A Review On Stability Indicating HPLC Method Development
A Review On Stability Indicating HPLC Method Development
A Review On Stability Indicating HPLC Method Development
ABSTRACT
Article Received on
26 May 2015, This article discusses strategies and issues pertinent to a review on
Revised on 17 June 2015, Stability indicating HPLC method development. High performance
Accepted on 09 July 2015
liquid chromatography (HPLC) is an essential analytical tool in
assessing drug product stability. HPLC methods should be able to
*Correspondence for separate, detect and quantify the various drug-related impurities that
Author
may be introduced during synthesis. It further understands the
B. Varsha Rao
chemistry of the drug substance and drug product and facilitates the
Department of
Pharmaceutical Analysis development of stability indicating analytical methodology. Various
& Quality Assurance, chromatographic factors were evaluated in order to optimize the
CMR College of detection of all potentially relevant degradants. The method should be
Pharmacy, JNTU (H)
carefully examined for its ability to distinguish the primary drug
University, Hyderabad,
components from the impurities. New chemical entities and drug
Telangana.
products must undergo forced degradation studies which would be
helpful in developing and demonstrating the specificity of such stability indicating methods.
At every stage of drug development practical recommendations are provided which will help
to avoid failures.
INTRODUCTION
High Performance Liquid Chromatography is now one of the most powerful tools in
analytical chemistry. It has the ability to separate, identify, and quantify the compounds that
are present in any sample that can be dissolved in a liquid.
High performance liquid chromatography (HPLC) is the most accurate analytical methods
widely used for the quantitative as well as qualitative analysis of drug product and used for
determining drug product stability.[1,11]
PRINCIPLE
Adsorption chromatography: When the stationary phase is a solid and mobile phase is a
liquid or gaseous phase, it is called as adsorption chromatography.
IMPORTANCE
HPLC is a versatile, reproducible chromatographic technique for the estimation of drug
products. It has wide applications in different fields in term of quantitative and qualitative
estimation of active molecules. HPLC has many applications in the field of pharmaceutical,
environmental, clinical, forensic and in food and flavor analysis.[11]
METHOD DEVELOPMENT
Before starting the method development, various physiochemical properties like pKa value,
log P, solubility and absorption maximum of the drug must be known, for it lays a foundation
for HPLC method development. Log P and solubility helps select mobile phase and sample
solvent while pKa value is important as it helps determine the pH of the buffer and pH related
changes in retention occur at pH values within 2 of pKa value.[17]
Reverse phase column is a preferred choice to start the separation of sample components as
the degradation is carried out in aqueous solution. Methanol, water and acetonitrile can be
used as mobile phase in various ratios for the initial stages of separation. Selection between
methanol and acetonitrile for organic phase is based on the solubility and properties of the
analyte. Initially the water: organic phase ratio can be kept at 50:50 and suitable
modifications can be made as trials proceed to obtain a good separation of peaks. Latter
buffer can be added if it is required to obtain better peak separation and peak symmetry.
Variation in column temperature affects the selectivity of the method as analytes respond
differently to temperature changes. A temperature in the range of 3040C is suitable to
obtain good reproducibility. Also a sufficient run time after the drug peak is to be allowed to
obtain the degradants peak eluting after the drug peak. During the method development it
may happen that the drug peak may hide an impurity or degradant peak that co-elutes with
the drug. This requires peak purity analysis which determines the specificity of the method.
Direct analysis can be done online by using photodiode array (PDA) detection. PDA provides
information of the homogeneity of the spectral peak but it is not applicable for the degradants
that have the similar UV spectrum to the drug. Indirect method involves change in the
chromatographic conditions like mobile phase ratio, column, etc. which will affect the peak
separation. The spectrum of altered chromatographic condition is then compared with the
original spectra. If the degradant peaks and area percentage of the drug peak remain same,
then it can be confirmed that the drug peak is homogeneous. The degradant that co-elutes
with the drug would be acceptable if it is not found to be formed in accelerated and long term
storage conditions. The method is then optimized for separating closely eluting peaks by
changing flow rate, injection volume, column type and mobile phase ratio.[13,17,18,19]
The purpose of stability testing is to provide evidence on how the quality of a drug substance
or drug product varies with time under the influence of a variety of environmental factors,
such as temperature, humidity, and light, and to establish a retest period for the drug
substance or a shelf life for the drug product and recommended storage conditions.
The choice of test conditions defined in this guidance is based on an analysis of the effects of
climatic conditions in the three regions of the EU, Japan, and the United States. The mean
kinetic temperature in any part of the world can be derived from climatic data, and the world
can be divided into four climatic zones, I-IV. This guidance addresses climatic zones I and II.
The principle has been established that stability information generated in any one of the three
regions of the EU, Japan, and the United States would be mutually acceptable to the other
two regions, provided the information is consistent with this guidance and the labeling is in
accord with national/regional requirements. A stability indicating method(SIM) is an
analytical procedure used to quantitate the decrease in the amount of the active
pharmaceutical ingredient(API) in drug product due to degradation. According to an FDA
guidance document, a stability-indicating method is a validated quantitative with time. A
stability-indicating method accurately measures the changes in active ingredients
concentration without interference from other degradation products, impurities and
excipients. Stress testing is carried out to demonstrate specificity of the developed method to
measure the changes in concentration of drug substance when little information is available
about potential degradation product. The development of a suitable stability indicating
method provides a back ground for the pre-formulation studies, stability studies and the
development of proper storage requirements.[2,3,18,19]
The FDA and ICH guidances state the requirement of stability testing data to understand how
the quality of a drug substance and drug product degradation studies are a regulatory
requirement and scientific necessity during drug development, it is not considered as a
requirement for formal stability program. It has become mandatory to perform stability
studies of new drug moiety before filing in registration dossier. The stability studies include
long term studies(12months)and accelerated (6months). But (6months) can be performed at
conditions milder than that used in accelerated studies. So the study of degradation products
like separation, identification and quantitation would take even more time. As compared to
stability studies, forced degradation studies help in generating degradants in much shorter
span of time, mostly a few weeks.[33,34]
Analytes
For a related substance method, determining the significant and relevant related substances
is very critical. Significant degradation products observed during testing should be
Resolution
A stability indicating method must resolve all significant degradation products from each
other. Typically the minimum requirement for baseline resolution is 1.5. This limit is valid
only for 2 Gaussian-shape peaks of equal size. In actual method development, Rs = 2.0
should be used as a minimum to account for day to day variability, non-ideal peak shapes and
differences in peak sizes.
Precision, Accuracy
Expectations for precision and accuracy should be determined on a case by case basis. For a
typical related substance method, the RSD of 6 replicates should be less than 10%. Accuracy
should be within 70 % to 130% of theory at the LOQ level.
Analysis time
A run time of about 5-10 minutes per injection is sufficient in most routine related substance
analyses. Unless the method is intended to support a high-volume assay, shortening the run
time further is not recommended as it may compromise the method performance in other
aspects (e.g., specificity, precision and accuracy).
Solvent type
Solvent type (methanol, acetonitrile and tetrahydro-furan) will affect selectivity. The choice
between methanol and acetonitrile may be dependent on the solubility of the analyte as well
as the buffer used. Tetrahydrofuran is least polar among these three solvent, often responsible
for large changes in selectivity and is also incompatible with the low wavelength detection
required for most pharmaceutical compounds.[14,15,16]
Mobile phase pH
Most pharmaceutical compounds contain ionisable functionalities such as amino, pyridine
and carboxylic acid. Introduction of new packing material that are stable over a wide range of
pH up to pH 12 allow for a broader applicability of a mobile phase pH as a
retention/selectivity adjustment parameter . When the sample is eluted with a mobile phase of
100% (organic), there is no separation, as the sample is eluted in the void volume. This is
because the sample is not retained; but retention is observed when the mobile phase solvent
strength is decreased to allow equilibrium competition of the solute molecules between the
bonded phase and the mobile phase. When the separation is complex, that is, many
components are to be separated, and when the solvent strength is decreased and there is still
no resolution between two close peaks, another organic solvent of a different polarity or even
a mixture of two organics may need to be tried to effect separation. Additionally, mobile
phase optimization can be enhanced in combination with bonded phase optimization (i.e.,
substituting C18/C8 with cyano or phenyl). A goal for the band spacing of a solute (K)
should be in the range of 4 to 9 and a run time of about 15 minutes or 20 minutes at most for
most routine product release or stability runs.[5]
Identifying the best stationary phase for separation is the most critical step of column
selection, and decision should be based on sample solubility and the chemical differences
among the compounds of interest. There are several types of matrices for support of the
stationary phase, including silica, polymers, alumina, and zirconium. Silica is the most
common matrix. Silica matrices are robust, easily derivatized, manufactured to consistent
sphere size, and does not tend to compress under pressure. Silica is chemically stable to most
organic solvents and to low pH systems. In recent years, silica supported columns have been
developed for use at high pH. The nature of the stationary phase will determine whether a
column can be used for normal phase or reverse phase chromatography. Common stationary
phases are C4 (butyl), C8 (MOS), C18 (ODS), nitrile (cyanopropyl), and phenyl
(phenylpropyl) columns. In general, longer alkyl chains, higher phase loading, and higher
carbon loads provide greater retention of non-polar analytes. Selectivity is most influenced by
the amount of accessible surface area of the derivatized silica gel particles and the carbon
load. Thus it is often a benefit to not only have columns with different stationary phases, but
columns with the same phase from different manufacturers.
Commonly used reverse phase columns and their uses are Propyl (C3), Butyl (C4), and
Pentyl (C5) phases are useful for ion-pairing chromatography (C4) (vide infra) and peptides
with hydrophobic residues, and other large molecules. C3C5 columns generally retain non-
polar solutes more poorly when compared to C8 or C18 phases. Examples include Zorbax
SB-C3, YMC-Pack C4, and Luna C5. These columns are generally less stable to hydrolysis
than columns with longer alkyl chains. Octyl (C8, MOS) phases have wide applicability. This
phase is less retentive than the C18phases, but is still quite useful for pharmaceuticals,
nucleosides, and steroids. Standard C18 Columns and similar stationary phases will undergo
phase collapse at highly aqueous mobile phases, typically at less than 5-10% organic
composition; this will decrease analyte-stationary phase interaction. Collapsed phases are
also difficult to re-equilibrate. To prevent phase collapse, C18 columns with a polar group
embedded in the alkyl chain have been developed to help solvate the hydrophobic chain in
>90% aqueous mobile phases. Examples include Zorbax SB-Aq, Synergi Hydro-RP and
YMC-Pack ODS-Aq.[26]
Column Temperature
Column temperature control is important for long-term method reproducibility as temperature
can affect selectivity. A target temperature in the range of 30-40C is normally sufficient for
good reproducibility. Use of elevated temperatures can bring benefits to HPLC, particularly
in instances where columns are stable over an extended temperature range. First, operating at
a temperature higher than ambient reduces the viscosity of the mobile phase and thus overall
backpressure on the column. Lower system pressures allow for faster flow rates and thus
faster analyses. The temperature may also effect the selectivity patterns because analytes will
While temperature is a variable that can affect selectivity , its effect is relatively small. Also
the k' generally decreases with an increase in temperature for neutral compounds but less
dramatically for partially ionized analytes. Some effect when there is a significant difference
in size and shape. Overall, it is better to use solvent strength to control selectivity than to use
temperature; its effect is much more dramatic. An increase of 1C will decrease the k' by 1 to
2%, a both ionic and neutral samples are reported to show significant changes in with a
temperature changes. Possible temperature fluctuations during method development and
validation, it is recommended that the column be thermo stated to control the temperature.[17]
Peak Purity
An essential requisite of a separation analysis is the ability to verify the purity of the
separated species, that is, to ensure that no co eluting or co migrating impurity contributes to
the peak response. Peak purity (or peak homogeneity) analysis of the main peak, to assess for
the presence of impurities under the main peak, is an essential part of the validation of a SIM.
Direct evaluation can be performed in-line by employing PDA detection, LC-MS or LC-
NMR. Indirect evaluation of peak purity can be accomplished by changing one or more
chromatographic parameters (column, mobile phase, gradient composition, etc.) that will
significantly impact the separation selectivity. The resulting impurity profile is then
compared against that of the original method. If the number of degradant peaks is the same in
both separations, and if the percent of the main component is the same in both separations,
then there can be reasonable confidence that all the degradants have been resolved from the
main component. Automated versions of this approach have been successfully utilized in a
multi-dimensional screening with instrumentation capable of systematically evaluating
several different columns and eluents for impurity analysis.[27,28,29,30]
Method Optimization
The experimental conditions should be optimized to get desired seperations and sensitivity
after getting appropriate seperations. The optimization of mobile phase parameters is always
considered first as this is much easier and convenient than stationary phase optimization.
Primary control variables (factors) in the optimization of liquid chromatography (LC)
methods are the different components of the mobile phase determining acidity, solvent
strength, gradient, flow rate, temperature, sample amounts, injection volume, and diluents
solvent type . This is used to find the desired balance between resolution and analysis time
after satisfactory selectivity has been achieved. The parameters involved include column
dimensions, column-packing particle size and flow rate. These parameters may be changed
without affecting capacity factors or selectivity.[4]
Method selection is the first step in establishing an analytical method and consideration must
be given to what is to be measured, and with what accuracy and precision. Method validation
must have a written and approved protocol prior to use.[7]
Method development and validation can be simultaneous, but they are two different
processes, both downstream of method selection. Analytical methods used in quality control
should ensure an acceptable degree of confidence that results of the analyses of raw
materials, excipients, intermediates, bulk products or finished products are viable. Before a
test procedure is validated, the criteria to be used must be determined.
Analytical methods should be used within good manufacturing practice (GMP) and good
laboratory practice (GLP) environments, and must be developed using the protocols set out in
the International Conference on Harmonization (ICH) guidelines (Q2A and Q2B, 2000 and
Monika Bakshi et al., 2002). The US Food and Drug Administration (FDA) John W Dolan et
al 2002 and Smela et al., 2005) and US Pharmacopoeia (USP) (Huynh Ba et al., 2009) both
refer to ICH guidelines.[13]
Limits of Degradation
The question of how much degradation is sufficient has been the topic of many discussions
amongst pharmaceutical scientists. Degradation of drug substances between 5% and 20% has
been accepted as reasonable for validation of chromatographic assays. It is not necessary that
forced degradation would result in a degradation product. The study can be terminated if no
degradation is seen after the drug substance or drug product has been exposed to stress
conditions than those conditions mentioned in an accelerated stability protocol. This is
indicative of the stability of the molecule under test. Over stressing a sample may lead to the
formation of a secondary degradation product that would not be seen in formal shelf-life
stability studies and under-stressing may not generate sufficient degradation products.[2,33]
Some conditions mostly used for forced degradation studies are presented in Table 1.
The primary degradants and their secondary degradation products can be distinguished by
testing at early time points and thus help in a better degradation pathway determination.
Studies should be repeated when formulations or methods change because the change may
lead to the production of new degradation products.
Degradation conditions
Typical degradation studies include four main degradation mechanisms: heat, hydrolytic,
oxidative, and photolytic degradation. Selecting suitable reagents such as the concentration of
acid, base, or oxidizing agent and varying the conditions (e.g.,temperature) and length of
exposure the preferred level of degradation can be achieved.
Hydrolytic conditions
Hydrolysis is one of the most common degradation chemical reaction over a wide range of
pH. Hydrolysis is a chemical process that includes decomposition of a chemical compound
by reaction with water. Hydrolytic study under acid or basic conditions involve catalysis of
ionizable functional groups present in the molecule. Acid or base stress testing involves
forced degradation of a drug substance by exposure to acidic or basic conditions which
generates primary degradants in desirable range. The selection of the type and concentrations
of acid or base depends on the stability of the drug substance. Hydrochloric acid or sulfuric
acids (0.11 M) for acid hydrolysis and sodium hydroxide or potassium hydroxide (0.11 M)
for base hydrolysis are suggested as suitable reagents. If the compounds for stress testing are
poorly soluble in water, then co-solvents can be used to dissolve them in HCl or NaOH. The
selection of co-solvent is based on the drug substance structure. Stress testing trial is
normally started at room temperature and if there is no degradation, elevated temperatures
(5070C) are applied. Stress testing should not exceed more than 7 days. The degraded
sample is then neutralized using suitable acid, base or buffer, to avoid further
decomposition.[2,18,35]
Oxidation conditions
Hydrogen peroxide is widely used for the oxidation of drug substances in forced degradation
studies but other oxidizing agents such as metal ions, oxygen, and radical initiators (e.g.,
azobisisobutyronitrile, AIBN) can also be used. Selection of an oxidizing agent, its
concentration, and conditions depends on the drug substance. It is reported that subjecting the
solutions to 0.13% hydrogen peroxide at neutral pH and room temperature for seven days or
up to a maximum of 20% degradation could potentially generate the relevant degradation
products. The oxidative degradation of drug substance involves an electron transfer
mechanism to form reactive anions and cations. Amines, sulfides and phenols are susceptible
to electron transfer oxidation to give N-oxides, hydroxylamine, sulfones and sulfoxide.The
functional group with labile hydrogen like benzylic carbon, allylic carbon, and tertiary carbon
or -positions with respect to hetero atom is susceptible to oxidation to form hydro peroxides,
hydroxide or ketone.[18,35,36]
Thermal conditions
Thermal degradation (e.g., dry heat and wet heat) should be carried out at more strenuous
conditions than the recommended ICH, Q1A accelerated testing conditions. Samples of solid-
state drug substances and drug products should be exposed to dry or wet heat, while liquid
drug products should be exposed to dry heat. Studies may be conducted at higher
temperatures for a shorter period. Effect of temperature on thermal degradation of a substance
is studied through the Arrhenius equation
k=AeEa/RT
Where k is specific reaction rate, A is frequency factor, Ea is energy of activation, R is gas
constant (1.987 cal/deg mole) and T is absolute temperature . Thermal degradation study
is carried out at 4080C.[2,18,35,36]
Photolytic conditions: The photo stability testing of drug substances must be evaluated to
demonstrate that a light exposure does not result in unacceptable change. Photo stability
studies are performed to generate primary degradants of drug substance by exposure to UV or
fluorescent conditions. Samples of drug substance and solid/liquid drug products should be
exposed to a minimum of 1.2 million lux hours. The most commonly accepted wavelength of
light is in the range of 300800 nm to cause the photolytic degradation. The maximum
illumination recommended is 6 million lux hours. Light stress conditions can induce photo
oxidation by free radical mechanism.[2,36]
CONCLUSION
Stability-indicating method is an analytical procedure that is capable of discriminating
between the major active (intact) pharmaceutical ingredients (API) from any degradation
(decomposition) product(s) formed under defined storage conditions during the stability
evaluation period.
REFERENCES
1. Azim Md Sabir, HPLC method development and validation: A Review.
2. Blessy M, Development of forced degradation and stability indicating studies of drugs
A review.
3. B. Prathap, A Review on stability indicating HPLC method development. International
Journal of Innovative Pharmaceutical Research. 2012; 3(3): 229-237.
4. Changhe Wen, Designing HPLC Methods for Stability Indication and Forced
Degradation Samples For API, Collected from American Pharmaceutical Review at
http://www.americanpharmaceuticalreview.com.
5. Donald D Hong and Mumtaz Shah, Development and validation of HPLC Stability
indicating Assays, In: Sens T. Carstensen, C.T. Rhodes, editors Drug Stability-Principle
& Practice. 3rd Edition. New York: Marcel Dekker Inc. 2008; 332.
6. FDA Guidance for Industry: Analytical Procedures and Methods Validation (draft
guidance), August 2000.
7. GA Shabir. Validation of HPLC Chromatography Methods for Pharmaceutical Analysis.
Understanding the Differences and Similarities between Validation Requirements of
FDA, the US Pharmacopeia and the ICH. J. Chromatogr. A. 2003; 987(1-2): 57-66.
8. Georg nagva, Forced degradation studies as a integral part of HPLC stability indicating
method development. Drug delivery technology. 2010.
9. Huynh K Ba (ed.). Development of Stability indicating methods. Handbook of Stability
Testing in Pharmaceutical Development; Springer 2009: 154.
10. Huynh K Ba. Development of Stability indicating methods; In: Handbook of Stability
Testing in Pharmaceutical Development, Springer 2009; 153.
11. Satinder Ahuja, Michael W.dong, Handbook of Pharmaceutical analysis by HLPC.
12. ICH guidelines Q1A (R2). Stability Testing of New Drug Substances and Products
(revision 2), November 2003.
13. International Conference on Harmonisation of Technical Requirements for Registration
of Pharmaceuticals for Human Use (ICH), Quality Guidelines, http://www.ich.org/
products/guidelines/quality/ article/ quality- guidelines.html.
14. John W Dolan. Stability-Indicating Assays. LC Troubleshooting. 2005:275.
15. John W Dolan. Stability-IndicatingAssays. LC Troubleshooting. LC-GC North America.
2002; 20(4): 346-349.
16. JW Dolan. Journal of Chromatography A. 2002; 965: 195-205.
17. LR Snyder, JL Glajch, JJ Kirkland. Practical HPLC method Development. New York:
John Wiley; 1988; 227-251.
18. Monika Bakshi and Saranjit Singh: Development of validated stability-indicating assay
methods-critical review. J. Pharm. Biomed. Anal. 2002; 28(6): 1011-1040.
19. Patel Riddhiben M, Stability indicating HPLC method development, IJRP, 2011; 2(5):
79-87.