Stability Indicating HPLC Method Development A Review

International Journal of Trend in Scientific Research and Development (IJTSRD)
Volume 5 Issue 5, July-August 2021 Available Online: www.ijtsrd.com e-ISSN: 2456 – 6470
@ IJTSRD | Unique Paper ID – IJTSRD46310 | Volume – 5 | Issue – 5 | Jul-Aug 2021 Page 2286
Stability Indicating HPLC Method Development - A Review
Suraj Nagwanshi1
, Smita Aher2
, Rishikesh Bachhav3
1
Department of Quality Assurance Techniques, R. G,
Sapkal College of Pharmacy, Anjaneri, Nashik, Maharashtra, India
2
Department of Pharmaceutical Chemistry, R. G, Sapkal College of Pharmacy, Anjaneri, Nashik, Maharashtra, India
3
Department of Pharmacology, R. G, Sapkal College of Pharmacy, Anjaneri, Nashik, Maharashtra, India
ABSTRACT
High-performance liquid chromatography (HPLC) is an essential
analytical tool for evaluating drug stability. HPLC methods must be
able to isolate, detect, and quantify drug-related degradation products
that may form during storage or production, and identify drug-related
impurities that may form during synthesis. .. This article describes
strategies and challenges for designing HPLC methods to
demonstrate drug stability. It will deepen our understanding of drugs
and medicinal chemistry and demonstrate advances in stability that
reflect an analytical approach. Several important chromatographic
parameters were investigated to improve the detection of potentially
related degradants. It is necessary to find suitable solvent and mobile
phase samples that provide sufficient stability and compatibilitywith
each component and potential impurities and degradants. This
method should be carefully considered as it has the ability to
distinguish between primary and secondary decomposers. The study
of forced destruction of chemicals and new drugs is essential for the
development and characterization of these immobilization methods.
Practical guidance is provided at each stage of drug development to
develop a forced-disposal protocol and avoid common issues that
might impede data interpretation.
KEYWORDS: HPLC, Forced degradation, Stability indicating
method
How to cite this paper: Suraj Nagwanshi
| Smita Aher | Rishikesh Bachhav
"Stability Indicating HPLC Method
Development - A Review" Published in
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and Development
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INTRODUCTION
Drug stability testing requires an accurate analytical
method to determine the amount of a
pharmaceutically active substance (API) without the
interference of degradants, process contaminants, and
other potential contaminants. With the introduction of
guidelines from the International Council for
Coordination Harmonization (ICH), the need to
establish a Stability Assessment Methodology
(SIAM) has become increasingly clear. The
guidelines specifically call for essential degradation
studies to be performed under various conditions such
as pH, light, oxidation and dry heat. It separates the
drug from its breakdown products. Stability
Demonstration Methods Stability demonstration
experiments are quantitative analytical methods that
can detect changes in drugs and drug properties over
time. Stability tests accurately determine the active
ingredient without affecting the handling of
degradation products, impurities, auxiliary ingredients
or other potential impurities. In addition to
demonstrating specificity, forced degradation studies
are used to facilitate the formulation, production and
development of packaging by identifying degradation
pathways and degradation products of active
ingredients that may occur during storage. These
studies often
STABILITY INDICATING METHOD
DEVELOPMENT STRATEGIES
Provide methods to produce specific hydrolysis
products that are needed to validate methods.
There is no “but if not all” sustainable development
formula that relates to the analysis of growth
strategies for sustainability indicators. It is advisable
to look at the development of this method from a
broader perspective before embarking on actual
experiments. Bakshi and Singh discussed several
important issues related to the development of
IJTSRD46310

International Journal of Trend in Scientific Research and Development @ www.ijtsrd.com eISSN: 2456-6470
fixation techniques. Dolan 3 provided feedback on the
stability of the measurements. Discussing Smella 4
from an organizational point of view.
Figure 1: Overview of the Method Development Process
Step I - Understand the chemistry/ Physicochemical properties of drug
Knowledge of physical and chemical properties and API expression is essential to support method development.
Information on various properties was collected to generate relevant information through systematic programs or
literature searches to support drug discovery, company drug specifications, spectral libraries, and drug discovery
reports. Information for element selection for study of dissociation constants, partition coefficients, fluorescence
properties (if applicable), chromatographic behavior, spectral properties, redox potentials to prepare initial test
conditions, and stresses, or information suggesting useful dissociation mechanisms. [5,6] Dissociation constants
and dissociation constants can be used to develop efficient sampling methods to determine optimal mobile phase
pH for good separation. Fluorescence properties, spectroscopy, chromatography, and redox data can be used to
determine the best way to measure and measure the assay of interest. The structure of the analyte, particularly
functional groups, reflects the potential active degradation sites and the drug's susceptibility to hydrolysis,
oxidation, and pyrolysis. Compatibility testing is performed to evaluate the stability of the state when mixed
with traditional adjuvants and lubricants and to determine the interaction of the drug with the raw (inactive)
ingredient. First-class testing should be performed to determine procedures for subsequent experiments based on
past experience.
Step II – Set up Preliminary HPLC condition
The first empirical situation can be adopted from the literature in a formal or informal manner and as a starting
point. Officially published USP methods are acceptable and can be used for stability testing after stability and
suitability for use have been demonstrated. If that path is not available, you must create a new path. Test
conditions should be based on API properties and impurities, if known. Choosing the right tree and the right
mobile phase is very important. There is a lot of information about many HPLC columns today, and you can
choose the right column for each API type. Choose the column and phase group you are moving to get the
correct separation position. The development of computational methods is very useful for rapidly developing
initial HPLC conditions. As the goal of this phase is to rapidly develop HPLC conditions for subsequent method
development experiments, scientists will focus on isolating important related substances to improve the accuracy
of all related substances. A good beta level saves a lot of time in the early development phase.[8]
Step III – Preparation of samples required for method development
SIM cards are typically designed using API controls under conditions other than those used for rapid reliability
testing. In addition to being displayed on the SIM card, it can generate experimental stress, also known as forced
disassembly, to provide information about the product and disassembly pathway during storage to aid
development. Used package. In the early stages of development, it is difficult to find real examples. Focusing on
the API creates a more realistic prototype in terms of the memory used to develop SIM cards. [9] These studies
typically aim to analyze 5-10% of APIs. Conduct pyrolysis, hydrolysis, oxidation, photolysis, and/or forced
degradation studies under harvest conditions. Forced dissolution samples should be tested under initial HPLC
conditions using appropriate reagents, preferably PDA reagents. Common formulations - solid (tablets/capsules),
semi-solids (ointments/creams) or slurries (cough syrup/ophthalmic solutions) - solid phase extraction (SPE) are
used for sample preparation, but it is very important that they are used specifically for the sample. One is for
replacement. director. .. in many ways the US Environmental Protection Agency (EPA).[10]

Step IV – Developing Separation – Stability Indicating Chromatography
Prerequisites The most important factor in choosing a SIM card chromatography basis for a new device is to
ensure the separation and identification of degraded substances in solution. To this end, a 1:1 dilution of
water:organic solvent is a good starting point as it increases the solubility of most of the related substances and
ensures good dissolution of solid formulations. The second step is to obtain separation conditions so that we can
identify as many different peaks as possible in the experimental sample set. The most common dissociation
variables are solvent type, pH of the mobile phase, column type, and temperature.[1]
Isocratic or Gradient Mode The choice between step mode or step mode depends on the number of active
ingredients to be dissolved or separated. To determine if calibration is required or if a stoichiometric mode is
appropriate, an initial slope is generated and the ratio of the total calibration time to the difference in
calibration time between the first and last components is calculated. The calculated ratio is 0.25, and a slope
is useful as shown in Figure 2. Typically, conformal mode is used to launch a product, and gradient mode is
used to evaluate stability. This is because isometric methods usually involve passwords. No wear is checked
unless the product initially molds within 15 minutes. Over time, decomposition products are formed that
must be controlled. This requires a gradient process to completely dissolve the mixture. Thus, the gradient
process is a stabilization or conditioning process.
Figure 2: Isocratic or Gradient?
Solvent type The solvent type (methanol, acetonitrile, tetrahydrofuran) affects the selectivity. The choice
between methanol and acetonitrile depends on the solubility of the analysed material and the buffer used.
Tetrahydrofuran is the least polar of these three solvents, often produces large changes in selectivity, and is
not compatible with the short wavelength detection required for most active substances.[5, 12]
Mobile phasepH When filtering a sample in mobile phase 100 (organic), if the sample is placed in a volume
under vacuum, separation does not occur due to insufficient sample retention, but retention occurs when the
solvent strength decreases in the mobile phase. Collision between dissolved molecules between the
conjugate and the mobile phase preparation: d. If Harry is complicated. Separation should be attempted if
there is another organic solvent of different polarity, or a mixture of the two organic substances. The target
bandgap (K') for the dissolved material should be 4-9 and the run time is about 15 minutes or up to 20
minutes for most conventional or stationary products.[5]
Role of the column and column temperature The heart of the HPLC system is the column. Column
changes have the greatest impact on analytical accuracy during method development. The three main
components of an HPLC column are material (shaft housing), matrix, and stationary phase. Typically,
modern reverse-phase HPLC columns are produced by filling the column jacket with spherical silica gel
coated with a hydrophobic solid phase. The reaction of chlorosilanes with hydroxyl groups on the silica gel
surface introduces a stationary phase into the matrix. In general, the characteristics of the stationary phase
have the greatest influence on capacity, selectivity, efficiency and leaching factors. There are several types
of solid-phase matrices, including silica, polymer, alumina, and zirconium. Silica is the most commonly used
matrix in HPLC columns. The silica matrix is strong, easily deformed, formed into a rigid bead shape, and is
not compressed under pressure. Silica is chemically stable in most organic solvents and low pH systems. A
short-term solution for solid silica supports is to melt at pH 7 or higher. Recently, silica-based columns have
been developed for use at high pH values. The type, size and shape of the particles support the silica
separation effect. The smaller the particles, the more theoretical pages and the higher the separation
efficiency. However, using smaller particles increases the reflux pressure during chromatography and
increases access to the column. For this reason, development work uses more than three or five pillars. A
narrower particle size distribution of the silica particles results in higher accuracy. Thus, different

combinations of similar phase columns from different manufacturers or columns from the same plant can
have very different separation properties due to different matrix manufacturing processes. The character of
the scene has been proven.[14]
Column temperature Controlling column temperature is important for long-term reproducibilityof methods
as temperature can affect selectivity. A target temperature in the range of 30-40 °C is usually sufficient for
good measurements. Using a higher temperature can be beneficial for a number of reasons. First, working at
a higher ambient temperature reduces the viscosity of the mobile phase and reduces the pressure across the
shaft. Low system pressure results in faster flow rates and faster analysis. Temperature can also affect
selectivity models because analytes react differently at different temperatures. Finally, using a vertical oven
eliminates deviations due to normal temperature fluctuations around the axis. Temperature is a variable that
can affect selectivity, but the effect is relatively small. Also, k generally decreases with increasing
temperature of neutral compounds, but is less pronounced in partial ionization analyses. If there is a big
difference in size or shape, it will take some damage. In general, it is better to use the strength of the solvent
rather than the temperature to control the selectivity. The effect is more dramatic. An increase of 1 °C
decreases k from 1% to 2%, and the ionic and neutral samples show large changes in temperature. Possible
temperature changes during the process.
Peak Purity Analyzing the peak purity (or peak asymmetry) of the central peak is an important part of
validating the SIM card to assess the presence of contaminants below the central peak. Direct linear
evaluation can be performed using PDA16, LC-MS17 or LC-NMR detection. However, PDA only works
well with hydrophobic substances that have a different UV spectrum than the drug itself. If the molecular
weight is the same as that of Detromere, or if the ionization of the digester is suppressed bythe existing API,
the digester will not work. An indirect assessment of peak purity can be accomplished by modifying one or
more chromatographic parameters (column, mobile phase, gradient structure, etc.) that significantly affect
separation selectivity. The resulting impurity profile is compared to the original method. If the two classes
have the same number of decomposition peaks and the percentage areas of the principal components are the
same in both classes, then we can logically conclude that all decompositions are solved by the principal
components. Automated versions of this approach have been successfully used on multidimensional sieves
equipped with various columns and tools to systematically assess mass for the analysis of impurities 18, 19,
20. Other approaches to alternative separation techniques with similar objectives as the chapter on LiLi
chromatography, thin layer chromatography (TLC), natural phase HPLC, capillary electrophoresis (CE) and
supercritical liquid chromatography (SFC).[21].
Step V –Method Optimization
The experimental conditions should be optimized to get desired separations and sensitivity after getting
appropriate separations. Stability-indicating assay experimental conditions will be achieved through
planned/systematic examination on parameters including pH (if ionic), mobile phase components and ratio,
gradient, flow rate, temperature, sample amounts, injection volume, and diluents solvent type.[8]
Step VI – Validation of analytical method
The method must be validated according to USP/ICH guidelines to show the accuracy, precision, specificity,
linearity, range, detection limit, quantification limit, robustness and robustness of the method. A verification plan
must be developed and acceptance criteria must be defined. If the degradation product is above the identification
threshold (usually 0.1%), it is necessary to separate, identify, characterize and identify it. [22, 23] There are a
variety of techniques that can be used to identify and characterize impurities and degradation products, such as
HPLC with PDA (photodiode array) detector, IR (infrared) spectroscopy, elemental analysis, MS (mass
spectrometry), NMR (resonance nuclear magnetic field) ), GC/MS, LC/MS, LC/MS/MS, LC/NMR, etc. Method
development and validation are cyclical activities. If new problems are found in the method or the results do not
meet the acceptance criteria during the verification process, the method should be modified and re-verified until
the method is suitable for use.
FORCED DEGRADATION STUDIES IN STABILITY-INDICATING METHOD DEVELOPMENT
Forced degradation studies usually involve exposing a drug or a representative sample of a drug to light, heat,
humidity, acid/base hydrolysis, and oxidation, and other related pressure conditions. These experiments play an
important role in the drug development process to promote: the development of stability indicator methods, the
design of drug formulations, the selection of storage and packaging conditions, and a better understanding of the
potential responsibilities of drug molecule chemistry and stability- Related issues are resolved. 9.24-26 The

mandatory degradation of APIs and products (in addition to establishing specificity) will also provide the
following information:
1. Determination of degradation pathways of drug substances and drug products;
2. Discernment of degradation products in formulations that are related to drug substances versus those that are
related to non-drug substances(e.g., excipients);
3. Structure elucidation of degradation products;
4. Determination of the intrinsic stability of a drug substance molecule in solution and solid state;
5. reveal the thermolytic, hydrolytic, oxidative, and photolytic degradation mechanism of the drug substance
and drug product.[27]
According to the guidance documents of ICH and FDA, mandatory degradation studies are mainlyused for three
purposes: to provide assessment of the stability of drug substances or preparations; to clarify the possible
degradation pathways of active pharmaceutical ingredients in drug substances or drug products; and to
investigate applicable to drug substances and drug products. The stability index capability of the drug analysis
program.
Although FDA Guide 28 and ICH Guide provide useful definitions and general comments on mandatory
degradation studies, their guidelines on scope, timing, and best practices are very general and lack details. Test
conditions and schedule for conducting research related to the drug development phase.
Experimental Design to Forced Degradation Studies Study protocol
A general protocol for conducting forced degradation studies, shown in figure 3 is arranged according to the type
of test material (drug substance, drug product) and the type of degradation (hydrolysis, oxidation, etc.)
Figure 3: An illustrative diagram showing the different forced degradation conditions to be used for
drug substance and drug product
Condition for stress Testing
Initial experiments should focus on determining the conditions that will degrade the drug by approximately 10%.
Table 1 summarizes the different pressure conditions and exposure times commonlyused for forced degradation.
The concentration of the drug in the pressure sample solution will affect the final target degradation level
achieved. Dilute sample concentrations generally produce more extensive degradation than more concentrated
solutions, as shown in Figure 4. Therefore, reducing the drug concentration when necessary can help increase
degradation.[16,17]
Table 1: Conditions generally employed for forced degradation
Stress Type Condition Time
Acid hydrolysis 0.1 N HCL (upto 5.0N) 1-7 days
Base Hydrolysis 0.1 N naOH/KOH (upto 5.0 N) 1-7 days
Thermal Hydrolysis 70 0
C 1-7 days
Oxidative Solution
O2 + Initiator (AIBN) in ACN/water, 80/20, 400
C,
RT, protected from light
Few hrs to 7 days
Thermal 700
C Upto 2 weeks
Thermal / Humidity 700
C/75%RH Upto 2 weeks

Figure 4: Thermal hydrolysis profile of an API (Structure not shown) at 700C: degradation vs. time at
three sample concentrations
Timeline for conducting studies
The ICH guidelines do not mention any regulatory
requirements for mandatory degradation studies in the
first or second phase of development. There are good
reasons to initiate the forced degradation study of
drug substances in the first phase. The most important
reason is to support the development of a highly
discriminatory preliminary method because it can
detect most, if not all, degradation products. . This
method will have stability indicator capabilities, and
at this stage only requires minimal verification. The
compulsory degradation study of APIs and
preparations should be completed before the
registration stability study. It will be helpful to
determine the main degradation products at that
time.[23,24]
CONCLUSION
The ICH guidelines do not mention any regulatory
requirements for mandatory degradation studies in the
first or second phase of development. There are good
reasons to initiate the forced degradation study of
drug substances in the first phase. The most important
reason is to support the development of a highly
discriminatory preliminary method because it can
detect most, if not all, degradation products. . This
method will have stability indicator capabilities, and
at this stage only requires minimal verification. The
compulsory degradation study of APIs and
preparations should be completed before the
registration stability study. It will be helpful to
determine the main degradation products at that time.
REFERENCES
[1] FDA Guidance for Industry. Analytical
Procedures and Methods Validation (draft
guidance), August 2000.
[2] Monika Bakshi and Saranjit Singh.
Development of validated stability-indicating
assay methods--critical review. J. Pharm.
Biomed. Anal. 2002; 28(6):1011-1040
[3] John W. Dolan. Stability-Indicating Assays. LC
Troubleshooting. LCGC North America, 2002;
20(4):346-349.
[4] Michael J. Smela. Regulatory Considerations
for Stability Indicating Analytical Methods in
Drug Substance and Drug Product Testing.
American Pharmaceutical Review. 2005;
8(3):51-54.
[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 &
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[6] K. Huynh-Ba, Development of Stability
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[7] http://www.cvg.ca/images/HPLC_Method_Dev
elopment.pdf - Effective HPLC method
development.
[8] Changhe Wen, Designing HPLC Methods for
Stability Indication and Forced Degradation
Samples For API, Collected from American
Pharmaceutical Review at
http://www.americanpharmaceuticalreview.co
m
[9] Swartz M. and Krull I., “Developing and
Validating Stability Indicating Methods”.
LCGC North America, 2005; 23(6):586- 593.
[10] Supplement to LC/GC. Current trends and
developments in sample preparation, May1998.

[11] K. Huynh-Ba (ed.), Development of Stability
indicating methods; In: Handbook of Stability
Testing in Pharmaceutical Development,
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[12] John W. Dolan, “Stability-Indicating Assays”,
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[13] LR Snyder, JL Glajch, JJ Kirkland. Practical
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[19] Stepensky D, Chorny M, Dabour Z,
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