Patent Application
20200115412
This invention relates to a chromatographic method for the separation of vancomycin and its degradation products.
Vancomycin is a potent antibiotic reserved for serious drug-resistant bacterial infections including intravenous infusion for complicated infection (including MRSA) and oral administration for severe gastro-intestinal (GI) infections caused by Clostridium difficile. It was first isolated from soil bacterium (Amycolatopis orientalis) by Kornfeld in 1953, and first commercialized by Eli Lilly in 1954. Vancomycin, which is listed on the WHO's List of Essential Medicines, is a complex glycopeptide derived from N. orientalis with significant analytical challenges, including the presence of at least 12 identified impurities and a greater number of unknown impurities. Vancomycin is unstable at room temperature, hygroscopic and amorphous. Vancomycin has six ionizable groups and some of the impurities have seven. It is difficult to handle (high surface energy) and difficult to formulate. AeroVanc is a dry-powder inhalation product (DPI) under development for the treatment of methicillin resistant S. aureus (MRSA) infections in the lungs of cystic fibrosis patients. AeroVanc (vancomycin hydrochloride inhalation powder) contains the antibiotic and a single excipient, L-leucine. AeroVanc comprises a dry powder formulation which is delivered to the lungs by oral inhalation using a unit dose delivery device.
Various HPLC methods are listed in the United States Pharmacopeia (USP), European Pharmacopoeia (EP) and the British Pharmacopoeia (BP) monographs, and in the scientific literature for the assessment of vancomycin impurities. However, none of the procedures provide acceptable separations for the determination of the impurities of vancomycin in vancomycin drug substance and in AeroVanc.
US20160264620A1 and U.S. Pat. No. 9,428,291B2 teach the purification of vancomycin using reversed phase HPLC. Diana et al., HPLC, Rapid Communication Mass Spectrometry, 2006, 20(4), 685-693, and Diana et al., Journal of Chromatography A, 2003, 996(1-2), 115-131 teach the quantification of vancomycin and related substances using reversed phase HPLC with a C18 column and mass-spectrometry (MS) detection. Backes et al., Journal of Pharmaceutical and Biomedical Analysis 1998, 16 (8), 1281-1288 teaches the quantification of vancomycin and its degradation products CDP-1 Major and CDP-1 Minor using reversed phase HPLC with a C18 column. Hadwiger et al., Antimicrobial Agents and Chemotherapy, 2012, 56(6), 284-2830 and Nambiar et al., 2012, 56(26) 2819-2823, teach the quantification of vancomycin and related substances using reversed phase HPLC with a C18 column and mass-spectrometry detection.
There remains a need for improved separation of complex compounds such as vancomycin from known and unknown impurities to provide high quality medicaments.
The invention provides method for separating a mixture of compounds each having at least one ionizable group, the method comprising: treating the mixture with reversed phase high pressure liquid chromatography on a stationary phase comprising a reversed phase chromatography column in the presence of a mobile phase comprising (a) a first mobile phase component comprising an aqueous buffer system comprising a weak acid and optionally a conjugate base, and at least one organic solvent miscible with water, and (b) a second mobile phase component comprising an aqueous buffer system comprising a conjugate base and optionally a weak acid, and a different concentration of at least one organic solvent miscible with water, wherein the ratio of weak acid to conjugate base in the first mobile phase component is different from the ratio of weak acid to conjugate base in the second mobile phase component and the ratio of the first mobile phase component to the second mobile phase component is varied during the separation.
A detailed description of various aspects, features and embodiments of the subject matter described herein is provide with reference to the accompanying drawings, which are briefly described below. The drawings are illustrative and are not necessarily drawn to scale, with some components being exaggerated for clarity. The drawings illustrate various aspects and features of the present subject matter and may illustrate one or more embodiment(s) or example(s) of the present subject matter in whole or in part. Together with the description, the drawings serve to explain the principles of the disclosed subject matter.
The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Office upon request and payment of the necessary fee.
The contents of all references herein are hereby incorporated by reference in their entirety.
The invention provides an analytical method designed to separate and quantify over 12 impurities and degradation products of vancomycin in vancomycin hydrochloride, an active pharmaceutical ingredient (API) and the inhalation powder form of vancomycin, AeroVanc, developed by Savara Inc.
Described herein are procedures for the determination of vancomycin impurities in vancomycin hydrochloride API and vancomycin hydrochloride inhalation powder (AeroVanc) both in bulk powder and filled into capsules.
Treating a mixture of compounds with reversed phase high pressure liquid chromatography comprises applying the mixture to one end of a column comprising a solid stationary phase and passing a liquid mobile phase through the length of the column, thereby eluting the compounds through the stationary phase to the end of the column. Because the compounds partition between the stationary phase and the mobile phase at different proportions, each of compounds in the mixture reach the end of the column at different retention times, resulting in their separation. The compounds can be detected by one or more detectors, which may also allow for quantification by comparison to standards. The retention times can be also used to identify the separated compounds by comparison to known samples of one or more of the compounds.
As used herein, the term “impurity” refers to a minor compound in a mixture with a major compound, wherein the major compound is a desirable material, such as a pharmaceutical or therapeutic agent. For example, the impurity may be present in a mixture from a finite, non-zero amount up to about 10 weight % relative to the major compound, preferably less than 5.0, 2.0, 1.0, 0.5 or 0.1 weight %. Impurities may arise from process byproducts or degradation of the major compound.
As used herein, the term “excipient” refers to an inactive or inert substance that serves as the vehicle or medium for a drug or other active substance. Pharmaceutical excipients are substances other than the active pharmaceutical ingredient (API) that have been appropriately evaluated for safety and are intentionally included in a drug delivery system or formulation. Excipients may be included, for example, for the purpose of long-term stabilization, bulking up solid formulations that contain potent active ingredients in small amounts (thus often referred to as “bulking agents”, “fillers”, or “diluents”), or to confer a therapeutic enhancement on the active ingredient in the final dosage form, such as facilitating drug absorption, reducing viscosity, or enhancing solubility. Excipients can also be useful in the manufacturing process, to aid in the handling of the active substance such as by facilitating powder flowability or non-stick properties, in addition to aiding in vitro stability such as prevention of denaturation or aggregation over the expected shelf life. The selection of appropriate excipients also depends upon the active ingredient, the route of administration, the dosage form, and other factors.
As used herein, the term “gradient” refers to one or more change in the composition of the mobile phase used during a HPLC separation over time. A “step” gradient refers to a gradient wherein the mobile phase is changed to a new composition almost instantaneously and then held at the new composition for a period of time. A “linear” gradient refers to a gradient wherein the mobile phase is changed at a constant “ramp” rate or slope for a period of time. In a “non-linear” gradient, the mobile phase is changed in a non-linear fashion. For a given separation method, the overall gradient may comprise one or more of these types of gradients. Depending on the compositions of the mobile phase components used to produce the gradient, a gradient may be considered as a linear gradient for one condition or characteristic of the mobile phase and be non-linear for a second characteristic of the mobile phase. For example, a linear gradient comprising two different pH-modifying mobile phase components may result in a non-linear gradient in pH even though the solvent gradient may be linear.
The term “isocratic” refers to a mobile phase that is held constant over a period of time during a separation.
The method is suitable for the analysis of vancomycin free base, and any other salts of vancomycin, especially the hydrochloride salt. The method can be used to analyze vancomycin in various pharmaceutical formulations.
Embodiments include the following.
The method of the Summary of the Invention wherein the first mobile phase component comprises an aqueous buffer system comprising a weak acid and no conjugate base and the second mobile phase component comprises an aqueous buffer system comprising a weak acid and a conjugate base.
The method of the Summary of the Invention wherein the first mobile phase component comprises an aqueous buffer system comprising a weak acid and a conjugate base and the second mobile phase component comprises an aqueous buffer system comprising a conjugate base and no weak acid.
The method of the Summary of the Invention wherein the first mobile phase component comprises an aqueous buffer system comprising a weak acid and a conjugate base and the second mobile phase component comprises an aqueous buffer system comprising a weak acid and a conjugate base.
The method of the Summary of the Invention or any of Embodiments 1 through 3 wherein the at least one miscible organic solvent is selected from the group consisting of alcohols, acetonitrile, dioxane, tetrahydrofuran and mixtures thereof.
The method of Embodiment 4 wherein the at least one miscible organic solvent is selected from the group consisting of tetrahydrofuran, acetonitrile and mixtures thereof.
The method of Embodiment 5 wherein the first mobile phase component comprises tetrahydrofuran and acetonitrile and the second mobile phase component comprises tetrahydrofuran and acetonitrile in different percentages than in the first mobile phase.
The method of the Summary of the Invention or any of Embodiments 1 through 6 wherein the buffer systems comprise formic acid, sodium formate, sodium acetate, acetic acid, ammonium formate, ammonium acetate or combinations thereof.
The method of Embodiment 7 wherein the buffer systems comprise sodium acetate and acetic acid.
The method of Embodiment 8 wherein the first mobile phase component comprises acetic acid and sodium acetate as buffer components.
The method of Embodiment 9 wherein the second mobile phase component comprises acetic acid and sodium acetate as buffer components in a different ratio than in the first mobile phase.
The method of Embodiment 9 wherein the second mobile phase component comprises sodium acetate and no acetic acid as buffer components.
The method of the Summary of the Invention or any of Embodiments 1 through 11 wherein the pH of the first mobile phase component is controlled between 2 and 8.5.
The method of Embodiment 12 wherein the pH of the first mobile phase component is controlled between 2.5 and 7.
The method of Embodiment 12 wherein the pH of the first mobile phase component is controlled between 3 and 5.
The method of Embodiment 12 wherein the pH of the first mobile phase component is controlled between 3.5 and 4.5.
The method of the Summary of the Invention or any of Embodiments 1 through 15 wherein the pH of the second mobile phase component is controlled between 2.5 and 9.5.
The method of Embodiment 16 wherein the pH of the second mobile phase component is controlled between 6.0 and 9.0.
The method of Embodiment 16 wherein the pH of the second mobile phase component is controlled between 7.5 and 9.0.
The method of the Summary of the Invention or any of Embodiments 1 through 18 wherein the reversed phase chromatography column comprises a stationary phase comprising silica gel particles having a chemically modified surface comprising octadecyl-pentafluorophenyl-silyl (C18 PFP) moieties.
The method of the Summary of the Invention or any of Embodiments 1 through 19 wherein the second mobile phase component comprises 0% of the total mobile phase for an initial period of time and is then increased in one or more linear ramps to comprise a major portion (at least 50%; at least 60% at least 70% or at least 80%) of the total mobile phase over a second period of time.
The method of Embodiment 20 wherein the second mobile phase is 0% of the total mobile phase for a third period of time.
The method of the Summary of the Invention or any of Embodiments 1 through 21 wherein the second mobile phase component comprises 0% of the total mobile phase for an initial period of time and is then increased in a single step to comprise a major portion (at least 50%; at least 60% at least 70% or at least 80%) of the total mobile phase over a second period of time.
The method of Embodiment 22 wherein the second mobile phase is 0% of the total mobile phase for a third period of time.
The method of the Summary of the Invention or any of Embodiments 1 through 23 comprising quantifying the amount of each of the compounds in the mixture.
The method of the Summary of the Invention or any of Embodiments 1 through 24 comprising identifying at least one impurity in the mixture.
The method of the Summary of the Invention or any of Embodiments 1 through 25 comprising detecting the compounds of the mixture using an ultraviolet-visible light detector.
The method of the Summary of the Invention or any of Embodiments 1 through 25 comprising detecting the compounds of the mixture using a diode-array detector.
The method of the Summary of the Invention or any of Embodiments 1 through 25 comprising detecting the compounds of the mixture using a mass spectrometer.
The method of the Summary of the Invention or any of Embodiments 1 through 28 wherein at least one of the compounds in the mixture has at least two ionizable groups.
The method of Embodiment 29 wherein each of the compounds in the mixture has at least two ionizable groups.
The method of the Summary of the Invention or any of Embodiments 1 through 28 wherein at least one of the compounds in the mixture has at least three ionizable groups.
The method of Embodiment 31 wherein each of the compounds in the mixture has at least three ionizable groups.
The method of the Summary of the Invention or any of Embodiments 1 through 28 wherein at least one of the compounds in the mixture has at least four ionizable groups.
The method of Embodiment 33 wherein each of the compounds in the mixture has at least four ionizable groups.
The method of the Summary of the Invention or any of Embodiments 1 through 28 wherein at least one of the compounds in the mixture has at least five ionizable groups.
The method of the Summary of the Invention or any of Embodiments 1 through 28 wherein at least one of the compounds in the mixture has at least six ionizable groups.
The method of the Summary of the Invention or any of Embodiments 1 through 36 wherein the mixture of compounds comprises a glycopeptide antibiotic and one or more impurities or degradation products.
The method of Embodiment 37 wherein the mixture of compounds comprises vancomycin or vancomycin hydrochloride, and one or more impurities.
The method of Embodiment 38 wherein the mixture further comprises leucine.
The method of Embodiment 39 wherein at least one impurity in a vancomycin composition can be measured in the range of 0.05% to 10.0% relative to vancomycin (i.e. at least one impurity in a vancomycin mixture is present in the range of 0.05% to 10.0% relative to vancomycin).
Embodiments of this invention, including Embodiments 1 through 40 above as well as any other embodiments described herein, can be combined in any manner, and the descriptions of variables in Embodiments 1-40 above as well as any other embodiments described herein, and any combination thereof, pertain to the methods of the present invention. Notably, any of the embodiments above can be further embodied by any other embodiment above, such as wherein any embodiment above can further embody any of the embodiments preceding it.
A notable method for separating a mixture of compounds each having at least two ionizable groups comprises treating the mixture with reversed phase high pressure liquid chromatography on a stationary phase comprising a reversed phase chromatography column in the presence of a variable mobile phase comprising (a) a first mobile phase component comprising an aqueous sodium acetate/acetic acid buffer system and at least one organic solvent miscible with water, and (b) a second mobile phase comprising an aqueous sodium acetate/acetic acid buffer system, and a higher concentration of at least one organic solvent miscible with water, wherein the ratio of sodium acetate/acetic acid in the first mobile phase component is different from the sodium acetate/acetic acid in the second mobile phase component and the ratio of the first mobile phase component to the second mobile phase component is varied during the separation.
Vancomycin and vancomycin salts, alone or in combination with other antibiotics, are useful in treating staphylococcal, streptococcal and enterococcal infections or diphtherial endocarditis. An indication of oral vancomycin therapy includes the treatment of pseudomembranous colitis caused by staphylococci when it is unresponsive to vancomycin for injection. Vancomycin for injection may be applicable to all of the other indications. An inhalable powder form of vancomycin currently in development, AeroVanc, may be useful for treatment of methicillin resistant S. aureus (MRSA) infections in the lungs of cystic fibrosis patients.
The vancomycin molecule is composed of two basic structures, including a disaccharide group, α-o-vancosamine-β-o-glucosyl, and a heptapeptide backbone. The structure of vancomycin determines its instability and the ease with which it may be degraded under acidic conditions, alkaline conditions, and/or high temperature conditions. Vancomycin is produced by microbial fermentation, which may produce impurities with structures different from vancomycin. The impurities include process impurities and degradation products. Sometimes, impurities and degradant products may have different pharmacologic properties and toxicologic properties from the main ingredient. Thus, it is important to be able to characterize the purity of various vancomycin preparations. Table 1 summarizes vancomycin and known impurities contained in commercial preparations. It is important to be able to separate these peaks to monitor purity and/or degradation of vancomycin in pharmaceutical products to ensure good product quality, safety and efficacy.
Desvancosaminyl-vancomycin and agluco-vancomycin are degradation products that result from the loss of the disaccharide moiety and the vancosamine sugar, respectively, by hydrolysis. Vancomycin can degrade to des-amido-succinimido-vancomycin by deamidation (Harris et al., Journal of the American Chemical Society, 1983 105 (23), 6915-6922 and Antipas et al., International Journal of Pharmaceutics, 1994, 109, 261-269). Des-amido-succinimido-vancomycin can further degrade to a mixture of two isomers of des-amido-isoaspartyl-vancomycin (CDP-1 Minor and CDP-1 Major). A number of other degradation or process impurities can be found in preparations of vancomycin hydrochloride, some of which are shown in Table 1.
This disclosure discusses the importance of design-of-experiments (DOE) combined with a good understanding of the physicochemical properties of vancomycin (especially the relationship between the charge of the molecule and the mobile phase pH) in the rational development of a robust analytical method for the separation of complex mixtures in a solid dosage form. A reversed HPLC column packed with an octadecyl-penta-fluorophenyl-silyl-bonded phase (C18-PFP) such as available from ACE (Advanced Chromatography Technologies, Ltd., Aberdeen, Scotland) proved to be particularly suitable due to its high functional group selectivity and its ability to separate positional and geometric isomers. The first design-of-experiments (DOE-1) involving the investigation of pH (2.7 to 7.0), and organic solvent composition (acetonitrile, THF and methanol) and concentration (0-100%) identified the optimum conditions for separation of vancomycin and impurities on a 10-cm long C18-PFP column.
Careful control of mobile-phase pH and solvent composition is important to the HPLC separation in the analysis of the impurities.
Factors to consider when developing a robust analytical method for separating complex mixtures include the following.
Because the compounds in the mixture may have multiple ionizable groups, the mobile phase pH needs to be controlled to provide a pH region that provides the best separation depending on the pKa values of the various ionizable groups.
Organic modifier solvent type and concentration controls selectivity (elution order) and overall retention time. There is a limited number of solvents to choose from because they should be miscible with water. Methanol, tetrahydrofuran (THF) and acetonitrile are preferred solvents in reversed phase HPLC.
Selecting the ideal combination of mobile phase pH and modifier is challenging. Commercial software packages are available but they are expensive and do not consider small differences in chemical structures of the drug and impurities. It is important to have knowledge of chromatographic theory, chromatographic practice and physical organic chemistry to develop methods for each separation problem, especially separations of very complex mixtures of structurally very similar compounds, some of which the structures of some compounds are known and structures of other compounds are unknown. Good separation of closely related impurities is necessary for sensitive, accurate and precise measurements.
The composition of the HPLC column also needs to be considered in combination with the mobile phase composition. For developing the methods described herein, we chose a PFP-C18 column because of the ability of the stationary phase to separate closely related compounds, especially isomers.
The mobile phases used in this invention comprise a combination of aqueous buffers and water-miscible organic solvents selected from alcohols, such as methanol (MeOH), ethanol, propanol, isopropanol, acetonitrile (MeCN), dioxane and tetrahydrofuran (THF).
Buffer solutions may include formic acid, providing a pH of about 2.7, sodium acetate/acetic acid mixture, providing a pH of about 4.5, and ammonium formate, providing a pH of about 7.0. Another aqueous system may comprise ammonium acetate. Mobile phases comprise mixtures of the buffer solutions and one or more of the organic solvents.
The mobile phases can be selected to provide baseline resolution of various impurities by modifying the amounts of buffer and organic solvents in each mobile phase. During the chromatographic separation, the mobile phase(s) may be run under isocratic conditions (constant mobile phase composition), gradient conditions (variable mobile phase composition) or a combination of both.
The precise control of pH is important for separating compounds with one or more ionizable groups (notably two or more), such as vancomycin, which could significantly alter their interaction with the column depending on their charged state. A pH buffer is either an aqueous mixture of a weak acid and its conjugate base or a mixture of a weak base and its conjugate acid. In this invention, two or more mobile phase compositions having different organic-solvent compositions and different pH values are used. This allows the solvent composition and the pH to be decoupled in the combined mobile phase. The different mobile phase compositions are mixed together by programming the HPLC pumps in order to change both the organic-solvent strength and the pH of the combined mobile phase flowing through the column. As a result, the pH of the combined mobile phase and the solvent strength depend on the ratio of the two (or more) mobile phase compositions at any point during the chromatographic run. In this invention the ratio of the weak acid and the conjugate base is changed during the gradient region of the separation. The pH of the combined mobile phase flowing through the column is determined by the pH of the first mobile phase composition and the pH of the second mobile phase composition. The rate of change of pH of the combined mobile phase is controllable because the pH is related to the pKa value of the buffer and the ratio of the concentrations of the two components in the buffer. Similarly, the solvent strength of the combined mobile phase also changes based on the ratio of the first mobile phase composition and the second mobile phase composition. However, solvent strength is an additive property, while pH is logarithmic. Even though the rate of change of the organic solvents by changing the ratio of the first and second mobile phase compositions may be linear, the rate of change of pH with time is non-linear due to the complex relationship between pH and the ratio of the two concentrations of the components in the buffer.
By proper selection of the pH and organic solvent components of the first and second mobile phase compositions, and their ratio during a chromatography run, the pH and solvent strength can be customized to provide effective separations of complex mixtures. For example, two mobile phases compositions used in this invention are acetate buffer systems wherein the pH of the first mobile phase component is kept around 3 to 5, preferably from about 3.9 to 4.5, or about 4.0 to about 4.3; and the pH of the second mobile phase component is kept around 3 to 10, preferably from about 6.0 to 9.5, or about 8.0 to 9.0, allowing one to modify the pH of the combined mobile phase by changing the ratio of the two mobile phases. The organic solvent strength (composition) is also different in the first and second compositions, so that the solvent strength of the combined mobile phase can be modified, but at a different rate than the pH. This invention provides a way to change multiple components of a mobile phase composition using only two mobile phase compositions.
Examples of using this technique are demonstrated by the following separations of vancomycin from associated impurities. In order to develop an improved separation method for vancomycin, we studied separations by varying factors including pH and solvent under gradient conditions, using a statistical design of experiments and two mobile phases containing an aqueous buffer (pH 2.7, 4.5 or 7.0) and one of three solvents: acetonitrile, methanol or tetrahydrofuran (THF). The column temperature, gradient shape and flow rate were held constant. An improved method was developed by a design of experiments (DOE-1) investigation in which we conducted six experiments in a two-thirds factorial design (six binary combinations of one solvent and one buffer). General chromatographic parameters for the first improved method for the vancomycin impurities studied in DOE-1 are summarized below.
Choice of solvent and pH also affected peak shape, retention times and retention-time order. Chromatography at pH of 2.7 exhibited peak tailing compared to separations at higher pH (
t
predicted
=f
MeOH
t
MeOH
+f
MeCN
t
MeCN
+f
THF
t
THF
where tMeOH, tMeCN, and tTHF are the retention times in the mobile phase containing buffer and one solvent and fMeOH, fMeCN and fMeOH, are the volume fractions of the solvents in mobile phase containing one, two or three solvents.
The dissociation constants of vancomycin and des-amido-isoaspartyl-vancomycin (CDP-1 Minor and CDP-1 Major) are assumed to have very similar pKa values and illustrate why the pH needs to be very carefully controlled. While vancomycin shows a plateau in net charge between about 3 and 6, des-amido-iso-aspartyl-vancomycin (CDP-1 Minor and CDP-1 Major) does not show a similar plateau due to its additional ionization site at about 4.5. The net charge of the two compounds intersects at a pH of about 3.6. This narrows considerably the range of pH where an effective separation can be achieved.
The first optimized analytical method utilizes reversed phase HPLC with an ACE Excel 2 C18-PFP column with the specific parameters shown in Table 4.
We also wished to develop a single method for the analysis of vancomycin impurities in both AeroVanc and in vancomycin hydrochloride drug substance, the active pharmaceutical ingredient (API) in AeroVanc. The previous method was acceptable for AeroVanc but was not acceptable for drugs substance analysis, which requires the analysis of all known and unknown impurities in vancomycin hydrochloride, including separation of several pairs of peaks not well separated by the original method developed for AeroVanc.
Preliminary studies indicated that a different approach was required. The same stationary phase (PFP C18) was used due to its ability to separate closely structures, but a longer 15-cm column was required to give greater separating power.
We chose to investigate a combination of pH gradient and solvent gradient. Ion-exchange chromatography commonly uses pH gradients. Solvent gradients are standard in reversed phase chromatography. A combined pH/solvent gradient is an unconventional approach in reversed phase chromatography. The combination of solvent gradient and pH gradient was achieved by mixing two different mobile phase compositions having different pH values and different solvent strengths to provide a combined mobile phase in which pH and solvent strength could be varied depending on the ratio of the two mobile phase compositions.
A second even more improved method was developed using a more complex DOE (DOE-2), exploring additional variabilities such as flow rate, gradient shape, and temperature. A second design of experiment (DOE-2), more extensive than the first DOE-1 used to develop the original method, examined the effects of acetonitrile, THF, buffer pH, column length, temperature and gradient profile on the separation. The second design of experiments (DOE-2) study suggested that isocratic (constant solvent strength) was required to separate peaks eluting before vancomycin and a gradient (increasing solvent strength) was required to separate peaks eluting after vancomycin. This dramatically increased the number of potential variables to be optimized. Additional studies indicated that a different buffer pH was required for the isocratic regions compared with the buffer pH in the gradient region, leading to a concomitant pH gradient and a solvent gradient as the overall strength of the mobile phase was increased.
These studies predicted an improved method could be obtained with an initial isocratic region (constant mobile phase conditions) to separate the early eluting peaks followed by a gradient region to separate the late eluting peaks. Initial experiments also showed a longer 15-cm column compared with the 10-cm column used previously was needed to separate all the peaks. The two regions of the chromatography were optimized separately, using an isocratic region for early peak resolution and a gradient region for peaks eluting after vancomycin.
The results in
As examples,
Both
The improved HPLC method was validated according the Q2(R1) guideline of the International Council on the Harmonization (ICH) of the Technical Requirements for Pharmaceuticals for Human Use (ICH Q2(R1)) and shown to be fit for the purpose.
The improved method can accurately and precisely measure the concentration of each impurity within the range 0.05% to 10.0% relative to vancomycin.
HPLC Instruments
The retention time of vancomycin and the impurities vary among instruments. Therefore, the gradient start times may be adjusted, within the ranges specified in the method, to achieve the required retention times and to meet the system suitability criteria. The start time of the first gradient (ST1) (Table 5) is defined in initial instrument set up-conditions. The gradient slopes of each region are constant defined by the value of ST2, ST3, ST4, ST5 and ST6 in Table 6.
HPLC Columns
The retention times of the vancomycin and the impurities can increase very gradually over time with repeated use for analysis of routine samples, and the selectivity of the column changes subtly over time as the column ages. The method is more flexible than the original method and conditions can be re-adjusted (Table 6 below) when using one column for a period of time or when a new column is used. The gradient, acetic acid concentration and sodium acetate concentration in the mobile phase can be adjusted to achieve the required retention times and to meet the system suitability criteria. Other factors related to the column itself can influence the separations. For example, changes in column manufacture may slightly change their composition, which can have a significant effect on separations.
Procedures
Reference Standards
Vancomycin HCl and its impurities are light sensitive and hygroscopic.
Reference standards are handled in a humidity chamber or controlled humidity room that has been purged with nitrogen or low relative humidity air prior to use and confirmed to have a relative humidity less than 10% (as measured with the Vaisala Hygrometer, or a similar device).
The water content of the vancomycin reference standard is re-measured by a separate technique each time the standard solutions are prepared.
All standard and sample solutions are prepared in Class A volumetric glassware, stored at 2-8° C. and protected from light by wrapping in aluminum foil. HPLC vials containing the solutions are protected from light by covering the HPLC vials with foil on the bench-top prior to transferring the vials to the autosampler.
Retention Time Markers
Vancomycin has 12 impurities that are known to be present in samples of vancomycin hydrochloride and in vancomycin hydrochloride inhalation powder and capsules, as well as a number of unidentified impurities.
Six of the 12 known impurities are potential degradation products of vancomycin:
Des-amido-isoaspartyl vancomycin (minor isomer, CDP-1 Minor) (EP Impurity B)
Des-amido-isoaspartyl vancomycin (major isomer, CDP-1 Major) (EP Impurity B)
Des-amido-succinimido vancomycin
Des-vancosamino vancomycin (EP Impurity D)
Epi-26(R) vancomycin
Agluco vancomycin (EP Impurity C)
The other six impurities arise from the drug substance:
Cis-chloro-(2) vancomycin
N-demethyl vancomycin (EP Impurity A)
Mono-dechloro-(2) vancomycin
De-(L-Asn)-L-Gln vancomycin
N-methyl vancomycin
Mono-dechloro-(6) vancomycin
Mono-dechloro-(6) vancomycin sometimes elutes as a pair of poorly resolved peaks in all the samples as well as in the reference standard of mono-dechloro-(6) vancomycin, suggesting the compound is a mixture of two compounds. The two peaks should be integrated together as one peak and reported as mono-dechloro-(6) vancomycin.
The peaks for vancomycin and five of the known impurities are located by the injection of reference standards as follows:
Des-amido-iso-aspartyl vancomycin (a mixture of CDP-1Minor and CDP-1Major in the approximate ratio of 3:7)
N-demethyl vancomycin
Des-vancosamino vancomycin
Agluco vancomycin
The expected retention times of the other known impurities are calculated from the known relative retention times as described below. Unidentified (unknown) impurities may be present in samples of vancomycin formulations. The retention times of the expected unidentified impurities are calculated from the retention times of the reference standards as described below.
General Procedures for chromatographic separations are described below.
Materials and Equipment
Equipment
Shimadzu HPLC System, or equivalent, comprising the following components or equivalents.
LC-20AD, binary HPLC pumps with 180 μL mixer
SIL-20AC, autosampler
CTO-20A, column heater
DGU-20A, inline degasser
SPD-20A, UV/Vis detector or SPD-M10A diode array detector
CBM-20A communications Bus Module
Computer or other suitable data collection system
ACE Excel 2 C18-PFP HPLC column (part number EXL-1010-1502U) having an internal diameter of 2.1 mm, length of 150 mm and particle size of 2 μm.
Analytical balance: AND HM-202 or equivalent
Sartorius ME5 Semi-micro analytical balance or equivalent
Top-loading Balance, Mettler Toledo PB4002-S or equivalent
Humidity chamber (Nitrogen Glove Box)
pH Meter, Fisher Scientific AR25 or equivalent
Refrigerator capable of maintaining temperature of 2-8° C.
Freezer capable of maintaining temperature of −20° C.
Vaisala hygrometer or other device capable of measuring relative humidity below 10%
Gilson positive displacement adjustable micropipets, MR-1000 and MR-250 or equivalent.
Class A volumetric flasks having volumes of 2, 5, 25 and 250 mL
Class A 5.0 mL volumetric pipets
Scintillation vials, clear glass, 20 mL
Pointed Glass Rod, EMD part number 1.09998 or equivalent
Chemicals and Reagents
Vancomycin hydrochloride API reference standard
Des-amido-isoaspartate vancomycin reference standard
Agluco vancomycin reference standard
N-demethyl vancomycin reference standard
Des-vancosamino vancomycin reference standard
Vancomycin hydrochloride inhalation bulk powder (AeroVanc Lot 195A01-NJ00011-S3)
Water, HPLC grade
Acetonitrile, HPLC grade
Tetrahydrofuran, 99.9+%, anhydrous, inhibitor-free
Sodium Acetate 3M Solution, BioUltra Grade (Sigma P/N 71196-100ML or equivalent)
Acetic Acid, Ampules to make 500 ml of 1 N Acetic Acid, (EMD Titrisol part number 1.09951.0001 or equivalent)
Sodium phosphate monobasic, monohydrate, HPLC Grade or equivalent
Phosphoric acid, 85%, ACS grade or equivalent
Solutions were prepared according to procedures described below. Quantities were scaled as needed to prepare different volumes of the solutions.
1N Acetic Acid Solution
Rinse a 500 ml volumetric flask well with water. Add approximately 250 ml of water to the flask. Pierce one ampoule of Titrisol acetic acid in the flask using a pointed glass rod and rinse out the ampoule contents and the rod with sufficient amounts of water to transfer the acid completely to the flask. Dilute the flask to volume with water and mix well. Store at room temperature and assign an expiration date of seven days from the date of preparation.
Buffer A: Sodium Acetate Buffer, pH 4.10
Rinse a 2 L volumetric flask well with water and add approximately 200 ml of water to the flask. Dry the outside of the flask completely and tare the flask on the top-loading balance. Add 150.00 g±0.05 g of 1 N Acetic Acid Solution to the flask. Record the weight of 1 N Acetic Acid Solution in grams to two decimal places. Calculate the target weight of 3 M sodium acetate solution in grams from the certificate of analysis using the following formula
Where:
Sodium Acetate Solution, 125 mM
Rinse a 1 L volumetric flask well with water and add approximately 200 ml of water to the flask. Dry the outside of the flask completely and tare the flask on the top-loading balance. Calculate the target weight of 3 M sodium acetate solution in grams from the certificate of analysis using the formula
Where:
Add the calculated target weight W±0.05 g of 3 M sodium acetate solution to the flask. Record the target weight and experimental weight of 3 M sodium acetate solution in grams to two decimal places. Dilute the solution to volume using water and mix well by inverting at least twenty times. Store at room temperature and assign an expiration date of 7 days from the date of preparation.
THF Stock Solution: THF/Buffer A, 1:4 (w/w), to Prepare 250 Milliliters
Rinse a 0.5 L mobile phase bottle well with water and drain completely. Dry the outside of the bottle well. Tare the 0.5 L mobile phase bottle on the top-loading balance. Add 200.00 g±0.05 g of Buffer A into the 0.5 L glass bottle. Tare the balance again and add 50.0 g±0.05 g THF into the 0.5 L glass bottle. Cap and mix the solution thoroughly using a stir-bar. Store at room temperature and assign an expiration date of 7 days from the date of preparation.
Mobile Phase A: THF/Buffer A/Acetonitrile 2.5/979.9/17.3 (w/w/w), to Prepare 1.8 Liters
Rinse a 2 L mobile phase bottle well with water and drain completely. Dry the outside of the bottle well. Tare the 2 L mobile phase bottle on the top-loading balance. Add 1745.64 g±0.05 g of Buffer A into the 2 L glass bottle. Tare the balance again and add 22.68 g±0.05 g THF Stock Solution into the 2 L glass bottle. Tare the balance again and measure 31.24±0.05 g acetonitrile into the 2 L glass bottle. Cap and mix the solution thoroughly using a magnetic stir-bar. Store at room temperature and assign an expiration date of 7 days from the date of preparation.
Mobile Phase B: THF/125 mM Sodium Acetate/Acetonitrile 19.0/820.5/120.7 (w/w/w), to Prepare 2 Liters
Rinse a 1 L mobile phase bottle well with water and drain completely. Dry the outside of the bottle well. Tare the 1 L mobile phase bottle on the top-loading balance. Add 820.50 g±0.05 g of 125 mM Sodium Acetate Solution into the 1 L glass bottle. Tare the balance again and add 19.00 g±0.05 g THF into the 1-liter glass bottle. Tare the balance again and add 120.70±0.05 g acetonitrile into the 1 L glass bottle. Cap and mix the solution thoroughly using a magnetic stir-bar. Store at room temperature and assign an expiration date of 7 days from the date of preparation.
Weigh 3.45 g of sodium phosphate, monobasic, monohydrate and add to the 1 L glass bottle. Add 1000 mL water to the 1 L glass bottle. Stir until dissolved. Adjust the pH of the solution to 3.2 using 85% phosphoric acid while stirring. Store at room temperature and assign an expiration date of 30 days from the date of preparation.
Measure 250 ml Diluent 1 into a 500 mL glass bottle. Measure 250 ml acetonitrile and add to the 500 mL glass bottle. Mix thoroughly. Store at room temperature and assign an expiration date of 30 days from the date of preparation.
The nominal concentration of standard solution is approximately 90 μg/mL without correction for water and purity. Quantities may be scaled as appropriate to prepare different volumes of the solutions.
Determine the water content of the vancomycin HCl reference standard by Karl-Fisher titration and record the value. Obtain two moisture values, one before weighing the standards and one after weighing the standards. Use the mean value of the moisture value in the calculations. Accurately weigh approximately 22.50±1.00 mg of vancomycin HCl reference material and record the weight in mg to two decimal places. Transfer to a 250 mL volumetric flask with aid of Diluent 1. Dissolve and adjust to 250 mL with Diluent 1. Mix well and label as Standard A.
Prepare a second standard solution by weighing approximately 22.50±1.00 mg of vancomycin HCl reference material and recording the weight in mg to two decimal places. Transfer to a 250 mL volumetric flask with aid of Diluent 1. Dissolve and adjust to 250 mL with Diluent 1. Label the second standard solution as Standard B. Store both solutions at 2-8° C., protect from light and assign an expiration date of 14 days from the date of preparation.
Des-Amido-Isoaspartate Vancomycin (approximately 500 μg/mL)
Accurately weigh 1.000 to 1.200 mg des-amido-isoaspartate vancomycin using the microbalance. Record the weight in mg to three decimal places. Transfer to a 2 mL volumetric flask, with the aid of Diluent 2. Mix thoroughly until dissolved. Adjust the volume to 2 mL with Diluent 2. Mix thoroughly. Store at −20° C. until needed.
N-Demethyl Vancomycin (Approximately 500 μg/mL)
Accurately weigh 1.000 to 1.200 mg N-demethyl vancomycin using the microbalance. Record the weight in mg to three decimal places. Transfer to a 2 mL volumetric flask, with the aid Diluent 1. Mix thoroughly until dissolved. Adjust the volume to 2 mL with Diluent 1. Mix thoroughly. Store at −20° C. until needed.
Des-Vancosamino Vancomycin (Approximately 500 μg/mL)
Accurately weigh 1.000 to 1.200 mg desvancosamino-vancomycin using the microbalance. Record the weight in mg to three decimal places. Transfer to a 2 mL volumetric flask, with the aid of Diluent 2. Mix thoroughly until dissolved. Adjust the volume to 2 mL with Diluent 2. Mix thoroughly. Store at −20° C. until needed.
Agluco Vancomycin (Approximately 500 μg/mL)
Accurately weigh 1.000 to 1.200 mg agluco vancomycin using the microbalance. Record the weight in mg to three decimal places. Transfer to a 2 mL volumetric flask, with the aid of Diluent 2. Mix thoroughly until dissolved. Adjust the volume to 2 mL with Diluent 2. Mix thoroughly. Store at −20° C. until needed.
Prepare the Impurity Marker Solution containing the following mixture:
Des-amido-isoaspartate vancomycin approximately 45 μg/mL (total CDP-1Minor+CDP-1Major), Agluco vancomycin approximately 45 μg/mL, Des-vancosamino vancomycin approximately 45 μg/mL, N-demethyl vancomycin approximately 45 μg/mL, Vancomycin approximately 900 μg/ml.
Accurately weigh 4.500±0.500 mg vancomycin HCl reference standard on the microbalance. Transfer to a 5 mL volumetric flask with the aid of Diluent 1. Mix thoroughly until dissolved. Pipet 450 μL des-amido-isoaspartate vancomycin, approximately 500 μg/mL, into the 5 mL volumetric flask. Pipet 450 μL N-demethyl vancomycin, approximately 500 μg/mL into the 5 mL volumetric flask. Pipet 450 μL des-vancosamino vancomycin approximately 500 μg/mL into the 5 mL volumetric flask. Pipet 450 μL agluco vancomycin approximately 500 μg/mL into the 5 mL volumetric flask.
Prepare the QL Check Solution containing approximately 0.45 μg/mL CDP-1Major (approximately 0.05% level relative to Vancomycin in impurities sample preparations). Pipet 128 μL des-amido-isoaspartate vancomycin 500 μg/mL into a 100 mL volumetric flask. Adjust to 100 mL with Diluent 1 and mix well. Protect from light by wrapping the flask in aluminum foil. Transfer an aliquot of approximately 100 μL of the solution to an HPLC vial for HPLC analysis. The remaining solution may be divided into approximately 500 μL aliquots and stored at −20° C. for future use.
Accurately weigh approximately 25.00±1.00 mg of SA-182-003-14-068 vancomycin hydrochloride inhalation bulk powder for system suitability. Quantitatively transfer to a 25 mL volumetric flask using Diluent 1. Adjust to 25 mL with Diluent 1. Mix thoroughly and label System Suitability Solution. Protect from light by wrapping the flask in aluminum foil. Transfer an aliquot of approximately 100 μL of the solution to an HPLC vial insert in an HPLC vial for HPLC analysis.
The remaining solution may be divided into approximately 100 μL portions and stored at −20° C. for future use.
Impurities: Vancomycin Hydrochloride API (approximately 900 μg/mL)
Accurately weigh 22.50±1.00 mg of vancomycin hydrochloride API. Record the weight in mg to two decimal places. Quantitatively transfer to a 25 mL volumetric flask using Diluent 1. Adjust to 25 mL with Diluent 1. Mix thoroughly and label API 1A. Prepare two additional sample solutions and label API 2A and API 3A.
Pipet 5.0 mL of API 1A to a 50 mL volumetric flask, add approximately 15 mL Diluent 1, mix thoroughly, adjust to volume, mix thoroughly and label API 1B. Prepare two additional sample solutions from the API 2A and API 3A and label API 2B and API 3B, respectively.
Protect from light by wrapping the flasks in aluminum foil. Transfer aliquots of each sample preparation to separate HPLC vials. Store the flasks at 2-8° C., protect from light and assign an expiration date of 7 days from the date of preparation.
Impurities: Vancomycin hydrochloride inhalation powder (powder from bulk or from capsules, approximately 900 μg/mL)
For bulk powder, accurately weigh 25.00±1.00 mg of vancomycin hydrochloride inhalation powder from the bulk powder container. For powder from capsules, open 4 capsules and transfer the powder to a 20 mL scintillation vial. Weigh 25.00±1.00 mg of vancomycin hydrochloride inhalation powder from the scintillation vial. Record the weight in mg to two decimal places. Quantitatively transfer into a 25-mL volumetric flask using Diluent 1. Add approximately 15 mL Diluent 1, mix thoroughly until dissolved, adjust to volume with Diluent 1, mix thoroughly and label Powder 1A (or Capsule 1A). Prepare two additional sample solutions and label Powder 2A (or Capsule 2A) and Powder 3A (or Capsule 3A).
Pipet 5.0 mL from Powder 1A (or Capsule 1A) into a 50 mL volumetric flask. Dilute to 50 mL with Diluent 1, mix thoroughly, and label Powder 1B (or Capsule 1B). Prepare two additional solutions from Powder 2A (or Capsule 2A) and Powder 3A (or Capsule 2A) and label Powder 2B (or Capsule 2B) and Powder 3B (or Capsule 3B), respectively. Protect from light by wrapping the flasks in aluminum foil. Transfer aliquots of each sample solution to separate HPLC vials. Store the flasks at 2-8° C. and assign an expiration date of 7 days from the date of preparation.
Before running samples, equilibrate the column and establish the correct instrument settings and the correct compositions of Mobile Phase A and Mobile Phase B as follows.
Install the column onto the HPLC instrument and set the column oven to 40° C. Flush the column with 97% Mobile Phase B (Section 5.1.6) at 0.2 mL/min for at least 20 minutes but not more than 30 minutes, allowing the column to come to temperature during this time. Flush the column with 100% Mobile Phase A at 0.4 mL/min for at least 10 minutes but not more than 30 minutes.
Before running samples establish the correct gradient profile as follows:
Set up the instrument with the initial setting shown in Table 5.
Inject the QL Check Solution and run the gradient with the gradient start times shown in Table 5 with a start time for the first gradient (ST1) of 44 minutes.
Inject Standard Solution A and run the gradient with a start time for first gradient (ST1) of 44 minutes and the other gradient start times as shown in Table 5.
Compare the chromatograms obtained with reference chromatograms.
Adjust the gradient start times (ST1 to ST6) in appropriate increments, keeping the difference between each start time the same as shown in Table 5 and re-inject the QL Check Solution and the Standard Solution A.
Compare the chromatograms obtained with the reference chromatograms and repeat until the separation between vancomycin and the gradient-related peak shown in the reference chromatogram is obtained.
Once a gradient start time for a particular column-instrument combination has been established, the conditions may be used as a starting point for future HPLC analyses using that particular column-instrument combination.
Before running samples establish the correct compositions of Mobile Phase A and Mobile Phase B as follows:
Starting with the compositions of Mobile Phase A and Mobile Phase B and the gradient profile established above, make one injection of the Impurities Marker Solution and one injection of the System Suitability Solution.
Calculate the resolution factor (R2,1) for the following pairs of peaks in the System Suitability Solution, using the procedures outlined below as guide to the identifying the peaks in the System Suitability solution and using the following equation. If the electronic integrator is unable to measure the widths at half height of the two peaks, use the tangent-extrapolated width at half height for the larger of the two peaks for both w1 and w2.
a. CDP-1Major/vancomycin
b. Unknown Impurity 9/des-amido-succinimido-vancomycin
c. Des-amido-succinimido-vancomycin/unknown Impurity 10
d. Des-vancosamino-vancomycin/unknown impurity 22
where:
The mean value for the separation of CDP-1Major and vancomycin should be not less than 1.5. The mean value for the separation of unknown impurity 9 and des-amido-succinimido-vancomycin should be not less than 0.6. The mean value for the separation of des-amido-succinimido-vancomycin and impurity 10 should be not less than 0.6. The mean value for the separation of des-vancosamino-vancomycin and unknown impurity 22 should be not less than 0.8. If all the acceptance criteria are met, analysis can proceed.
If one or more of the acceptance criteria are not satisfied, adjust the pH of Mobile Phase A and/or Mobile Phase B.
It may be necessary to adjust the pH of Mobile Phase A by adjusting the concentration of acetic acid in Mobile Phase A in an iterative fashion until all the acceptance criteria are satisfied. For each iteration, a fresh Buffer A solution should be made and the THF Stock Solution and Mobile Phase A should be prepared from this fresh Buffer A.
If the R2,1 value of CDP-1Major and vancomycin is less than 1.5 increase the pH of Mobile Phase A by decreasing the concentration of acetic acid in Buffer A solution using Table 7 as a guide, up to a maximum of pH 4.15. If the value of unknown impurity 9 and des-amido-succinimido-vancomycin is less than 0.6 decrease the pH of Mobile Phase A by increasing the concentration of acetic acid in Buffer A, using Table 10 as a guide, down to a minimum of 4.05. If the value of R2,1 for the separation of des-amido-succimido-vancomycin and unknown 10 is less than 0.6 increase the pH of Mobile Phase A by decreasing the concentration of acetic acid in Buffer A, using Table 10 as a guide, up to a maximum of 4.15.
If value of R2,1 for the separation of des-vancosamino-vancomycin and unknown 12 is less than 0.8 increase the pH of Mobile Phase B by increasing the concentration of sodium acetate solution used in the preparation of mobile phase B up to a maximum of 150 mM.
Repeat calibration steps, if necessary, until the acceptance criteria of the resolution factors are satisfied. If attempts to satisfy the acceptance criteria are unsuccessful, the column should be replaced. It may be necessary to adjust the compositions of both Mobile Phase A and Mobile Phase B in an iterative fashion until the resolution factors are achieved. If mobile phase composition is adjusted, the gradient start time should be re-evaluated as above to verify the gradient is still acceptable.
Once a mobile phase composition for a particular column-instrument combination has been established, the composition may be used as a starting point for future HPLC instrument setup evaluations using that particular column-instrument combination.
Sample Analysis
Analysis Sequence
Using the instrument settings and mobile phase compositions established above, inject the standards and samples according to the injection sequence in Table 8.
System Suitability
Standard Precision
Calculate the mean and the percent relative standard deviation (% RSD) of the peak areas of the vancomycin peak in Standard A. The % RSD (n=6) of the vancomycin peak in Standard A initial injections of Standard A must be no more than 1.0% to accept the results.
The check standard agreement between Standard A and Standard B must be 100.0%±2.0% to accept the results. Bracketing Standard Agreement: The bracketing standard agreement between the six initial Standard A injections and each Standard A bracketing standard injection after sample injections must 100.0%±2.0% to accept the results.
Calculate the mean (n=2) resolution factor (R2,1) for the following pairs of peaks in the System Suitability Solution, using the equation above. The mean value for R2,1 for the separation of CDP-1Major and vancomycin should be not less than 1.5 to accept the results. The mean value for R2,1 for the separation of unknown impurity 9 and des-amido-succinimido-vancomycin should be not less than 0.6 to accept the results. The mean value for R2,1 for the separation of des-amido-succinimido-vancomycin and impurity 10 should be not less than 0.6 to accept the results. The mean value for R2,1 for the separation of des-vancosamino-vancomycin and unknown impurity 22 should be not less than 0.8 to accept the results. If all the System Suitability Criteria are satisfied, calculate the S/N ratio as described below. If one or more of the System Suitability Criteria are not satisfied, adjust the composition of Mobile Phase A or Mobile Phase B as described above.
Calculate the signal-to-noise ratio (S/N) of CDP-1Major in the QL Check Solution (Table 11). The S/N should be not less than 5 to accept the results.
Calculate the USP <621> Tailing Factor of the vancomycin peak in the first injection of Standard A. The USP Tailing Factor of the vancomycin peak Standard A should be between 0.85 and 1.15 to accept the results.
The elution order of the six peaks in the Impurities Marker Solution is given in Table 9.
Identify vancomycin and the five impurities in the Impurities Marker Solution using the elution order in Table 9. Use the average RT of impurities in the Impurities Marker Solution Injections and the example chromatograms as a guide to identifying known impurities in Table 10 if present in sample chromatograms.
Retention times of impurities in the Impurities Marker Solution are used to predict retention times and identify the other known impurities not included in the Impurities Marker Solution as well as unknown impurities as described below.
Except where indicated, compare the retention time of the peaks eluting before vancomycin with the expected retention times calculated using the relative retention times (RRTs) in Table 11 and the following equation:
RT(Predicted)=RT(NDMV)×RRT
Where:
Except where indicated, compare the retention time of the peaks eluting after vancomycin with the expected retention times calculated using the relative retention times (RRTs) in Table 11 and the following equation:
RT(Predicted)=RT(DVA)×RRT
Where:
Calculations
The calculated values are left un-rounded when used in subsequent calculations and calculations of averages, standard deviations, etc. to avoid the impact of multiple intermediate rounding steps on the final results.
Concentration of Standard A and Standard B Solution Preparation (Cws)
Calculate the concentration of vancomycin in Standard A and Standard B, as follows:
Where:
Report the concentration of Vancomycin in Standard A and Standard B in μg/mL to 2 decimal places.
Impurity Concentration
Calculate the concentration of each individual impurities in the samples solutions 1A, 1B and 1C, as follows:
Where:
Calculate the total concentration of all the impurities in sample solutions 1A, 2A and 3A as follows (include only those impurities present at concentrations equal to or greater (≥) 0.45 μg/mL):
Where:
Report the total impurity concentration (μg/mL) in impurity solutions 1A, 2A and 3A to three decimal places in the project notebook.
Concentration of Vancomycin in the Samples
Calculate the concentration of vancomycin the samples 1B, 2B and 3B as follows:
Where:
Concentration of Each Individual Impurity in the Sample (Impurity %)
Calculate the concentration of each individual impurity in samples 1A, 2A and 3A, as follows:
Where:
Calculate the average concentration as a percentage of each individual impurity in the sample (vancomycin hydrochloride, API, vancomycin hydrochloride inhalation powder or capsules).
Total Concentration of Individual Impurities in the Sample
Calculate the total concentration of the impurities in the samples, as follows.
Where:
Include only the reportable impurities in the calculation of total reportable impurities.
Data Reporting
Impurities in Vancomycin Hydrochloride, API
Report the impurities having concentration that exceed the Reporting Threshold of 0.05%. Therefore, report all values equal to or greater than 0.06%. Report all values equal to or less that the reporting threshold as “≤0.05%”. For impurities below 1.0%, report value to two decimal places (e.g. 0.06%, 0.13%). At or above 1.0% report values to one decimal place (e.g. 1.0%, 1.3%).
Impurities Vancomycin Hydrochloride in Vancomycin Hydrochloride Inhalation Powder and Capsules
Report the impurities having concentration that exceed the Reporting Threshold of 0.05% in samples of vancomycin drug substance and greater than 0.1% in samples of AeroVanc.
The method disclosed herein was successfully applied to the determination of degradation products of vancomycin in the solution and solid states.
The method disclosed herein was also applied to the determination of degradation products of AeroVanc vancomycin powder stored for three months at 5° C. and 25° C.
This application claims the benefit of U.S. Provisional Application No. 62/745,772, filed Oct. 15, 2018, the contents of which are hereby incorporated by reference in its entirety.
| Number | Date | Country | |
|---|---|---|---|
| 62745772 | Oct 2018 | US |
