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Ahmed L. Al-Aoufi Teaching Assistant Pharmaceutical Dept. PHT 351
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Sterilization Definition: It is the process of killing or removing bacteria and all other forms of living micro-organisms and their spors from the pharmaceutical products (preparation). Sterile product: It is free from all living microorganism and passes the sterility test.
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Other terms used in relation to sterilization: *Antiseptics: These are the substance used to inhibit the growth or destroy germs. They are used on the skin. *Bactericides: These are the substance used to kill the microorganism. *Bacteriostatic Agents: These are the substance which inhibit the growth of bacteria. Different bacteriostatic agent used against different bacteria.
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*Disinfectants: These are the substance used to kill bacteria and other infectious agents from the non- living material. they are too strong to be applied to the human body. as: phenol, cresol, eresol with soap solution and chloroxylenol. *Fungicides: These are substance which kill fungi. *Mycocides : These are the substance which kill molds. *Viricides : These are the substance which kill viruses.
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Aseptic Processing : These operation performed between the sterilization of an object or preparation and the final sealing. These operation are carried out in the complete absence of microorganisms.
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The product or materials which require sterilization 1-All parenteral preparation & its contents. 2-All ophthalmic preparations & its contents 3-surgical instruments 4-surgical dressing & gloves. 5-parentral adminstration sets as syrings [ I.V. sets etc]
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Difference between sterilization and disinfection: In sterilization there is complete destruction or removal of all bacteria & their spors, but in disinfection there is destruction of bacteria but not their spors
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Methods of Sterilization 1- Dry heat sterilization. 2- Moist heat sterilization. 3- Gas sterilization. 4- Sterilization by ionizing radiation. 5- Sterilization by ionizing radiation.
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Comparison Between Different Methods. *process occur: How can sterilization? *lag time *mechanism *advantages *disadvantages *material which can be sterilized *material which can not be sterilized
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Sterilization Efficiency Microbial Death Kinetic: D- value : It is the time (for heat) or dose (for radiation) require for the microbial population to reduce by one logarithm unit. Log N u -D= u/Log N o
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Ex 1 After 5 min of product exposure to temperature of 121 C˚ the m.o was reduced from 2x10 ⁵ to 6 x10³ calculate D-value at 121 C˚
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Solution D = 5/ 5.30 – 3.778 = 3.285 min
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Ex2: After 10 min of exposure to temperature of 121 C˚ the m.o was reduced from 2x10⁵ to 6x10³ calculate D-value at 121 C˚ and write yuor comment?!!
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Solution D = 10/ 5.30 – 3.778 = 6.67 min Comment: at 121 C˚ the microbial population is decrease 90% every 6.57 min
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Ex 3: After 15 min of product exposure to 126.5 C˚ the population is reduced from 5x 10⁵ to 2x10³ Calculate your D and write your comment?(6.25min)
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Resistance value (Z) The number of degree ( C˚) required for 1 log reduction in the D value Z= T 1 - T 2 / log D 2 - log D 1
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After certain experiments at 121.5 C˚ the D was 3.2 min & at 126.5 C˚ the D was 2.3 min. Calculate Z value?
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Z-value: = 126.5 – 121.5 / 0.505 – 0.361 = 5/0.144 = 34.7
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Ex2: After certain experiments at 121.5 C˚ the D was 6.3 min at 126.5 C˚ the D was 1.5 min Write your comment
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Z = 126.5 -121.5 / 0.799 – 0.176 = 5/0.623 = 8
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Parenteral Preparation Definition: Are sterile preparations intended for administration by injection, infusion or implementation into human or animal body. Special Requirement of P.P. :
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Classification of P.P. IV … IM … S.C Site of injection, Onset response, Injection volume, vehicle used, Duration
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Disadvant.AdvantagesInjection volume Onset response Site of injection -Need proff. -High SE. -Direct to sys -Avoid 1ts pass metab. -Bioavialab. ↑↑↑Vein IV -Painful e some drugs. - Need local anesthetics -Less SE comparing e IV. ↑↑ -Arm. -Thigh -Buttocks IM - Easy to do. - Can inject at home. -Less painful ↑Subcutaneous tissues SC ( for Insulin)
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Quality Control of Parenteral 1- Volume in Container. 2- Sterility testing. 3- Pyrogen testing: Pyrogenic substances are lipid polysaccharide products of the metabolism of m.o. Pyrogen destroy at 175 C ̊̊ for 3 hr, less effective method (2) filtration (3) chemical oxidation or combination of these.
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Practical: 1- 10 ml /kg of tested solution (at 37 C) is injected in the ear vein of 3 healthy rabbits ( temp. not exceeding 39.8 C ). 2- Rectal temp. is recorded at 1,2 and 3 hr. Solution is apyrogenic if : - no rabbit shows an individual rise in temp. of 0.6 and - sum of rise in 3 rabbit not exceeding 1.4 C If 2nd limit pass go to doubling so doubling… If temp. rise exceeds these limits, the test is repeated using 5 rabbits, the sample is accepted if: - no individual rise exceed 0.6 C and - sum of rise in the 8 rabbits does not exceed 3.7 C
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After 1st exam. Ophthalmic paper. Power point
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