AN ISOLATED VALACYCLOVIR IMPURITY, PROCESS FOR THE
PREPARATION OF VALACYCLQVIR IMPURITY AND USE AS A
REFERENCE STANDARD
CROSS-REFERENCE TO RELATED APPLICATIONS
This application claims the benefit of provisional application Serial
Number 60/607,279, filed September 3,2004, which is incorporated herein by reference.
FIELD OF THE INVENTION
The present invention relates to an isolated impurity of valacyclovir; N-formyl
valacyclovir, its preparation and its use as a reference standard.
BACKGROUND OF THE INVENTION
Valacyclovir is an L-valyl ester prodrug of acyclovir. Acyclovir is an acyclic
analog of a natural nucleoside which has been found to have high anti-viral activity.
Acyclovir is widely used in the treatment and prophylaxis of viral infections in humans,
particularly infections caused by the herpes group of viruses. See Goodman and Oilman's,
The Pharmacological Basis of Therapeutics 1193-1198 (9th ed. 1996).
Valacyclovir has the chemical name 1-valine, 2-[(2-amino-l,6-dihydro-6-oxo
-9H-purin-9-yl)methoxy]ethyl ester. (CAS Registry No. 124832-26-4.) Valacyclovir is
currently marketed as VALTREX®. The chemical structure of valacyclovir is shown as
Structure I.
Structure I
It is well known in the art that, for human administration, safety considerations
require the establishment, by national and international regulatory authorities, of very low
limits for identified, but toxicologically uncharacterized impurities, before an active
pharmaceutical ingredient (API) product is commercialized. Typically, these limits are
less than about 0.15 percent by weight of each impurity. Limits for unidentified and/or
uncharacterized impurities are obviously lower, typically, less than 0.1 percent by weight.
Therefore, in the manufacture of APIs, the purity of the products, such as valacyclovir, is
required before commercialization, as is the purity of the active agent in the manufacture
of formulated pharmaceuticals.
It is also known in.the art that impurities in an API may arise from degradation of
the API itself, which is related to the stability of the pure API during storage, and the
manufacturing process, including the chemical synthesis. Process impurities include
unreacted starting materials, chemical derivatives of impurities contained in starting
materials, synthetic by-products, and degradation products.
In addition to stability, which is a factor in the shelf life of the API, the purity of
the API produced.in the commercial manufacturing process is clearly a necessary
condition for commercialization. Impurities introduced during commercial
manufacturing processes must be limited to very small amounts, and are preferably
substantially absent. For example, the ICH Q7A guidance for API manufacturers requires
that process impurities be maintained below set limits by specifying the quality of raw
materials, controlling process parameters, such as temperature, pressure, time, and
stoichiometric ratios, and including purification steps, such as crystallization, distillation,
and liquid-liquid extraction, in the manufacturing process.
The product mixture of a chemical reaction is rarely a single compound with
sufficient purity to comply with pharmaceutical standards. Side products and by-products
of the reaction and adjunct reagents used hi the reaction will, in most cases, also be
present in the product mixture. At certain stages during processing of an API, such as
Valacyclovir, it must be analyzed for purity, typically, by HPLC or TLC analysis, to
determine if it is suitable for continued processing and, ultimately, for use in a
pharmaceutical product. The API need not be absolutely pure, as absolute purity is a
theoretical ideal that is typically unattainable. Rather, purity standards are set with the
intention of ensuring that an API is as free of impurities as possible, and, thus, is as safe
as possible for clinical use. As discussed above, in the United States, the Food and Drug
Administration guidelines recommend that the amounts of some impurities be limited to
less than 0.1 percent.
Generally, side products, by-products, and adjunct reagents (collectively
"impurities") are identified spectroscopically and/or with another physical method, and
then associated with a peak position, such as that in a chromatogram, or a spot on a TLC
plate. (Strobel p. 953, Strobel, H.A.; Heineman, W.R., Chemical Instrumentation: A
Systematic Approach, 3rd dd. (Wiley & Sons: New York 1989)). Thereafter, the
impurity can be identified, e.g., by its relative position in the chromatogram, where the
position in a chromatogram is conventionally measured in minutes between injection of
the sample on the column and elution of the particular component through the detector.
The relative position in the chromatogram is known as the "retention time."
The retention tune can vary about a mean value based upon the condition of the
instrumentation, as well as many other factors. To mitigate the effects such variations
have upon accurate identification of an impurity, practitioners use the "relative retention
time" ("RRT") to identify impurities. (Strobel p. 922). The RRT of an impurity is its
retention time divided by the retention time of a reference marker. It may be
advantageous to select a compound other than the API that is added to, or present in, the
mixture in an amount sufficiently large to be detectable and sufficiently low as not to
saturate the column, and to use that compound as the reference marker for determination
of the RRT.
Those skilled in the art of drug manufacturing research and development
understand that a compound in a relatively pure state can be used as a "reference
standard." A reference standard is similar to a reference marker, which is used for
qualitative analysis only, but is used to quantify the amount of the compound of the
reference standard in an unknown mixture, as well. A reference standard is an "external
standard," when a solution of a known concentration of the reference standard and an
unknown mixture are analyzed using the same technique. (Strobel p. 924, Snyder p. 549,
Snyder, L.R.; Kirkland, JJ. Introduction to Modern Liquid Chromatography, 2nd ed.
(John Wiley & Sons: New York 1979)). The amount of the compound in the mixture can
be determined by comparing the magnitude of the detector response. See also U.S. Patent
No. 6,333,198, incorporated herein by reference.
The reference standard can also be used to quantify the amount of another
compound in the mixture if a "response factor," which compensates for differences in the
sensitivity of the detector to the two compounds, has been predetermined. (Strobel p.
894). For this purpose, the reference standard is added directly to the mixture, and is
known as an "internal standard." (Strobel p. 925, Snyder p. 552).
The reference standard can serve as an internal standard when, without the
deliberate addition of the reference standard, an unknown mixture contains a detectable
amount of the reference standard compound using the technique known as "standard
addition."
In a the "standard addition technique", at least two samples are prepared by
adding known and differing amounts of the internal standard. (Strobel pp. 391-393,
Snyder pp. 571, 572). The proportion of the detector response due to the reference
standard present in the mixture without the addition can be determined by plotting the
detector response against the amount of the reference standard added to each of the
samples, and extrapolating the plot to zero concentration of the reference standard. (See,
e.g., Strobel, Fig. 11.4 p. 392).
As is known by those skilled in the art, the management of process impurities is
greatly enhanced by understanding their chemical structures and synthetic pathways, and
by identifying the parameters that influence the amount of impurities in the final product.
Like any synthetic compound, valacyclovir can contain extraneous compounds or
impurities that can come from many sources. They can be unreacted starting materials,
by-products of the reaction, products of side reactions, or degradation products.
In this application the reference marker is the impurity N-formyl valacyclovir in
the API. Detection or quantification of the reference marker serves to establish the level
of purity of the API. Use of a compound as a reference marker requires recourse to a
sample of substantially pure compound.
SUMMARY OF THE INVENTION
In one aspect, the present invention relates to an isolated N-fonnyl valacyclovir.
In a further aspect, the present invention relates to a method of making N-formyl
valacyclovir including the steps of reacting valacyclovir and ammonium formate to obtain
a reaction mixture, combining the reaction mixture with hot water, heating the
combination of reaction mixture and hot water, and cooling the combination to obtain a
precipitate of N-formyl valacyclovir.
In a further aspect, the present invention relates to the use of N-formyl
valacyclovir as a reference marker in a qualitative analysis of valacyclovir.
In another embodiment, the invention is directed to a method of using N-formyl
valacyclovir as reference standard to analytically quantify the purity of valacyclovir.
In yet a further aspect, the invention is directed to a method for the quantification
of the purity of valacyclovir, comprising the use of N-formyl valacyclovir as reference
standard, where the reference standard may be either external standard or internal
standard.
BRIEF DESCRIPTION OF THE FIGURES
Figure 1 is a representative HPLC chromatogram from an analysis of a standard
solution of N-formyl valacyclovir.
Figure 2 is a representative HPLC chromatogram of a marker solution of Nformyl
valacyclovir.
Figure 3 is a representative HPLC chromatogram of valacyclovir sample
containing N-formyl valacyclovir.
DETAILED DESCRIPTION OF THE INVENTION
As used herein, the term "isolated" refers to a compound that is at least 90 area-%,
as judged by HPLC.
A "reference marker" is used in qualitative analysis to identify components of a
mixture based upon their position, e.g., in a chromatogram or on a Thin Layer
Chromatography (TLC) plate (Strobel pp.- 921,922, 953). For this purpose, the
compound does not necessarily have to be added to the mixture if it is present in the
mixture. A "reference marker" is used only for qualitative analysis, while a reference
standard may be used for quantitative or qualitative analysis, or both. Hence, a reference
marker is a subset of a reference standard, and is included within the definition of a
reference standard.
As used herein, the term "reference standard" refers to a compound that may be
used both for quantitative and qualitative analysis of an active pharmaceutical ingredient.
For example, the HPLC retention time of the compound allows a relative retention tune to
be determined, thus making qualitative analysis possible. The concentration of the
compound in solution before injection into an HPLC (or GC) column allows the areas
under the HPLC (or GC) peaks to be compared, thus making quantitative analysis
possible.
Reference standards are described in general terms above. However, as will be
understood by those skilled in the art, a detector response can be, for example, the peak
heights or integrated peak areas of a chromatogram obtained, e.g., by UV or refractive
index detection, from the eluent of an HPLC system or, e.g., flame ionization detection
(FID) or thermal conductivity detection, from the eluent of a gas chromatograph, or other
detector response, e.g., the UV absorbance of spots on a fluorescent TLC plate. The
position of the reference standard may be used to calculate the relative retention time for
valacyclovir and impurities of valacyclovir.
In one embodiment the present invention provides N-fonnyl valacyclovir, an
impurity of valacyclovir that is isolated from valacyclovir and, in preferred embodiments,
substantially free of valacyclovir. In another embodiment, the present invention provides
a method for the preparation of N-fonnyl valacyclovir. In a further embodiment, the
present invention relates to the use of N-formyl valacyclovir as a reference marker in a
qualitative analysis of valacyclovir. In another embodiment, the invention is directed to a
method of using N-formyl valacyclovir as reference standard to analytically quantify the
purity of valacyclovir. In yet a further aspect, the invention is directed to a method for
the quantification of the purity of valacyclovir, comprising the use of N-formyl
valacyclovir as reference standard, where the reference standard may be either external
standard or internal standard.
N-formyl valacyclovir, although mentioned in the NDA for valacyclovir
(Valtrex®), has never been obtained in substantially pure form, isolated from (that is
separate and apart from) valacyclovir. To the best of Applicants' knowledge, the structure
of N-formyl valacyclovir has never been discovered before (the location of N-formyl
group being unknown).
N-formyl valacyclovir can form during the synthesis of valacyclovir or upon
storage, especially if the valacyclovir contains residual process solvents.
The present invention provides an isolated valacyclovir impurity, N-formyl
valacyclovir, having the structure (IT). To the best of Applicants' knowledge, the structure
of N-formyl valacyclovir has never been reported and the compound has never been
possessed separate and apart from valacyclovir.
Preferably, the isolated N-formylvalacyclovir comprises from about 0.03 area-%
to 5 area-% valacyclovir as judged by HPLC.
More preferably, the isolated N-formyl valacyclovir comprises about 0.03 area-%
to about 2 area-% valacyclovir or the isolated N-formyl valacyclovir is at least 95 area-%
pure as judged by HPLC.
In a further embodiment, the present invention provides a method of making
isolated N-formyl valacyclovir comprising the steps of: reacting valacyclovir with
ammonium formate, heating the reaction mixture, combining the resulting hot reaction
mixture with hot water, further heating the reaction mixture, cooling the reaction mixture
and recovering the N-formyl valacyclovir. Optionally, a solvent is added to the reaction
mixture. Preferably, the reaction mixture is obtained in the absence of a solvent.
Preferably, the reaction time is of about 1 to about 10 hours. More preferably, the reaction
time is of about 2 to about 4 hours. Preferably, the reaction mixture of valacyclovir with
ammonium formate is heated to a temperature of about 125°C to about 145°C. Preferably,
the hot water are at a temperature of about 100°C. Preferably, the resulting combination
of the reaction mixture with hot water is filtered while hot. Preferably, the reaction
mixture is cooled to room temperature. The N-formyl valacyclovir can be recovered
(isolated) by any means known in the art, for example filtration (gravity or suction) or
centrifugation, to mention just two.
Prefaerbly, N-formyl valacyclovir is recrystallized. More preferably N-formyl
valacyclovir is recrystallized from water, to obtain isolated N-formyl valacyclovir.
Manufacturing lot release criteria can be established with reference to a
particular amount or concentration of a reference standard in the bulk product. Detection
and quantification of the reference standard in the API of a pharmaceutical dosage form
can serve as a measure of the shelf-life of the pharmaceutical dosage form. That is,
detection of the reference standard at some concentration signals that the API has begun
to deteriorate and that efficacy of the API may be compromised. As used herein, HPLC
refers to the well-known technique of high-performance liquid chromatography, also
referred to as high pressure liquid chromatography. HPLC can be applied to detection
and quantification of components of a mixture, for example detection and quantification
of impurities in a principal compound such as an active pharmaceutical ingredient (API).
Detection and especially quantification of components of a mixture can be
accomplished with the use of response factors. The response of a detector in HPLC (e.g.
UV detectors or refractive index detectors) can be and typically is different for each
compound eluting from the HPLC column. Response factors, as known, account for this
difference in the response signal of the detector to different compounds eluting from the
column.
The present invention provides various methods involving the use of N-formyl
valacyclovir as reference marker or reference standard.
Provided is a method of identifying N-formyl valacyclovir in a sample of
valacyclovir comprising:
(a) providing a reference sample comprising a reference marker and valacyclovir;
(b) carrying out HPLC or TLC on the reference sample to determine the relative
retention time of the reference marker compared to valacyclovir;
(c) carrying out HPLC or TLC on the sample of valacyclovir to determine the relative
retention time of the N-formyl valacyclovir compared to valacyclovir;
(d) comparing the relative retention times determined in steps (b) and (c);
where, if the relative retention tunes determined in steps (b) and (c) are substantially the
same, the N-formyl valacyclovir is identified as being the same as the reference marker.
Also provided is a method of determining the amount of an impurity in a sample
of valacyclovir comprising:
(a) adding a known amount of a reference standard to the valacyclovir sample;
(b) subjecting the valacyclovir to HPLC;
8
(c) identifying and measuring the area of an HPLC peak associated with the N-formyl
valacyclovir;
(d) identifying and measuring the area of an HPLC peak associated with the reference
standard;
(e) calculating the amount of the impurity in the valacyclovir sample based on the
results of steps (c) and (d);
where the reference standard is N-formyl valacyclovir.
Also provided is a method of determining the amount of N-formyl valacyclovir in
a sample of valacyclovir comprising:
(a) providing a sample of valacyclovir containing an unknown concentration of the Nformyl
valacyclovir;
(b) providing a sample of a known concentration of the N-formyl valacyclovir;
(c) subjecting a portion of the sample of valacyclovir and a portion of the sample of
the N-formyl valacyclovir to HPLC;
(d) measuring the area of the N-formyl valacyclovir peaks obtained from the sample
of valacyclovir and from the sample of the N-formyl valacyclovir; and
(e) calculating the concentration of the N-formyl valacyclovir in the sample of
valacyclovir from the measurements of step (d).
Also provided is a method of determining the amount of N-formyl valacyclovir in a
sample of valacyclovir comprising:
(a) providing a first reference solution of known concentration of substantially pure
valacyclovir,
(b) providing a second reference solution of known concentration of substantially
pure N-formyl valacyclovir of known concentration;
(c) subjecting an aliquot of each of the first and second reference solutions to HPLC
analysis and detennining the response factors of valacyclovir and N-formyl
valacyclovir;
(d) providing a solution of known overall concentration of the valacyclovir;
(e) subjecting the solution to HPLC analysis under substantially the same conditions
used in step (c); and
(t) calculating the amount of N-ibrmyl valacyclovir in the solution using the
respective peak areas and the response factors.
The response factor is calculate as follows: If Y is the primary or principal
component, the relative response factor of compound X, i.e. an impurity in Y and
especially a reference marker for the purity of Y, can be expressed as:
Ry/x=[Mx/MY]/[Ax/AY]
where MX and My are the known molar amounts or concentrations of X and Y in a
standard solution (a solution having known amount of X and Y) and AX and Ay are the
detector responses, for example peak areas in HPLC, for species X and Y, respectively.
Then, in a solution having a known total amount of sample but unknown relative
amounts of Y and X:
where M'x and M'y are the amounts of X and Y, respectively, in the solution and A'x and
A'y are the associated detector responses for X and Y.
Determination of response factors requires access to samples of substantially pure
X and Y, especially when X is a reference marker for the purity of Y. The present
invention provides N-formyl valacyclovir in isolated form, suitable for use as a reference
standard.
Determination of the purity of valacyclovir in a pharmaceutical dosage form that
includes valacyclovir, for example to evaluate shelf life and residual potency, requires
that the valacyclovir be separated from excipients and other intentionally added
* ingredients in the dosage form. This can be accomplished by, for example, combining a
suitable quantity of the dosage form, comminuted if desired, with a suitable solvent.
Suitable solvents dissolve valacyclovir and impurities therein^ especially N-formyl
valacyclovir, but do not dissolve excipients and other intentionally added ingredients
The present invention provides a process for preparing a pharmaceutical
composition comprising valacyclovir or a pharmaceutically acceptable salt thereof which
comprises formulating valacyclovir or a pharmaceutically acceptable salt, tested
according to any of the methods, which are part of this invention, above with an excipient
of carrier.
10
Detection and especially quantification of components of a mixture by HPLC
requires that the peaks for the components be sufficiently separated (resolved). This can
be checked by performing a system suitability check to determine the resolution factors
according to a method such as described below.
The well-known technique of thin layer chromatography (TLC) can also be
applied to assessment of the purity of an API. In this case, presence of an impurity, e.g. a
reference marker, is established by the presence of a suitably-visualized "spot" at the
same, simultaneously determined relative position, RF, (relative to the solvent front) of
the reference marker.
In yet another embodiment, the present invention provides a method of testing or
proofing the purity of valacyclovir, either in bulk or isolated from a pharmaceutical
dosage form that includes valacyclovir. The method includes the step of testing the
valacyclovir by HPLC or TLC to determine the presence of N-formyl valacyclovir in the
valacyclovir. The herein below described HPLC method is an example of an analytical
technique suitable for this testing or proofing.
EXAMPLES
Example 1: Quantitative analysis of N-formyl valacyclovir in valacvclovir
A. Chromatographic Method
Quantitative analysis of valacyclovir maybe performed using the following
achiral HPLC method:
The chromatograpbic method utilizes a suitable chromatography column such as the
reverse phase column CIS and gradient HPLC mode.
Column & Packing: Ihertsil ODS-3V 5jo, 250x4.6mm
Eluent A: 98% 0.01M Potassium Dihydrogen Phosphate in water
adjusted to pH-3.5 with 10% H3PO4 and 2% Acetonitrile
(Table Removed)
B. Standard Solution preparation of N-formyl-valcyclovir for identification of Nformyl-
valcyclovir:
A solution of N-formyl-valcyclovir standard in diluent was prepared. The peak of Nformyl-
valcyclovir was identified at RT=27.4 minutes. A chromatogram of the standard is
shown in Figure 1.
C. Marker Solution preparation for identification of N-formyl-valcyclovir:
Marker Solution of valacyclovir containing N-formyl-valcyclovir in a
concentration of about 0.8 mg/ mL of a diluent was prepared. The marker solution
containing N-formyl-valcyclovir was injected in order to identify peak of N-formylvalcyclovir
impurity in Valcyclovir sample. The peak of N-formyl-valcyclovir was
identified (according to the peak obtained in the Standard Solution) at RT=28.345
minutes. A typical chromatogram of marker containing N-formyl-valacyclovir is shown
in Figure 2.
D. Sample Solution preparation :
A solution of valacyclovir for analysis with a concentration of about O.Smg/ of a
diluent was prepared.
E. Procedure:
Marker and sample solutions were injected into chromatograph continuing the
chromatogram of samples up to the end of gradient program.
The sample chromatogram is shown in Figure 3.
The peaks areas are determined using a suitable integrator as known in the art.
Calculations:

A 150-ml one necked round-bottomed flask were equipped with magnetic stirring
bar and closed with CaCk tube was charged with! 0.8 g (.03M) g valacyclovir, and 2.1 g
(.033M) ammonium formate. The heterogeneous reaction mixture was heated in an oil
bath thermostatted at 125°C for 2.5 hrs with vigorous stirring of the contents of the flask.
The solid mixture melted with the release of ammonia gas and water vapors.
The reaction mixture was transferred while hot with 30 ml boiling water into the
crystallization flask to which 250 ml hot water were added. The mixture was heated until
it turns clear. Any insoluble impurities were removed by quick, hot filtration through a
glass wool plug. The filtrate was allowed to stand for 8 hrs at room temperature to give,
after filtration, white powder, 9.5 g with a purity of 85.39%.
The same crystallization procedure was repeated twice, from hot water (150 ml
and 75 ml respectively), and yielded 4.5 g with a purity of 95.85 area-%.
The !H and 13C-NMR together with the 2D experiments data indicate that the
CHO group is attached to the valine-NH2 moiety in the valacylovir molecule.
A 150-ml one necked round-bottomed flask were equipped with magnetic stirring
bar and closed with CaCfe tube was charged withlO.8 g (.03M) g valacyclovir, and 2.1 g
(.033M) ammonium formate. The heterogeneous reaction mixture was heated in an oil
bath thermostatted at 145°C for 2.5 hrs with vigorous stirring of the contents of the flask.
The solid mixture melted with the release of ammonia gas and water vapors.
The reaction mixture was transferred while hot with 30 ml boiling water into the
crystallization flask to which 250 ml hot water were added. The mixture was heated until
it turns clear. Any insoluble impurities were removed by quick, hot filtration through a
glass wool plug. The filtrate was allowed to stand for 8 hrs at room temperature to give,
after filtration, white powder, 10.4 g with a purity of 80%.
The same crystallization procedure was repeated, from hot 150 ml water, and
yielded 9.0 g with a purity of 92.4 area-%.
4: preparation ot JN-^ormvl Valacyclovir
A 100 ml round bottom flask equipped with magnetic stir bar is charged with 7.25 gr
Valacyclovir (20 mrnol), 1.97 gr ammonium formate (31.2 mmol), NMP (N-Methylpyrrolidone)
(15 ml) is added and stirring is started. The resulting mixture is placed in an
oil bath that is heated to 125C for 2 hrs. The mixture is removed from the oil bath,
allowed to cool to room temperature, and the solvent is removed under reduced pressure
using high vac. pump. The residue is crystallized from 150 ml boiling water to give

CLAIMS
1. Isolated N-formylvalacyclovir.
2. The isolated N-formylvalacyclovir of claim 1, comprising from about 0.03 area-% to
5 area-% valacyclovir as judged by HPLC.
3. The isolated N-formyl valacyclovir of claim 2, comprising about 0.03 area-% to about
2 area-% valacyclovir as judged by HPLC.
4. The isolated N-formyl valacyclovir of claim 1, which is at least 95 area-% pure as
judged by HPLC.
5. A method of preparing N-formylvalacyclovir comprising:
a) reacting valacyclovir with ammonium formate;
b) heating the reaction mixture;
c) combining the reaction mixture from step a) with hot water;
d) heating the reaction mixture;
e) cooling the reaction mixture; and
f) recovering the N-formyl valacyclovir.
6. The method of claim 5, wherein a solvent is added in step a).
7. The method of claim 5 further comprising the step of isolating the N-formyl
valacyclovir.
8. The method of claim 5 wherein the reaction time is about 1 to about 10 hours.
9. The method of claim 8 wherein the reaction time is about 2 to about 4 hours.
10. The method of claim 5 wherein the reaction mixture of valacyclovir and ammonium
formate is heated to about 125°C to about 145°C.
11. The method of claim 5 wherein the hot water in step c) is at a temperature of about
100°C.
12. The method of claim 5 wherein the reaction mixture in step d) is filtered while hot.
13. The method of claim 5 wherein the reaction mixture in step e) is cooled to room
temperature.
14. The method of claim 5 wherein the N-formyl valacyclovir is recrystallized.
15. The method of claim 14 wherein the N-formyl valacyclovir is recrystallized from
water.
16. A method of identifying an impurity in a sample of valacyclovir comprising:
a) providing a reference sample comprising a reference marker and
valacyclovir;
b) carrying out HPLC or TLC on the reference sample to determine the
relative retention time of the reference marker compared to valacyclovir;
c) carrying out HPLC or TLC on the sample of valacyclovir to determine the
relative retention time of the N-formyl valacyclovir compared to
valacyclovir;
d) comparing the relative retention times determined in steps (b) and (c);
where, if the relative retention times determined in steps (b) and (c) are
substantially the same, the N-formyl valacyclovir is identified as being the
same as the reference marker.
17. The method of claim 16, wherein in both steps (b) and (c) HPLC is carried out.
18. A method of determining the amount of N-formyl valacyclovir in a sample of
valacyclovir comprising:
(a) adding a known amount of a reference standard to the valacyclovir sample;
(b) subjecting the valacyclovir to HPLC;
(c) identifying and measuring the area of an HPLC peak associated with the N-formyl
valacyclovir;
(d) identifying and measuring the area of an HPLC peak associated with the reference
standard;
(e) calculating the amount of the impurity in the valacyclovir sample based on the
results of steps (c) and (d);
where the reference standard is N-formyl valacyclovir.
19. A method of determining the amount of N-formyl valacyclovir in a sample of
valacyclovir comprising:
a) providing a sample of valacyclovir containing an unknown concentration
of the impurity;
b) providing a sample of a known concentration of N-formyl valacyclovir;
c) subj ecting a portion of the sample of valacyclovir and a portion of the
sample of N-formyl valacyclovir to HPLC;
d) measuring the area of N-formyl valacyclovir peaks obtained from the
sample of valacyclovir and from the sample of the impurity; and
e) calculating the concentration of N-formyl valacyclovir in the sample of
valacyclovir from the measurements of step (d).
20. A method of determining the amount of an impurity in a sample of valacyclovir
comprising:
a) providing a first reference solution of known concentration of substantially
pure valacyclovir;
b) providing a second reference solution of known concentration of
substantially pure N-formyl valacyclovir of known concentration;
c) subjecting an aliquot of each of the first and second reference solutions to
HPLC analysis and determining the response factors of valacyclovir and
N-formyl valacyclovir;
d) providing a solution of known overall concentration of the valacyclovir;
e) subjecting the solution to HPLC analysis under substantially the same
conditions used in step (c); and
f) calculating the amount of N-formyl valacyclovir in the solution using the
respective peak areas and the response factors.
21. The method of claim 16 wherein the sample of valacyclovir is bulk valacyclovir.
22. The method of any of claims 18,19 and 20 wherein the valacyclovir is bulk
valacyclovir.
23. The method of any of claims 18,19 and 20 wherein the sample of valacyclovir is
taken from a batch or production lot of valacyclovir, the amount of N-formyl
valacyclovir is determined to be less than 10 area-% as judged by HPLC, and the
batch or production lot is released for sale / export.
24. The method of claim 16 wherein the valacyclovir is valacyclovir separated from one
or more pharmaceutical dosage forms comprising valacyclovir.
25. The method of any of claim 18,19 and 20 wherein the valacyclovir is valacyclovir
separated from one or more pharmaceutical dosage forms comprising valacyclovir.
26. The method of claim 25 wherein the pharmaceutical dosage forms comprising
valacyclovir is taken from a batch or production lot, the amount of N-formyl
valacyclovir is determined to be less than 10 area-% as judged by HPLC, and the
batch or production lot is released for sale / export.
11. A process for preparing a pharmaceutical composition comprising valacyclovir or
pharmaceuticaUy acceptable salt thereof which comprises formulating valacyclovir or
apharmaceutically acceptable salt, tested according to any of fee methods of claims
16,18,19 and 20 with an excipient of carrier.