron sucrose are high in pH (e.g., pH values of 10.5-11), and have an osmolarity of 1250 mOsmol/L. These formulations can be diluted with 0.9% sodium chloride to provide a therapeutically-desired concentration.
  • Iron sucrose is conventionally packaged in glass. Glass vessels are known to be air-impermeable, and therefore protect the iron sucrose from oxidation. Generally, glass containers are visually inspected for sediment and damage before use. Only those containing a sediment free and homogeneous solution should be used. Because iron sucrose is a dark opaque solution, the presence of glass particulate as the result of delamination is not readily recognized by visual inspection alone. Also, the light obscuration technique is not sensitive enough to detect the delaminated particles in iron sucrose formulations due to the inherent opacity of the solution.
  • Delaminated glass particles can be identified using, among other methods, scanning electron microscopy equipped with an energy dispersive X-ray analyzer (SEM/EDS). Scanning electron microscopy (SEM) can also be used to map the surface morphology within glass vials and to screen surface integrity. Glass surfaces can be characterized by SEM before and after exposure to drug product. Additionally, solutions can be filtered through an appropriate filter membrane and the retained glass particulates can be detected using the SEM technique. However, these methods of detection of glass delamination are impractical for routine inspection of commercially packaged iron sucrose solutions.
  • the inventors have determined that iron sucrose formulations packaged in conventional glass vessels can develop glass particulates over time due to the delamination of glass from the interior glass surface. Accordingly, the inventors have identified a need in the art to provide a glass package for iron sucrose solutions that avoids glass delamination.
  • One aspect of the invention involves a packaged iron sucrose product including a container constructed from a material including glass, the container having an inside surface having formed thereon a layer of a material containing silicon dioxide or a silicone polymer. Inside the container is an iron sucrose formulation in contact with the layer of the material.
  • the iron sucrose formulation is an aqueous formulation, such as iron sucrose and water for injection.
  • the solution may have a pH of 9 or greater.
  • the iron concentration may be in the range of 0.1 mg/mL to 50 mg/mL.
  • the material coating the interior inside surface of the container includes a polyalkylsiloxane, such as polydimethylsiloxane, having a thickness of about 150 nm to about 50 ⁇ m.
  • a silicon dioxide layer may have a thickness in the range of about 50 nm to about 20 ⁇ m.
  • a further aspect of the invention is directed to a method for storing an iron sucrose formulation.
  • the method includes packaging a high pH iron sucrose in a container according to the invention.
  • FIG. 1 is cross-sectional view of a pharmaceutical product constructed in accordance with the present invention.
  • FIGS. 2A-2D are SEM photographs of delaminated glass flakes collected on filter paper and obtained from individual containers of VENOFER® Iron Sucrose Injection, USP. Samples were obtained five months prior to product expiration from containers stored at room temperature.
  • FIGS. 3A-3D are SEM photographs of delaminated glass flakes collected on filter paper and obtained from individual containers of VENOFER® Iron Sucrose Injection, USP. Samples were obtained eighteen months prior to product expiration from containers stored at room temperature.
  • FIG. 4 is an SEM photograph of glass flakes collected on filter paper and obtained from a solution of Iron Sucrose Injection, USP, packaged in a USP Type 1 glass container (tubing vial) stored for 2 months at 25° C.
  • FIG. 5 is an SEM photograph of glass flakes collected on filter paper and obtained from a solution of Iron Sucrose Injection, USP, packaged in a USP Type 1 tubing vial and stored at 25° C. for 12 months.
  • FIG. 6 is an SEM photograph of filter paper used to filter a solution of Iron Sucrose Injection, USP, that was packaged in a CARPUJECT® syringe and stored for 12 months at room temperature.
  • the CARPUJECT® container is a USP Type I glass container that is coated with silicone.
  • FIG. 7 is an SEM photograph of filter paper used to filter a solution of Iron Sucrose Injection, USP, that was packaged in a Wheaton siliconized USP glass container (molded vial) that was stored for 3 months at 40° C.
  • FIG. 8 is an SEM photograph of filter paper used to filter a solution of Iron Sucrose Injection, USP, packaged in a SCHOTT siliconized USP glass tubing vial and stored for 3 months at 40° C.
  • FIG. 9 is an SEM photograph of filter paper used to filter a solution of Iron Sucrose Injection, USP, that was packaged in a SCHOTT TYPE I PLUS silicon dioxide (SiO 2 ) coated glass container made from tubing glass and stored for 2 months at 25° C.
  • the invention is related to the use of a glass vessel for the packaging and storage of iron sucrose formulations.
  • the interior surface of the vessel is coated with a layer of a material containing silicon, such as silicon dioxide or a silicone polymer.
  • the packaged products and storage methods of the invention provide iron sucrose formulations in a storage stable container that reduces or prevents the formation of glass particulate matter over the storage life of the product.
  • a packaged iron sucrose product can be constructed in accordance with the invention as generally depicted in FIG. 1 .
  • Product 10 includes container 12 having an interior surface 14 .
  • Interior surface 14 defines an interior space 16 within container 12 .
  • An iron sucrose formulation 18 is contained within interior space 16 of container 12 .
  • formulation 18 is at or above a pH of approximately 9.
  • opening 20 facilitates the filling of container 12 and provides access to the contents of container 12 , thereby allowing the contents to be removed from container 12 when they are needed.
  • opening 20 is a mouth of a bottle or vial.
  • opening 20 can have a variety of known configurations without departing from the scope of the present invention.
  • the glass vessel is made from a material that includes glass, which is used herein in its ordinary sense.
  • materials include soda-lime glass, borosilicate glass, or fused silica. Numerous other types of specialty glass are available including materials where glass is not 100% of the composition. All of these materials are contemplated as appropriate materials for a container for iron sucrose that can be coated with a material containing silicon.
  • the material forming the layer on the interior surface of the container is semi-inorganic polymer based on the structural unit R 2 SiO, where R is an organic group, for example alkyl, characterized by wide-range thermal stability, high lubricity, extreme water repellence, and physiological inertness.
  • R is an organic group, for example alkyl, characterized by wide-range thermal stability, high lubricity, extreme water repellence, and physiological inertness.
  • R polydimethylsiloxane
  • R silicone polymers where R is other alkanes are readily available.
  • R can be a functionalized moiety that can be cross-linked in situ on the interior surface of the container.
  • Many silicone polymers will work as long as polymer layer can be rendered pharmaceutically compatible and inert to high pH iron sucrose formulations following application of the polymer to the surface.
  • Materials containing silicone may include co-polymers of polyalkylsiloxanes and other compounds which render the inside of the container pharmaceutically compatible and inert
  • the material forming the layer on the interior surface of the container is a silicone polymer, also known as silicone oil.
  • Suitable polymers include, for example, PDMS, alpha-trimethylsilyl)-poly(oxy(dimethylsilylene))-omega-methyl, and dimethylpolysiloxane hydrolyzate.
  • Commercially available examples of such materials include materials in the Baysilon family of silicone polymers (Bayer AG), and Dow Corning® Medical Fluids (Dow Corning, Midland, Mich.), such as Dow Corning® 360 and 365 Medical Fluids.
  • a layer of silicone polymer can have a thickness in the range of 150 nm to 50 ⁇ m, more particularly from about 1 ⁇ m to about 35 ⁇ m, and even more particularly about 5 ⁇ m to 25 ⁇ m.
  • a common method for applying a silicone polymer to a surface includes diluting Dow Corning® 360 Medical Fluid to 0.1-5% and then using this solution for rinsing, dipping or spraying containers.
  • the solution can be diluted in aliphatic (e.g. hexane, or preferably heptane) and aromatic (e.g. toluene or xylene) solvents. Certain chlorinated solvents can also be used.
  • Dow Corning® Q7-9180 Silicone Fluids volatile short-chain linear polydimethylsiloxanes
  • Dow Corning® 365 Medical Fluid is an emulsion composed of 35% Dow Corning® 360 Medical Fluid in water with non-ionic surfactants, Tween®20 and Triton®X-100, and preservatives, sodium benzoate and parabens (propyl and methyl p-hydroxy-benzoates).
  • this emulsion can be further diluted with sterile, pyrogen-controlled (WFI) water to a concentration of 0.1-5.0% silicone in the final treatment solution.
  • WFI pyrogen-controlled
  • the solution can be applied to surfaces by known methods of rinsing, dipping or spraying. Delivery to the surface of just enough silicone to achieve a uniform coating is sufficient.
  • FTIR Fourier-Transform Infrared Spectroscopy
  • a layer of material is formed on the interior glass surface of a container. While some studies suggest that heat treatment can result in a small percentage of fluid to become bound to the surface, it is generally considered that the material can be removed from the surface with appropriate solvents and detergents.
  • the container is heated following the application of the silicone polymer to ensure complete removal of any solvents and to allow the silicone fluid to become more intimately associated with the substrate.
  • the input heat energy assists small aggregates or droplets of the fluid to spread out evenly over the surface and create a more uniform film.
  • the moisture present on the surface of an article due to humidity from the air is displaced. Heating or baking is done at a temperature and over a time sufficient to remove this moisture from the surface. It is understood that no chemical bonding results. Rather, a strong physical attraction between the surface and initial monolayer of fluid is created.
  • the amount of silicone fluid required is only that needed to achieve a uniform coating of the silicone.
  • the interior surface of the container itself should be clean and free of contaminants before treatment.
  • the baking temperature is kept below 150-350° C. Temperatures at the lower end of the range will minimize any possibility of oxidation and/or the formation of formaldehyde.
  • the time needed for baking is related to the temperature used, usually 20-120 minutes, and can be substantially shortened at higher temperatures.
  • One skilled in the art can readily perform time/temperature studies in order to identify the optimum conditions for the container being siliconized.
  • Some increase in durability or decrease in mobility can be achieved by using a fluid with a higher viscosity. Higher viscosity fluids will not flow as easily across a surface (migrate) and will not tend to be removed into suspension as easily as lower viscosity fluids.
  • the relative number of repeating siloxane units in the polymer chain will determine the molecular weight and viscosity of a particular fluid. As the number of units increases the polymer obviously becomes longer and the viscosity also increases.
  • Another method for coating a surface with a polymer includes using a polymer having a functional group that renders the polymer capable of being cross-linked in situ upon activation of the polymer by, for example, heating or irradiation.
  • the polymer is sprayed or otherwise applied to the inside surface of a container by any conventional method and subjected to an activation step of heating or irradiation.
  • the glass treatment entails the formation of a layer of silicon dioxide material.
  • the silicon dioxide material is SiO 2 (>95%, or even >99%).
  • the silicon dioxide material is substantially pure SiO 2 .
  • the silicon dioxide layer can be formed, for example, by a vapor deposition process.
  • the layer of silicon dioxide can have a thickness, for example, in the range of 50 nm to 20 ⁇ m.
  • the layer of the material covers substantially the entire interior surface of the storage container.
  • SCHOTT TYPE I PLUS® glass containers are made of pharmaceutical Type I glass having a chemically bonded, substantially invisible, ultrathin layer (0.1-0.2 ⁇ m) of pure SiO 2 on their inner surface. As a result, loss of active components due to adsorption, degradation, etc. is significantly reduced.
  • the container can be washed, depyrogenated, filled and sterilized.
  • Iron sucrose mixtures include, for example, water and polynuclear iron (III) hydroxide in sucrose.
  • the iron sucrose mixture has a pH greater than 7, more particularly greater than about 9.0 and even more particularly greater than about 10.5.
  • the iron concentration (measured as elemental iron) can be, for example, in the range of 0.1 mg/mL to 50 mg/mL. In one embodiment of the invention, the iron concentration is in the range of 0.1 mg/mL to 10 mg/mL. In another embodiment of the invention, the iron concentration is in the range of 5 mg/mL to 50 mg/mL.
  • the aqueous iron sucrose mixture can have a pH in the range of 10.5-11 and an iron concentration of about 20 mg/mL, as in a commercial product marketed under the trademark VENOFER® (American Reagent, Inc., Shirley, N.Y.).
  • the aqueous iron sucrose mixture includes only iron sucrose and water for injection.
  • the aqueous iron sucrose mixture is substantially free of proteins, dextran or other polysaccharides or preservatives (e.g. benzyl alcohol).
  • FIGS. 2-9 are SEM photographs of filter paper used to collect the solid contents of individual vials of iron sucrose formulations using a 0.45 micron polycarbonate filter. The photographs of the filter paper and the filtrate are shown at various magnifications.
  • the inventors have identified particulate flakes having a diameter from 1 ⁇ m to about 1000 ⁇ m in iron sucrose formulations packaged in conventional glass packages. Depending upon the size and number of flakes that can be counted, a relative extent of glass delamination can be obtained. The presence of sodium, potassium, oxygen, aluminum and silicon in the flakes is also indicative of delamination.
  • FIGS. 2A-2D are SEM photographs of filter paper that collected the glass flakes from individual containers of VENOFER® iron sucrose formulation. The photographs show, at various magnifications, the development of glass particulate matter in samples at 5 months prior to the expiration of the formulation.
  • FIGS. 3A-3D are SEM photographs of filter paper that collected the glass flakes from individual containers of VENOFER® iron sucrose formulations at various magnifications, in samples 18 months prior to expiration. The newer samples of FIGS. 3A-3D showed glass flakes but to a lesser extent than the sample shown in FIGS. 2A-2D .
  • FIGS. 4 and 5 are SEM photographs of the filter paper that collected the glass flakes from an untreated tubing vial used for storage of a high pH iron sucrose formulation.
  • the formulation was stored in the vial for 2 months at 25° C.
  • the formulation was stored in the vial for 12 months at 25° C. The difference in the number of flakes that developed between 3 and 12 months is apparent from the photographs.
  • FIGS. 6-9 show the filter paper that was used to filter the contents of siliconized containers according to the present invention.
  • FIG. 6 shows absence of glass flakes in a CARPUJECT® glass container treated with a silicone polymer that contained an iron sucrose formulation for 12 months at room temperature.
  • FIG. 7 shows the absence of glass flakes in a solution of an iron sucrose injection packaged in a Wheaton siliconized USP glass container (molded vial) that was stored for 3 months at 40° C.
  • FIG. 8 shows the absence of glass flakes in a solution of Iron Sucrose Injection, USP, packaged in a SCHOTT USP siliconized glass container (glass tubing vial) and stored for 3 months at 40° C.
  • FIG. 9 shows glass flakes from a SCHOTT TYPE I PLUS® glass container that stored the formulation for 2 months at 25° C.
  • the iron sucrose formulation after filling the glass vessel with the iron sucrose formulation, the iron sucrose formulation remains in the glass vessel for an extended period of time without measurable glass delamination.
  • the aqueous iron sucrose formulation can be left in the glass vessel for at least several weeks, and preferable several months, without appreciable glass delamination.
  • the product is free of glass particulate as the result of glass delamination for at least three months, more particularly, 6 months, even more particularly 12, 18, 24, 30 or 36 months without measurable delamination.
  • Another aspect of the invention relates to a method for storing an aqueous iron sucrose formulation.
  • the method includes providing a glass vessel having an inside surface coated with a layer of material comprising a silicone polymer or silicon dioxide.
  • the glass vessel and the layer of the material can be substantially as described above with respect to the packaged iron sucrose product of the present invention.
  • the method further comprises at least partially filling the glass vessel with the aqueous iron sucrose formulation.
  • the aqueous iron sucrose formulation can be substantially as described above with respect to the packaged iron sucrose products of the present invention.
  • the glass vessel is then sealed, for example with a cap or stopper of known construction.
  • the cap or stopper preferably has a product contact surface constructed from a material that does not interact with the iron sucrose contained within the container.
  • the cap or stopper has a product contact surface that includes a layer of material substantially as described above with respect to the container.
  • the container 12 has a closure (shown as cap 22 ) constructed to seal opening 20 , thereby fluidly sealing the iron sucrose formulation 16 within container 12 .
  • Cap 22 can be constructed of a variety of known materials. However, it is preferable that cap 22 be constructed of a material that minimizes the transmission of vapor therethrough and that minimizes the likelihood of interaction with and/or degradation of formulation 18 . For instance, cap 22 is a material having vapor barrier characteristics sufficient to minimize the transmission of atmospheric components therethrough.
  • the inner surface of the cap, stopper, lid or cover can be formed from or coated by a base-resistant material, such as polymethylpentene or fluoropolymer. Cap 22 and container 12 can be constructed such that cap 22 can be threadingly secured thereto.
  • cap 22 and container 12 are well known.
  • Alternative embodiments of cap 22 and container 12 are also possible and will be immediately recognized by those of ordinary skill in the relevant art. Such alternative embodiments include, but are not necessarily limited to, caps that can be “snap-fit” on containers, caps that can be adhesively secured to containers, and caps that can be secured to containers using known mechanical devices, e.g., a ferrule.
  • cap 22 and container 12 are configured such that cap 22 can be removed from container 12 without causing permanent damage to either cap 22 or container 12 , thereby allowing a user to reseal opening 20 with cap 22 after the desired volume of formulation 18 has been removed from container 12 .
  • cap 22 is constructed as a stopper for a pharmaceutical vial, thereby allowing medical personnel to access the contents of container 12 by inserting a hypodermic needle through cap 22 .
  • cap 22 is constructed of a material that substantially seals itself upon removal of a hypodermic needle that has been inserted therethrough in order to access the contents of container 12 .
  • container 12 is to contain formulation 18 .
  • container 12 is in the shape of a bottle or standard pharmaceutical vial.
  • container 12 can have a variety of configurations, closures and volumes without departing from the spirit and scope of the invention.
  • container 12 can be configured as a shipping vessel for large volumes (e.g., tens or hundreds of liters) of formulation 18 .
  • Such shipping vessels can be rectangular, spherical, or oblong in cross-section without departing from the intended scope of the invention.
  • the glass vessel can have any desired form.
  • the glass vessel can have the shape of a vial.
  • the vial can have, for example, a capacity in the range of 1 mL to 30 mL.
  • the glass vessel has the foam of an ampoule.
  • the glass vessel can have other forms, such as a tube, a bottle, a jar, or a flask.
  • the glass vessel is a syringe.
  • any headspace in the glass vessel can be charged with a non-oxidizing gas, such as nitrogen or argon.
  • a glass delamination study was performed under accelerated stability conditions.
  • An iron sucrose solution (20 mg elemental iron and 300 mg sucrose per ml of water) at pH 11.0 was packaged in the containers along with a control wherein delamination is expected.
  • Four different coated containers were evaluated to determine prevention of delamination under various packaging conditions. Molded glass vials (Wheaton Science Products, Milleville, N.J.), and glass tubing vials (Schott AG). were coated with silicone by rinsing the containers with the DOW CORNING® 365 Medical Fluid and baking the containers for a predetermined time and temperature.
  • a third container was a CARPUJECT® syringe (Hospira, Inc., Lake Forest, Ill.).
  • the syringe has a siliconized glass surface that is prepared by spraying the DOW CORNING® 365 medical fluid on the interior of the syringe and baking.
  • the fourth container was a container of Schott TYPE 1 PLUS® tubing glass (Schott, AG), which is prepared with a pure silicon dioxide coating.
  • the control was a container made of conventional, non-coated tubing glass from Gerresheimer AG (Dusseldorf, Germany).
  • samples of Iron Sucrose Injection were prepared as described above and packaged in glass CARPUJECT® syringe containers that were coated with a silicone polymer as described in Example 1.
  • the samples were subject to both accelerated and long term stability storage. Five units of each sample were collected at various time points and analyzed for glass flakes as described above. As shown in Table 2, some delamination was found in all samples stored at accelerated 40° C. storage after 6 months. However, as shown in Table 3, no delamination was found in all samples at 25° C. and 30° C. at 12 months of storage, and minimal delamination was found after 18 months of storage.
  • Very thin flakes were Very thin flakes were Some thicker particles found in 2 out of 5 found in 2 out of 5 were found in 2 out of syringe cartridges; syringe cartridges; 5 syringe cartridges; 10-30 ⁇ m in length. 10-200 ⁇ m in length. 15-60 ⁇ m in length. One cartridge had 4 One cartridge had about No definite evidence and the other had 2 12 flakes and the other of glass delamination. flakes. had about 8 flakes.
US12/993,592 2008-05-23 2009-05-22 Packaged Iron Sucrose Products Abandoned US20110226658A1 (en)

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US12/993,592 US20110226658A1 (en) 2008-05-23 2009-05-22 Packaged Iron Sucrose Products

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US5564808P 2008-05-23 2008-05-23
US12/993,592 US20110226658A1 (en) 2008-05-23 2009-05-22 Packaged Iron Sucrose Products
PCT/US2009/045006 WO2009143439A1 (fr) 2008-05-23 2009-05-22 Produits conditionnés fer-sucrose

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EP (1) EP2296998A1 (fr)
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US20140069886A1 (en) * 2012-06-28 2014-03-13 Corning Incorporated Delamination resistant glass containers with heat-tolerant coatings
US20140151371A1 (en) * 2012-11-30 2014-06-05 Corning Incorporated Glass containers with delamination resistance and improved strength
US8980777B2 (en) 2011-10-25 2015-03-17 Corning Incorporated Glass compositions with improved chemical and mechanical durability
US20150197371A1 (en) * 2012-09-26 2015-07-16 Katholieke Universiteit Leuven Bottles with means to prevent gushing
US9145329B2 (en) 2011-10-25 2015-09-29 Corning Incorporated Alkaline earth alumino-silicate glass compositions with improved chemical and mechanical durability
US20160184183A1 (en) * 2008-05-23 2016-06-30 Hospira, Inc. Packaged Iron Sucrose Products
US9517966B2 (en) 2011-10-25 2016-12-13 Corning Incorporated Glass compositions with improved chemical and mechanical durability
US9603775B2 (en) 2013-04-24 2017-03-28 Corning Incorporated Delamination resistant pharmaceutical glass containers containing active pharmaceutical ingredients
US9668936B2 (en) 2012-02-28 2017-06-06 Corning Incorporated Glass articles with low-friction coatings
US9700486B2 (en) 2013-04-24 2017-07-11 Corning Incorporated Delamination resistant pharmaceutical glass containers containing active pharmaceutical ingredients
US9700485B2 (en) 2013-04-24 2017-07-11 Corning Incorporated Delamination resistant pharmaceutical glass containers containing active pharmaceutical ingredients
US9707155B2 (en) 2013-04-24 2017-07-18 Corning Incorporated Delamination resistant pharmaceutical glass containers containing active pharmaceutical ingredients
US9707154B2 (en) 2013-04-24 2017-07-18 Corning Incorporated Delamination resistant pharmaceutical glass containers containing active pharmaceutical ingredients
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AU2009248885B2 (en) 2015-02-05
JP2011523866A (ja) 2011-08-25
US20160184183A1 (en) 2016-06-30
JP5568551B2 (ja) 2014-08-06
EP2296998A1 (fr) 2011-03-23
CA2725147C (fr) 2019-06-11
CA2725147A1 (fr) 2009-11-26
AU2009248885A1 (en) 2009-11-26
US20200222282A1 (en) 2020-07-16

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