Skip to main content

Role of RH and Temperature in Dry Powder Injection Manufacturing

Role of RH and Temperature in Dry Powder Injection Manufacturing

Relative humidity and temperature plays a significant role in pharmaceutical manufacturing and it is a critical parameter in dry powder injection manufacturing.

role of rh and temperature in dry powder
RH

Moisture remains to be a great risk to the pharmaceutical industry. Moisture is known to cause deterioration of hygroscopic substances, it activates reactions between containers and the pharmaceutical substances contained in them and it is also known to cause solidification of dry powder injection.

Drugs are chemicals and they chemically change when subjected to unfavorable conditions. Due to this, pharmaceutical products should be kept in environments with the right temperatures ranges that will not alter their quality or functionality. But why should RH and temperature be controlled in dry powder injection manufacturing? Find out below the role of RH and temperature in dry powder injection manufacturing. 

Moisture in Powder Causes Poor Grinding 

In the manufacturing processes, pharmaceutical substances that absorb moisture from the environment are hard to grind. The substance will, therefore, cling to the grinding machine there leading to defying of pneumatic transfer.

This means the end powder that is going to be produced will not dissolve well when the time to inject it into the patient. Powder injections that do not dissolve perfectly normally have a low bioavailability in the body of the patients and their pharmacokinetics attributes are always poor. 

Prevents Low-Quality Powder Injection Production

The presence of moisture in the substance impairs the reactions that are involved in the competent manufacturing of the powder. When the manufacturing processes are compromised, the end quality of the powder will be generally low. Low-quality powder has a short shelf-life and it might end up expiring before the estimated expiry date reaches.

Besides the short shelf-life, the product might also cause adverse reactions to the patients and it might be ineffective in performing the purported role. Control of humidity is therefore important to the pharmaceutical companies so as to facilitate the production of high-quality powder.

The Role of RH and temperature in dry powder injection manufacturing is therefore to facilitate the production of high-quality powder that will not only work excellently but that will also last long without reducing quality.

Every pharmaceutical company should be in a position to install an automatic humidity and temperature control systems so that the manufacturing machines will always be producing the high-quality product.

Most of the humidity range required is between 30 to 45% RH depending on the drug powder that is being manufactured. There are standard requirements for every powder injection manufacturing so it is good to check before starting the process. Most pharmaceutical companies are located in the wet and cold regions where it is always required to have humidity control systems.

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...

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...