Skip to main content

Pyrogen Test and Its Determination Using Rabbits

Pyrogen Test and Its Determination Using Rabbits

Learn how to determine the pyrogen in parenteral preparations by injecting the sample in rabbits for pyrogen testing.

Introduction:

Pyrogen test is performed to check the presence or absence of pyrogens in all aqueous parenterals. Rabbits are used to perform the test because their body temperature increases when pyrogen is introduced by the parenteral route.

For this test, three healthy rabbits are selected each weighing at least 1.5 kg. No rabbit should be selected if:

  1. It has a normal temperature greater than 49.8°C.
  2. It was used in a positive test during last two weeks or negative test during last two days.
Method for Pyrogen Test:

The pyrogen testing is performed in an air-conditioned room. The food and water is withheld to rabbit overnight. A clinical thermometer is inserted in the rectum of each rabbit to a depth of not less than 7.5 cm. Two readings of the temperature of rabbit in normal conditions should be taken at the interval of half an hour before start the test and mean of the both should be calculated to determine the initial temperature.

The equipment, injectors and needles used in the test should be pyrogen-free. These should be washed with water for injection and then heated at  260°C for two hours. The injection is warmed to 38°C before injecting to the rabbits. 0.5 to 1.0 ml per kg dose should be injected through the ear vein. Six reading of temperature is recorded at an interval of half an hour.

Pyrogen Test Results:

The response of each rabbit is detected by the difference of initial temperature and the highest temperature recorded. The response of all three rabbits gives the sum of responses and can be concluded as:

  • If the sum of responses does not greater than 1.4°C and any of rabbit shows the response less than 0.6° C, the product passes the test.
  • I sum of responses is greater than 1.4 °C or any of rabbit shows the response 0.6 or greater, continue the test using 5 rabbits.
  • If the test is done using 5 rabbits, then if the sum of responses of all 5 rabbits is greater than 3.7°C and the individual response of not more than three rabbits is greater than 0.6°C, the product passes the test.

Comments

Popular posts from this blog

Checklist for Audit in Sterile Area

Checklist for Audit in Sterile Area Checklist to verify the sterile manufacturing area before the audit. 1. Is there any SOP giving details for activity/ movement in the sterile area. 2. Verify the suitability of system for sanitization of hands. 3. Is there the SOP on entry-exit; gowning and de-gowning into the critical area available? 4. Verify the availability of following records:  Air pressure differential  Particulate monitoring  Temperature  Humidity  Microbiological monitoring by settle plate 5. Are these records available and maintained as per SOPs? 6. Check the above mentioned individual records. Are the entries within specifications mentioned in SOP/ MTPs. 7. Is the controlled copy of MTP pertaining to monitoring by settle plate available to plant person? 8. Are the location for settle plates identified and the chart/ layout available with plant? 9. Are the following areas monitored for parameters mentioned in step 4:  Air-lock to the critical ar...

Aseptic Filling Process (Media Fill) Validation Protocol in Sterile Pharmaceuticals

Aseptic Filling Process (Media Fill) Validation Protocol in Sterile Pharmaceuticals Validation of sterile manufacturing process by media fill validation test as per PICS guidelines for aseptic validation or aseptic process simulation. 1.0 OBJECTIVE 1.1 To define procedures for validating and maintaining the validation of all aseptic filling processes and qualification of the quality of the product by system/facility/equipment. 2.0 SCOPE 2.1 This procedure applies to all aseptically filled sterile products intended for human use. 3.0 RESPONSIBILITY 3.1 The Validation personnel coordinate the aseptic filling validation program and write the sterile media aseptic filling processes reports. 3.2 Manufacturing personnel the sterile media aseptic filling processes and performs the sterile media fills. 3.3 QA personnel perform the sampling and assist with the IPQA monitoring required for each sterile media fill. 3.4 QC personnel to perform the testing and assist with the monitoring required fo...

MSDS (Material Safety Data Sheet)

MSDS   What Is an MSDS? An MSDS (Material Safety Data Sheet) is a document that provides detailed information about a chemical substance, including its hazards, safe handling procedures, storage requirements, and emergency measures. Today, MSDS is more commonly called SDS (Safety Data Sheet) under the Globally Harmonized System (GHS). Why MSDS / SDS Is Important Protect workers and employees Ensure safe handling and storage of chemicals Prevent accidents and injuries Provide emergency response information Comply with workplace safety regulations.  MSDS (Material Safety Data Sheet)  International safety standards.  GHS – Globally Harmonized System Full form: Globally Harmonized System of Classification and Labelling of Chemicals Develop by United Nations (UN).  OSHA (USA) – Hazard Communication Standard (HCS) Factories Act & Chemical Rules (India) Factories Act, 1948 Manufacture, Storage and Import of Hazardous Chemical Rules, 1989 REACH (Europe) REACH Regula...

Steps for HPLC Method Development

Steps for HPLC Method Development Know about the different steps of the HPLC analytical method development in pharmaceutical analysis. Analytical method development is considered as a critical process in pharmaceuticals. Availability of the different types of columns, operating  parameters, mobile phase composition, diluent and pH values make it critical to develop an analytical method. A good analytical method should be  simple, used column, mobile phase and buffer should be common. It can be done easily step by step. Following are the common HPLC method development steps. 1. Selection of HPLC Analytical Method 2. Selection of Chromatographic Conditions 3. Parameter Optimization 1. Selection of HPLC Analytical Method: First of all consult the literature that is available on the product. It will help you to understand the nature of  the product that will help to select the different parameters. A. Sample Preparation: Select method to prepare the sample according to its ...

Blow Fill Seal (BFS) and Form Fill Seal (FFS) Technology in Sterile Manufacturing

Blow Fill Seal (BFS) and Form Fill Seal (FFS) Technology in Sterile Manufacturing Know about sterile pharmaceutical production using Blow Fill Seal (BFS) and Form Fill Seal (FFS) technology. Both of these techniques are used to manufacture  sterile pharmaceutical products   as parenteral (LVP & SVP), infusions, ophthalmic and inhalation products. These are automated techniques to prepare sterile products. The basic concept of the  FFS   and BFS is to reduce the  contamination   by forming the container, filling and sealing in a closed sterile chamber of the machine. There is no personnel intervention to reduce the chances of the contamination during the manufacturing of sterile products. It gives more production at very low operational cost with the high assurance of  sterility . Blow fill seal technology is widely used and accepted by the various pharmaceutical regulatory authorities as US-FDA and MHRA. The system is being used for over 30 years a...