1 / 9

Sterilization

Sterilization. on a practical basis means the absence of any detectable viable organism. : only the desired organism is detectably present. Sterilization methods : Medium & equipment: .

jermaine-haney
Download Presentation

Sterilization

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Sterilization on a practical basis means the absence of any detectable viable organism. : only the desired organism is detectably present. Sterilization methods: Medium & equipment: . Heat-sensitive materials in medium: (microfiltrator pore sizes<0.2μm). Heat-sensitive equipment: UV radiation (energy intensive) or chemical agents (toxic to the desired culture. e.g.70% ethanol-water, and ethylene oxide (gas). Gas (air): sterilized through adiabatic compression process for supplying oxygen (~2200C) followed by (e.g. glass wool filter).

  2. Sterilization Thermal deactivation The probability of an unsuccessful sterilization: 1- P0(t) The probability of extinction (successful sterilization): P0(t)=[1-p(t)]N0 where p(t) is the probability that an individual will still be viable at time t. N0 is the number of individuals (cells or spores) initially present. Assume first order death rate: p(t)=e-kdt 1- P0(t)=1-[1-p(t)]N0 = 1-[1-e-kdt]N0 where the specific death rate kd = αe-E0d/RT(1/time), constant at specified T. Eod is the activation energy for the death of the organism.

  3. Sterilization (D): time for the number of viable cells to decrease tenfold. E[N(t)] = N0 p(t) E[N(t)] = N0 e-kdt 0.1= e-kdD D=2.303/kd E[N(t)] is the expected value of the number of individuals present at time t.

  4. Sterilization 1- P0(t)= 1-[1-e-kdt]N0 kd = αe-E0d/RT From the above equation: • Known N0, T, t, determine Kd, the probability of an unsuccessful sterilization is determined. • Given N0, T, acceptable probability of failure e.g. 10-3, required time can be determined • Higher Kd tends to achieve low probability of sterilization failure. Normally at 121oC. Kd of vegetative cells > 1010 min-1, spores 0.5-5 min-1. The major concern is spores.

  5. Sterilization Chart e.g. N0=108, Kd=1min-1 (1210C), t=26min Kdt=26 Probability of failure: 1-P=0.001 e.g. N0=108, Kd=1min-1 (1210C), 1-P=0.001 Kdt=26 Required sterilization time: t=kdt/kd=26 min (M. Shular, Textbook, p.319)

  6. holding cooling heating T (K) t time Kd2 Kd3 Kd1 T (K) t time Batch Sterilization Temperature verse time in a batch sterilization process Simplified calculations for deactivation of spores and medium components

  7. Sterilization Degradation of components in the medium in sterilization process. vitamin and growth factor The inactivation of viability is much more sensitive to temperature changes than the degradation of important growth factors in the medium It is important to assure complete killing of foreign organisms without the destruction of important components in the medium.

  8. Sterilization Degradation of components in medium Assume the degradation rate of such components is first order. dC/dt=-kdC The degradation rate constant kd can also be related to temperature by Arrhenius equation. Integrating the above equation, ln C/C0=-kdt or C=C0e-kdt where C0 is the initial concentration of the component. To determine the components remaining active: the temperature T → determine kd → with known t, determine C.

  9. Sterilization Degradation of components in the medium. T (K) t time C1 Δt2 C2 Kd,2 C0 C1 Δt1 C2 Δt3 C3 Kd,3 Kd,1 kd = αe-E0d/RT

More Related