loopfull is removed from each dilution and transferred to capable of killing the test organism in 10 minutes but not GERMICIDAL SUBSTANCES

Similar documents
Gye and Cramer (1919) found that the ionizable salts of calcium injected together with the washed spores of Cl. tetani or of certain

6.0 ANTIBACTERIAL ACTIVITY OF CAROTENOID FROM HALOMONAS SPECIES AGAINST CHOSEN HUMAN BACTERIAL PATHOGENS

The Disinfecting Effect of Electrolyzed Water Produced by GEN-X-3. Laboratory of Diagnostic Medicine, College of Medicine, Soonchunhyang University

SUMMARY OF PRODUCT CHARACTERISTICS. Lincomycin (as Lincomycin hydrochloride) Neomycin (as Neomycin sulphate) Excipients Disodium edetate

Summary of Product Characteristics

Determination of antibiotic sensitivities by the

Controlling Bacterial Growth

DISSEMINATION OF PULLORUM DISEASE IN THE INCUBATOR

METRIGUARD. Technical Bulletin

Klett-Summerson photoelectric colorimeter. The presence of the glucose RESISTANCE AND SYNERGISM IN STREPTOMYCIN

Burn Infection & Laboratory Diagnosis

SENSITIVE AND -RESISTANT TUBERCLE BACILLI IN LIQUID MEDIUM SENSITIVITY TESTS

SUMMARY OF PRODUCT CHARACTERISTICS

EXPERIMENT. Antibiotic Sensitivity-Kirby Bauer Diffusion Test

Australian and New Zealand College of Veterinary Scientists. Fellowship Examination. Veterinary Anaesthesia and Critical Care Paper 1

against Clinical Isolates of Gram-Positive Bacteria

Summary of Product Characteristics

TEAT DIP- POST DIP- PRE DIP- STRIPING

SUMMARY OF PRODUCT CHARACTERISTICS. 1. NAME OF THE VETERINARY MEDICINAL PRODUCT Vetrisulf powder for oral solution for chickens, turkeys and geese

Antibacterial Agents & Conditions. Stijn van der Veen

Quality Control Testing with the Disk Antibiotic Susceptibility Test of Bauer-Kirby-Sherris-Turck

suis. The multiple amino acid media devised by these workers (KBD and MMHRB) contained cystine and methionine as organic sources of sulfur.

SUMMARY OF PRODUCT CHARACTERISTICS

BACTERIOLOGY OF THE HEALTHY CONJUNCTIVA*

averaged 10 ticks each. In addition, a considerable number of ticks

THE STABILITY OF E1VROFLOXA CIN University Undergraduate Research Fellow. A Senior Thesis. Texas ASM University.

ANNEX I SUMMARY OF PRODUCT CHARACTERISTICS 1/18

CORAL ESSENTIALS INFORMATION

USE OF GERMICIDES IN HOME AND HEALTHCARE SETTINGS: IS THERE A RELATIONSHIP BETWEEN GERMICIDE USE AND ANTIMICROBIAL RESISTANCE

Staphylococcus aureus

Test Method Modified Association of Analytical Communities Test Method Modified Germicidal Spray Products as Disinfectants

AviagenBrief. Best Practice Management in the Absence of Antibiotics at the Hatchery. October Aviagen Veterinary Team.

Mastitis and On-Farm Milk Cultures - A Field Study - Part 1

ANNEX I SUMMARY OF PRODUCT CHARACTERISTICS

ANNEX I SUMMARY OF PRODUCT CHARACTERISTICS

Should you have any questions, please contact Edith Chang, Ph.D., Senior Scientific Liaison ( or

Chapter 8 Antimicrobial Activity of Callus Extracts of Justicia adhatoda L. in Comparison with Vasicine

ANNEX I SUMMARY OF PRODUCT CHARACTERISTICS

Summary of Product Characteristics

Media Issued by: LABORATORY MANAGER Original Date: April 11, 2001 Approved by: Laboratory Director Revision Date: February 27, 2004

Fluoroquinolones resistant Gram-positive cocci isolated from University of Calabar Teaching Hospital, Nigeria

Susceptibility Pattern of Some Clinical Bacterial Isolates to Selected Antibiotics and Disinfectants

DO NOT WRITE ON or THROW AWAY THIS PAPER!

UCD VET VIEWS CALIFORNIA CATTLEMEN S MAGAZINE APRIL 2005 COW/CALF BIOSECURITY

Some Antibacterial Agents Used with Koi (oz refers to weight unless otherwise specified)

Introduction to Chemotherapeutic Agents. Munir Gharaibeh MD, PhD, MHPE School of Medicine, The university of Jordan November 2018

Chapter 2. Disk diffusion method

Susceptibility Testing

Effect of Calcium Level of the Developing and Laying Ration on Hatchability of Eggs and on Viability and Growth Rate of Progeny of Young Pullets 1

SURVIVABILITY OF HIGH RISK, MULTIRESISTANT BACTERIA ON COTTON TREATED WITH COMMERCIALLY AVAILABLE ANTIMICROBIAL AGENTS

AMOXICILLIN AND CLAVULANIC ACID TABLETS Draft proposal for The International Pharmacopoeia (February 2018)

UNIVERSITY OF PITTSBURGH Institutional Animal Care and Use Committee

IT HAS been well established that

(From the Department of Bacteriology, Hoagland Laboratory, Brooklyn)

Fluoroquinolones ELISA KIT

TOLYPOMYCIN, A NEW ANTIBIOTIC. V IN VITRO AND IN VIVO ANTIMICROBIAL ACTIVITY. Masahiro Kondo, Tokiko Oishi and Kanji Tsuchiya

No-leaching. No-resistance. No-toxicity. >99.999% Introducing BIOGUARD. Best-in-class dressings for your infection control program

THE ROLE OF WATER IN THE EVOLUTION OF THE TERRESTRIAL VERTEBRATES

SUMMARY OF PRODUCT CHARACTERISTICS. Bottle of powder: Active substance: ceftiofur sodium mg equivalent to ceftiofur...

A solution for current veterinary challenges

Antibacterial susceptibility testing

- { PAGE } - GOVERNMENT OF RAJASTHAN DIRECTORATE MEDICAL, HEALTH F.W. SERVICES RAJASTHAN, JAIPUR

Dosing Your Cat with Azithromycin Pediatric Suspension. By Lorraine Shelton

Shortly after the demonstration of a therapeutic

Gram-positive cocci Staphylococci and Streptococcia

Quad Plate User s Manual

Irish Medicines Board

STUDIES ON HATCHABILITY OF SCHISTOSOMA JAPONICUM EGGS IN SEVERAL EXTERNAL ENVIRONMENTAL CONDITIONS

Molecular Characterization of Staphylococcus aureus of Camel (Camelus dromedarius) Skin Origin

Observations on the Mode of Action of Antibiotic Synergism and Antagonism

2 0 hr. 2 hr. 4 hr. 8 hr. 10 hr. 12 hr.14 hr. 16 hr. 18 hr. 20 hr. 22 hr. 24 hr. (time)

revealed a population of particles apparently of considerable homogeneity with

206 Adopted: 4 April 1984

Rutgers University, New Brunswick, N. J.) All these cultures proved to be highly active against mycobacteria.

International Journal of Advances in Pharmacy and Biotechnology Vol.3, Issue-2, 2017, 1-7 Research Article Open Access.

Milk Quality Evaluation Tools for Dairy Farmers

Ultra-Fast Analysis of Contaminant Residue from Propolis by LC/MS/MS Using SPE

APPLICATION FOR LIVE ANIMAL USE IN TEACHING AT FAULKNER STATE COMMUNITY COLLEGE

BIOLACTAM. Product Description. An innovative in vitro diagnostic for the rapid quantitative determination of ß-lactamase activity

Summary of product characteristics As per Annex C. SUMMARY OF PRODUCT CHARACTERISTICS Doc. No. SPC/71108 Ver.1

I. ITs CONCENTRATION IN BLOOD CELLS AND PLASMA AND RELATION TO THE INCUBATION PERIOD BY J. FURTH, M.D.

Public Assessment Report. Scientific discussion. Xiflodrop 5 mg/ml eye drops, solution. Moxifloxacin hydrochloride DK/H/2221/001/DC

Wheat and Wheat By-Products for Laying Hens

DREXEL UNIVERSITY COLLEGE OF MEDICINE ANIMAL CARE AND USE COMMITTEE POLICY FOR PREOPERATIVE AND POSTOPERATIVE CARE FOR NON-RODENT MAMMALS

PRACTICAL APPLICATION OF ARTIFICIAL INSEMINATION IN CONJUNCTION WITH SYNCHRONIZATION OF HEAT CYCLE IN THE EWE

Public Assessment Report Scientific discussion. Amlodipin Accord (amlodipine besilate)

SZENT ISTVÁN UNIVERSITY. Doctoral School of Veterinary Science

THE POULTRY ENTERPRISE ON KANSAS FARMS

Explanation of Down and Feather Tests (Includes References to International and Country Specific Standards)

LipoClear Testing. Don Newton, MS, MT Brockton Hospital Laboratory, Brockton, Massachusetts

GENTAMICIN: ACTIVITY IN VITRO AGAINST GRAMNEGATIVE ORGANISMS AND CLINICAL EXPERIENCES IN THE TREATMENT OF URINARY TRACT INFECTIONS

Microscopy Directions

Isolation of antibiotic producing Actinomycetes from soil of Kathmandu valley and assessment of their antimicrobial activities

NAFCILLIN AND OXACILLIN COMPARATIVE ANTISTAPHYLOCOCCAL ACTIVITY IN MICE. J. A. YURCHENCO, M. W. HOPPER, T. D. VINCE and G. H.

by adding different antibiotics to sera containing

Evaluation of a computerized antimicrobial susceptibility system with bacteria isolated from animals

,omb White Leghorn Layers in Three Types of Houses in Oregon

Using SCC to Evaluate Subclinical Mastitis Cows

Summary of Product Characteristics

VLLM0421c Medical Microbiology I, practical sessions. Protocol to topic J05

Transcription:

A NEW METHOD FOR THE EVALUATION OF GERMICIDAL SUBSTANCES A. J. SALLE, W. A. McOMIE AND I. L. SHECHMEISTER Department of Bacteriology, University of California, Berkeley, California Received for publication March 27, 1937 The usual procedure in testing the germicidal strength of a compound is to note its effect on one or more species of bacteria and to compare the results with those obtained from phenol. A value known as the phenol coefficient may be calculated from the results of such a test. The phenol coefficient is defined as the killing power of a germicide, towards a specified organism, as compared to that of phenol. If the organism, Eberthella typhosa (B. typhosus) is used as the test organism the result will be an Eberthella-typhosa phenol coefficient, etc. The phenol coefficients will vary, naturally, with the test organism employed. Several methods are used to determine the phenol coefficient. That proposed by Reddish (1928), and recommended by the American Public Health Association, was followed by us in every case. Briefly, the phenol coefficient is determined by inoculating various dilutions of the germicide in sterile distilled water with the test organism. After an interval of five minutes a standardized loopfull is removed from each dilution and transferred to broth. This is repeated after ten minutes and again after fifteen minutes. The tubes are examined for turbidity after 48 hours. The same procedure is followed for phenol. The phenol coefficient is determined by dividing the greatest dilution of disinfectant capable of killing the test organism in 10 minutes but not in five minutes by the phenol dilution found to effect this result. 1 A 4 mm. loop, outside diameter. 267

268 A. J. SALLE, W. A. McOMIE AND I. L. SHECHMEISTER Various factors must be controlled in order that the results shall be of value. These include: species of organism, viability of the organism, temperature of incubation, proportion of culture to disinfectant, size of the inoculation loop, and composition of the culture medium. It is customary to rate disinfectants on the basis of their phenol coefficients. The method may be justifiable if the germicides are to be employed on external skin surfaces or in connection with the sterilization of non-living material. On the other hand, if disinfectants are internally administered or used on mucous surfaces, the above method presents serious objections. A germicide possessing a high phenol coefficient is usually preferred to one less potent. There would be no advantage in using a compound with a coefficient of 10 on mucous surfaces if it possessed ten times the toxicity of phenol. Phenol could be employed to equal advantage, with probably a considerable saving in the cost of the disinfectant. It is believed that a more accurate method of rating those germicides, recommended for internal administration or for use on mucous membranes, would be to test them for their effect on the growth of living embryonic tissue as well as for their ability to kill bacteria. A number, known as the toxicity index is determined by dividing the highest dilution required to prevent the growth of embryonic chick heart tissue during 48 hours by the highest dilution required to kill the test organism after an exposure of 10 minutes. For the preparation of tissue cultures it is necessary to have: (1) Plasma, (2) Tyrode solution, (3) tissue fragments and, (4) diluted embryonic fluid. 1. Plasma. Guinea-pig plasma is satisfactory and easily obtained. Ten cubic centimeters of blood are mixed with 1.0 cc. of a 1:1000 heparin solution. This prevents rapid coagulation of the plasma. The blood is centrifuged, the plasma removed and refrigerated until used. 2. Tyrode solution. This is a physiological salt solution containing 0.1 per cent glucose. It is used probably more than any other physiological salt solution for tissue culture work.

EVALUATION OF GERMICIDAL SUBSTANCES 269 3. Tissue fragments. Chick hearts removed from 9-day-old embryos are used in pieces from 0.5 to 1.0 mm. in diameter. The size should be as uniform as possible, never larger than 1.0 mm. in diameter. 4. Dilute embryonic fluid. This is prepared by mincing chick embryos in a tissue grinder and diluting with 5 parts of Tyrode solution. The suspension is then centrifuged and the clear supernatant fluid removed. The embryonic fluid serves as food for the tissues. The various dilutions of the germicide under examination are made in the embryonic fluid. The tissue cultures are prepared as follows: The fragments are embedded in guinea-pig plasma diluted with three parts of Tyrode solution in Carrel flasks. The plasma coagulates shortly after the addition of the tissue. The fibrin matrix holds the fragments. The coagulated plasma is then covered with a layer of embryonic fluid containing a known concentration of the germicide. The flasks are capped to prevent evaporation and incubated at 380C. The plasma, Tyrode solution and embryonic extract are carefully measured so that the final concentration of germicide in each flask is known. The flasks are examined for tissue growth after an incubation period of 48 hours.2 The highest dilution of the germicide showing no growth of the tissue is taken for the calculation of the toxicity index. The following example will show the method for determining the index. The highest dilution of disinfectant preventing growth of tissue in 48 hours is 1: 5000. The highest dilution of the chemical showing no growth of the test organism, Staphylococcus aureus, after 10 minutes' exposure,' is 1:2500. The toxicity index is calculated by dividing 5000 by 2500. The result, 2.0, means that the germicide is twice as toxic for the tissues 2 A period of 24 to 48 hours is required in order to determine if the tissue fragments show proliferation. 3 The exposure time of the organisms to germicide was limited to 10 minutes because it is not believed that a chemical in contact with a mucous membrane or the cut surfaces of an incision will remain effective for a longer period of time.

270 A. J. SALLE, W. A. MoOMIE AND I. L. SHECHMEISTER as for the bacteria. If the toxicity index was 0.5 it would mean that the disinfectant was twice as toxic for the bacteria as for the tissue. Theoretically, the smaller the toxicity index the more nearly perfect the germicide. An index greater than one indicates that the germicide is more toxic to the tissue than to the bacteria. An index less than one indicates that the germicide is more toxic to the bacteria than to the tissue. In previous communications (Salle and Lazarus, 1935, a-h) comparisons were made of the resistance of Staphylococcus aureus and embryonic chick heart tissue to the following germicides: 1. Phenol (carbolic acid, C6H5OH) 2. Iodine (12) 3. Iodine trichloride (I Cls) 4. Merthiolate (sodium ethyl-mercuri thiosalicylate, C2H5. Hg.S. C6H4 *COONa, manufactured by Eli Lilly and Company) 5. Metaphen (the anhydride of 4,nitro-5-hydroxy-mercuri-ortho cresol, C2H2. CH3ONO2.Hg, manufactured by Dermatological Research Laboratories) 6. Hexylresorcinol (Normal hexylresorcinol, C6H3(OH)2C6H13, manufactured by Sharp and Dohme). 7. Mercurochrome (The disodium salt of 2:7 dibromo-4-hydroxymercuri-fluorescein, NaOOC * C6H4C: C6H2Br: OC6HBr(ONa) l I HgOH * 3H20, manufactured by Hynson, Westcott and Dunning) 8. Potassium mercuric iodide (K2HgI4) 9. Mercuric chloride (HgCl2) The Staphylococcus aureus phenol coefficients and their corresponding toxicity indices are recorded in table 1. When E. typhosa was substituted for S. aureus as the test organism a different set of figures was obtained. The germicides fall in a different order on the basis of their toxicity indices. The results are recorded in table 2. The results show that the simple inorganic compounds rate considerably better than some of the newer organic preparations. In both series iodine gave the lowest toxicity index while mercurochrome proved to be the most toxic.

EVALUATION OF GERMICIDAL SUBSTANCES 271 TABLE 1 Toxicity of germicides to chick heart tissue and Staphylococcus aureus GERMICID DILUTION SHOWING NO TOXICITY COCCUS ESHOWING GROWTH OF INDEX =/ ARU NO TIRSUE STAPHYLO- A/B PHENOL GROWTH = A COCCUS COEFFICIENT AUREUS = B Iodine... 1:1,800 1:20,000 0.09 308 Iodine trichloride... 1:2,400 1:6,000 0.40 92 Mercuric chloride... 1:45,000 1:16,000 2.8 246 Hexylresorcinol... 1:21,000 1:7,000 3.0 108 Metaphen... 1:76,000 1:6,000 12.7 92 Phenol... 1:840 1:65 12.9 Potassium mercuric iodide... 1:12,000 1:900 13.3 13.8 Merthiolate... 1:176,400 1:5,000 35.3 70 Mercurochrome... 1:10,500 1:40 262.0 0.6 TABLE 2 Toxicity of germicides to chick heart tissue and E. typhosa HIGHEST HGET DILUTION HIGHEST TOXICITY E. TYPHOSA GERMICIDE SHODIN SHOWING NO INDEX - PHENOL GETCIESH NONTIS EH. GROWTH TYPHOSA OF A/B COEFFICIENT GROWTH =A - B Iodine... 1:1,800 1:24,000 0.08 240 Potassium mercuric iodide... 1:12,000 1:110,000 0.11 1,100 Mercuric chloride... 1:45,000 1:180,000 0.25 1,800 Iodine trichloride... 1:2,400 1:8,500 0.28 85 Metaphen... 1:76,000 1:90,000 0.84 900 Hexylresorcinol... 1:21,000 1:7,500 2.8 75 Phenol... 1:840 1:100 8.4 Merthiolate... 1:176,000 1:5,000 35 50 Mercurochrome... 1:10,500 1:300 35 3 DISCUSSION HIGHEST HIGHEST DILUTION STAPHYLO- The determination of the phenol coefficient is not an accurate basis for evaluation of disinfectants employed under all conditions. The method is practical for rating disinfectants to be employed for the sterilization of non-living material. On the other hand the method fails to take into account the toxicity of germicides for living tissues when used internally or on mucous surfaces. A more valuable expression would be one based on a

272 A. J. SALLE, W. A. McOMIE AND I. L. SHECHMEISTER combination of the killing power of the disinfectant for bacteria with its toxic action toward living embryonic tissue. This method gives a figure which is known as the toxicity index. The toxicity index is defined as the ratio of the highest dilution of disinfectant required to prevent the growth of embryonic chick heart tissue during 48 hours to the dilution required to kill a given test organism in 10 minutes. The toxicity indices are not always proportional to the phenol coefficients. Iodine trichloride and metaphen have the same phenol coefficient yet metaphen is about 32 times more toxic to embryonic chick heart tissue than the iodine compound (table 1). As a germicide merthiolate is over 100 times more potent than mercurochrome but only about one-eighth as toxic to tissue. An important conclusion is that the older and simpler germicides rate considerably higher than the newer and more complex compounds. Iodine is one of the oldest germicides known. It is usually employed as tincture of iodine, an alcoholic solution, which is quite irritating, due to the presence of the alcohol. Because of this irritating property the alcoholic solution is gradually losing favor. In aqueous solution, however, the iodine is non-irritating and relatively non-toxic to tissue. It is the most ideal of any of the compounds studied when tested by the tissue culture technique. Of the newer organic preparations examined hexylresorcinol gave the lowest toxicity index on Staphylococcus aureus (grampositive), while metaphen gave the lowest figure when tested on Eberthella typhosa (gram-negative). The above germicides are being retested in an attempt to control some of the more obvious variables. Some of these are, (1) temperature, (2) time of action of chemical on bacteria and tissue, and (3) presence of organic matter. REFERENCES REDDISH, G. F. 1928 Article on the Standardization of Disinfectants and Antiseptics, in Newer Knowledge of Bacteriology and Immunology, edited by E. 0. Jordan and I. S. Falk. University of Chicago Press. SALLE, A. J., AND LAZARUS, A. S. 1935a A comparison of the resistance of bacteria and embryonic tissue to germicidal substances. I. Merthiolate. Proc. Soc. Exper. Biol. and Med., 32, 665-667.

EVALUATION OF GERMICIDAL SUBSTANCES 273 SALLE, A. J., AND LAZARUS, A. S. 1935b A comparison of the resistance of bacteria and embryonic tissue to germicidal substances. II. Metaphen. Proc. Soc. Exper. Biol. and Med., 32, 937-938. SALLE, A. J., AND LAZARUS, A. S. 1935c A comparison of the resistance of bacteria and embryonic tissue to germicidal substances. III. Mercurochrome. Proc. Soc. Exper. Biol. and Med., 32, 1057-1060. SALLE, A. J., AND LAZARUS, A. S. 1935d Comparison of resistance of bacteria and embryonic tissue to germicidal substances. IV. Hexylresorcinol. Proc. Soc. Exper. Biol. and Med., 32, 1119-1120. SALLE, A. J., AND LAZARUS, A. S. 1935e Comparison of resistance of bacteria and embryonic tissue to germicidal substances. V. Iodine. Proc. Soc. Exper., Biol. and Med., 32, 1481-1483. SALLE, A. J., AND LAZARUS, A. S. 1935f Resistance of bacteria and embryonic tissue to germicidal substances. VI. Iodine trichloride. Proc. Soc. Exper. Biol. and Med., 33, 8-9. SALLE, A. J., AND LAZARUS, A. S. 1935g A comparison of resistance of bacteria and embryonic tissue to germicidal substances. VII. Potassium mercuric iodide. Proc. Soc. Exper. Biol. and Med., 33, 393-395. SALLE, A. J., AND LAZARUS, A. S. 1935h Comparison of resistance of bacteria and embryonic tissue to germicidal substances. VIII. Mercuric chloride. Proc. Soc. Exper. Biol. and Med., 37, 371-374. Downloaded from http://jb.asm.org/ on March 17, 2019 by guest