R. VIJAYAKUMAR., M Pharm,
Research Scholar
department of Pharmaceutical Technology.
Anna university- BIT
Tiruchirappalli
B Pharm / 2nd Year ,III Semester.
UNIT-I / Colloidal dispersion's
R. VIJAYAKUMAR., M Pharm,
Research Scholar
department of Pharmaceutical Technology.
Anna university- BIT
Tiruchirappalli
B Pharm / 2nd Year ,III Semester.
UNIT-I / Colloidal dispersion's
Introduction
Definition
Features desired in pharmaceutical suspension
Advantage/Disadvantages of pharmaceutical suspension
Flocculated and deflocculated suspension
Interfacial properties of suspending particles
Settling in suspensions
Effect of Brownian movement,
Sedimentation of flocculated particles,
Sedimentation parameters
Formulation of suspensions
Wetting of Particles,
Controlled flocculation,
Flocculation in structured vehicle
Classification of dispersed systems & their general characteristics, size & shapes of colloidal particles, classification of colloids & comparative account of their general properties. Optical, kinetic & electrical properties. Effect of electrolytes, coacervation, peptization& protective action.
Solid State of matter,
Crystalline, Amorphous & Polymorphism Forms,
Classification of solid state of matter On the basis of Internal Structure,
PHYSICAL PHARMACEUTICS-I,
Habet,
B.Pharm,
State of matter and properties of matter (Part-7)(Solid-crystalline, Amorpho...Ms. Pooja Bhandare
CRYSTALLINE SOLID, Types of Crystalline solid, AMORPHOUS SOLID, Difference between crystalline solid and amorphous solid, Why does the amorphous form of drug have better bioavaibility that crystalline couterpaerts?, Polymorphism,
TYPES OF POLYMORPHISM, PROPERTY OF POLYMORPHS, Methods of preparation of Polymorphs, Methods to determine Polymorphism Characterization of Polymorphs, Pharmaceutical Application
Introduction
Definition
Features desired in pharmaceutical suspension
Advantage/Disadvantages of pharmaceutical suspension
Flocculated and deflocculated suspension
Interfacial properties of suspending particles
Settling in suspensions
Effect of Brownian movement,
Sedimentation of flocculated particles,
Sedimentation parameters
Formulation of suspensions
Wetting of Particles,
Controlled flocculation,
Flocculation in structured vehicle
Classification of dispersed systems & their general characteristics, size & shapes of colloidal particles, classification of colloids & comparative account of their general properties. Optical, kinetic & electrical properties. Effect of electrolytes, coacervation, peptization& protective action.
Solid State of matter,
Crystalline, Amorphous & Polymorphism Forms,
Classification of solid state of matter On the basis of Internal Structure,
PHYSICAL PHARMACEUTICS-I,
Habet,
B.Pharm,
State of matter and properties of matter (Part-7)(Solid-crystalline, Amorpho...Ms. Pooja Bhandare
CRYSTALLINE SOLID, Types of Crystalline solid, AMORPHOUS SOLID, Difference between crystalline solid and amorphous solid, Why does the amorphous form of drug have better bioavaibility that crystalline couterpaerts?, Polymorphism,
TYPES OF POLYMORPHISM, PROPERTY OF POLYMORPHS, Methods of preparation of Polymorphs, Methods to determine Polymorphism Characterization of Polymorphs, Pharmaceutical Application
Discussion on the 2 kinds of Disperse Systems 1. Suspensions 2. Emulsions. The principles of emulsification, types and examples of emulsifying agents used.
Electro osmosis ,colligative propertries of colloids ,electrokinetic properti...Anand P P
electro osmosis.that topics deals with colloids and their one of the colligative properties that is electro kinetic property.under the electrokinetic colligative property of colloids consist 2 properties mainly electrophoresis and elecoosmosis.the electro osmosis have several application properties.the electroosmosis is mainly deals with the charge of colloidal system and their movements opposite charges.electrical double layer theory.
A colloid is a substance microscopically dispersed throughout another substance.
The word colloid comes from a Greek word 'kolla', which means glue thus colloidal particles are glue like substances.
These particles pass through a filter paper but not through a semipermeable membrane.
Colloids can be made settle by the process of centrifugation.
Here almost full every topics interrelated with colloid chemistry has been discussed.The slides have been made showing question pattern taking Begum Rokeya University Chemistry Department previous year questions to appear the slides easy towards the viewers.Stay join with me.Thank you.
Colloidal Dispersion, Its Types and Method of PreparationChitralekhaTherkar
Dispersion
Definition of Colloids
Shapes and Sizes of Colloids
Classification of Colloids
Properties of Colloids
1. Optical Properties.
2. Electrical Properties.
3. Kinetic Properties
Purification of Colloids
Method of Preparation of Colloids.
Physical Stability of Colloids.
Factors affecting Colloidal Dispersion.
Colloids are crucial to both ordinary living and pharmacological formulations. the study of both big molecules
and intricately divided multiphase systems is known as colloidal science. the intersection of colloid and
surface science is the multi-phase system. a colloid is a mixture in which one material is suspended within
another substance and has insoluble particles scattered over a tiny scale. between genuine solutions and
suspensions, colloidal solutions or colloidal dispersions represent a middle ground. the dispersed phase of
colloids is distributed throughout the dispersion medium. in many facets of chemistry, colloidal chemistry
knowledge is necessary. this article provides information on what colloids are, their types, sizes, forms,
qualities, and uses.
Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
NVBDCP.pptx Nation vector borne disease control programSapna Thakur
NVBDCP was launched in 2003-2004 . Vector-Borne Disease: Disease that results from an infection transmitted to humans and other animals by blood-feeding arthropods, such as mosquitoes, ticks, and fleas. Examples of vector-borne diseases include Dengue fever, West Nile Virus, Lyme disease, and malaria.
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
Adv. biopharm. APPLICATION OF PHARMACOKINETICS : TARGETED DRUG DELIVERY SYSTEMSAkankshaAshtankar
MIP 201T & MPH 202T
ADVANCED BIOPHARMACEUTICS & PHARMACOKINETICS : UNIT 5
APPLICATION OF PHARMACOKINETICS : TARGETED DRUG DELIVERY SYSTEMS By - AKANKSHA ASHTANKAR
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
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micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
ARTIFICIAL INTELLIGENCE IN HEALTHCARE.pdfAnujkumaranit
Artificial intelligence (AI) refers to the simulation of human intelligence processes by machines, especially computer systems. It encompasses tasks such as learning, reasoning, problem-solving, perception, and language understanding. AI technologies are revolutionizing various fields, from healthcare to finance, by enabling machines to perform tasks that typically require human intelligence.
2. Colloidal Dispersions
• Dispersed systems consist of :
a) particulate matter (dispersed phase).
b) dispersion medium (continuous medium).
• Classification of dispersed systems (according to
particle size):
MOLECULAR COLLOIDAL COARSE
DISPERSION DISPERSION DISPERSION
- Less than 1 um - 1 um to 500 um - Greater than 500 um
- Particles undergo - Very slow diffusion - Don’t diffuse
rapid diffusion e.g. O2 e.g. colloidal silver sol. e.g. suspension &
& glucose emulsion
3. Colloidal Dispersions
MOLECULAR COLLOIDAL COARSE
DISPERSION DISPERSION DISPERSION
-Particles invisible -Particles resolved -Particles are
in electron by electron visible under
microscope. microscope. ordinary
microscope.
-Pass through - Pass through
semipermeable filter paper but not - Do not pass
membranes and pass through through filter
filter paper. semipermeable paper or
membrane. semipermeable
membrane.
4. Types of colloidal systems:
o According to the interaction between particles of
dispersed phase & those of dispersion medium:
1) Lyophilic (solvent loving).
2) Lyophobic (solvent hating).
3) Association (amphiphilic).
6. 1) Lyophilic colloids
• Colloidal particles interact to an appreciable extent with the molecules of the
dispersion medium (solvent loving).
• Obtained simply by dissolving the material in the solvent ( due to the high
affinity).
Types of lyophilic colloids;
(According to type of solvent)
•Hydrophilic colloids; •Lipophilic colloids;
•Solvent: water. •Solvent: non- aqueous,
organic solvent.
•Example: acacia,
insulin…. in water. •Example: rubber
&polystyrene.
SO; material that form lyophilic colloid in a certain solvent may not do so
in another solvent, e.g.; acacia + water lyophilic colloid (hydrophilic type).
acacia + benzene NO lyophilic colloid formed.
7. 1) Lyophilic colloids
o the dispersed phase does not precipitate easily
o the sols are quite stable as the solute particle
surrounded by two stability factors:
a- negative or positive charge
b- layer of solvent
o If the dispersion medium is separated from the
dispersed phase, the sol can be reconstituted by
simply remixing with the dispersion medium.
Hence, these sols are called reversible sols
8. 2) Lyophobic colloids
o Colloidal particles have very little or no attraction for the dispersion
medium (solvent hating).
o Colloidal particles: inorganic particles (e.g. gold, silver, sulfur….)
Dispersion medium: water.
- These colloids are easily precipitated on the addition of small
amounts of electrolytes, by heating or by shaking
- Less stable as the particles surrounded only with a layer of
positive or negative charge
- Once precipitated, it is not easy to reconstitute the sol by
simple mixing with the dispersion medium. Hence, these sols
are called irreversible sols.
o Not obtained simply i.e need special method for preparation
9. 2) Lyophobic colloids
o Methods to prepare lyophobic
colloids:
A) Dispersion methods:
o coarse particles are reduced in size by;
1) Ultrasonic generator
2) Electric arc.
3) Colloid mill.
10. 1) Ultrasonic generator:
• Dispersion achieved by high intensity UG at frequency more than
20,000 cycles/second
2) Electric arc:
• Involves production of an electric arc within the liquid and
dispersion achieved by intense heat generated by the arc so some
metal of the electrodes dispersed as vapor then condense to colloidal
particles.
3) Colloidal mill:
• Material sheared between 2 rapidly rotating close plates.
• Low efficiency & reduce the size of small proportion of particles
only.
12. • B) Condensation methods:
• materials of sub colloidal dimensions are caused to aggregate into
particles with colloidal size range by;
1) Change in solvent.
2) Chemical reaction.
1) Change in solvent:
• Change in solvent Super saturation Formation &growth of nuclei.
( colloidal system formation)
e.g. sulfur and alcohol in
excess of water
2) Chemical reaction:
• Hydrogen sulfide Oxidatn. Sulfur atoms Sulfur sol.
Br2 + H2S S + 2 HBr
HNO3 + H2S H2O + NO2 + S
• Ferric chloride + water Hydrolysis Ferric oxide sol. (red color).
• Hydrogen sulfide + arsenous acid Double decomp. Arsenous sulfide sol.
13. 3. Association colloids:
o Certain molecules or ions termed amphiphile
(surface active agent SAA) are characterized by two
distinct regions of opposing solution affinities within
the same molecules or ions.
14. 3. Association colloids:
- At low concentration: amphiphiles exist
separately (subcolloidal size)
- At high concentration: form aggregates or
micelles (50 or more monomers) (colloidal
size)
16. As with lyophilic sols, formation of association colloids is
spontaneous, provided that the concentration of the
amphiphile in solution exceeds the cmc.
Amphiphiles may be
1. Anionic (e.g., Na. lauryl sulfate)
2. Cationic (e.g., cetyl triethylammonium bromide)
3. Nonionic (e.g., polyoxyethylene lauryl ether)
4. Ampholytic (zwitterionic) e.g., dimethyl dodecyl
ammonio propane sulfonate.
17. Comparison of properties of colloidal sol
Lyophilic Lyophobic Association (amphophilic).
(solvent-loving). (solvent-hating).
Dispersed Large organic Inorganic particles Aggregates (micelles) of small
phase molecules lying within such as gold or organic molecules or ions
colloidal size silver whose size is below the
colloidal size
Solvation Solvated little Hydrophilic or lipophilic portion
of the molecules is solvated
depending on the medium
Preparation Spontaneous by Needs special Spontaneous when conc. Of
dissolving in solvent procedure amphiphiles exceeds cmc
Viscosity Viscosity increased as Not greatly Increased as conc. Of
the conc. increase. At increased due to amphiphile increase as
certain conc. Gel sol unsolvation micelles no. increase &
gel formation. become asymmetric.
Effect of Stable in presence of Unstable due to Cmc is reduced and salting
electrolytes neutralization of
electrolytes out occur at high salt conc.
Desolvation and salting out charges on particles
in high conc.
18. Shape of colloidal particles:
o The more extended the
particle, the greater its
specific surface & the greater
the opportunity for attraction.
o Properties of colloids as Flow,
sedimentation rate & O.P. are
all affected by the shape of
the particles.
19. Purification of colloids
o 1) Why?
Many lyophobic sols contain more or less material in true
solution. which may be undesirable for any number of
reasons; e.g.,
n electrolyte impurities : cause the flocculation of the
sol.
• 2) How?
a) Dialysis.
b) Electro dialysis.
c) Ultra filtration.
20. a)- Dialysis:
o Depend on difference in size between colloidal
particles & molecular particles (impurities).
o Technique;
1) use semi permeable membrane (e.g. collodion
(nitrocellulose), cellophane).
2) pore size of used semi permeable membrane prevent
passage of colloidal particles & permit passage of
small molecules & ions (impurities) such as urea,
glucose, and sodium chloride, to pass through.
o A type of dialysis equipment; “Neidle dialyzer”
o At equilibrium, the colloidal material is retained in
compartment A, while the subcolloidal material is
distributed equally on both sides of the membrane.
By continually removing the liquid in compartment
B, it is possible to obtain colloidal material in A
that is free from subcolloidal contaminants
21. b)- Electro dialysis:
o Technique;
o An electric potential may be used to
increase the rate of movement of ionic
impurities through a dialyzing
membrane and so provide rapid
purification.
o Electrodialysis is carried out in a three-
compartment vessel with electrodes in
the outer compartments containing
water and the sol in the center
compartment.
oA typical apparatus is shown in the figure. Application of electrical potential
causes cations to migrate to the negative electrode compartment and anions to
move to the positive electrode compartment, in both of which running water
ultimately removes the electrolyte.
22. c) Ultra filtration:
• Technique;
Apply pressure (or suction) Solvent &
small particles forced across a membrane while
colloidal particles are retained.
N.B.
• The membrane must be supported on a
sintered glass plate to prevent rupture
due to high pressure.
• Pore size of the membrane can be increased
by soaking in a solvent that cause swelling
•e.g. cellophane swell in zinc chloride
solution.
e.g. collodion (nitrocellulose) swell in
alcohol.
23. Artificial kidney machine:
• patient’s blood (arterial) pass through Cellophane coils (ideal semi
permeable membrane for
haemodialysis).
• cellophane pass urea, glucose, electrolytes but don’t pass
plasma proteins & blood cells
• pure dialyzed blood enter the body again through a vein.
N.B.
• success of the artificial kidney machine
depends on its ability to reduce blood urea.
• Cellophane coils are supported on a drum
rotating in electrolyte solution (rinsing
fluid).
24. • Suit artificial kidney machine;
• Importance of the rinsing solution:
• Substances present in excess in blood (e.g. urea) diffuse from blood to
the rinsing solution.
• Substances which are deficient in blood (e.g. bicarbonate) diffuse from
the rinsing solution to blood.
• Substances which are present in normal amounts in blood are kept
unaltered have the same conc. In both blood and rinsing solution.
25. Pharmaceutical applications of colloids;
1) Colloidal silver iodide, silver chloride & silver protein are
effective germicides & not cause irritation as ionic silver salts.
2) Colloidal copper used in cancer.
3) Colloidal gold used as diagnostic agent.
4) Colloidal mercury used in syphilis.
5) Association colloids (SAA) are used to increase solubility &
stability of certain compounds in aqueous & oily
pharmaceutical preparations.
26. Suit Pharmaceutical applications of
colloids;
6) Efficiency of certain substances is increased when used in
colloidal form due to large surface area.
e.g. efficiency of kaolin in adsorbing toxins from GIT.
e.g. efficiency of aluminum hydroxide as antacid.
7) Blood plasma substitutes as dextran, PVP & gelatin are
hydrophilic colloids used to restore or maintain blood volume.
8) Iron - dextran complex form non-ionic hydrophilic sols
used for treatment of anemia.
28. A) Kinetic properties:
Which relate to the motion of the particles within the
dispersion medium as following:
• Brownian motion.
• Diffusion.
• Sedimentation.
• Osmotic pressure.
• The Donnan membrane effect.
• Viscosity.
29. 1) Brownian motion:
o Definition: colloidal particles are subjected to
random collision with molecules of the dispersion
medium (solvent) so each particle move in irregular
and complicated zigzag pathway.
o First observed by Robert Brown (1827) with pollen
grains suspended in water.
o The velocity of particles increases with
decreasing particle size and viscosity.
o Increasing the viscosity of dispersion
medium (by glycerin) decrease then stop
Brownian motion.
30. 2) Diffusion:
o Definition:
o As a result of Brownian motion
particles pass (diffuse) from a region of
higher concentration to one with lower
conc.
o Rate of diffusion is expressed by;
Fick’s first law:
dm/dt = -DA dc/dx
Where dm is the mass of substance
diffusing in time dt across an area
A under the influence of a
concentration gradient dC/dx.
The minus sign denotes that
diffusion takes place in the
direction of decreasing
concentration.
D is the diffusion coefficient.
31. 3) Sedimentation:
o Stoke’s law;
V = 2r2 ( p-po) g / 9 η
• v: velocity of sedimentation of spherical particles.
• p: density of the spherical particles.
• po: density of the medium.
•η: viscosity of the medium.
• g: acceleration due to gravity.
At small particle size (less than 0.5 um) Brownian motion is
significant & tend to prevent sedimentation due to gravity &
promote mixing in stead.
• so, we use an ultracentrifuge which provide stronger force so
promote sedimentation in a measurable manner.
32. 4) Osmotic pressure:
o The method is based on Van's Hoff's law;
P = RTC / M
o From the equation;
a) The osmotic pressure (P) depends on molar conc. Of the
solute (C) & on absolute temp. (T).
b) The osmotic pressure is inversely proportional to
molecular weight (M).
R= molar gas constant
o The equation is valid for very dilute solutions in which
the molecules do not interact mutually.
33. 5) The Donnan membrane effect.
o Definition:
Diffusion of small ions through a
membrane will be affected by the
presence of a charged macromolecule
that can’t penetrate the membrane
due to its size.
Application:
1) Facilitating the absorption of
ionizable drugs from GIT by co-
administration of macromolecules of
same charge so mutual ionic
repulsion occurs e.g
co-administration of anionic
macromolecule e.g. sodium carboxy
methyl cellulose, with a diffusible
anion e.g. potassium benzyl penicillin
to enhance diffusion of the later
across body membranes.
34. 6) viscosity
o Definition:
o The resistance to flow of a system under an
applied pressure
o Viscosity of colloid allows 1- calculation of the
molecular weight.
2- Provide useful information about the shape of
the colloidal particles.
o N.B.
o Spherocolloidal dispersions are of relatively low
viscosity.
o On the other hand Linear colloidal dispersions are of
high viscosity.
o If linear colloidal particles coil up into spheres
The viscosity of the system falls due to changing the
shape.
35. B) Optical properties:
1) Light scattering (Tyndall effect).
1) Ultra microscope.
2) Electron microscope.
36. 1) Light scattering (Tyndall effect)
o True solutions do not scatter light and
appear clear but colloidal dispersions
contain opaque particles that do scatter
light and thus appear turbid.
o Tyndall effect:
when a beam of light pass through a colloidal
sol, scattered light cause the sol to appear
turbid.
o Importance of light scattering
measurements:
1) Estimate particle size.
2) Estimate particle shape.
3) Estimate particles interactions.
37.
38. 3) Electron
microscope:
2) Ultra microscope:
o Particles appear as spots o Give actual picture of the
of light against the dark particles (up to 5A).
background of the o Used to observe the size,
microscope. shape and structure of
sols.
o High energy electron
o Used in the technique of beams are used. (have
micro electrophoresis for greater resolving power)
measuring particle
charge. o One disadvantage is;
only dried samples can be
examined. Not give
information on
solvation.
40. a) Electrical properties of interfaces:
Most surfaces acquire a surface electric charge
when brought into contact with an aqueous
medium, the principal charging mechanisms
being as follows:
1) Ion dissolution.
2) Ionization.
3) Ion adsorption.
41. 1) Ion dissolution:
o Surface charge of colloidal particle is controlled by the charge of ion
present in excess in the medium.
o Examples; 1) AgNo3 + NaI AgI +NaNo3
a) silver iodide in a solution with excess iodide Particles acquire - ve
charge & vice versa. if excess Ag the charge will be +ve since the conc.
Of Ag and I determine the electric potential
b) Aluminum hydroxide in a solution with excess hydroxide
particles acquire – ve charge & vice versa.
Potential determining ions: ions whose conc. determine the
electric potential at the particle surface (e.g. Ag+ , I -, H+, OH- )
42. 2) Ionization
o Surface charge of colloidal particle is controlled by the
ionization of surface groupings
o Examples;
a) polystyrene latex has carboxylic acid group at the surface, ionize to give
negatively charged particles.
b) acidic drugs as ibuprofen & nalidixic acid acquire surface negative
charged.
c) Amino acids & proteins have carboxyl & amino groups whose ionization
depend on the pH as follow;
- + - +
NH2-R-COO NH3-R-COO NH3-R-COOH
At high PH Zwitter ion At low PH
Alkaline medium Iso electric point Acidic medium
Negatively charged Zero charge Positively charged
COOH COO- NH2 NH3+
43. Suit ionization;
o Iso electric point:
o pH at which +ve charges = -ve charges,
o i.e. net charge of the amino acid = zero.
o It is a definite pH specific for each protein.
o At this pH protein is least soluble & precipitated.
o Q; How can you precipitate insulin???
o BY ADJUSTING THE pH OF the SOLUTION
TO THE ISO ELECTRIC POINT OF INSULIN
(PH 5.2).
44. 3) Ion adsorption:
o Surface charge of colloidal particle is controlled by the
unequal adsorption of oppositely charged ions
o Examples;
o Surfaces of sol in water are more often –ve charged
than +ve charged ?!!!
Because cations are more hydrated than anions so
cations reside in the bulk while less hydrated anions
adsorbed on the surface.
45. b) The electrical double layer:
• Definition:
• Development of a net charge at the particle surface affects the
distribution of ions in the surrounding interfacial region,
• As a result: concentration of counter ions increase at the
surface,
• Thus, an electrical double layer exists around each particle.
• Example;
AgNO3 + NaI AgI +NaNO3
•At xs NaI :
Na+
AgI I-
AgI AgI
AgI AgI AgI AgI ( N.B. Vice versa if xs AgNO3 )
46. o Silver iodide sols can be prepared by the reaction,
n AgN03 + Nal---- Agl + NaN03
o In the bulk of AgI particles 1 : 1 ratio of Ag+ and I-
o If the reaction is carried out with an excess silver nitrate,
there will be more Ag+ than l- ions in the surface of the
particles The particles will thus be positively charged
and the counterions surrounding them will be N03-.
o The combination of the positively charged surface and the
atmosphere of counter ions surrounding it is called the
electric double layer.
o If the reaction is carried out with an excess NaI, there will
be more l- than Ag+ ions in the surface of the particles
The particles will thus be negatively charged and the
counter ions surrounding them will be Na+.