PREFORMULATION STUDIES

Definition:
Preformulation is the first step in the rational development of dosages form of a drug
substance. It can be defined as an investigation of physical and chemical properties of the
drug substances alone and when combined with excipients, in order to develop a stable, safe,
effective and affordable dosage form.
Objectives:
The overall objective of Preformulation is to generate information useful to the formulator in
developing stable and bioavailable dosage form that can be mass produced.
Principal areas of Preformulation

SL NO PRINCIPAL AREAS EXAMPLES

Crystallinity and polymorphism
Hygroscopicity
1 BULK CHARACTERIZATION
Fine particle characterization
Powder flow
Ionization constant – pKa
pH solubility profile
Common ion effect – KSP.
2 SOLUBILITY ANALYSIS Thermal effects
Solubilization
Partition coefficient
Dissolution
Stability in toxicology formulation
Solution stability
pH stability profile
3 STABILITY ANALYSIS
Solid state stability
Bulk stability
Compatibility

1. BULK CHARACTERIZATION
When a drug molecule is discovered all the solid-forms are hardly identified. So during bulk
characterization the following characteristics are studied.
(i) Crystallinity and polymorphism
Chemical Compounds

Habit Internal Structure

Crystalline Amorphous

Single Entity Molecular Adduct

POLYMORPHS

Non-stoichiometric Stoichiometric
Inclusion compounds solvates / hydrates

Channel Layer Cage

(Clathrate)
 Flow ability of powder and chemical stability depends on the habit and internal structure of a
drug.

Habit is the description of the outer appearance of a crystal. A single internal-structure for a
compound can have several different habits, depending on the environment for growing crystals.
Different habits of crystals are given below.

Needle or Acicular
Platy
Tabular

Bladed
Equant or Massive
Fig. 1 Prismatic

Internal Structure

Crystalline state
In this state of matter atoms or molecules are arranged in highly ordered form and is associated with
three-dimensional periodicity.

[N.B. Atoms or molecules tend to organize themselves into their most favorable thermodynamic state, which under certain
conditions results in their appearance as crystals.
N.B. The repeating three-dimensional patterns are called crystal lattices. The crystal lattice can be analyzed from its X-ray
diffraction pattern.]

Amorphous forms
In this forms the solids do not have any fixed internal structure. They have atoms or molecules
randomly placed as in a liquid.
e.g. Amorphous Novobiocin
[N.B. Amorphous forms are prepared by rapid precipitation, lyophillization or rapid cooling of molten liquids
e.g. glass]

Difference between crystalline and amorphous form

Crystalline forms Amorphous forms
(i) Fixed internal structure (i) Do not have any fixed internal structure
(ii) More stable than its amorphous forms. (ii) Higher thermodynamic energy than its
(iii) More stable than its amorphous forms. crystalline form.
(iv) Lesser solubility than its amorphous form. (iii) Less stable than its crystalline forms.
(v) Lesser tendency to change its form during (iv) Greater solubility than its crystalline forms.
storage. (v) Tend to revert to more stable forms during
storage.

Polymorphs
When a substance exists in more than one crystalline form, the various forms are called Polymorphs
and the phenomenon as polymorphism.
e.g. Chloramphenicol palmitate has three polymorphs A, B and C .
Depending on their relative stability, one of the several polymorphic forms will be physically more
stable than the others. Such a stable polymorph represents the lowest energy state, has highest melting
point and least solubility. The representing polymorphs are called metastable forms which represent
higher energy state; the metastable forms have a thermodynamic tendency to convert to the stable
form. A metastable form cannot be called unstable because if it is kept dry, it will remain stable for
years.
Molecular Adducts
During the process of crystallization, some compounds have a tendency to trap the solvent
molecules.
1. Non-Stoichiometric inclusion compounds (or adducts)
In these crystals solvent molecules are entrapped within the crystal lattice and the number of
solvent molecules are not included in stoichiometric number. Depending on the shape they are of
three types :-
(1) Channel
When the crystal contains continuous channels in which the solvent molecule can be included.
e.g . Urea forms channel.
(2) Layers:- Here solvent molecules are entrapped in between layers of crystals.
(3) Clathrates(Cage):- Solvent molecules are entrapped within the cavity of the crystal from all sides.

2. Stoichiometric inclusion compounds (or stoichiometric adducts)

This molecular complex has incorporated the crystallizing solvent molecules into specific sites
within the crystal lattice and has stoichiometric number of solvent molecules complexed.
When the incorporated solvent is water, the complex is called hydrates and when the solvent is
other than water, the complex is called solvates. Depending on the ratio of water molecules within a
complex the following nomenclature is followed.
(i) Anhydrous : 1 mole compound + 0 mole water
(ii) Hemihydrate: 1 mole compound + ½ mole water
(iii) Monohydrate: 1 mole compound + 1 mole water
(iv) Dihydrate : 1 mole compound + 2 moles water

Properties of solvates / hydrates

(i) Generally, the anhydrous form of a drug has greater aqueous solubility than its hydrates. This is
because the hydrates are already in equilibrium with water and therefore have less demand for
water. e.g. anhydrous forms of theophyline and ampicillin have higher aqueous solubility than the
hydrates.
(ii) Non aqueous solvates have greater aqueous solubility than the non-solvates. E.g. chloroform
solvates of griseofulvin are more water soluble than their nonsolvate forms.

ANALYTICAL METHODS FOR CHARACTERIZATION OF SOLID FORMS

Methods of studying solid forms are listed as below:

Method Material required per sample

Microscopy 1 mg
Hot stage microscopy 1 mg
Differential Scanning Calorimetry (DSC) 2 – 5 mg
Differential Thermal Analysis (DTA) 2 – 5 mg
Thermogravimetric Analysis 10 mg
Infrared Spectroscopy 2 – 20 mg
X-ray Powder Diffraction 500 mg
Scanning Electron Microscopy 2 mg
Dissolution / Solubility Analysis mg to gm

Microscopy
In this type of microscope light passes through cross-polarizing filters.
Amorphous substances (e.g. super-cooled glass and non-crystalline organic compounds or substances
with cubic crystal lattices e.g. NaCl ) have single refractive index. Through this type of microscope
the amorphous substances do not transmit light, and they appear black. They are called isotropic
substances.
Hot-stage microscopy
In this case, the polarizing microscope is fitted with a hot stage to investigate polymorphism,
melting points, transition temperatures and rates of transition at controlled rates.
It facilitates in explaining the thermal behavior of a substance from the DSC and TGA curves.

[N.B. A problem often encountered during thermal microscopy is that organic molecules can degrade during the melting
process, and recrystallization of the melt may not occur, because of the presence of contaminant degradation products. ]

Thermal Analysis

Differential Thermal Analysis

In DTA instrument a record is
produced where temperature
difference (T) (between the sample
and reference material) is plotted
against temperature (T) when two
specimens are subjected to an
identically controlled temperature
regime.
The reference material is alumina,
keiselguhr.

Differential Scanning Calorimetry

In DSC method the difference in energy inputs (H) into a sample and reference material is
measured as a function of temperature as the specimens are subjected to a identically controlled
temperature programme.

Samples that may be studied by DSC or DTA

are:
Powders, fibres, single crystals,
polymer films, semi-solids or liquids.

Applications of DTA / DSC in preformulation

studies
1. To determine the purity of a sample
2. To determine the number of
polymorphs and to determine the ratio
of each polymorph.
3. To determine the heat of solvation
4. To determine the thermal degradation of a drug or excipients.
5. To determine the glass-transition temperature (tg) of a polymer.

Thermogravimetric Analysis (TGA)

TGA measures the changes in sample weight as a function of time (isothermal changes) or
temperature.

Application of TGA in preformulation study

1. Desolvation and decomposition processes
are monitored.
2. Comparing TGA and DSC data recorded under identical conditions can greatly help in the
explanation of the thermal process.

TGA and DSC analysis of an acetate salt of

an organic amine that has two crystalline
forms, anhydrous and dihydrate are shown
above. Anhydrous / dihydrate (10:1) mixture
was prepared by dry blending. Heating rate
was 50C/min.
From DSC curve, it is evident that
the dihydrate form loses two molecules of
water via an endothermic transition between
700C and 900C. The second endotherm at
1550C corresponds to melting process.
From TA curve, it is evident that at
70 – 900C weight-loss was due to the loss
two molecules of water and the weight loss
at 1550C was due to vaporization of acetic
acid and decomposition.

X-RAY POWDER DIFFRACTION

When a X-ray beam falls on a powder the
beam is diffracted. This diffraction in found
only in case of crystalline powder.
Amorphous forms do not show X-ray
diffraction.
Uses:
(i) Each diffraction pattern is characteristic of a specific
crystalline lattice for a given compound. So in a 6 Fig. 6
mixture different crystalline forms can be analyzed 5
using normalized intensities at specific angles.
4
(ii) Identification of crystalline materials by using their Intensity
diffraction pattern as a ‘finger print’. First, the powder 3
diffraction photograph or diffractometer trace are taken 2
and matched with a standard photograph. All the lines 1
and peaks must match in position and relative intensity.
20 40 60 80 100
% From B
HYGROSCOPICITY

Definition: Many pharmaceutical materials have a tendency to adsorb atmospheric moisture

(especially water-soluble salt forms). They are called hygroscopic materials and this
phenomenon is known as hygroscopicity.
Equilibrium moisture content depends upon:
(i) the atmospheric humidity
(ii) temperature
(iii) surface area
(iv) exposure time
(v) mechanism of moisture uptake.

Deliquescent materials:
They absorb sufficient amount of moisture and dissolve completely in it. (e.g. anhydrous calcium
chloride).
Tests of hygroscopicity
powder sample
Procedure desiccator
Bulk drug samples are placed in open containers shallow
with thin powder bed to assure maximum container
atmospheric exposure. These samples are then
saturated salt
exposed to a range of controlled relative solution
humidity (RH) environments prepared with
saturated aqueous salt solutions. Fig. 7

The amount of moisture adsorbed can be determined by the following methods:

(i) Gravimetry
(ii) Thermogravimetric analysis (TGA)
(iii) Karl-Fischer titration (KF-titration)
(iv) Gas chromatography (GC)
Time of monitoring depends on the purpose:
(i) For the purpose of ‘handling’ data points from 0 to 24 hours are taken
(ii) For the purpose of ‘storage’ data points from 0 to 12 weeks are taken.

Significance of hygroscopicity test

(a)

To decide special handling procedure

mg H 2O % weight (with respect to time).
g sample gain

time time
Fig. 8
(b)

Equilibrium To decide
moisture (i) the storage condition i.e. at low humidity environment.
content Fig. 9 (ii) special packaging – e.g. with desiccant.
mg H 2O
g sample
(c) Moisture level in a powder sample may affect the flowability
and compactibility which, are important factors during tableting
RH and capsule filling.

(d) After adsorption of moisture, if hydrates are formed then solubility of that powder may change
affecting the dissolution characteristics of the material.
(e) Moisture may degrade some materials. So humidity of a material must be controlled.

FINE PARTICLE CHARACTERIZATION

Parameters those are measured:

(i) particle size and size-distribution
(ii) shape of the particle
(iii) surface morphology of the particles
Instrumental methods of particle size characterization

(i) Light microscope

First a standard graticule (BS 3625) is standardized with a stage micrometer. Then snall
number of particles are spread over a glass slide and placed on the stage of the microscope. Particles
are focussed and the particle diameters are measured. Several hundred particles are measured and
reported as a histogram.
Disadvantage: The procedure is time consuming.

(ii) Stream counting devices

Examples: (a) Coulter counter – electrical sensing zone method
(b) HIAC – counter – optical sensing zone
(c) Malvern particle & droplet sizer – Laser diffraction method.

Procedure: To vacuum
Samples prepared for analysis are dispersed in a
conducting medium (e.g. saline) with the help of ultrasound
and a few drops of surfactant (to disperse the particles
uniformly). A known volume (0.5 to 2 ml) of this suspension is
then drawn into a tube through a small aperture (0.4 to 800 m
To amplifier
diameter) across which a voltage is applied. and counter
As each particle passes through the hole, it is counted and
sized according to the resistance generated by displacing that
particle’s volume of conducting medium.
Size distribution is reported as histogram. Stirrer
(iii) Sieve analysis
A powder sample is passed through a standard sieve set. The
particle size is plotted against % weight retained on each sieve. . . .. Electrodes
Use: This method is used generally for large samples.
. .. . .
. . . Orifice
.
. . .. .
Instrumental method for determination of specific surface
area Fig. 10 Coulter counter

Brunauer, Emmett and Teller (BET) nitrogen adsorption method:

A layer of nitrogen molecules is adsorbed to the sample surface at –1960C. Once the surface
is saturated, the sample is heated to room temperature, the nitrogen gas is desorbed, and its volume is
measured and converted to the number of adsorbed molecules via the gas law. Since each N2 molecule
occupies an ara of 16 A2, one may readily compute the surface area per gram of each pre-weighed
sample.

Instrumental method for characterization of surface morphology

The scanning electron microscope creates the magnified images by using electrons instead of light
waves. The images are black and white.
Procedure
 Biological materials are dried in a special way that prevents them from shrinking.
 Since SEM illuminates them with electrons, they are made conductive by coating with a very thin
layer of gold by a machine called sputter-coater.
 The sample is placed inside the microscope’s vacuum column through an airtight door.
 After the air is pumped out of the column, an electron gun emits a beam of high-energy electrons.
This beam travels downward through a series of magnetic lenses designed to focus the electrons
to a very fine spot.
 Electron gun
 Near the bottom, a set of scanning coils
moves the focussed beam back and forth Vacuum column
across the specimen, row by row.
Condensing
 As the electron beam hits each spot on the lenses Monitor
sample, secondary electrons are knocked
loose from its surface. A detector counts
these electrons and sends the signals to an Scan coils
amplifier.
 The final image is built up from the
number of electrons emitted from each Objective lens
spot on the sample. Secondary
Electron
Electron
beam

Target Detector &

Amplifier

BULK DENSITY Fig. 11 Scanning Electron Microscope

Apparent Bulk Density (g/cm3)
Bulk drug powder is sieved through 40 mesh screen. Weight is taken and poured into a graduated
cylinder via a large funnel. The volume is called bulk volume.
Weight of the powder
Apparent Bulk Density 
Bulk Volume
Tapped density (g/cm3)
Bulk powder is sieved through 40 mesh screen. Weight is taken and poured into a graduated cylinder.
The cylinder is tapped 1000 times on a mechanical tapper apparatus. The volume reached a minimum
– called tapped volume.
Weight of the powder
Tapped density 
Tapped volume
True density (g/cm3)
Solvents of varying densities are selected in which the powder sample is insoluble. Small quantity of
surfactant may be mixed with the solvent mixture to enhance wetting and pore penetration. After
vigorous agitation, the samples are centrifuged briefly and then left to stand undisturbed until
floatation or settling has reached equilibrium.
The samples that remains suspended (i.e. neither suspended not floated) is taken. So the true density
of the powder are equal. So the true density of the powder is the density of that solvent. The density of
that solvent is determined accurately with a pycnometer.
Source of variation of bulk density
Method of crystallization, milling, formulation.
Methods of correction
By milling, slugging or formulation.
Significance
(i) Bulk density
Bulk density is required during the selection of capsule size for a high dose drug.
In case of low dose drug mixing with excipients is a problem if the bulk densities of the drug
and excipients have large difference.
(ii) Tapped density Fig. 12
Knowing the dose and tapped 000 1.4
density of the formulation, the
00 1.2
capsule size can be determined.
0 1.0
(iii) True density Capsule 8
Capsule
1
From bulk density and true density size volume
of powder, the void volume or 2 6 (ml)
porosity can be measured. 3 4
4
5 2

0.4 0.5 0.6 0.7 0.8 0.9

Packed density (g/ml)
 m m   1 1 
Void volume      m   
  bulk  ture    bulk  true 
 1 1 
m   
  
  bulk true 
Void volume
Porosity   1  bulk
Bulk volume m  true
 bulk

Powder flow properties

Powder flow properties depends on
(i) particle size
(ii) density
(iii) shape
(iv) electrostatic charge and adsorbed moisture
that may arise from processing or formulation.
A free-flowing powder may become cohesive during development. This problem may be solved by
any of the following ways.
(i) by granulation
(ii) by densification via slugging
(iii) by filling special auger feed equipment (in case of powder)
(iv) by changing the formulation.

Procedure Fig. 13
For free flowing powder
A simple flow rate apparatus consisting of a grounded
metal tube from which drug flows through an orifice onto an g/sec
electronic balance, which is connected to a strip chart recorder.
Several flow rate (g/sec) determinations at various orifice sizes time
(1/8 to ½ inch) should be carried out. Nozzle Plotter
The grater the standard deviation between multiple flow Powder
rate measurements, the greater will be the weight variation of the
product (tablets or capsules).
Compressibility :-
t  0
% compressibility  x100
t
t = tapped bulk density Digital Balance
0 = Initial bulk density
Solubility Analysis

Determination of equilibrium solubility of a drug

Equilibrium
The drug is dispersed in a solvent. The solubility conc.
suspension is agitated at a constant temperature.
Samples of the suspension are withdrawn as a function Plateau Fig. 14
of time, clarified by centrifugation, and assayed to Conc.
establish a plateau concentration.

Solvents taken Time

(i) 0.9% NaCl at room temperature
(ii) 0.01 M HCl at RT
(iii) 0.1 M HCl at RT
(iv) 0.1 M NaOH at RT
(v) At pH 7.4 buffer at 370C

Drug concentration is determined by the following analytical methods

(i) HPLC
(ii) UV –Spectroscopy
(iii) Fluorescence Spectroscopy
(iv) Gas Chromatography

Solubility depends on
(i) pH
(ii) Temperature
(iii) Ionic strength
(iv) Buffer concentration

Significance
(i) A drug for oral administrative should be examined for solubility in an isotonic saline solution
and acidic pH. This solubility data may provide the dissolution profile invivo.
(ii) Solubility in various mediums is useful in developing suspension or solution toxicologic and
pharmacologic studies.
(iii) Solubility studies identify those drugs with a potential for bioavailability problems. E.g. Drug
having limited solubility (7 %) in the fluids of GIT often exhibit poor or erratic absorption
unless dosage forms are tailored for the drug.

pKa Determination

When a weakly acidic or basic drug partially ionizes in GI fluid, generally, the unionized molecules
are absorbed quickly.
Handerson-Hasselbach equation provides an estimate of the ionized and unionized drug concentration
at a particular pH.
For acidic drug : e.g. + -
HA + H 2O H3O + A
Weak Strong
acid base

[ionized ] [ A ] [base]
pH  pKa  log  pKa  log  pKa  log
[unionized ] [ HA] [acid ]
 For basic compounds e.g.
B + H 3O+ BH+ + H2O
Weak Strong
base acid

[unionized] [ B] [base]
pH  pKb  log  pKa  log 
 pKa  log
[ionized ] [ BH ] [acid ]

Drug Stomach Plasma Duodenum

PH 1.5 PH = 7.4 PH = 5.0

Weak acid [HA] = 100 [HA] = 100 [HA] = 100

e.g. Ibuprofen
pKa = 4.4
[A--] = 0.13 [A--] = 100,000 [A--] = 398.1

[Total] = 100.13 [Total] = 100,100 [Total] = 498.1

Weak base [B] = 100 [B] = 100 [B] = 100

e.g. Nitrazepam
pKa = 3.2
[BH +] = 5012 [BH +] = 0.006 [BH +] = 1.6
[Total] = 5112 [Total] = 100.006 [Total] = 101.6

Method of determination of pKa of a drug

(i) Detection of spectral shifts by UV or visible spectroscopy at various pH.

Advantage: Dilute aqueous solutions can be analyzed by this method.
(ii) Potentiometric titration
Advantage: Maximum sensitivity for compounds with pKa in the range of 3 to 10.
Disadvantage: This method is unsuccessful for candidates where precipitation of the
unionized forms occurs during titration. To prevent precipitation a co-solvent
e.g. methanol or dimethylsulfoxide (DMSO) can be incorporated.
(iii) Variation of solubility at various pH.

Effect of temperature on stability

Heat of solution, HS represents the heat released or absorbed when a mole of solute is dissolved in a
large quantity of solvent.

Significance
 Most commonly, the solubility process is endothermic, e.g. non-electrolytes, unionized forms of
weak acids and bases  H is positive  Solubility increases if temperature increases.
 Solutes that are ionized when dissolved releases heat
 the process is exothermic  HS is negative  Solubility increases at lower temperature.
Determination of HS.
H S 1
The working equation ln S      C where, S = molar solubility of the drug at T0K
R T 
and R = gas constant
S is detemined at 50C, 250C, 370C and 500C.
HS = – Slope x R Hs
Slope =
R
Solubilization lnS
For drug candidates with poor water solubility, preformulation
studies should include limited experiments to identify the possible 1
mechanisms for solubilization.
Means of increasing the solubility are: T
(i) Addition of a cosolvent to the aqueous system e.g. ethanol, propylene glycol and glycerin.
MOA: These co-solvents disrupt the hydrophobic interactions of water at the non-polar solute
/ water interfaces.
(ii) Solubilization in micellar solutions such as 0.01 M Tween 20 solution.
(iii) Solubilization by forming molecular complexes e.g. benzoic acid forms complex with caffeine.

Partition coefficient
Partition coefficient is defined, as the ratio of un-ionized drug concentrations between the organic and
aqueous phases, at equilibrium.
 C 
K O / W   oil  at equilibriu m Generally, octanol and chloroform are taken as the oil phase.
 C water 
Significance
Drug molecules having higher KO/W will cross the lipid cell membrane.

Dissolution
The dissolution rate of a drug substance in which surface area is constant during disintegration is
described by the modified Noyes-Whitney equation.
dc DA
 ( CS  C )
dt hV
where, D = diffusion coefficient of the drug in the dissolution medium
h = thickness of the diffusion layer at the solid/liquid interface
A = surface area of drug exposed to dissolution medium.
V = volume of the medium
CS = Concentration of saturated solution of the solute in the dissolution medium at the
experimental temperature.
C = Concentration of drug in solution at time t.
When A = constant and CS >> C the equation can be rearranged to
dC DA V dC DA D
 CS or ,  CS or , W  k A t where, k 
dt hV dt h h
where, W = weight (mg) of drug dissolved at time t
 mg 
k = intrinsic dissolution rate constant  2  Slope = kA
 min cm  W

Determination of k
 Pure drug powder is punched in a die and punch apparatus to
time (t)
give a uniform cylindrical shape. The tablet is covered with wax in all sides. One circular face is
exposed to the dissolution medium. Thus, as dissolution proceeds, the area, A, remains constant.
 Time to time dissolution medium is taken out and fresh medium added to the chamber.
 With two types of assembly, the experiments can be carried
out.

Stability analysis
Preformulation stability studies are the first quantitative
assessment of chemical stability of a new drug. This may involve . ... ...
1. Stability study in toxicology formulation
2. Stability study in solution state .. ... ....
3. Stability study in solid state.
Static disc Rotating disc
Stability study in toxicology formulation dissolution dissolution
A new drug is administered to animals through oral route either aparatus apparatus
by
(i) mixing the drug in the feed
(ii) in the form of solution
(iii) in the form of suspension in aqueous vehicle
 Feed may contain water, vitamin, minerals (metal ions), enzymes and different functional groups
that may severely reduce the stability of the new drug. So stability study is should be carried out
in the feed and at laboratory temperature.
 For solution and suspension, the chemical stability at different temperature and pH should be
checked.
 For suspension-state the drug suspension is occasionally shaken to check dispersibility.

Solution stability
Objective: Identification of conditions necessary to form a stable solution.
Stability of a new drug may depend on:
(i) pH (ii) ionic strength (iii) co-solvent
(iv) light (v) temperature (vi) oxygen.

pH stability study
(i) Experiiments to confirm decay at the extremes of pH and temperature. Three stability studies are
carried out at the following conditions
(a) 0.1N HCl solution at 900C
(b) Solution in water at 900C
(c) 0.1 N NaOH solution at 900C
These experiments are intentionally done to confirm the assay specificity and for maximum rates of
degradation.
(ii) Now aqueous buffers are used to produce solutions with wide range of pH values but with
constant levels of drug concentration, co-solvent and ionic strength.
All the rate constants (k) at a single temperature are then plotted as a function of pH.
(ii) Ionic strength
Since most pharmaceutical solutions are intended for parenteral routes of administration, the pH-
stability studies should be carried out at a constant ionic strength that is compatible with body
fluids. The ionic strength () of an isotonic 0.9%w/v sodium chloride solution is 0.15.
Ionic strength for any buffer solution can be calculated by
1
 
2
mi Z i
2
where, mi = molar concentration of the ion
Zi = valency of that ion
For computing,  all the ionic species of the buffer solution and drugs are also taken into calculation.

(iii) Co-solvents
Some drugs are not sufficiently soluble to give concentrations of analytical sensitivity. In those
cases co-solvents may be used. However, presence of co-solvents will influence the rate constant.
Hence, k values at different co-solvent concentrations are determined and plotted against % of co-
solvent. Finally, the line is extrapolated to 0% co-solvent to produce the actual k value (i.e. in pure
solvent).

(iv) Light
Drug solutions are kept in
(a) clear glass ampoules
(b) amber color glass container
(c) yellow-green color glass container
(d) container stored in card-board package or wrapped in aluminium foil – this one acts as the
control.
Now the stability studies are carried out in the above containers.

(v) Temperature
The rate constant (k) of degradation reaction of a drug varies with temperature according to Arrhenius
equation.
Ea
 Ea  1 
k  Ae RT
or , ln  ln A   
R T 
where, k = rate constant
A = frequency factor Ea
Ea = energy of activation
Slope =
ln k R
R = gas constant
T = absolute temperature

Procedure 1/ T
Buffer solutions were prepared and kept at different temperatures. Rate constants are determined at
each temperature and the ln k value is plotted against (1/T)).
Inference
 The relationship is linear  a constant decay mechanism over the temperature range
has occurred.
 A broken or non-linear relationship  a change in the rate-limiting step of the reaction or change
in decay mechanism.

Uses
Shelf life of the drug may be calculated.
e.g. Time Concentration of drug remaining
0 100 %
t10% 90%
Therefore, ln C = ln C0 – k1t
Ln C/C0 = – k1t
90 ln 0.90 0.105
or, ln   k1t10% or, t10%  
100  k1 k1
where, t10% = time for 10% decay to occur if the reaction follows 1st order kinetics

Conclusion
If the drug is sufficiently stable, liquid formulation development may be started at once.
If the drug is unstable, further investigations may be necessary.

Solid state stability

Objectives
Identification of stable storage conditions for drug in the solid state and identification of compatible
excipients for a formulation.
Characteristics
Solid state reactions are much slower, so the rate of appearance of decay product is measured (not the
amount of drug remaining unchanged).
 To determine the mechanism of degradation thin layer chromatography (TLC), fluorescence or
UV / Visible spectroscopy may be required.
 To study polymorphic changes DSC or IR-spectroscopy is required.
 In case of surface discoloration due to oxidation or reaction with excipients, surface reflectance
equipment may be used.

A sample scheme for determining the bulk stability profile of a new drug:

Storage condition 4 weeks 8 weeks 12 weeks

50C – Refrigerator
220C – Room Temperature
370C – Ambient humidity
370C / 75% RH (Relative Humidity)
Light box
Clear box
Amber glass
Yellow-Green glass
No exposure (Control :- Card-board box or wrapped with aluminium foil)
50 C – Ambient Humidity
0

– O2 Head Space
– N2 Head Space
700C – Ambient Humidity
900C – Ambient Humidity

Procedure
1. Weighed samples are placed in open screw-capped vials are exposed to a variety of temperatures,
humidities an dlight intnesities. After the desired time samples are taken out and measured by
HPLC (5 – 10 mg), DSC (10 to 50mg), IR (2 to 20mg).
2. To test for surface oxidation samples are stored in large (25ml) vials for injection capped with
Teflon-lined rubber stopper. The stoppers are penetrated with needles and the headspace is
flooded with the desired gas. The resulting needle holes are sealed with wax to prevent degassing.
3. After fixed time those samples are removed and analyzed.

Drug-excipient stability profile

Hypothetical dosage forms are prepared with various excipients and are exposed to various conditions
to study the interactions of drug and excipients.