HiEncap™ Mueller Hinton Broth

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EC391D
To determine the susceptibility of bacteria to Sulphonamides by the tube dilution method.


Intended Use

Recommended to determine the susceptibility of bacteria to Sulphonamides by the tube dilution method.

Composition

Ingredients Gms / Litre
HM infusion B from# 300.000
Acicaserm $ 17.500
Starch 1.500
Final pH (at 25°C) 7.3±0.1

**Formula adjusted, standardized to suit performance parameters

# Equivalent to Beef infusion from

$ Equivalent to Casein acid hydrolysate

Directions

Each capsule contains 10.5 gms of medium. Suspend 1 capsule in 500 ml (2 capsules in 1000 ml) distilled or purified water. Heat to boiling to dissolve the medium completely. Dispense into tubes or flasks as desired. Sterilize by autoclaving at 15 lbs pressure (121°C) for 15 minutes.

Principle And Interpretation

The Mueller Hinton formulation was originally developed as a simple, transparent agar medium for the cultivation of pathogenic Neisseria species (3). Other media were subsequently developed that replaced the use of Mueller Hinton Agar for the cultivation of pathogenic Neisseria species, but it became widely used in the determination of sulfonamide resistance of gonococci and other organisms. Mueller Hinton Broth is recommended for dilution antimicrobial susceptibility testing of all species of most commonly encountered aerobic and facultatively anaerobic bacteria (4,5).

HM infusion B from and Acicase™ provide nitrogenous compounds, carbon, sulphur and other essential nutrients. Starch acts as a protective colloid against toxic substances present in the medium. Starch hydrolysis yields dextrose, which serves as a source of energy. These ingredients are selected for low thymine and thymidine content as determined by MIC values for Enterococcus faecalis with sulfamethoxazoletrimethoprim (SXT). Calcium and magnesium ion concentrations are adjusted to provide the amounts recommended by CLSI to give the correct MIC values with aminoglycosides and Pseudomonas aeruginosa (5).

Type of specimen

Clinical isolates

Specimen Collection and Handling

For clinical samples follow appropriate techniques for handling specimens as per established guidelines (1,2). After use, contaminated materials must be sterilized by autoclaving before discarding.

Warning and Precautions :

In Vitro diagnostic Use only. Read the label before opening the container. Wear protective gloves/protective clothing/eye protection/face protection. Follow good microbiological lab practices while handling specimens and culture. Standard precautions as per established guidelines should be followed while handling clinical specimens. Safety guidelines may be referred in individual safety data sheets.

Limitations :

  • Cation adjusted broth is recommended for antibiotic susceptibility of certain antibiotics.

Performance and Evaluation

Performance of the medium is expected when used as per the direction on the label within the expiry period when stored at recommended temperature.

Quality Control

Appearance
Gelatin capsule containing cream to yellow coloured granular media

Colour and Clarity of prepared medium

Light amber coloured clear solution in tubes

Quantity

Each capsule contains 10.5 gms of medium sufficient for 500 ml media

Reaction

Reaction of 2.1% w/v aqueous solution at 25°C. pH : 7.3±0.1

pH

7.20-7.40

Cultural Response

Cultural characteristics observed after an incubation at 35-37°C for 18-24 hours.

Organism Inoculum
(CFU)
Growth
Escherichia coli ATCC 25922 (00013*) 50-100 good-luxuriant
Haemophilus influenzae ATCC 49247 50-100 good-luxuriant
(in Mueller Hinton Chocolate Broth)
Neisseria gonorrhoeae ATCC 49226 50-100 good-luxuriant
Pseudomonas aeruginosa ATCC 27853 (00025*) 50-100 good-luxuriant
Staphylococcus aureus subsp. aureus ATCC 25923 (00034*) 50-100 good-luxuriant
Enterococcus faecalis ATCC 19433 (00009*) 50-100 good-luxuriant
Streptococcus pneumoniae ATCC 6305 50-100 good-luxuriant
(in Mueller Hinton Blood Broth)

Key: *Corresponding WDCM numbers.

Storage and Shelf Life

Store between 10-30°C in a tightly closed container and the prepared medium at 15-25°C. Use before expiry date on the label. On opening, product should be properly stored dry, after tightly capping the bottle in order to prevent lump formation due to the hygroscopic nature of the product. Improper storage of the product may lead to lump formation. Store in dry ventilated area protected from extremes of temperature and sources of ignition. Seal the container tightly after use. Product performance is best if used within stated expiry period.

Disposal

User must ensure safe disposal by autoclaving and/or incineration of used or unusable preparations of this product. Follow established laboratory procedures in disposing of infectious materials and material that comes into contact with clinical sample must be decontaminated and disposed of in accordance with current laboratory techniques (1,2).

More Information
Product Name HiEncap™ Mueller Hinton Broth
SKU EC391D
Application/ Industry Clinical
Product Type HiEncap™
Physical Form Granulated Media in Gelatin Capsule
Origin Animal
Packaging type HDPE Jar
References 1. Murray P. R., Baron J. H., Pfaller M. A., Jorgensen J. H. and Yolken R. H., (Ed.), 2003, Manual of Clinical Microbiology, 8th Ed., American Society for Microbiology, Washington, D.C. ,,
2.Mueller J. H. and Hinton J., 1941, Proc. Soc. Exp. Biol. Med., 48:330.
3.National Committee for Clinical Laboratory Standards, 2000, Approved Standard: M7-A
5.Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria that grow aerobically, 5th Ed., NCCLS, Wayne, Pa.
Customized Product Available No
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