Method of preventing lamellar silica formation in glass container
AssigneeAmgen Inc.
InventorsYasser Nashed-Samuel, Jeremy Gastwirt
Life of this patent
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Abstract
Methods of preventing the formation of lamellar silica formation in a borosilicate glass container storing a pharmaceutical formulation in an interior of the glass container in accordance with embodiments of the disclosure can include washing the container and drying the container under extended dry conditions of at least 3000 ms.
Claims33
A method for preventing lamellar silica formation in a borosilicate glass container storing a pharmaceutical formulation in an interior of the glass container, comprising:
- prior to filling the glass container with the pharmaceutical formulation, washing the interior of the glass container with a pressurized water jet;
- and
- drying the glass container by blowing compressed air into the interior of the glass container for at least 3000 ms wherein the glass container is washed and dried using a batch washer.
A method for preventing lamellar silica formation in a borosilicate glass container storing a pharmaceutical formulation in an interior of the glass container, comprising:
- prior to filling the glass container with the pharmaceutical formulation, washing the glass container with a pressurized water jet under conditions sufficient to remove contaminants, drying the washed glass container;
- and
- depyrogenizing the glass container by heating the dried glass container in an oven at a temperature of at least about 250° C., wherein the glass container remains stationary in the oven during heating.
A method of preventing lamellar silica formation in a borosilicate glass container containing a pharmaceutical formulation in an interior of the glass container, comprising:
- prior to filling the glass container with the pharmaceutical formulation, washing the glass container with a pressurized water jet under conditions sufficient to remove contaminants,
- drying the washed glass container by blowing compressed air into the interior of the glass container for at least 3000 ms,
- placing the dried glass container in a heat-safe container and covering the heat-safe container containing the dried glass container with a lid;
- depyrogenizing the dried glass container contained in the covered heat-safe container.
The method of any one of the preceding claims, comprising drying the glass container using at least 3 drying cycles, each drying cycle comprising blowing compressed air into the interior of the glass container for at least 3000 ms.
The method of any one of the preceding claims, comprising drying the glass container using 3 to 10 drying cycles, each drying cycle comprising blowing compressed air into the interior of the glass container for at least 3000 ms.
The method of any one of the preceding claims, wherein the glass container is dried by blowing compressed air into the interior of the glass container for about 3000 ms to about 10,000 ms.
The method of any one of the preceding claims, wherein the glass container is washed by exposing the interior of the container to the pressurized water jet for a duration greater than 1000 ms.
The method of any one of the preceding claims, wherein the glass container is washed by exposing the interior of the container to the pressurized water jet for a duration of greater than 1000 ms to about 6000 ms.
The method of any one of the preceding claims, wherein the pressurized water jet has a temperature of at least 72° C.
The method of any one of the preceding claims, wherein the glass container is washed using at least 3 washing cycles, each washing cycle comprising exposing the interior of the container to the pressurized water jet for greater than 1000 ms.
The method of any one of the preceding claims, wherein the glass container is washed using 3 to 10 washing cycles, each washing cycle comprising exposing the interior of the container to the pressurized water jet for greater than 1000 ms.
The method of any one of the preceding claims, further comprising filling the glass container with the pharmaceutical formulation, wherein the pharmaceutical formulation comprises an acid selected from the group comprising citric acid, phosphoric acid, acetic acid, or salts thereof.
The method of any one of the preceding claims, wherein filled glass container remains free of lamellar silica after storage of a pharmaceutical formulation comprising citric acid and polysorbate 80 within the glass container for at least 30 days at 40° C.
The method of any one of the preceding claims, wherein the glass container is dried with compressed air.
The method of any one of the preceding claims, wherein an interior surface of the glass is substantially free of a silica gel after depyrogenation.
The method of any one of the preceding claims, wherein the glass container has a volume of 10 cc, and the glass container is washed by exposing the interior of the glass container to a pressurized water jet for at least 3000 ms.
The method of any one of the preceding claims, wherein the glass container has a volume of 10 cc and the glass container is dried by blowing compressed air into the interior of the glass container for about 3000 ms to about 6000 ms.
The method of any one of claims 1 to 24 and 27, wherein the glass container has a volume of 50 cc and the glass container is dried by blowing compressed air into the interior of the glass container for about 5000 ms to about 8000 ms.
The method of any of the preceding claims, wherein the pressurized water jet has a pressure of at least 7.25 psi.
A method of screening a glass container storing a pharmaceutical formulation for susceptibility to lamellar silica formation when filled with a pharmaceutical formulation, comprising:
- filling a washed and depyrogenized glass container with a buffer for the pharmaceutical formulation, wherein the glass container comprises ions selected from the group comprising sodium, calcium, hydroxide, silicate, and combinations thereof;
- storing the filled glass containers at a temperature of 40° C. for at least 14 days;
- optically analyzing the buffer after storage for formation of one or more particles in the buffer;
- when particle formation is observed, isolating the one or more particles from the buffer for structural and elemental analysis;
- analyzing the isolated one or more particles using one or more of optical microscopy, scanning electron microscopy/energy dispersive X-ray spectroscopy (SEM/EDS), Fourier-transform infrared spectroscopy (FTIR), x-ray photoelectron spectroscopy (XPS), differential interference contrast microscopy (DIC), microflow imaging (MFI), and combinations thereof to determine a morphology of the particles and chemical composition;
- and
- analyzing an interior surface of the glass container, once emptied and after isolating the one or more particles, for delamination-type deformation of the interior surface, wherein the presence of particles having a chemical composition comprising silicon, oxygen, and carbon, and the absence of delamination-type deformation of the interior surface of the glass container indicates susceptible to lamellar silica formation.
The method of claim 30 wherein the glass container is a borosilicate glass container.
The method of claim 30, wherein the interior surface of the glass container is analyzed using one or more of stereomicroscopy, secondary ion-mass spectrometry (SIMS) depth profiling, and scanning electron microscopy (SEM).
Dependencies are inferred from the claim text.