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Production of Insulin Reverse Phase – High Pressure Liquid Chromatography Unit (RP-HPLC) Presented by:Justin McComb Rachelle Bolton Young Chang
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Overview Purpose of the Unit Principles of RP-HPLC Design Validation Equations Organic Modifiers Resin Design Options Process Design Considerations Cost Analysis Final Process Final Design
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Purpose of Unit The unit purifies native insulin by removing impurities such as: insulin ester denatured insulin partially cleaved precursor components The second RP-HPLC used in the production of insulin is used to purify the human insulin that has been produced.
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Principles of RP-HPLC RP-HPLC is a technique by which differences in polarity of compounds can be used to separate them from a mixture into their components Chromatography functions through mass transfer between a mobile and stationary phase Stationary phase (packing): non-polar resin Mobile phase (solvent): polar liquid As the mobile phase passes through the column, the components within that phase will have different affinities for the stationary phase.
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Principles of RP-HPLC This will affect the elution time of each compound, and will cause the mixture to separate into its components.
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Principles of RP-HPLC
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Design Validation Equations Re p = Reynolds f p = friction factor Q = volumetric flowrate A = x-sectional area ρ = density μ = viscosity L = column length ΔP = pressure drop ε = void fraction D p = resin diameter Ergun Equation Laminar Flow Validation Pressure Drop Calculation
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Summary Table of Organic Modifiers 1 poise = dyne s/cm 2 = g/cm s = 1/10 Pa s 1 p = 100 centiPoise Density(g/cm 3 )Viscosity(cP) @ Room Temperature Isopropanol0.782.5 Acetonitrile0.7860.38 Ethanol0.7891.2
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Resin Design Option #1
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Resin Design Option #2
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Scale Up Constant Length Constant Linear Flowrate Process Design Considerations
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Cost Analysis Capital Cost (Hamilton estimates): 20 units x $20000/unit = $400,000 Operating Costs Resin Cost: $10,000/unit Solvent Cost: Encompasses 80% of total operating cost Energy Cost: Cold water Pump (vs. pressure drop)
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Final Process 20,000 mg of the insulin solution is dissolved in 1.5 L water, 10% 2-propanol Column is regenerated with 0.5N NaOH, washed with water, then washed with 80% isopropyl alcohol containing 0.1% trifluoroacetic acid Column is equilibrated with 5 column volumes of Buffer A Insulin solution is applied at 100 cm/h flow rate Column washed with 3 column volumes of 20% Buffer B and 80% Buffer B Buffer B increased from 20% to 40% in 1 column volume Native insulin eluted in a linear gradient of 40-50% buffer B in 30 column volumes 16,000 mg insulin (98% purity) generated
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Final Design
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Questions ????
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