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PHARMACEUTICAL WATER
The quality attributes of water for a particular application are dictated by the requirement of its usage. Sequential processing steps that are used water for different pharmaceuticals are shown in the figure below
Preparation of Media
Use purified water for preparation of media. Weigh accurately quantity as mentioned in table, after weighing the required amount take it slowly from the pan without spilling the dehydrated media and transfer it into a clean container wash weighing vessel if required. Add a small volume of purified water and swirl to dissolve completely. Make up the required volume by adding purified water from the side walls of the container. Boil the media if required to dissolve completely using, a hot plate/water bath. Allow the media to cool to about 250C and check the pH with the help of a pH meter, the pH meter should lie within the range specified on individual container on dehydrated media adjust if required with 0.1 N HC1/0.1N NaOH. Dispense the media as per the requirement sterilize by loading the media bottles/ flasks in the autoclave as per the validated load cycle diagram by autoclaving at 1210C at 15 lbs pressure for 15 mins. Label the media container/flask/bottle/test tube as follows : Media Name : Batch No. : Sterilized Load No. : Use Before Date :
1. 2.
1.1 W.F.I (Water for injection) 2.1 CSSP (Clean Steam Purified Water)
C. Sterility Testing:
The sterility test is used to detect the presence of viable forms of bacteria, fungi and yeast in or on pharmaceutical preparation. 1. Membrane Filtration Technique 2. Direct Inoculation Technique
1.
Plate Method
1 ml of the final dilution onto each of two sterile Petri dishes. Promptly add to each dish 15 to 20 ml of Soyabean Casein Digest Agar medium that previously has been melted and cooled to approximately 45C, & solidify at room temp invert the Petri dishes and incubate for 48hr to 72 hours. Following incubation, examine the plates for growth, count the no. of colonies.
2. Membrane Filtration
Use membrane filters 50mm in diameter and having a normal pore size of not greater than 0.45 um the effectiveness of which in retaining bacteria . Sterilize and assemble the filtration apparatus. Transfer 10m1 to membrane filter and filter immediately.
Primary Test
Prepared Mac Conkey broth & distribute it in 100 ml test tube. Transfer 1 ml of the pre enriched medium into the sterile Mac Conkey broth and incubate it at 42 2C for 48 hours. If any growth occurs, carry out for further identification of E.coli. Streak the growth over Mac Conkey agar, EMB & incubate it for 24hrs at 36 2C.
Confirmative Test
Reagent :
Kovacs reagent.
Method : To 5 ml of 24 hr old peptone culture, add 0.5 ml of Kovacs reagent shake gently and incubated at 43.5 deg .And stand for 1min if red colour ring is observed then indole is +nt, which confirm E.coli presence.
Indole Test
Environmental Monitoring
MICROBIOLOGICAL ENVIRONMENTAL MONITORING:
Environmental monitoring carried out in non-sterile drug product and drug substance manufacturing areas
Procedure
1) Media of EM : Preincubated plates of Soyabean Casein Digest agar medium can be used. 2)Frequency for EM : Environment monitoring shall be performed IN CLASS 100 DAILY IN 10000 TWICE A WEEK IN 100000 OCNE IN A WEEK. 3)Sampling area, sapling locations and EM schedule: Adjacent to doors At low level return air grilles Between HEPA's in clean rooms an corners of rooms.
Incubation of plates :
Environmental monitoring operator shall ensure that all plates are incubated with in 4 hours from the time plate exposure completed. Incubate the plates in an inverted position at 20-350C for 72 hours. Further incubate the same plates in an inverted position at 30-350C for another 48 hours.
Observation:
Observe the plates for bacterial and fungal count and note down the observations in environmental monitoring record. The total no. of colony forming unit (CFU) shall be calculated as a sum of bacterial (CFU) and fungal (CFU).
1.Exotoxin
Exotoxins are water-soluble, heat-labile and high molecular weight proteins. Exotoxin may travel from the site of infection to other body tissues or target cells in which they exert their effects. Exotoxins usually are : Synthesized by specific bacteria (mainly Gram ve) Heat labile proteins inactivated at 60-800C Associated with specific diseases and have specific mechanism of action. Highly immunogenic and stimulate the production of neutralizing antibodies called antitoxins. Unable to produce a fever in the host directly.
2.Endotoxin
Endotoxin is the structural element of bacteria, called Lipopolysaccharide (LPS). Lipopolysaccharide is contained in the outer membrane of most bacterial cell walls, but the greatest amount found in Gram-ve bacteria.
Under certain conditions, this Lipopolysaccharide is toxic to specific hosts. This LPS is called an endotoxin because it is bound to the bacterium and released when the microorganism lyses.
The toxic component of LPS is the lipid protein, called Lipid A The lipid component exhibits all the properties associated with endotoxicity.Bacterial endotoxins are :
Heat stable. Toxic only a high doses (milligram per kilogram amount). Weakly immunogenic. Usually capable of producing general systemic effects: fever (are pyrogenic), shock, blood coagulation, weakness, diarrhea, inflammation, intestinal hemorrhage and fibrinolysis Bacterial endotoxin has a number of physiological effects following intravenous injections including the following; activation of cytokine system; endithelial cell damage; permeability of vascular leading to a drop in blood pressure; and intravascular coagulation. Incases where the body is subjected to massive doses, such as in the case of gram negative bacterial infection; endotoxin release may cause ultimately death from septic shock.
LAL TESTING
The limulus Amoebocyte Lysate (LAL) test is used for detection and quantification of gram-negative endotoxin using limulus amoebocyte lysate A Multi enzyme Complex, is derived from cytoplasm of circulating Amoebocyte cells (WBCs) of Horse Shoe Crab (Limulus polyphemus). Limulus Amoebocyte Lysate --Large North American Horse Shoe Crab. WBC in the blood of crab. A lysed preparation of cells.
--
Endotoxin
PROENZYME COAGULASE
Ca++
COAGULOGEN COAGULIN
MATERIAL USED:
REAGENT REQUIRED FOR LAL TEST Limulus Amoebocyte Lysate (sensitivity 0.125 EU/ ml). Endotoxin standard (LPS from E. coil 0113 of 100 EU). LAL reagent Water (LRW). Sample of product to be tested.
PREPARATION OF LAL
Reconstitute the lyophilized lysate by adding 1.9 ml LAL reagent water. Swirl gently but thoroughly for at least 30 sec. Do not shake as the content give rise to foam formation.
PREPARATION OF CSE
Reconstitute endotoxin by adding 5 ml. LRW. Vortex the vial of endotoxin for at least 15 seconds. Dilute the endotoxin with LRW to a concentration of 1 EU/ml. Using the 1 EU/ml. endotoxin solution prepare a serial to fold dilution series that brackets the end point of lysate.
Procedure
Take 100 l of each dilution as prepared above in 10 x 75 mm sterilized test tubes & in each test tube add 100 l of Lysate. Stir each test tube on vortex mixture for a second. Then incubate all the test tubes in a dry heat incubator block at 37+100C for 60+2
OBSERVATION
After incubation and end point determination (manually), the sensitivity of the LAL reagent will be confirmed if the test results are positive to with in one two fold dilution of the stated labeled potency. If a gel clot is formed in one of the 0.06 dilution tube, it means that given lysate is over sensitive than the labeled potency. Now, the actual lysate sensitivity is determined as follows :
RESULTS
Each tube in gel clot method is interpreted as either positive or negative. A positive test is defined as the formation of a film gel . A negative test is characterized by the absence of gel .
PRECAUTIONS
All the glassware should be thoroughly cleaned and depyrogenated. Reaction temperature should not exceed 36-38C. pH of the reaction mixture must be in the range of pH 5-7. cis Reaction time should be no longer than one hour. Each test must be accompanied by positive and negative controls Strict aseptic condition must be used.
INTRODUCTION
The sterility test is used to detect the presence of viable forms of bacteria, fungi and yeast in or on pharmaceutical preparation. The working conditions in which the tests are performed should be free from any microbial form & should be monitored regularly by sampling the air & surfaces The tests must be carried out under conditions designed to avoid accidental contamination of
the product during the test. A batch is defined, as a collection of sealed containers that are same in the nature i.e. the risk of the contamination is same for each of the unit in it.
PRINCIPLE
The test is based upon the principle that if bacteria & fungi are placed in the medium, which provides nutritive material & water the organisms will grow and their presence can be indicated by turbidity in the originally clear medium.
CULTURE MEDIA
The following culture media are found to be suitable for the test of sterility: Fluid Thioglycollate Medium (FTGM)
After dissolving media in distilled water, distribute it into suitable vessels. Sterilize by autoclaving for 18-20 minutes at 1210C. Cool promptly to 250C C & store at 20-30 0C.
Procedure
METHODS
Membrane Filtration Technique Direct Inoculation Technique
Filtration
Filterate aseptically then remove the membrane from the holder, cut the membrane in half with the help of tong & scissors, immerse one half of the membrane in 100ml of soybean casein digest medium (SCDM) & incubate at 20-25Cfor not less than 14 days. Similarly other half of the membrane in 100ml of Fluid Thioglycollate medium (FTGM) & incubate at 30-35 C for not less than 14 days. Aseptically transfer the specified volume of the material from each container to a vessel of culture medium
Mix the liquid with the medium & Incubate in the specified media for not less than 14 days. And check the turbidity for the presence & absence of microbial growth . Application For bacterial detection For Fungal Detection Fluid Thioglycollate Medium Soyabean Casein Digest Medium
Incubation Temp. Incubation Period Positive Control 30 350C 14 days 1. Staphylococcus aureus 2. Pseudomonas aeruginosa 20 250C 14 Days 1. Bacillus subtitles 2. C.albicans
Result: The positive LALgel clot is characterized by the formation of a solid gel , which remains intact in the bottom of the tube upon incursion. From this study it was concluded that:
CFU and Endotoxin level of raw, finished product and water sample respectively tested from different poilll nr sources. No microorganism recovered from the raw, finished Product. No microorganism recovered from any of the water Sample and Products. .
Sterility Test : Result: The above sample complies the sterility test. Environmental monitoring :Result : for class 1, 00, 000 should not exceed more than 10cfu \plate.The alert limit should not
exceed more than 50 cfu/plate.. action limit of plate exposure for class 10,000 should not exceed more than 50 cfu per plate & the alert limit for the same class should not exceed more than 25 cfu per plate. The action limit for the class 100 should not be more than 01 cfu per plate.