Skip to main content

Relative Response Factor (RRF) and its Calculation in HPLC Analysis

Relative Response Factor (RRF) and its Calculation in HPLC Analysis
Know about the relative response factor and its calculation in system suitability parameters in HPLC analysis of pharmaceutical substances and pharmaceutical products.

During the manufacturing process of active pharmaceutical ingredients, some unwanted substances are produced those are known as impurities. 
Some impurities are raised due to the degradation of the actual drug.

Impurities in pharmaceutical drug substances and drug products are required to be analyzed for the quantity of the impurities. To determine the actual quantity of the impurity it is required to have impurity standard. In the absence of the impurity standard relative response factor (RRF) may be used to calculate the actual quantity of the impurity.

Q3B R2 of ICH Guidelines also says that if the response factor is determined correctly, it can be used to measure the actual amount of impurity. Identification threshold, quantification threshold and reporting threshold are given by ICH and it is important to determine the impurities within these thresholds.

Relative Response Factor (full form of RRF) is an alternate method for the determination of the quantity of the impurities present in pharmaceutical products and amount of the impurity can be calculated with the help of peak area of the components.

Relative response factor is the ratio of the response of the impurity and the active pharmaceutical ingredient (API) under the identical chromatographic conditions (chromatographic column, temperature, mobile phase, flow rate etc).

Relative response factor is determined by analyzing the impurity standard and API standard of equal concentration. The following formula is used to determine the response factor:

Response Factor (RF) =             Peak Area            
                                           Concentration in mg/ml


Relative Response Factor (RRF) = Response Factor of impurity
                                                         Response Factor of API


RF in chromatography for different products are different and should be determined for individual substance. Relative response factor determined on a particular detector cannot be used in the calculation of product determined on another detector because different detectors show the difference in the response of the same compound.

Solutions of at least three different concentrations of standard and impurity are prepared and injected in HPLC. The slop of area and concentration of impurity and standard are calculated to determine the relative response factor.
Also see: Theoretical Plates and their Determination in HPLC Analysis

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...