Validation of sterelization_equipment
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This document discusses the validation of sterilization equipment, including dry heat sterilizers and steam sterilizers. It provides definitions of key terms like sterilization and depyrogenation. It also outlines the process for validating different types of sterilization equipment, including design qualification, installation qualification, operational qualification, and performance qualification. The validation process involves tests to evaluate temperature distribution, heat penetration, and lethalities to verify sufficient sterilization is achieved.
Validation of sterelization_equipment
- 1. VALIDATION OF – Slide: 1/51 STERILIZATION EQUIPMENTS Aseptic Area Validations Pharmaceutical & Chemical Industry Research and Development Foundation
- 2. Content: – Slide: 2/51 • Definition of Sterilization and Depyrogenation • Microbiological aspects of Sterilization and Depyrogenation, Lethality calculation, • D- Value, FH & F0 Values • Z- Value and use of microbiological indicators.
- 3. – Slide: 3/51 Content: - Dry Heat Ovens - Dry Heat Sterilization Tunnels - Steam Sterilizator (Autoclaves) 1. Design Qualification 2. Installation Qualification 3. Operational Qualification 4. Performance Qualification 4.1. Thermodynamical aspects of Sterilization 3.2. Temperature Distribution and Heat Penetration studies.
- 4. – Slide: 4/51 Definitions: • 1. Sterilization: Validated process used to render a product free of living microorganisms including bacterial endospores. • 2. Depyrogenation: Removal or inactivation of bacterial endotoxin.
- 5. Sterilization Only: • The cycle is designed to assure that the probability of survival of the native microflora is no greater than one cell in one million units of the commodity. (10-6 probability of nonsterility) • Dry Heat Sterilization, Theoretical requirement: 170 0C, 32 min. • Steam Sterilization Theoretical requirement: 121 0C, 15 min. – Slide: 5/51
- 6. – Slide: 6/51 Sterilization - Overkill • The overkill approach provides assurance of sterilization well in excess of the 10-6 probability of non- sterility. For example an FH provided by an overkill cycle may produce a 12- log reduction of a biological indicator that exhibits a high resistance to dry heat.
- 7. – Slide: 7/51 Sterilization & Depyrogenation • Applies to the cycles where the purpose is both sterilization and depyrogenation. Whenever depyrogenation is a desired end point, relatively high temperatures and/or extended heating times are necessary. Thus, microbial lethality delivered by these cycles provides a margin of safety far in excess of a 10- 6 probability of nonsterility. • Dry Heat Depyrogenation Theoretical requirement: 250 0C-30 min.
- 8. D - Value : Time required for one log (or 90%) reduction of microorganism population at base temperature. Microbial Death Curve 1000000 100000 10000 1000 100 10 1 0,1 0,01 0,001 0,0001 0,00001 0,000001 0,0000001 0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 Minutes at Base Temp. Log numb. of Survivors D-Value= 1.0 min. – Slide: 8/51
- 9. – Slide: 9/51 Determination of Z - Value: • Determine the D - value of an organism at min. three different temperatures. • Construct a Thermal Death Curve by plotting the logarithm of the D- Value versus temperature.
- 10. – Slide: 10/51 Z-Value: Death Rate Constant Assesment of Z Value 100 10 1 0,1 D130 0C : 10 min. 120 130 140 150 160 170 Temperature 0C Log D Value Z Value = 20 0C D150 0C : 1.0 min.
- 11. – Slide: 11/51 Z-Value: • In general, for Dry Heat sterilization, Z- Value may be assumed as 20 0C. And for Steam Sterilization as 10 0C. • However, it will be appropriate to verify for the biological indicators when they are used to measure the integrated lethality of a dry heat or steam sterilization cycle.
- 12. – Slide: 12/51 LETHALITY RATE: Also defined as : • FH For Dry Heat Sterilization • Fo For Steam Sterilization • The equivalent sterilization time spent at the base temperature. • Tb : 170 oC (For Dry Heat Sterilization) • Tb : 121 oC (For Steam Sterilization)
- 13. LETHALITY CALCULATION “Patashnik Method” Lethality Rate : 10 (T-Tb)/Z FH = Δt x Lethality Rate Δt : Cycle time T : Actual Cycle temperature Tb : Base Temperature Z : Microbial Death Rate Constant – Slide: 13/51
- 14. – Slide: 14/51 LETHALITY CALCULATION Example: Determination of FH of a 3 min. dry heat sterilization cycle at 175 0C t = 3 min T = 175 0C FH = 4 x 10 (175-170)/20 Tb = 170 0C FH = 5.31 z = 20 0C Sterilization at 175 0C for 3 min. is equivalent to 5.31 min. at 170 0C .
- 15. Lethality in Dry Heat Sterilization Time Temperature Lethality Rate (min) (0C) min. at 170 0C 5 105 0,0006 10 110 0,0010 15 120 0,0032 20 135 0,0178 25 150 0,1000 30 165 0,5623 35 170 1,0000 40 172 1,2589 45 174 1,5849 50 174 1,5849 55 174 1,5849 60 175 1,7782 65 165 0,5623 70 150 0,1000 75 140 0,0316 80 130 0,0100 85 110 0,0010 90 105 0,0006 – Slide: 15/51 – Σ of Lethal Rates : 10.1912 –FH = Δt x Σ of Lethal Rates –Δt = 5 min. –FH = 5 x 10.192 –FH = 50.961 min. at 170 0C .
- 16. PART-1 DRY HEAT STERILIZATION AND – Slide: 16/51 DEPYROGENATION VALIDATION
- 17. – Slide: 17/51 DRY HEAT STERILIZATION & DEPYROGENATION • Dry heat is often the agent of choice for sterilizing items which will tolerate high temperatures. Dry heat sterilization processes are generally less complicated than steam processes, although higher temperature and/or longer exposure times are required because microbial lethality associated dry heat is much lower than that for saturated steam at the same temperature.
- 18. – Slide: 18/51 Thermodynamical Aspects of Heating Process: 1. Convection Heating Process: • The heat transfer through a medium by motion of it ‘s parts. Natural convection is a result of differences in density caused by temperature gradients in the fluid mass. • Forced convection heating is effected by the action of a mechanical device.
- 19. – Slide: 19/51 Thermodynamical Aspects of Heating Process: 2. Conduction Heating Process: • Conduction is accomplished ether by a molecular interaction from higher energy level to a lower energy level or by free electrons. • Thus, the ability of solids to conduct heat varies directly with the free electron concentration. Pure metals are best conductors and non- metals are the poorest.
- 20. – Slide: 20/51 Thermodynamical Aspects of Heating Process: 3. Radiant Heating Process: • Radiant heating is the process which energy flows from high temperature body to a lower temperature. • The geometry of both source and the exposure section of the unit will affect the uniformity of the radiation density in a unit.
- 21. Dry Heat Sterilization Equipment Validation • Batch Sterilizers Dry Heat Ovens • Continuous Sterilizers – Slide: 21/51 Sterilization Tunnel • The basics of the Batch and Continuous sterilizers are mainly the same. Since the continuous (Tunnel) sterilizer validation is more complicated, the topics will concentrate on the Convection continuous process qualification.
- 22. – Slide: 22/51 Batch & Continuous Processing –1. BATCH PROCESSING: –Washing –Sterilization Dry Heat Oven (Double Door) –Manuel Transfer – Filling –Manuel Transfer –1. CONTINUOUS PROCESSING: –Washing –Sterilization –Washing –Filling (Tunnel) –Filling –Continuous Transfer –Continuous Transfer
- 23. Dry Heat Sterilization Validation 1. Design Qualification: – Slide: 23/51 • Facility layout, decision of batch or continuous process. • Utility requirements and specifications. • Pressure differential requirements. • Required capacity of the sterilizer. • Type of materials to be sterilized. • Any requirements for presterilization.
- 24. Dry Heat Sterilization Validation 2. Installation Qualification: – Slide: 24/51 • The equipment should comply with the original purchase specifications. • Exceptions should be appropriately documented. • The structural installation like; Leveling, insulation, and air flow requirements should meet manufacturer’s specifications.
- 25. Dry Heat Sterilization Validation 2. Installation Qualification: – Slide: 25/51 • All utility connections such as electrical and HVAC should meet the design specifications. • Materials of construction of both the sterilizer and the facility should meet the design specifications.
- 26. – Slide: 26/51 Dry Heat Sterilization Validation 2. Installation Qualification- CALIBRATIONS: The following pieces of equipment should be calibrated by removing or in situ: • Temperature sensors and recording devices • Temperature Controllers (in situ) • Pressure gauges • Belt speed controller and recorder • Cycle set point switches • Velometers
- 27. Dry Heat Sterilization Validation 3. Operational Qualification: – Slide: 27/51 • The actual operational performance of the electro/mechanical components should be verified and documented. • Electrical Logic: Ensure that each step is in the correct sequence and it’s repeatable. • Cycle Set Point Adjustability: Limit Switch sequencing should be verified.
- 28. Dry Heat Sterilization Validation 3. Operational Qualification: – Slide: 28/51 • Overload interlocks: Should not allow excess commodity build- up during processing. • Gasket Integrity: Zone to zone leak rate should be within the limits at all panel gaskets. • Air Balance Ability: Check that, the baffle/linkage mechanisms can be adjusted for balance.
- 29. Dry Heat Sterilization Validation 3. Operational Qualification: – Slide: 29/51 • Blower Rotation: Check that the blowers rotated in the specified direction and speed. • Vibration Analysis: Check the dynamic balancing of the blowers to minimize the vibration in each phase. • Air Balance: Check that the ΔP is positive with respect to the preparation side of the tunnel.
- 30. Tunnel Sterilizer Pressure Differential – Slide: 30/51
- 31. Dry Heat Sterilization Validation 3. Operational Qualification: – Slide: 31/51 • Heater Elements: Check that all the heater elements are properly operating. • Belt Speed: Check that the belt and belt speed recorder are operable. • HEPA Filters: Verify the integrity of the filters.
- 32. Dry Heat Sterilization Validation 4. Performance Qualification: – Slide: 32/51 • In a conductive dry heat sterilization and depyrogenation process, significant variations may occur depending on the load configuration. • Initial load temperature, specific heat of the load components, and the load variations should be tested for delta temperature and slowest to heat zone.
- 33. Dry Heat Sterilization Validation 4. Performance Qualification: – Slide: 33/51 Temperature Distribution: • External monitoring and recording instruments shall be calibrated before and after the OQ/PQ studies (3 point calibration, ± 0.5 0C tolerance). • Uniformity of the temperature distribution in case of Min&Max. loading should be verified by using Thermocouples with 3 replicates. • T/C (Thermocouple) placement shall be documented on a diagram.
- 34. Dry Heat Sterilization Validation 4. Performance Qualification: – Slide: 34/51 Temperature Distribution: • Min. 10-12 T/C ‘s shall be used and they should not be inserted in the load. Data should be recorded during the whole cycle at 1 min. intervals. • At least one T/C shall be placed adjacent to the equipment temperature controller. • Location of the “cold spot” should be determined and documented.
- 35. Dry Heat Sterilization Validation 4. Performance Qualification: – Slide: 35/51 Heat Penetration- Acceptance Criteria: • Thermocouples should be inserted into the load. • At least three biological indicators and T/C’s shall be placed around the cold spot. • External T/C readings should comply with manufacturer’s specifications (with Max ± 3 0C difference) • Biological indicator inactivation results should assure 6-log reduction for Bacillus Subtilis and 3-log reduction for endotoxin. Lethality calculation should verify the Equivalent FH value for defined cycle.
- 36. – Slide: 36/51 HEAT PENETRATION STUDIES
- 37. HEAT PENETRATION STUDIES LOAD CONFIGURATION a13 b13 S7 S4 7 b14 a14 a15 b15 S8 S5 8 b16 a16 a17 b17 9 S9 S6 b18 a18 a7 b7 4 b8 a8 a9 b9 5 b10 a10 a11 b11 6 b12 a12 a1 b1 1 b2 a2 a3 b3 2 b4 a4 a5 b5 3 b6 a6 S1 S2 S3 END MIDDLE START – Slide: 37/51 –S1-S9 : Thermocouples –a1-a18: Bio- Indicators (Bacillus Subtilis) –b1-b18: Endotoxin challenged containers.
- 38. PART-2 STEAM STERILIZATION VALIDATION – Slide: 38/51
- 39. – Slide: 39/51 STEAM STERILIZATION Various types of steam sterilzers are commercially available; • Saturated Steam • Water Immersion • Water Cascade System • Air-Steam Mixtures • Gravity Air Displacement (unpacked materials sterilization) • Vacuum air Displacement (Packed materials)
- 40. STEAM STERILIZATION – Slide: 40/51 • Microbiological aspects of Steam Sterilization and Dry Heat Sterilization are basically the same; • D- Value is determined in the same way • Z- Value = 10 0C • Tb = 121 0C • Lethality (F0 ) can be calculated in the same way.
- 41. Lethality in Steam Sterilization Time Temperature Lethality Rate (min) (0C) min. at 121 0C 5 100 0,0080 6 103 0,0160 7 106 0,0320 8 109 0,0630 9 112 0,1260 10 115 0,2510 11 118 0,5010 12 121 1,0000 13 121 1,0000 14 121 1,0000 15 118 0,5010 16 115 0,2510 17 112 0,1260 18 109 0,0630 19 106 0,0320 20 103 0,0160 21 100 0,0080 – Slide: 41/51
- 42. Steam Sterilization Validation 1. Design Qualification : – Slide: 42/51 • Facility layout. • Utility requirements and specifications. • Required capacity of the sterilizer. • Type of materials to be sterilized (Liquids, wrapped ,hollow or porous materials) • Requirement for Gravity and/or Prevacuum cycles.
- 43. – Slide: 43/51 Steam Sterilization Validation 2. Installation Qualification- CALIBRATIONS: The following pieces of equipment should be calibrated by removing or in situ: • Pressure Gauges • Timing Devices • Temperature Recording Devices • Verification of safety Systems and Devices (EN- 61010 Part- 1 and EN- 61010- 2-041)
- 44. Steam Sterilization Validation 3. Operational Qualification: – Slide: 44/51 • The actual operational performance of the electro/mechanical components and utilities should be verified and documented. • Clean Steam Generator (Free from non- condensables EN- 285) • Air Filtration Systems and compressed air • Power Source • Heat Exchanger, Cooling Water
- 45. Steam Sterilization Validation 4. Performance Qualification: – Slide: 45/51 Temperature Distribution: • External monitoring and recording instruments shall be calibrated before and after the OQ/PQ studies (3 point calibration, ± 0.5 0C tolerance). • Uniformity of the temperature distribution in case of Min&Max. loading should be verified by using Thermocouples with 3 replicates. • T/C placement shall be documented on a diagram.
- 46. Steam Sterilization Validation 4. Performance Qualification: – Slide: 46/51 Temperature Distribution: • At least one T/C shall be placed located in the steam exhaust line or adjacent to the equipment temperature controller. • Min. 10-12 T/C ‘s shall be used and they should not be inserted in the load. Data should be recorded during the whole cycle at 1 min. intervals. • Location of the “cold spot” should be determined and documented.
- 47. Steam Sterilization Validation 4. Performance Qualification: – Slide: 47/51 Heat Penetration- Acceptance Criteria: • Thermocouples should be inserted into the load. • At least three biological indicators and T/C’s shall be placed around the cold spot. • External T/C readings should comply with manufacturer’s specifications (with Max ± 1 0C difference) • Biological indicator (bacillus stearothermophilus) results should ensure the 6-log reduction and Lethality calculation should verify the Equivalent F0 (15 min. at 121 0C) value for defined cycle.
- 48. Steam Sterilization Validation 4. Performance Qualification: – Slide: 48/51 AIR REMOVAL TEST: • The ability of the pre-vacuum autoclaves to effectively remove the air and non-condensable gases should be tested. If the air is not effectively removed, air pockets will occur in the chamber and sterilization conditions will not be attained. • Bowie-Dick or DART Test pack, the uniformity of the colour change on the indicator sheet should be checked. (3.5 min. at 134 0C )
- 49. Steam Sterilization Validation 4. Performance Qualification: – Slide: 49/51 LEAK RATE TEST: • The presence of air prevents proper penetration of of the load by steam and thus inhibits sterilization. • Air leaking from outside into the chamber at the end of sterilization cycle will contaminate the load. • A leak rate equivalent to a rate of change in pressure of 1 mm Hg/min. over a period of 10 min. after stabilization is the maximum permitted rate.
- 50. – Slide: 50/51 STERILIZATION VALIDATION-GENERAL CHANGE CONTROL AND REVALIDATION • Any changes to the sterilization equipment and/or related utilities should be evaluated by a Change Control Procedure. Typical Changes Requiring Revalidation • Any changes in operating cycle (i.e:temperature , time, belt speed, chamber pressure) • Change in load configuration. • Change in sterilized materials. • Major maintenance work on critical instruments/elements or utilities.
- 51. – Slide: 51/51 …………..The END………….. Thanks For Your Attention, Any Questions Please? ………………………………….