Quality-by-design-based development and validation of a stability-indicating UPLC method for quantification of teriflunomide in the presence of degradation products and its application to invitro dissolution

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Quality-by-design-based development and
validation of a stability-indicating UPLC method
for quantification of teriflunomide in the presence
of degradation products and its application to in-
vitro dissolution
Nukendra Prasad Nadella, Venkata Nadh Ratnakaram & N. Srinivasu
To cite this article: Nukendra Prasad Nadella, Venkata Nadh Ratnakaram & N. Srinivasu (2017)
Quality-by-design-based development and validation of a stability-indicating UPLC method for
quantification of teriflunomide in the presence of degradation products and its application to in-
vitro dissolution, Journal of Liquid Chromatography & Related Technologies, 40:10, 517-527, DOI:
10.1080/10826076.2017.1330211
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JOURNAL OF LIQUID CHROMATOGRAPHY & RELATED TECHNOLOGIES
2017, VOL. 40, NO. 10, 517–527
https://doi.org/10.1080/10826076.2017.1330211
Quality-by-design-based development and validation of a stability-indicating UPLC
method for quantification of teriflunomide in the presence of degradation products
and its application to in-vitro dissolution
Nukendra Prasad Nadellaa,b
, Venkata Nadh Ratnakaramc
, and N. Srinivasua
a
Department of Science and Humanities, VFSTR, Vignan’s University, Guntur, Andhra Pradesh, India; b
Department of Analytical Research and
Development, AET Laboratories Pvt Ltd, Hyderabad, Telangana, India; c
Department of Chemistry, GITAM University, Bengaluru, Karnataka, India
ABSTRACT
A systematic design-of-experiments was performed by applying quality-by-design concepts to determine
design space for rapid quantification of teriflunomide by the ultraperformance liquid chromatography
(UPLC) method in the presence of degradation products. Response surface and central composite
quadratic were used for statistical evaluation of experimental data using a Design-Expert software. The
response variables such as resolution, retention time, and peak tailing were analyzed statistically for the
screening of suitable chromatographic conditions. During this process, various plots such as perturbation,
contour, 3D, and design space were studied. The method was developed through UPLC BEH C18
2.1 � 100 mm, 1.7-µ column, mobile phase comprised of buffer (5 mM K2HPO4 containing 0.1%
triethylamine, pH 6.8), and acetonitrile (40:60 v/v), the flow rate of 0.5 mL minÀ 1
and UV detection at
250 nm. The method was developed with a short run time of 1 min. Forced degradation studies revealed
that the method was stability-indicating, suitable for both assay and in-vitro dissolution of a drug product.
The method was found to be linear in the range of 28–84 µg mLÀ 1
, 2.8–22.7 µg mLÀ 1
with a correlation
coefficient of 0.9999 and 1.000 for assay and dissolution, respectively. The recovery values were found in
the range of 100.1–101.7%. The method was validated according to ICH guidelines.
GRAPHICAL ABSTRACT
KEYWORDS
Assay and in-vitro
dissolution; design of
experiments; method
validation;
stability-indicating;
teriflunomide; UPLC
Introduction
Teriflunomide is chemically (Z)-2-cyano-3-hydroxy-but-2-
enoic acid-(4-trifluoro methyl phenyl)-amide with molecular
formula C12H9F3N2O2 and relative molecular mass of
270.2 g molÀ 1
(Figure 1). Teriflunomide appears as white to
almost white, odorless, nonhygroscopic powder. It is a
none defined
CONTACT Nukendra Prasad Nadella prasadnn14@gmail.com Department of Science and Humanities, VFSTR, Vignan’s University, Vadlamudi,
Guntur-522213, Andhra Pradesh, India.
Color versions of one or more of the figures in this article can be found online at www.tandfonline.com/ljlc.
© 2017 Taylor & Francis
Downloadedby[115.99.18.65]at07:1508August2017

class-2 compound of biopharmaceutical classification system
due to its low solubility and high permeability.[1–4]
Terifluno-
mide is weakly acidic with pKa 3.1 at room temperature and
having a pH-dependent solubility. In aqueous buffers at 25°C,
the solubility of teriflunomide increases from 0.02 µg mLÀ 1
at pH 1.2 to 8 mg mLÀ 1
at pH 7.6.[3]
Teriflunomide is an
immunomodulatory agent with anti-inflammatory properties,
inhibits dihydroorotate dehydrogenase, a mitochondrial
enzyme involved in de novo pyrimidine synthesis.[5–16]
Teriflu-
nomide contains two degradation products (Figure 1) namely
4-trifluoromethyl aniline (“leflunomide impurity-A Ph. Eur.”)
and 2-cyano-N-[4-(trifluoromethyl) phenyl]-acetamide (“leflu-
nomide impurity-H Ph. Eur.”).[1,17,18]
A stability-indicating method is a quantitative analytical
procedure used to detect a decrease in the amount of active
pharmaceutical ingredient present due to degradation.
According to Food and Drug Administration (FDA) guide-
lines,[19,20]
stability-indicating method is defined as a validated
analytical procedure that accurately and precisely measures
active ingredients free from potential interferences like degra-
dation products, process impurities, excipients, or other
potential degradation products. Quality-by-design (QbD) is a
systematic approach to development that begins with prede-
fined objectives and emphasizes product, process understand-
ing, and process control, based on sound science and quality
risk management. Key benefits of QbD are as follows.[21–23]
. High level of assurance of analytical method.
. The method is designed to meet predefined needs and
performance requirements.
. The impact of different reagents and method parameters
on analytical method quality is understood.
. Development of robust and cost-effective analytical method.
. Regulatory flexibility.
Teriflunomide is not official in pharmacopoeia such as
United States Pharmacopoeia (USP), BP, JP, and Ph. Eur. A
wide variety of analytical methods have been reported in the
literature for analysis of teriflunomide include estimation of
teriflunomide in biological fluids such as human plasma,
rabbit plasma, and human blood by high performance liquid
chromatography (HPLC) and LC–MS.[24–29]
However, there
are no methods reported in a study of the effect of stress on
pharmaceutical dosage forms, and there is no validated ultra-
performance liquid chromatography (UPLC) method on the
basis of QbD approach, which enables a stability-indicating
UPLC method for quantification of teriflunomide in bulk
and pharmaceutical dosage forms. To speed up the analysis,
UPLC method gives faster product development for the
pharmaceutical industry. In general, an UPLC method
provides 3 � higher efficiency and generates a 9 � increase
in throughput with no loss in resolution with sub-2-µ
particle-size columns than 5-µ particle sizes.[30,31]
The primary objective of the proposed research work is to
develop a stability-indicating UPLC method using QbD
approach for rapid estimation of assay content and in-vitro
dissolution release in the presence of degradation products
for pharmaceutical tablet dosage forms and to validate the
method as per ICH guidelines.[32]
Development of shorter
chromatography run time reduces the analysis time, cost effec-
tiveness, low solvent consumption altogether increases the
pharmaceutical productivity in routine quality control.
Experimental
Materials and reagents
Teriflunomide working standard and teriflunomide
film-coated tablets were provided by AET Laboratories Pvt
Ltd, Hyderabad, India. Dipotassium hydrogen phosphate
(K2HPO4), triethylamine, hydrochloric acid, sodium hydrox-
ide (NaOH), phosphoric acid, potassium dihydrogen phos-
phate (KH2PO4), and potassium chloride of Emparta grade
were purchased from Merck, India. Acetonitrile, methanol of
HPLC grade were procured from Merck, India, and Milli-Q-
water was collected from Merck Millipore ELIX 10 system.
Instrumentation
Ultraperformance liquid chromatography system with
Empower-3 software, UPLC BEH-C18 100 � 2.1 mm, 1.7-µ
column was used for chromatographic analysis. UV spectro-
photometer (Lambda 25, Perkin Elmer) was used for the
spectroscopic analysis. Analytical balance (XP-205 dual-range
model, Metler Toledo), dissolution apparatus (TDT-08 L,
Electrolab), Vacuum oven (Thermolab), vacuum filtration unit
(Millivac-Maxi 230 V, Millipore), pH meter (Orion-Star-A211,
Thermo), Rotary shaker (RS-24BL, REMI), water bath
(MSI-8, Meta Lab), photo-stability chamber (NEC103RSPSI,
Newtronics), and sonicator (9L250H, PCI) were used.
Chromatographic conditions
Chromatographies conditions were optimized based on
design-of-experiments (DoE) studies. The chromatographic
Figure 1. Molecular structure of teriflunomide and its degradation products.
518 N. P. NADELLA ET AL.

separation was achieved on UPLC BEH-C18 100 � 2.1 mm,
1.7-µ column using mobile phase composed of buffer (5 mM
K2HPO4 containing 0.1% triethylamine, pH 6.8) and acetoni-
trile in the ratio of 40:60 v/v. The flow rate was set at
0.5 mL minÀ 1
, and UV detection wavelength was performed
at 250 nm. Injection volume was 1 µL with a column tempera-
ture of 35°C. Total run time of method was 1 min. Fifty mM
phosphate buffer (pH 6.8) and acetonitrile in the ratio of
60:40 v/v were used as a diluent.
Standard and sample preparation
Weighed and transferred about 56 mg of teriflunomide working
standard into a 100-mL volumetric flask. Added 60 mL of dilu-
ent, sonication was done to dissolve and made up to volume
with diluent. From this solution, 5 mL was diluted to 50 mL
with diluent to obtain a concentration of 56 µg mLÀ 1
of teriflu-
nomide. Taken 20 tablets of the test sample into a mortar and
pestle, and then crushed to a fine powder. Weighed and trans-
ferred powder equivalent to 14 mg of teriflunomide into a
250-mL clean and dry volumetric flask. Then added 150 mL
of diluent and sonication was performed for 10 min with inter-
mittent shaking for extraction of the drug. The volume was
made up to 250 mL with diluent. The sample solution was
filtered through 0.2-µ polyvinylidene difluoride (PVDF) syringe
filter and collected the sample with a concentration of
56 µg mLÀ 1
of teriflunomide. Teriflunomide was quantified
using the following formula, where, “Ax” is the area obtained
from sample chromatogram, “As” is the average area obtained
from standard chromatograms, “Wstd” is weight of teriflunomide
standard in mg, “Wspl” is weight of sample in mg, “AW” is the
average weight of drug product, “LC” is label claim, and “P” is
the percentage assay of teriflunomide standard on as is basis.
Assay % label claimð Þ ¼
Ax
As
�
Wstd
100
�
5
50
�
250
Wspl
�
AW
LC
� P
In-vitro dissolution
The standard solution was prepared at a concentration of
14 µg mLÀ 1
of teriflunomide in phosphate buffer solution of
pH 6.8. The in-vitro dissolution test was performed using a
phosphate buffer solution of pH 6.8 as dissolution media with
a medium volume of 1000 mL and media temperature of 37°C.
The type of dissolution apparatus used is a paddle with a
rotation speed of 50 rpm. The sample was collected after
30 min time point, and samples were filtered through 0.2-µ
PVDF syringe filter.
Method validation
The developed UPLC method for quantification of terifluno-
mide was validated according to a current international con-
ference on harmonization guideline ICH Q2 (R1) validation
of analytical procedures.[32]
The method was validated for its
system suitability, specificity, linearity, accuracy, precision,
and robustness. Before analyzing the sample, system suitability
criteria were performed to verify whether the analytical system
(analytical solutions, UPLC system, column) is suitable or not
for giving accurate and consistent precise results. The system
suitability of the proposed method was evaluated by calculat-
ing parameters such as theoretical plates not less than 2000,
tailing factor not more than 2.0, and percentage relative stan-
dard deviation (RSD) from five standard injections should not
be more than 2.0.[33,34]
The specificity of the analytical method
was determined by verifying the interference of blank/placebo,
impurity peaks at the retention time of teriflunomide. Stan-
dard and sample solutions were prepared at a concentration
of 56 µg mLÀ 1
of teriflunomide. Placebo solution was prepared
similarly as sample preparation by taking a placebo and omit-
ting drug substance. Individual preparations of impurity-A
and impurity-H solutions were performed at a concentration
of 2.8 µg mLÀ 1
, i.e., 5% level with respect to sample concen-
tration. Solutions were injected into the chromatography sys-
tem by giving 200–400-nm wavelength ranges in photodiode
array (PDA) system. Recorded the chromatograms, verified
for peak purity of teriflunomide as well as interferences of
the blank, placebo and impurity peaks.
Forced degradation studies
Performed the forced degradation studies and all the
degradation samples were diluted with diluent after
completion of the degradation process. Blank and placebo
solutions were prepared in the same manner in respective
degradation to exclude any contribution from the process.
All the degradation sample solutions were injected into
UPLC-PDA system and recorded the chromatograms. Peak
purity was determined for teriflunomide and verified for any
interference of placebo/degradation products at the retention
time of teriflunomide. The total percentage of degradation
products and a percentage of the assay were calculated. Mass
balance was performed by adding together the assay value
and total percentage of degradation products to make up to
about 100% of the initial assay value of the drug product.
Linearity and range
The linearity of the analytical procedure is its ability (within a
given range) to obtain test results which are directly
proportional to the concentration of an analyte in the sample.
The linearity of the proposed analytical method was
determined by preparing five concentration levels from 28 to
84 µg mLÀ 1
of teriflunomide. The correlation coefficient (r),
regression coefficient (r2
), y-intercept, and slope of regression
line were calculated. The range of the method was proved by
performing the linearity, precision, and accuracy at the
proposed minimum 50% and maximum 150% concentration
levels with respect to sample concentration. Weighed and
transferred about 56 mg of teriflunomide into a 100-mL
volumetric flask. Dissolved and diluted to volume with diluent
to obtain a concentration of 560 µg mLÀ 1
of teriflunomide
(linearity stock). To prepare 50, 80, 100, 120, and 150% levels,
respectively, 5, 8, 10, 12, and 15 mL of linearity stock solutions
were diluted to 100 mL.
Accuracy
A known amount of teriflunomide drug substance was spiked at
50, 100, and 150% levels with respect to sample concentration
JOURNAL OF LIQUID CHROMATOGRAPHY & RELATED TECHNOLOGIES 519

to the placebo and analyzed by the proposed UPLC method.
Percentage recovery was calculated. Weighed and transferred
350 mg of teriflunomide into a 250-mL volumetric flask. Added
150 mL of diluent and sonication was performed to dissolve.
The diluent was added up to the mark to get the concentration
of 1400 µg mLÀ 1
of teriflunomide (accuracy stock solution).
Weighed and transferred placebo equivalent to one tablet
weight into a 250-mL clean and dry volumetric flask. Added
5, 10, and 15 mL of accuracy stock solution to 150 mL of diluent
to obtain 50, 100, and 150% concentration levels, respectively.
Solutions were sonicated for 10 min with intermittent shaking
and made up to volume with diluent.
Precision
The precision of an analytical procedure expresses the
closeness of agreement (degree of scattering) between a series
of measurements obtained from multiple sampling of the same
homogeneous sample under the prescribed conditions.
Precision was performed in repeatability and intermediate
precision methods. Repeatability for assay method was
demonstrated by preparing six assay sample solutions at a
concentration of 56 µg mLÀ 1
(100% level of sample concen-
tration) and injected into an UPLC system over a short
interval of time as per proposed method and calculated the
percentage RSD for assay results. Intermediate precision was
demonstrated by preparing six assay sample solutions at a con-
centration of 56 µg mLÀ 1
on a different day by different
analysts and then injected into a UPLC system as per proposed
method. Percentage RSD of assay results was calculated
between two analyst values.
Robustness
The robustness of an analytical procedure is a measure of
its capacity to remain unaffected by small, but deliberate var-
iations in method parameters, and it provides an indication of
its reliability during normal usage. Method robustness was
established by considering the variations in wavelength
(250 � 2 nm), flow rate (0.5 � 0.1 mL minÀ 1
), column oven
temperature (35 � 5°C), and a mobile phase ratio (40:60 v/v,
38:62 v/v, 42:58 v/v). Solution stability and filter interference
were established.
Results and discussion
Method development and optimization
Method development was initiated based on QbD concepts.
Quality target analytical profile (QTAP) forms the basis of
design for the development of analytical methods. QTAP
includes all the target requirements along with justification
and objectives of the method and are listed in brief in
Table 1.[21,35]
Method quality attributes were derived from
the QTAP. Critical method quality attributes (CMQA) are
the measurable parameters or characteristics of the method
that should be within predefined appropriate limits, ranges
or acceptance criteria. The CMQA for an analytical method
are primarily all the validation parameters of the method
including the robustness requirements.[32,35]
UV spectrum
of teriflunomide was determined in a solution containing
56 µg mLÀ 1
of teriflunomide in a diluent containing 50 mM
phosphate buffer of pH 6.8 and acetonitrile in the ratio of
60:40 v/v. PDA spectrum was collected from 200 to
400-nm wavelength (Figure 2). Wavelength maxima were
observed at 204.8, 248.8, and 295.7 nm. Though the highest
absorption is observed at 295 nm, degradation products
(impurity-A and impurity H) were observed at 250 nm.
Hence, 250 nm was selected as chromatographic detection
wavelength for teriflunomide peak. Since all peak responses
are at 250 nm, the method is suitable for mass balance
studies.
Method optimization
The solubility of teriflunomide was performed in aqueous
media with a pH ranging from 1.2 to 6.8. The solubility of
teriflunomide in water, hydrochloric acid media of pH 1.2,
acetate buffer of pH 4.5 and phosphate buffer of pH 6.8 were
insoluble, insoluble, 0.1, and 3.9 mg mLÀ 1
, respectively. Based
on the solubility of teriflunomide, pH of diluent and the mobile
phase buffer was considered in pH above 6. During preliminary
method development trials, the chromatographic conditions
were used as follows. Mobile phase-A was 10 mM KH2PO4
containing 0.5% v/v of triethylamine with pH 6.5. Acetonitrile
was used as a mobile phase-B. UPLC BEH C18 2.1 � 50 mm,
1.7 µ column was used with a flow rate of 0.5 mL minÀ 1
, the
detection wavelength of 250 nm, and an injection volume of
1 µL. Different solvent compositions of mobile phase were
studied for teriflunomide peak shape. Poor peak shape was
observed in preliminary method development trials and further
proceeded with pH scouting studies to evaluate the peak tailing
and noninterference of degradation products. pH scouting
studies were performed to select the optimum mobile phase
pH, to obtain shorter run time with no interference of placebo
and impurity peaks at the retention time of teriflunomide.
Mobile phases with different pH of buffers were prepared by
mixing buffer and acetonitrile in the ratio of 50:50 v/v. The
results of pH scouting studies were given in Table 2. pH
scouting studies reveal that the retention time of impurity-A
and impurity-H was not changing with the change in pH of
mobile phase buffer. But, the retention time of teriflunomide
peak was moving to lower retention time by increasing pH of
mobile phase buffer. Comparatively, the higher USP plate
count was observed at buffer pH 2.0, but the impurity peaks
were eluted nearby the teriflunomide peak. And also, lower
pH was not suggestible due to poor solubility of teriflunomide.
Hence, pH of mobile phase buffer between 6.0 and 7.0 was
selected for optimization to achieve a lower retention time of
teriflunomide without the interference of degradation products
and to overcome any solubility issues due to lower pH.
Design-of-experiment studies
The design of experiments was executed to select robust and
rugged operational chromatographic conditions within the
design space. Ten mM KH2PO4 containing 0.5% v/v of
triethylamine with pH 6.8 was taken as a mobile phase buffer

for DoE studies. DoE study was executed by considering the
mobile phase composition, flow rate, column temperature as
control variables. USP tailing, the retention time of late eluting
impurity peak and resolution of nearby impurity with
teriflunomide were taken as response variables. Design Expert
8.0 software was used for the study. The selected design
parameters are response surface as study type, central
composite as design type and quadratic as design mode.
Proposed ranges of mobile phase solvent composition
50–70%, flow rate 0.4–0.7 mL minÀ 1
, and column temperature
25–45°C were selected to design. This data were fed into the
design expert software and software given twenty experiments.
All the DoE experiments were executed in UPLC and observed
results are tabulated in Table 3. The effect of control variables
on response variables was graphically evaluated in Figure 3.
The observations were derived from perturbation plot and
3D plot which describes the effect of method control variables
on the response variables.
Based on the desirability plot (Figure 4), column
temperature was set at 35°C. Design space plot (Figure 4)
suggests that flow rate of 0.5 mL minÀ 1
and mobile phase
composition of 40:60 v/v (buffer:acetonitrile) for a robust
chromatographic method. Teriflunomide peak was eluted at
0.5 min and run time was set at 1 min. Risk assessment is a
valuable scientifically based process used in quality risk
management. Risk assessment is helpful in identifying the
input material attributes (reagents/chemicals/columns) and
method parameters (flow, temperature, solution stability) that
are affecting CMQA. The first step of the risk-assessment
process involves identification of critical material attributes
and method parameters and performing risk assessments of
their attributes for the subsequent effect on CMQA. Based
on risk assessment, control strategy was established for the
selection of diluent pH at 6.8 for solubility of teriflunomide.
Method validation
Specificity
Diluent, placebo, standard, sample, impurity-A, impurity-H,
and impurity-spiked sample solutions were injected into
Table 1. Quality target analytical profile.
Analytical target profile
element Target/requirement Justification
Status of current study
(yes/no/remarks)
Type of method Quantification of teriflunomide in the
presence of degradation products
To quantify the teriflunomide in the
formulation
Yes
Mode of detection and
chromatography
UV, isocratic The molecule is having chromophoric groups
and can be detected by UV
Yes, UV detection at 250 nm
Specificity Blank, placebo, and impurity
interference should not be observed
ICH Q2 (R1) guideline requirements Yes
Precision of the method,
repeatability/
reproducibility
Should have a precision
withpercentage RSD below 2.0
ICH Q2 (R1) guideline requirements Yes
Accuracy Percentage recoveryshould be
between 98 and 102
The percentage recovery should be good for
the drug product and as per requirements
of ICH guidelines
Yes
Linearity Linearity at different concentration
levels should be obtained
The correlation coefficient should not be less
than 0.99 and as per requirements of ICH
guidelines
Yes
Robustness Assay results should not be affected
by small changes in method
parameters
Results should not be affected Yes
Stability indicating nature The principle peak should be pure
even after forced degradation
Purity angle should be less than purity
threshold and the mass balance should be
close to 100% of initial assay
Yes
Green chromatography Should use minimum percentage of
organic phase as possible
To avoid the use of more organic solvents and
to develop an environment-friendly method
Yes, low solvent consumption with
a shorter run time of 1 min
Figure 2. UV spectrum of teriflunomide.

UPLC-PDA system, and chromatograms were extracted. The
results are summarized in Table 4. The system suitability test
results observed during specificity and precision test are
tabulated in Table 5. Acidic, basic, oxidation, thermal, water,
humidity, and photodegradation samples were injected into
UPLC-PDA system and chromatograms were extracted. No
interference was observed with blank, placebo, and impurities
at the retention time of teriflunomide. Teriflunomide peak
passed the peak purity test for all degradation samples. The
results are summarized in Table 4. Mass balance was achieved
for all forced degradation samples and the results are
summarized in Table 4. The representative chromatogram of
specificity is given in Figures 5 and 6.
Linearity and range
Linearity solutions, i.e., 50, 80, 100, 120, and 150% levels were
injected into UPLC and chromatograms were recorded. The
regression line of analysis shows the linear relationship
between concentration and area response of teriflunomide.
Results of linearity and range are summarized in Table 5.
Accuracy and precision
Teriflunomide-spiked samples of 50, 100, and 150% levels
with respect to sample concentration to the placebo were
analyzed by the proposed UPLC method. Recovery of
teriflunomide was observed from 100.1 to 101.7% and all the
individual results were within the range of 98–102% criteria.
The results are summarized in Table 6. The precision of the
analytical method was determined by repeatability and
intermediate precision. The percentage RSD results for
repeatability, intermediate precision, and between two analyst
values were 1.03, 1.19, and 1.15, respectively (Table 6). Since
the percentage RSD of six assay results is not more than 2.0,
the method is repeatable. The percentage RSD of two analyst’s
assay results is less than 2.0, hence, intermediate precision is
acceptable.
Robustness
Method robustness was established by considering the changes
in wavelength, flow rate, column oven temperature, and mobile
phase ratio. Solution stability and filter interference were
studied. Hydrophilic polypropylene (GHP) and Millipore-
PVDF syringe filters were evaluated for filter interference and
no significant interference was observed. The percentage differ-
ences of area response from the unfiltered area for GHP and
PVDF were 0.28 and 0.38, respectively. The results of robust-
ness are tabulated in Table 5. Robustness test passed as a vari-
ation from initial results is not more than 2.0%.[36–40]
Table 3. Experimental results of DoE study and effect on response variables.
DoE experiments Results of response variables
Run no.
Column temperature
(°C)
Flow rate
(mL minÀ 1
)
Mobile phase
composition (v/v) USP tailing
Retention time of late
eluting impurity (min)
Resolution of nearby
impurity with teriflunomide
1 25 0.6 50:50 1.70 0.997 10.35
2 45 0.6 50:50 1.54 0.944 9.76
3 35 0.4 40:60 1.30 1.030 7.63
4 45 0.4 30:70 1.19 0.806 4.42
5 35 0.6 40:60 1.50 0.681 6.87
6 45 0.4 50:50 1.40 1.428 9.61
7 35 0.5 40:60 1.43 0.822 7.17
8 45 0.5 40:60 1.36 0.806 6.84
9 35 0.5 40:60 1.43 0.822 7.17
10 25 0.4 50:50 1.52 1.539 10.51
11 25 0.5 40:60 1.52 0.840 7.33
12 35 0.5 40:60 1.43 0.822 7.17
13 35 0.5 50:50 1.58 1.175 10.7
14 35 0.5 40:60 1.43 0.822 7.17
15 25 0.6 30:70 1.07 0.549 4.12
16 35 0.5 30:70 1.10 0.657 4.27
17 35 0.5 40:60 1.43 0.822 7.17
18 45 0.6 30:70 1.08 0.536 3.88
19 35 0.5 40:60 1.43 0.822 7.17
20 25 0.4 30:70 1.22 0.831 4.62
Increase of control variable
Effect on response variables
USP tailing RT of late eluting peak Resolution of nearby peak with teriflunomide
Observations from DoE study plots
A: Column temperature Decreases No effect No effect
B: Flow rate Increases Decreases No effect
C: Mobile phase solvent composition Decreases Decreases Decreases
DoE, design-of-experiments.
Table 2. Results of pH scouting experiments.
Buffer pH RT (retention time) of teriflunomide (min) RT of impurity-A (min) RT ofimpurity-H (min) USP tailing USP plate count
pH 2.0 1.388 1.263 1.130 1.59 9251
pH 3.0 0.808 1.322 1.130 2.02 4694
pH 4.0 0.661 1.329 1.133 1.90 3359
pH 5.0 0.590 1.332 1.134 1.90 3151
pH 6.0 0.587 1.327 1.136 1.90 3157
pH 7.0 0.579 1.333 1.134 1.38 3048

Comparison with reported methods
Ultraperformance liquid chromatography method was
developed for rapid quantification of teriflunomide in the
presence of degradation products in the pharmaceutical drug
product. The present method uses the shortest run time of
1 min with a retention time of teriflunomide of about
0.5 min compared to earlier reported methods which are
having a run time of minimum 2 min with an RT of
1.43 min (Table 7). The method was developed based on
QbD approach, and optimum chromatographic conditions
were selected based on design space obtained through DoE
studies. The developed method is stability indicating as there
is no interference in force degradation studies (Table 4). The
method was validated as per ICH guidelines and the results
of specificity, linearity, accuracy, precision, and robustness
were found satisfactory. No interference was observed with
blank, placebo, and degradation products at the retention time
of teriflunomide. The purity angle was less than the purity
threshold indicating that teriflunomide peak was free from
interference and passed the peak purity test (Table 4). The
reported methods were given for estimation of teriflunomide
release rate in biological fluids.[24–28]
Present method was
developed for rapid quantification of teriflunomide in the
presence of potential impurities by QbD in pharmaceutical
bulk and finished dosage form. Sample injection volume
(1 µL) in the present method is significantly lower, which helps
to maintain the good column performance compared to earlier
reported methods (minimum of 5 µL). A detailed comparison
of selected procedures with the present method is given in
Table 7. Teriflunomide contains no asymmetric centers,
Figure 3. Affect of control variables A (column temperature), B (flow rate), C (mobile phase solvent composition) on response variables a) USP tailing, b) resolution,
c) retention time of late eluting impurity.

Figure 4. Schematic representations of desirability plot and design space plot.
Table 5. System suitability evaluation, linearity, and robustness results.
Parameter Acceptance criteria[33]
Results of the test
RemarksSpecificity Precision
RSD (%) of area/five injections Not less than 2.0 0.38 0.38 Satisfactory
USP tailing factor Not more than 2.0 1.66 1.51 Satisfactory
Theoretical plates Not less than 2000 8134 9938 Satisfactory
Type of test Assay In-vitro dissolution
Linearity test results
Test concentration (µg mLÀ 1
) 28.02–84.06 2.84–22.70
Correlation coefficient (R) 0.9999 1.0000
Regression coefficient (R2
) 0.9998 0.9999
Slope 10124.6444 19885449.4184
Intercept 1919.441 1646.58
Parameter Change done Results Remarks
Robustness results
Solution stability Initial 100.6 Solutions are stable for 24 hr
After 24 hr 101.1
Wavelength (250 � 2 nm) 250 99.1 No significant variation in results
248 99.2
252 99.3
Flow rate (0.5 � 0.1 mL minÀ 1
) 0.5 99.1
0.4 99.8
0.6 100.1
Column oven temperature (35 � 5°C) 35 99.1
30 98.8
40 99.2
Mobile phase ratio (buffer:acetonitrile, v/v) 40:60 99.1
38:62 99.2
42:58 98.5
Table 4. Specificity, forced degradation studies, and mass balance results.
Sample name Retention time (min) Purity angle Purity threshold Peak purity Assay (%) Impurities (%) Total Mass balance
Impurity-A 0.813 — — — — — — —
Impurity-H 0.722 — — — — — — —
Teriflunomide standard 0.521 22.675 63.543 Pass — — — —
Sample 0.521 20.704 73.281 Pass 99.1 Nil 99.1 Yes
Acid-degradation 0.518 23.388 62.978 Pass 99.3 0.9 100.2 Yes
Alkali-degradation 0.524 1.509 72.977 Pass 99.2 Nil 99.2 Yes
Oxidation with KMnO4 0.517 22.161 90.000 Pass 91.6 6.6 98.2 Yes
Photo degradation-UV light 0.518 23.954 71.828 Pass 100.5 Nil 100.5 Yes
Photo degradation-visible light 0.519 21.555 66.176 Pass 100.2 Nil 100.2 Yes
Thermal-degradation 0.518 16.006 46.652 Pass 99.1 Nil 99.1 Yes
Water-degradation 0.519 21.389 59.804 Pass 96.8 2.3 99.1 Yes

Table 6. Accuracy and precision test results.
Level Theoretical concentration (µg mLÀ 1
, as teriflunomide) Experimental concentration (µg mLÀ 1
, as teriflunomide) Recovery (%)
50%-sample-1 27.814 28.101 101.0
50%-sample-2 27.814 28.164 101.3
50%-sample-3 27.814 27.875 100.2
50%-sample-4 27.814 28.278 101.7
50%-sample-5 27.814 28.288 101.7
50%-sample-6 27.814 28.503 101.1
100%-sample-1 55.628 55.999 100.7
100%-sample-2 55.628 55.771 100.3
100%-sample-3 55.628 55.703 100.1
150%-sample-1 83.442 83.538 100.1
150%-sample-2 83.442 83.807 100.4
150%-sample-3 83.442 83.697 100.3
150%-sample-4 83.442 84.207 100.9
150%-sample-5 83.442 84.166 100.9
150%-sample-6 83.442 84.338 101.1
Mean 100.8
RSD (%) 0.53
Preparation
In-vitro dissolution-precision Assay-repeatability Assay-intermediate precision
Labelled amount (%) Label claim (%) Label claim (%)
Precision results
1 97 99.1 98.5
2 98 99.8 97.6
3 98 99.5 98.5
4 100 101.7 99.8
5 98 99.2 99.6
6 99 100.8 100.9
Mean 98 100.0 99.2
RSD (%) 1.24 1.03 1.19
Mean between two analyst values 99.6
RSD (%) between two analyst values 1.15
Figure 5. Teriflunomide sample chromatogram.
Figure 6. Impurity spiked sample chromatogram.

therefore no enantiomers are possible, but can exist in E and Z
isomers. E-isomer will not separate in existing developed
method. As per literature review, there are no methods
available for the separation of these isomers. There is a scope
for future research work on separation of E and Z isomers of
teriflunomide.
Conclusions
The UPLC method was developed based on QbD concepts for
rapid quantification of teriflunomide in pharmaceutical drug
products. The developed method was validated as per ICH
guidelines. The method was found to be simple, selective, accu-
rate, precise, and robust. The developed method was stability
indicating as it was showing no interference of degradation pro-
ducts and placebo at the retention time of teriflunomide. Due to
the shorter run time of 1 min, this method provides faster analy-
sis, more work throughput, and reduces the cost of analysis due
to the reduction in solvent consumption. The method can be
used for in-vitro dissolution analysis. Therefore, the developed
method can be used for routine assay and in-vitro dissolution
analysis of quality control samples and stability samples of bulk
and finished pharmaceutical dosage form.
Acknowledgments
The authors wish to thank the management of AET Laboratories Private
Limited, Hyderabad, India for giving us an opportunity to carry out the
dissertation work.
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S. no.
Column, elution process, mobile phase, flow rate,
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Sample linear range,
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Run time (RT of
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1 Phenomenex Luna2 PFP, 2 � 100 mm, 3 µ,
gradient, mobile phase-A (0.1% formic acid),
mobile phase-B À 0.1% formic acid in
methanol:water:acetonitrile (0.5:0.5:9 v/v/v),
300 µL minÀ 1
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,
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rate in biological sample
[24]
2 Inertsil-ODS-3 C18 (50 � 4.6 mm, 5 µ); isocratic,
0.02 M CH3COONH4 pH 6.5: methanol (25:75
v/v); 0.8 mL minÀ 1
, 5 µL
10.1–4000 ng mLÀ 1
,
LC–ESI-MS/MS
2.0 min (1.43 min) For estimation of release
[25]
3 PolySULFOETHYL aspartamide strong cation
exchange column; isocratic, 10 mmol LÀ 1
KH2PO4 and 100 mmol LÀ 1
KCl in aqueous 25%
acetonitrile, acidified to pH 3 with o-phosphoric
acid. 0.7 mL minÀ 1
, 10 µL
0–200 µg mLÀ 1
, HPLC–
UV at 280 nm
[26]
4 XTerra-MS-C18 analytical column (100 � 3.9 mm,
5 µ), gradient, mobile phase-A-0.005 M
ammonium formate (pH 9.0) and B-acetonitrile
at 1.0 mL minÀ 1
, 10 µL
1–4000 ng mLÀ 1
,
LC–ESI-MS/MS
[27]
5 Nucleosil 100-5 C18-column, gradient, mobile
phase A-0.5 mM ammonium acetate in water–
acetonitrile–formic acid (9:5:0.02 v/v/v) and
mobile phase-B-0.5 mM ammonium acetate in
water–acetonitrile–formic acid (5:95:0.02 v/v/v),
0.5 mL minÀ 1
, 60 µL
5–500 µg mLÀ 1
,
LC–ESI-MS/MS
[28]
6 Acquity-UPLC BEH-C18 2.1 � 50 mm, 1.7 µ
column, isocratic, 5 mM K2HPO4 buffer
containing 0.1% triethylamine (pH 6.8) and
acetonitrile (40:60 v/v), 0.5 mL minÀ 1
, 1 µL
28–84.1 µg mLÀ 1
,
UPLC–UV at 250 nm
1 min (0.5 min) For quantification of
teriflunomide in the
presence of potential
impurities
Present
method

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