This document provides an overview of the Physical Pharmaceutics II course. It discusses key topics like colloidal dispersion, rheology, coarse dispersion, micromeritics, and drug stability. The course aims to help students understand physicochemical properties of drugs in designing dosage forms and apply principles of chemical kinetics to stability testing and expiry date determination. It covers various units including colloidal properties, rheology concepts, suspensions and emulsions, particle characterization, and factors influencing drug degradation. The assessment includes internal exams, assignments, and an end semester exam totalling 100 marks. The course equips students with formulation and evaluation skills by exploring physical and physicochemical principles involved in dosage forms.
R. VIJAYAKUMAR., M Pharm,
Research Scholar
department of Pharmaceutical Technology.
Anna university- BIT
Tiruchirappalli
III Semester.
UNIT-IV / Micromeritics
Powder Technology
Particle analysis in pharmaceuticals
Determination of particle size and surface area
Large scale equipment for powders
Types of powders
Decomposition and stabilization of pharmaceutical productsArshad Khan
Drug stability:Stabilization of medicinal agents against common reactions like hydrolysis & oxidation. Accelerated stability testing in expiration dating of pharmaceutical dosage forms. Photolytic degradation and its prevention.
R. VIJAYAKUMAR., M Pharm,
Research Scholar
department of Pharmaceutical Technology.
Anna university- BIT
Tiruchirappalli
III Semester.
UNIT-IV / Micromeritics
Powder Technology
Particle analysis in pharmaceuticals
Determination of particle size and surface area
Large scale equipment for powders
Types of powders
Decomposition and stabilization of pharmaceutical productsArshad Khan
Drug stability:Stabilization of medicinal agents against common reactions like hydrolysis & oxidation. Accelerated stability testing in expiration dating of pharmaceutical dosage forms. Photolytic degradation and its prevention.
PHYSICAL PHARMACEUTICS II COARSE DISPERSION VijayaKumarR28
R. VIJAYAKUMAR., M Pharm,
Research Scholar
department of Pharmaceutical Technology.
Anna university- BIT
Tiruchirappalli.
As per PCI syllabus for B Pharm / 2nd Year ,III Semester.
UNIT-III / Coarse dispersion
Preformulation Studies: Introduction to preformulation, goals and objectives, study of
physicochemical characteristics of drug substances.
a. Physical properties: Physical form (crystal & amorphous), particle size, shape, flow
properties, solubility profile (pKa, pH, partition coefficient), polymorphism.
b. Chemical Properties: Hydrolysis, oxidation, reduction, racemisation, polymerization
BCS classification of drugs & its significant
Application of preformulation considerations in the development of solid, liquid oral and
parenteral dosage forms and its impact on stability of dosage forms.
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
PHYSICAL PHARMACEUTICS II COARSE DISPERSION VijayaKumarR28
R. VIJAYAKUMAR., M Pharm,
Research Scholar
department of Pharmaceutical Technology.
Anna university- BIT
Tiruchirappalli.
As per PCI syllabus for B Pharm / 2nd Year ,III Semester.
UNIT-III / Coarse dispersion
Preformulation Studies: Introduction to preformulation, goals and objectives, study of
physicochemical characteristics of drug substances.
a. Physical properties: Physical form (crystal & amorphous), particle size, shape, flow
properties, solubility profile (pKa, pH, partition coefficient), polymorphism.
b. Chemical Properties: Hydrolysis, oxidation, reduction, racemisation, polymerization
BCS classification of drugs & its significant
Application of preformulation considerations in the development of solid, liquid oral and
parenteral dosage forms and its impact on stability of dosage forms.
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
It is a small presentation about the preformulation studies, which help students in their exams.
Preformulation is a crucial stage in pharmaceutical research and development that encompasses a series of scientific studies and experiments conducted before the formulation of a drug product begins. Its primary purpose is to gather essential information and data about the physical, chemical, and biopharmaceutical properties of a drug substance or active pharmaceutical ingredient (API).
Understanding the Drug Substance:
Preformulation starts with a comprehensive characterization of the drug substance. This includes identifying its chemical structure, molecular weight, and purity. Various analytical techniques are employed for this purpose, such as nuclear magnetic resonance (NMR) spectroscopy, mass spectrometry (MS), and high-performance liquid chromatography (HPLC).
2. Assessing Physicochemical Properties:
Preformulation studies delve into the physicochemical properties of the drug substance. Researchers investigate properties such as solubility, melting point, crystallinity, hygroscopicity, and polymorphism. These properties can profoundly affect formulation design and stability.
Preformulation and physicochemical property of the drugSHIVANEE VYAS
“It is the study of the physical and chemical properties of the
drug prior to compounding process”.
Preformulation commences when a newly synthesized drug shows sufficient pharmacologic promise in animal models towarrant evaluation in man.
These studies should focus on physicochemical properties of new compound that affect drug performance & development of efficaciouss dosage form.
This properties may provide;
A rationale for formulation design
Support the need for molecular modification.
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Letter from the Congress of the United States regarding Anti-Semitism sent June 3rd to MIT President Sally Kornbluth, MIT Corp Chair, Mark Gorenberg
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The US House of Representatives is deeply concerned by ongoing and pervasive acts of antisemitic
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Physical Pharmaceutics II
1. Physical Pharmaceutics II
Subject overview
MANIVASAKAM P
Assistant Professor,
Department of Pharmaceutics,
JKKMIHSCP, T.N PALAYAM -638504.
2. Introduction
❖ Physical pharmaceutics is a pharmaceutical material science that is concerned
with the physical and chemical principles of materials (drugs and other additives)
that go into the formulation of dosage forms.
❖ Historically, physical pharmacy has been associated with the area of pharmacy
that dealt with the quantitative and theoretical principles of physicochemical
science as they applied to the practice of pharmacy.
❖ A strong foundation in this subject helps the pharmacist in selecting the right kind
of materials.
❖ Physical pharmacy attempted to integrate the factual knowledge of pharmacy
through the development of broad principles of its own, and it aided the pharmacist
and the pharmaceutical scientist in their attempt to predict the solubility, stability,
compatibility and biological action of drug products.
3. Physical Pharmaceutics 2
❏ Colloidal dispersion
❏ Rheology
❏ Course dispersion
❏ Micromeritics
❏ Drug stability
Physical Pharmaceutics 1
❏ Solubility of drugs
❏ States of matter
❏ Surface and interfacial
phenomena
❏ Complexation and protein binding
❏ pH, buffer and isotonic solutions
4. Scope of PHY PHR - II
❖ The course deals with the physical and physicochemical properties
and principles involved in the dosage forms/formulations.
❖ Theory and practical components of the subject help the student to
get a better insight into various areas of formulation research and
development and stability studies of pharmaceutical dosage forms.
5. Objectives of PHY PHR - II
Upon the Completion of the course student shall be able to,
➔ Understand various physicochemical properties of drug molecules in
the designing the dosage forms.
➔ Know the principles of chemical kinetics & to use them for stability
testing and determination of expiry date of formulations.
➔ Demonstrate use of physicochemical properties in the formulation
development and evaluation of dosage forms.
6. Unit - I. Colloidal dispersion (10hrs)
❏ 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.
7. UNIT - II. Rheology (10hrs)
❏ Newtonian systems,
❏ Law of flow,
❏ Kinematic viscosity,
❏ Effect of temperature,
❏ non-Newtonian systems,
❏ Pseudo plastic, dilatant, plastic,
thixotropy, thixotropy in formulation,
❏ Determination of viscosity, capillary,
falling Sphere, rotational viscometers
Deformation of solids:
❏ Plastic and elastic deformation,
❏ Heckel equation,
❏ Stress,
❏ Strain,
❏ Elastic Modulus
8. Unit - III. Course dispersion (7 hrs)
❏ Suspension,
❏ Interfacial properties of suspended particles,
❏ Settling in suspensions,
❏ Formulation of flocculated and deflocculated suspensions.
❏ Emulsions and theories of emulsification,
❏ microemulsion and multiple emulsions
❏ Stability of emulsions,
❏ Preservation of emulsions,
❏ Rheological properties of emulsions and emulsion formulation by HLB
method.
9. Unit - IV. Micromeritics (10 hrs )
❏ Particle size and distribution,
❏ Mean particle size, number and weight distribution, particle number,
❏ Methods for determining particle size by different methods,
❏ Counting and separation method,
❏ Particle shape, specific surface,
❏ Methods for determining surface area,
❏ Permeability, adsorption,
❏ Derived properties of powders,
❏ Porosity ,
❏ Packing arrangement,
❏ Densities ,
❏ Bulkiness & flow properties.
10. Unit - V. Drug stability (10 hrs)
❏ Zero, pseudo-zero, first & second order,
❏ Units of basic rate constants,
❏ Determination of reaction order.
❏ Physical and chemical factors influencing the chemical degradation of
pharmaceutical product: temperature, solvent, ionic strength, dielectric
constant, specific & general acid base catalysis, Simple numerical problems.
❏ Stabilization of medicinal agents against common reactions like hydrolysis &
oxidation.
❏ Accelerated stability testing in expiration dating of pharmaceutical dosage
forms.
11. Reference Books
❏ Physical Pharmacy by Alfred Martin, Sixth edition.
❏ Tutorial pharmacy by Cooper and Gunn.
❏ Physical Pharmaceutics by Ramasamy C, and Manavalan R.
❏ Textbook of physical pharmaceutics by C V S Subrahmanyam.
❏ Aulton’s pharmaceutics- The design and manufacture of medicines.
❏ Remington education pharmaceutics.