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With drug delivery devices growing, it’s important to keep the factors surrounding filtration media in mind.
Released By Porex Corporation (Filtration Group)
July 20, 2022
By Sean Fenske, Editor-in-Chief Drug delivery technologies are growing in use across many segments of healthcare. They also bridge the gap between technology sectors—medical device to pharmaceuticals to biologics. These combination devices work due to a convergence of two of the aforementioned components, but a number of other technologies must be implemented to achieve a successful product. One of the most critical parts within a drug delivery device is the filtration media. As a rarely seen component in a finished device, it is not always considered as early in the development process as it should. Design engineers developing a drug delivery product, however, would be remiss if they didn’t invite their supply partner into the discussion early so as to optimize this component’s inclusion. With this in mind, Nadia Hajjar, category manager for life sciences at Porex, responded to a number of questions around the filtration media for drug delivery devices. She addresses the growth in this segment, what is accomplished by working with the supplier early, and the role filtration plays in the product. Sean Fenske: Where are you seeing growth in the drug delivery device sector? What is fueling this? Nadia Hajjar: One of the key areas where we are seeing growth in drug delivery devices is in the area of pharmaco-genomics—specifically in identifying biomarkers that can influence the development of drug treatments. Porous polymers play a key role in each of the main stages of this drug development process, including the research, extraction/purification, therapy development, processing, and final device design stage for drug delivery. The initiation of open-sourced CRISPR technology has fueled an explosion of biological therapies that are able to treat diseases formerly untreatable with synthetic medications, including certain types of cancer, Alzheimer’s, and MS. The use of whole blood versus synthetic drugs is a byproduct of this space, with treatments derived from tissue and DNA. The advent of more treatment therapies using whole blood, opens up a need for innovative materials that can separate, filter, wick and diffuse. A second key growth area within drug delivery is neurology. Traditionally we characterize medicine as a liquid going through our body, but by focusing on the brain, more innovative therapies have utilized frequency to target the nervous system and thereby treat conditions such as ADHD, migraines, and mental health disorders. These new treatment devices can require sensors, vents, and light filters to function. The third and final growth area is the increase in point-of-care devices being used for at-home diagnosis and treatment. There has been a steep growth in at-home care post-Covid, and an increased need for materials that can act as a vehicle for whole blood cell separation, pre-whole blood filtration, refined dosing, and increased dose accuracy. Fenske: When it comes to drug delivery devices, what role can filtration play? Hajjar: One of the key benefits of custom-engineered porous polymer components is that the role of filtration can be modified and adapted to take on additional responsibilities within the drug delivery device. The porous filtration media can impact device sterility, flow of both air and drug, shelf life, clogging, and metered dosing; it can even build a barrier for oil and water in or around the device. One porous component can also act as a vent or diffuser within the device in addition to filtration. Fenske: Are there an array of material options for porous filtration media in a drug delivery application or are they limited? What are they? Hajjar: There is a broad array of materials and additive options available for porous filtration media in drug delivery devices, including sintered porous plastics, porous fibers, and several types of porous membranes. Depending on the need, clean materials are available that are medically safe and will pass all FDA/regulatory device requirements. Based on the specifications of the specific device, our material science experts will work with you to decide what materials make the most sense to leverage, and we will work together to test on your device. Fenske: What are the most important factors designers need to consider in selecting the filtration material? Hajjar: When we work with a customer on designing their filtration media, we typically ask questions about the following areas:
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