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Chapter 4
Objectives
After reading this chapter, the student will be able to: 1. List reasons drugs are incorporated into various dosage forms. 2. Compare and contrast the advantages/disadvantages of various drug dosage forms. 3. Describe the information needed in preformulation studies to characterize a drug substance for possible inclusion into a dosage form. 4. Describe the mechanisms of drug degradation and provide examples of each. 5. Describe the five types of drug instability of concern to the practicing pharmacist. 6. Summarize approaches employed to stabilize drugs in pharmaceutical dosage forms. 7. Calculate rate reactions for various liquid dosage forms. 8. Categorize various pharmaceutical ingredients and excipients.
Copyright 2011 Wolters Kluwer Health | Lippincott Williams & Wilkins
Preformulation Studies
Chemical characterization Physical characterization
Physical Description
Solids, liquids, gases Chemical Properties Structure, form, reactivity Physical Properties Description, particle size, crystalline structure, melting point, solubility Biological Properties Ability to get to site of action and elicit a response
Microscopic Examination
Particle size Particle size range Crystal structure Particle shape
Heat of Vaporization
Vapor pressure Volatile drugs can migrate within a solid dosage form Personnel exposure
Particle Size
Dissolution rate Bioavailability Content uniformity Taste Texture Color Stability Flow characteristics Sedimentation rates
Polymorphism
Crystalline Amorphous Melting point variation Solubility differences
Solubility
Some aqueous solubility required for therapeutic efficacy Equilibrium solubility Solubility in different solvents
Solubility and pH
pH:solubility profiles are important. pH can affect solubility.
Dissolution
Dissolution may be rate-limiting step in the absorption of poorly soluble drugs. Can affect onset, intensity, and duration of response and control overall bioavailability of the drug from the dosage form
Membrane Permeability
pKa, solubility, and dissolution rate data can provide an indication of absorption.
Partition Coefficient
Octanol:water partition coefficient often used in formulation development
pKa/Dissociation Constants
Extent of dissociation or ionization Dependent on pH of medium Can affect absorption, distribution, and elimination
Rate Reactions
Change of drug concentration with respect to time
Stability Testing
Done at each stage of product development Product containers and closures must be considered Temperature and humidity studies Light studies Changes in physical appearance, color, odor, taste, texture Chemical changes of drug degradation Pharmacist is last professional to check for quality and stability prior to dispensing
Kinetics
The study of the rate of chemical change and the way this rate is influenced by conditions of concentration of reactants, products, and other chemical species that may be present and by factors such as solvent, pressure, and temperature
Importance of Kinetics
1. Selection of proper storage temperature Temperature Light Advising patient on storage conditions 2. Selection of proper container for dispensing Glass vs. plastic Clear vs. amber vs. opaque Cap liner selection
Stability: USP
The extent to which a product retains, within specified limits, and throughout its period of storage and use (i.e., its shelf life), the same properties and characteristics that it possessed at the time of manufacture
Definitions
Accelerated Testing Studies designed to increase the rate of chemical or physical degradation by using exaggerated storage conditions Bulk Drug Substance Active drug before formulation Drug Product Finished dosage form
Definitions (contd)
Expiration Date The date placed on the immediate container label of a drug product that designates the date through which the product is expected to remain within specifications Expiration Dating Period The interval that a drug product is expected to remain within the approved specifications after manufacture
Definitions (contd)
Primary Stability Data Data on the drug product stored in the proposed container-closure for marketing under storage conditions that support the proposed expiration date
Definitions (contd)
Stability-Indicating Methodology Quantitative analytical methods based on the characteristic structural, chemical, or biological properties of each active ingredient of a drug product, and that will distinguish each active ingredient from its degradation products so that the active ingredient content can be accurately measured
Definitions (contd)
Stability The capacity of a drug product to remain within specifications established to ensure its identity, strength, quality, and purity Strength A quantitative measure of active ingredient, as well as other ingredients requiring quantitation Supportive Stability Data Data other than primary stability data
Reaction Kinetics
Want two things from kinetic data:
Reaction Kinetics
The overall ORDER of a reaction is the SUM of the EXPONENTS of the CONCENTRATION terms of the RATE EXPRESSION. The ORDER with respect to EACH REACTANT is the EXPONENT of the INDIVIDUAL CONCENTRATION terms in the RATE EXPRESSION.
Order of a Reaction
An experimental quantity; merely provides information about the way in which the rate depends on concentration
Pure systems
Half-Life
Is meaningless to attempt to describe the time required for ALL material to decompose (i.e., infinity) Therefore, reaction rate can be described by K or halflife, t1/2
C = k0t + C0
Arrhenius Equation
log = k2\k1 = Ea (t2 T1)\2.3 RT1T2
<10 kcal/mole---------
Fast reactions stability problems in development Solvolytic process; most drug degradation
10-30 kcal/mole-------
50-70 kcal/mole-------
Pyrolytic reactions
Excipients
Coloring agents Sweetening agents Flavoring agents Surfactants Solubilizing agents Antioxidants Preservatives Thickening agents Suspending agents Binding agents Solvents Lubricants Perfumes Fats and oils
Harmonization of Standards
International harmonization of excipients Pharmaceutical industry is multinational Uniform standards needed
Flavoring Pharmaceuticals
Complex area Important for compliance Color and taste should generally match
Flavor
Taste Touch Smell Sight Sound
Greater sensitivity to odors than to tastes Females have greater sensitivity to odors than males
Flavor Selection
Immediate flavor identity Rapid full flavor development Acceptable mouthfeel Short aftertaste No undesirable sensations
Flavoring Techniques
Blending Fruit=========== Sour Salty/Sweet/Sour=== Bitter Salty=========== Decreases sourness Salty=========== Increases sweetness Overshadowing Methylsalicylate==== Glycyrrhiza
Sweetening Pharmaceuticals
Complex area Natural vs. synthetic Heat stability
Sweetening Agents
Dextrose Mannitol Saccharin Sorbitol Sucrose
Coloring Pharmaceuticals
Lighter shades preferred
Coloring Agents
Dyes: FD&C, D&C, Ext D&C Lakes: Calcium and aluminum salts Liquids: 0.001% to 0.0005% Powders: 0.1% Caramel Ferric oxide: Red/yellow
Preservatives
Sterilization and Preservation Preservative Selection General Preservative Considerations Mode of Action Preservative Utilization
Preservative Selection
Dosage form Route of administration Compatibility with excipients Container and closure compatibility
Mode of Action
Modification of cell membrane permeability Lysis and cytoplasmic leakage Irreversible coagulation of cytoplasmic constituents Inhibition of cellular metabolism Oxidation of cellular constituents Hydrolysis
Preservative Utilization
Benzoic acid/sodium benzoate Alcohol Phenylmercuric nitrate/acetate Phenol Cresol Chlorobutanol Benzalkonium chloride Methylparaben/propylparaben Others