Ointment
Ointment
Ointment
2 OINTMENTS
(I) DEFINITION:
preparations intended for application to skin
Ointments are soft, semisolid
inunction.
and mucous membrane with or without
Ointment serves mainly three functions.
1. Lubricating - Emollients.
2. Treat skin disorder (Medicinal effect).
3. Protective coverings.
236
PHARMACEUTICS - II (DISPENSING PHARMACY
1A) CLASSIFICATION OF OINTMENTS
Classification based on their composition, i.e. Base use.
OINTMENTBASES
(A) (B) (C) (D) (E)
Oleaginous
and Absorption Emulsion Water Soluble, Modern
Bases (cream) Bases Ointment
Hydrocarbons Bases
- Hydrous
Woolfat
Natural Synthetic - Woolfat - Rose water
origin - Bees wax Ointment
-Hydrophilic -Cold cream
petrolatum -USP
- Silicones - Wool
Alcohol
Ointment
(i) (ii) (iii)
Plant Animals Minerals
TG/OE
245
medicaments, 2. of
Anti-oxidants.
since proper withStability1. Emollient
:(B)properties. miscible
7. 6. 5.thisPH. secretions. 4.with 3.and prove 246
edicaments 1. Consistency
FORMULATION (V) : While
4.
: 3. div1ded
e.g. preservative. 2.
Solvent zinç Ease FreedomCompatibility Miscibility
It Emulsifying The O/W Pharmaceutical
Free
it As The The having TheEffect
Following shouldHydrocarbon
woolfat 2. 1. oxide will animal of irritant.
For most acid PH skin greasy on
Comp. throughout Property creams tend application cooling
from skin
have Phenol with in of secretions
with O/W
are can drugs and skin
Properties Mercury tooils irritant with base
the proper take bases water.
are reverse vegetable skin Function.
types Ointments base. are : may secretions rather
emulsion
good factors and skin interferes
consistency.
upare insoluble cause are
secretions
of to Ointment So th e removal, effect. secretions.
50% not : medium fats/oils oily heating
Ingredients if emulsion.trouble : is PHARMACEUTICS
bases
able as normal
skin
with
of possible in 5.5 and effect
water. to base. are water well are
for wi th So
take It sebum.
as
included And microbial miscible ointment aqueous. and more
up select can O/W liable
Olive
oil. so be to mix
aqueous, Animal compatible
in preventedcreamsoxidation. -
propershould it
bases base Emulsion readilyfunction. II
formulation growth (DISPENSING
or containing should
alcohol Vegetable vehicle be are with with
by It
present and prior can readily bases skin Greasy
of or not skin
ointment to so be PHARMACY)
glycerin. Oil. dissolve in trituration Zinc protected differ secretions.
are
require removed. functions base
finely Oxide, readily
: from may
SPECIAL
CASES*MORTAR-PESTLE an transferred
andTongue darkwhite, TwoSLAB-SPATULA medicament
spatula.smooth 1. 4 3. PREPARATIÖNS 2 1.
Perfumes. 6. Chelating Preservatives.
agent5. 4. 3.Base 2.SEMI
Powdered absorptionLarge medicaments
Mortars This This By (V) :
lular coloured so slabs A The Mainly Anti-oxidants
depressors glass Trituration Ointnent
mills.
By
Chemical
reactionBy ByBy eg. SOLID
light are slab-spatula ointment method method
extracts amounts from fusion-
Trituration there
to convenient, slab is DOSAGE
extracts base be over
coloured solid
i.e. used isslab is is is are Maleic
Acid Citric
Acid
should andpreferred obtained
perfomed and :
B.Unmedicated -BHA;
of lodine, white. preferable method than used A. OR four
should thenliquid when FORMs
ointments
Spatulas the mortar. insoluble Medicated BHT
be when incorporation
methods:
softened adding are when tannic
danger under OR
be because is by
best easy by
pulverized much acid, ofare can side triturating orsoft
mixture and rubbing liquid fats
with incorporated chermical of be of it
liquid salicylic steel. is no OR
small non-absorptive
made one lumpy in and
and to them the small MENTS ON Slab.
fatty is reactions Hard being oils
amounts by to acid over particles ingredients
made base.adding be onamount. are
and rubber printed the an
of
very incorporated. Mercurial between black part
spatulas black
and remain ointment
suitable fine. them in
easily of
coloured a the
gradually steel or and and mortar
slab
solvents. salts. base
wooden cleansed.
spatula of easy witha
and other until and 247
to to
about
40°C.to Using must oil, into
alcohol, Medicated
Ointment :M.P. the to 2. * * * 248
Soaps
4. by 3.
TripleOintment By substance melt
chemical ointmeFt. Qleated
Itmercury
Iodine 3. 2. 1.
Following Volatile th en When After With Levigation
When triturated
By Powders andpetroxolin Ichthammol
them Certain fluidity.Fluid
may involves à be such
roller Mills Chemical both
Fusion them
Strong smallfinely add different first extracts
are be methyl a
solids melting, hard
said to base of these fluid
type noL Mills reaction.
both
substancesportion it fusible : with is addwhich have with
to
mercuric is salicylate, powdered
the
Reaction containing are
previously highest a in are
mil used : the melting and a
process an and may
be
fusion list insoluble liquid small ar e been
is in Certain of fats/waxes
soft difficult
oil
fasterIndia made nitrate of such the ingredients M. P . insoluble semifluid
or be,
and preparations oleoresin : 60 points fats in amount found a heated
by
hydrophilic base melted an
as first which
than in mechanical mesh (Zincoxide, which fa t PHARMACEUTICS
to
chemical ointment perfumes, as oi!, to satisfactory in
dispensaries. base. it ingredients, and get are aids eg. are incoporate
which to
other shouldlevigating aand is should to it (Viscid) drive
advisable If adding a be Calamine,
is powdered
in
: incorporated calamine,
no smooth, insoluble.
preparing they
type reaction.bases mixing. menthol,be be incorprated off
oil th e it with eg. excess
of
They which added agent. is stired would for are
mills. Here present, starch) to others
homogeneous Zinc and soluble. this peruvian fats II-
are involve camphor,
after levigate until 'be smooth pass (DISPENSING
alcohol
new after in with oxide purpose.
the thexpected
e and
u_ed the the isdescending through Castor
product solid the to.be ointment soft, ointment. and separate balsam,
for the baseiodine, base and
solid it starch.
large formation has medicament incorporated th mixture.
at 1s l30 oil PHARMACY)
reduce
is congeals. necessary
scale, formed cooledcoaltar, with order
ismelting Solid (Sieve) and out. tar
the cool. solid Mix and their
of of is
PENETRATION: TESTEOR(A) penetration stforimp tubes Labeling(DX) Plastic
(X) Instructionrecommended
:label. : Ointments (PACKAGING):
CONTAINERS (VIII)
container. antioxidants.
can inproper
clude SEMI
Wild(1By
) (A)
(C) (B) EVALUATION The Jars Tin Ointments
Ointment They PRESERVATION
be (VIDi
LabelOn with tube SOLID
various are aluminium and prevented Oin tmentsget
Ointments
Unabsorbed
(Excess)
The weighed. skiandn TheRubbed gm.say X He Absorption RatPenetration
e must
for benzoin labelled now should
Say has of for jars DOSAGE
difference three are not
contaminatedalso contain
- on taken release experiments tubes. available. be are
usually react by
2. 1. tincture packed
Y fixed different
of of OF available antimicrobial. FORMS
gm. fixed the th e with-self tubeare with water
fats
(X-Y) of BASE Paper N(STORAGE):
Area the drug base EXTERNAL USE"
"STORE "FOR dispensed and
quantity functions. have or in the
drug into labels
lacquer adhesive used jars in
gm for through brown, Constituents
been uniformly
gave fixed from the IN are ointments
whichfor in
base of the permiting by so
blood conducted
t he A green either
amount various DRY difficult labels.
carefully
collected was time. micro-organisms easily
b¡se. skin.
stream. to
ointment
or ot
AND Self avoidopaque the oxidisable
penetrate. Base. to this affixto
adhesive ointment
elucidate COOL air
to are jars
dry to pockets.white
tubes. easily or of and and
absorption PLACE" and strip glass tubes. the spoiled.get get
Coating
apply
then labels extrudable.
fromthe or material rancid,
plastic.
and 249
the are of so
It
(2) 250
Two (C) (2) (1) (B)
Johnson(3)By
By ByTEST From By
) In RATE
vitro(b)Invivo(atypes * *
Experiment Bliss Strakosch
lodine Zeigler tor conditionsFixed
found
thatHe He The Fixd FOR above
Histological
OF Radioactive used:
Drugs 24
of miscible
Hydrocarbon
base water used Emulsion
: Emulsion l Lard
Woolfat AlmondoiParaffins
study
RELEASE
base Lardand
in concentration
ABSORPTION amount
: amount studies HRS
Radio paraffin was :
hydrochloride Pot.Iodine
Quinine Iodide made
substane Salicylate
Methyl of of BaseExaminations
it of
active carried
base was
OF medicated liquid to base
of ’
determine PHARMACEUTICS
DRUGS found
was sod.
was out drug paraffin Penetrate rubbed
Time Area
skinof
studied. on thatofhuman
chloride
measured measured base
Dog. the on
rubbed slowly skin
amount
as Penetrate
skin
absorption. in readily in -
absorption.
PoorRapid in the
biopsies II
the urine. on well
(DISPENSING
medicament. of
fixed penetration.
tissues defined
area at
and
different
for PHARMACY)
in fixed
the intervals
urine. time
vitro(b) In (a) SEMI
Peue
tra). Observe * * t (1) t t (1)
in
RelecSe
Rae 3 vivo SOLID
By
Note Plate CUPBored.CUP isAgar Micro Agar Intensity
More RubbedMixed He :
Bacteriostatic Skiusednner DOSAGE
sinne
OBy Ábsoopt\m O the is is plate CUP-
mu. By By organism pigmentation onwith
stakoSch Zone incubate filled of :
Contaminated Plate Na-fluorescein_as
fixed
Berneli with (Extent) different FORMS
BIfss of
Inhibition. medicatedfor selected drug
Method: area
zeigie. 24 was indicates of for Base.
hrs. selected pigmentation a
with must
fixed drug. a
Base. be more
micro time.
sensitive release.
- (coloration)
organism
to
drug.
made measured.
on
petridish.
251
Base Plain withFilled Bore Micro-org, withplate 252
Colony Agar
Greater Incubate
CONTROL
the
zone
PHARMACEUTICS
of
Inhibition BORE
Colony.
greaterInhibition
Zone of
-
Incubate TEST Il
release (DISPENSING
Ointment
Medicated WithFilled Micro
org withPlate Agar PHHARMAÇY)
Rag(4) (3)
Ramsay Bandelin(2) :SEMI
Prepared
* CUP * t * t t SOLID
CUP More Intensitysulpha.
colour
withWater Cube Made Used Sod.ointments.
Test Smear Sod.
Cup Used -
Waud DOSAGE
covered filled principle intensity placed
sulphonamide
of cube Chloride tube chloride
of test test
filled
with pink of tubes FORMS
of more tube(float)
sulphonamide used
Ointment
with release with
semi
dialysis color contains
release in as internally as
a a water
in a
permeable estimated test drug. water drug.
containing
Sulpha
Base
-Water
bath
Ehrlich's tube with maintain
Ehnich Waterbath Smear with
estimated
at fIlled Base.
membran Sod. different thin
at
(Indicator)
with constant layers
chloride. at
time. water. different
temperature. of
which
sodium
time
gives
chloride
pink 253
purified
water. trituration. Ointment
Oily() is or to 254
Creams ethylene
creams. prepared contain () phase. alcohol, creams
according 8.3
Washable. It
the It
Nonstaining.
5. 4. 3. 2. 1. Microbiological
Creams Aqueous Oily oll-in-water CREAMS
Oleagenous
a. NÍt Diluted contains Both skin is
Long should So emulsifying glycol
as fatty Permeable Sem1
occlusive tocreams viscousor Membrane Sod. CUP
have use oily the
emuslsion acid translucent.
chain with be Creams
oil-in-water mucous chloride float
ofderivative
cream. phases contain (aqueousemnlsion
Phase followingthroughlyproper ester
alcohol and water. contamination wax on
(Water- should Melt - of membrane. releasedwater
inhave and
characterspreservative. of
emulgent.
sorbitanwater a
creams)
(Cetyl,creams
emollient cleansed a of
bethe semi-solid
sorbitánalkali
removable) atfatty in-oil PHARMA
They in
stearyl). _are is 60°c. divalentor water
and liable
soap type.
:Apparatus It materialenmulgent
may
properties. fatty has Mix CEUTIGS
rinsed (Monovalent), consistency CUP
It be is
to acid creamy :aqueoussoap.Oily on has of (drUg
measured.
occur, ConstantWater at
Tenperature
water which the + -
with used ester. opaque Sample Base) II
white
particularly
freshly in phase bath. may water-in-oil
intended (DISPENSING
Aqueous
monostearin creams
the appearance.
to appearance,
preparation
boiled oily
Warm can be
wool for
in cream (0ily
phase
with the be application PHARMACY)
cooled aqueous or It aqueousprepared fat, creams)
also poly may wool while
of