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Pharmaceutical Water Systems

Pharmaceutical Water Systems. Mason P. Waterbury Nektar Therapeutics 28 June 05. Pharmaceutical Water Systems. Let’s talk about: What is High Purity Water? How do we make High Purity Water? How do we store and distribute High Purity Water? Specific challenges / solutions.

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Pharmaceutical Water Systems

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  1. Pharmaceutical Water Systems Mason P. Waterbury Nektar Therapeutics 28 June 05

  2. Pharmaceutical Water Systems • Let’s talk about: • What is High Purity Water? • How do we make High Purity Water? • How do we store and distribute High Purity Water? • Specific challenges / solutions

  3. Pharmaceutical Water Systems • What is High Purity Water? • Purified Water (PW) • Sterile Purified Water (SPW) • Water for Injection (WFI) • Sterile Water for Injection (SWFI) • Water for Irrigation • Future Monographs (e.g., Water for Hemodialysis)

  4. Pharmaceutical Water Systems • What is High Purity Water? • Purified Water (PW) • Sterile Purified Water (SPW) • Water for Injection (WFI) • Sterile Water for Injection (SWFI) • Water for Irrigation • Future Monographs

  5. Pharmaceutical Water Systems • Purified Water • USP: “. . .obtained by a suitable process” • Conductivity ≤ 1.3 µS/cm @ 25º C • Total Organic Carbon (TOC) ≤ 500 ppb • Microbial ≤ 100 cfu/ml • No endotoxin requirement • EP: “. . .prepared by distillation, by ion exchange, by reverse osmosis or by any other suitable method” • JP: “. . .purified by distillation, ion-exchange treatment, ultrafiltration or combination of these methods”

  6. Pharmaceutical Water Systems • Purified Water – Example System

  7. Pharmaceutical Water Systems • Water for Injection (WFI) • USP: “. . .distillation or a purification process that is equivalent of superior to distillation” • Conductivity ≤ 1.3 µS/cm @ 25º C • Total Organic Carbon (TOC) ≤ 500 ppb • Microbial ≤ 10 cfu / 100 ml • Endotoxin requirement < 0.25 EU/ml • EP: “. . .distillation” • JP: “. . .distillation. . .or by the Reverse Osmosis Ultrafiltration of Purified Water”

  8. Pharmaceutical Water Systems • Water for Injection (WFI) Distillation Techniques • Multi-Effect Still (MES) • Uses Plant Steam to convert feedwater to pure steam • Separators allow impurities to drop out of the pure steam • Pure steam from first effect used to convert feedwater to pure steam in subsequent effects

  9. Pharmaceutical Water Systems • Water for Injection (WFI) Distillation Techniques • Vapor Compression (VC) • Uses plant steam to convert initial feedwater to vapor (pure steam) • Pure steam is compressed, elevating temperature • Compressed vapor is used to evaporate new feedwater, giving up latent heat and condensing as WFI • Higher electrical demand, but lower steam demand

  10. Pharmaceutical Water Systems • High Purity Water Storage and Distribution • Materials of Construction (Chemical and Heat Compatibility) • Stainless Steel (316 or 316L) • Teflon, EPDM, Silicone, Viton (gaskets, diaphragms) • Fully Drainable (minimum slope 1/8” per foot, hygienic design of components) • Minimize Dead Legs (<= 2 pipe diameters) • Smooth Surfaces (Mechanical Polish vs. Electropolish) • Clean joints (sanitary Tri®Clamp, automatic orbital welding) • Passivate interior surfaces to form barrier between water and free iron

  11. Pharmaceutical Water Systems • Storage and Distribution – Sanitization • Heat (Continuous or Periodic, >81 deg. C for >1 hour) • Most popular – nothing added to system • If system continuously hot, all but eliminates concerns about sanitization • Can be a utility hog • Ozone • Gaining popularity • Ozone destruction and monitoring very important • Environmental concerns • Chemical • Must ensure that cleaning chemicals are completely removed from system • Rinsing post-sanitization time and cost intensive

  12. Pharmaceutical Water Systems • Storage and Distribution – Hot vs. Cold ? • Hot storage: • WFI produced through distillation is often generated hot, so why not store it hot? • Advantageous if there will be hot WFI distribution • Cold storage: • Periodic heat-up & cool-down of storage tank time- and energy-intensive • Could expedite heat-up by dumping tank contents, but this is wasteful • Best solution will vary depending on specific user requirements

  13. Pharmaceutical Water Systems Hot Storage, Hot and Ambient Distribution

  14. Pharmaceutical Water Systems Hot Storage, Hot and Ambient Distribution • Cost-effective when there are many ambient use points • Heat Sanitization of ambient loop by displacement of AWFI or by heating ambient loop • Two loops mean increased installation labor • Only one heat exchanger means all ambient users get water at same temperature, no local temperature selection

  15. Pharmaceutical Water Systems Hot Storage, Hot Distribution with Use Point Coolers

  16. Pharmaceutical Water Systems Hot Storage, Hot Distribution with Use Point Coolers • Cost-effective when there are few ambient use points • Main distribution loop is continuously hot, therefore self-sanitizing • Can have locally adjustable use point temperatures • Ambient point-of-use piping must be sanitized by flushing or pulsing HWFI through heat exchanger to drain • Additional heat exchangers means increased capital (and maintenance) cost • Some feel POU cooler piping is a dead leg, prone to microbial growth

  17. Pharmaceutical Water Systems Hot Storage, Hot Distribution with Use Point Cooler Sub-loops

  18. Pharmaceutical Water Systems Hot Storage, Hot Distribution with Use Point Cooler Sub-loops • Cost-effective when there are few ambient use points • Main distribution loop is continuously hot, therefore self-sanitizing • Heat exchanger piping kept hot when not in use • Can have locally adjustable use point temperatures • Dead leg question replaced by “turbulent flow” question – this becomes a balancing problem • Additional heat exchangers means increased capital (and maintenance) cost

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