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B. AmsdenCHEE 440 Stability The extent to which a product retains, within specified limits, and throughout its period of storage and use, the same properties and characteristics it possessed when manufactured. Types chemical physical microbiologic therapeutic toxicologic
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B. AmsdenCHEE 440 Degradation Mechanisms Hydrolysis cleavage of bonds by action of water esters procaine, atropine, aspirin amides chloramphenicol, penicillin, cephalosporins Oxidation molecule gains O or loses H susceptible compounds phenols, aromatic amines, aldehydes, ethers, unsaturated aliphatic compounds examples epinephrine, vitamin A, ascorbic acid
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B. AmsdenCHEE 440 Degradation Mechanisms photo-degradation light energy provides energy of activation reaction rate is independent of T photo-oxidation catalyzed by light nifedipine, colchicine, chlorpromazine, riboflavin isomerisation conversion of a drug into its optical isomer enantiomers often have significantly different ADME and pharmacological action often catalyzed by acid or a base ex. tetracycline, pilocarpine, cephalosporin esters
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B. AmsdenCHEE 440 Degradation Mechanisms Interactions between formulation compounds buffers general acid-base catalysts formation of amides benzocaine and citric acid accelerated photodecomposition riboflavin in presence of nonionic or anionic surfactant
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B. AmsdenCHEE 440 Factors governing stability Liquids pH temperature ionic strength solvent oxygen Solids excipients
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B. AmsdenCHEE 440 Effect Of pH Catalyst substance that influences rate of reaction but is not changed chemically either accelerates or inhibits reaction does not change position of equilibrium no change in G o forms a complex with reactant decomposes to form product + catalyst
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B. AmsdenCHEE 440 Acid-Base Catalysis accelerated decomposition in presence of acid or base often buffered therefore catalyzed specific acid-base catalysis rate law contains [H 3 O + ] or [OH - ]
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B. AmsdenCHEE 440 Hydrolysis of Ester acid-catalyzed degradation ester = S water = W product = P base-catalyzed degradation
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B. AmsdenCHEE 440 Example Drug X degrades by a base-catalyzed process in a buffer of pH 9 at room T. If the initial concentration of X was 0.1 M and after 4 days there was 0.099 M of X present, determine k 2 for this reaction.
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B. AmsdenCHEE 440 Solvent catalysis indicated by minimum region of k versus pH plot can occur along with both acid and base catalyzed degradation
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B. AmsdenCHEE 440 General Acid-Base Catalysis catalysis in buffered solution by other than H + or OH - k obs vs pH diagram deviates from expected behavior ex. streptozotocin in phosphate buffer
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B. AmsdenCHEE 440 Effect of T Arrhenius
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B. AmsdenCHEE 440 Example The rate constant for the decomposition of expensinin at 120 °C is 1.173 hr -1 and at 140 °C is 4.86 hr -1. Calculate the activation energy and the Arrhenius factor for this reaction.
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B. AmsdenCHEE 440 Other Influences Solvent polar solvents increase the rate of reaction where the products are more polar than the reactants nonpolar solvents increase the rate of reaction where the products are more nonpolar than the reactants Ionic strength, influences rate constant
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B. AmsdenCHEE 440 Solid Dosage Forms Stability concerns moisture hygroscopic excipients excipient catalyzed reactions ex. Mg stearate lubricant
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B. AmsdenCHEE 440 Drug Stabilization hydrolysis strategies optimum pH, buffer, solvent refrigeration complexation agent dosage form emulsion, suspensions oxidation add antioxidants sodium bisulfite, ascorbic acid ascorbyl palmitate, butylated hydroxytoluene (BHT), vitamin E
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B. AmsdenCHEE 440 Shelf-Life effective period of storage and use t 90 time required to degrade 10% of the drug 90% drug still active determined by reaction kinetics first order2nd orderzero order
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B. AmsdenCHEE 440 Example An ophthalmic solution has a mydriatic drug present at a 5 mg/ml concentration. The drug degrades by first order kinetics (k 1 = 0.0005/day). What is its shelf life?
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