End-to-end biopharma processing

Fluid management and freeze thaw solutions for biosimilar production

The growing demand for biosimilars and significant increases in the biosimilar market call for innovative solutions for their fluid management and freeze thaw processes. This relates to steps like filling and filtration, freezing and thawing, as well as cooling, storage and transport of biosimilars. While it is of utmost importance to produce high-quality products, manufacturers are also interested in finding ways to optimize production times and create a reliable process that is as cost-efficient as possible. In this article, we will highlight different filling and freezing approaches in biosimilar production and introduce effective and innovative fluid management and freeze thaw solutions.  Challenges in biosimilar fluid management Since biosimilar manufacturing is a costly and time intensive operation, it is important to design the whole process to be as efficient and safe as possible. This includes addressing biosimilar manufacturing challenges connected to fluid management like product loss, streamlining production to save time and navigating biosimilar regulatory requirements. More about challenges in manufacturing biosimilars Product loss in biosimilar production There are different occurrences to lose a product – either when carrying out tedious and monotonous tasks in fluid management manually or when primary packagings are damaged. To maximize safety and guarantee continuous product quality, it is essential for manufacturers to minimize the risks for contamination and product loss due to damaged primary packaging. This can be reached by minimizing the need for manual intervention and errors during production, integrating automated solutions for the entire process or different production steps. Further improvements are protective, durable cases that embed single-use bioprocess containers to prevent ruptures in the fragile when frozen container components. [[1]] Efficient manufacturing for shorter production times There are several factors to be considered when aiming to exploit the full potential of biosimilar manufacturing. These include upping vaccine production speed, as well as the ability to adjust to changing conditions and market demands. In terms of fluid management, this means relying on scalable fluid management solutions for biosimilars and biologics that are preferably automated to reduce downtime. Modular solutions are especially requested, as they can easily be scaled up without the need to replace every machine along the fluid pathway. [[2]]  Efficient strategies for manufacturing biosimilars Navigating regulations in biosimilar manufacturing There is an extensive regulatory framework involved in the production of biosimilars to ensure not only the similarity with its reference biologic, but also achieve continuous quality and safety of the product. Concerning biosimilar fluid management, strategies have to be found to ensure clean room requirements and aseptic filling processes, product protection and regular testing. Therefore, it is vital for manufacturers to find ways to integrate testing practices like pre-use post sterilization integrity testing (PUPSIT) for sterile filters in a way that consumes as little time and effort as possible, but with no compromise on safety.  Advantages of fluid management with single-use technology Single-use technology has proven to be a successful approach for advanced fluid management in bioprocessing. Costs and production times can be significantly reduced by falling back on automated solutions, which is bound to change the biopharmaceutical industry by lowering expenses for innovative treatment options. To ensure the safety of a biosimilar product, it is critical to provide protected and sterile manufacturing conditions. By integrating single-use technologies into the fluid management of biosimilars, it becomes possible to eliminate the process of cleaning and sterilization at the manufacturing site, which costs time and resources. Instead, single-use solutions rely on sterile tubing, connectors, and containers, along with other equipment to increase efficiency and safety that are easily disposable after usage. [[3]] Another important advantage of single-use solutions is their scalability. This addresses the challenge of up-scaling during production. As the size of production batches may significantly vary along development stages and manufacturing, modular single-use platform systems with easy plug & play racks allow for more freedom and flexibility. To summarize, the main advantages of fluid management with single-use technology are: Scalability Reducing production costs and time  Lowering contamination risks Compliance with cGMP regulations Single-use fluid management solutions for biosimilar production There are many ways in which manufacturers can benefit from integrating single-use fluid management solutions into biosimilar production. These range from automated homogenizing units to aseptic filling and filtration systems, as well as robust protective secondary packaging for single-use bags. Homogenizing liquids with RoSS.PADL Achieving a consistently homogeneous mixture in biosimilar solutions is essential to guarantee uniformity in high-quality products. Since process reproducibility is key, Single Use Support has developed RoSS.PADL, a homogenizing platform that gently kneads and cools single-use bags simultaneously. The cooling process prevents product alterations during massaging by maintaining the appropriate temperature for the biosimilar product. This automated homogenizing solution removes the need for human intervention, for instance during draining, and operates in a standardized and reproducible way. It is also possible to combine several RoSS.PADL units with each other and control them with one single operating system.  RoSS.PADL | Homogenizing Solution RoSS.PADL is a scalable massaging platform for achieving a uniform mixture in single-use bags. With integrated cooling and heating, it maintains optimal temperatures consistently. More information Aseptic filling and filtration with RoSS.FILL By integrating automation into aliquotation processes, it becomes possible to minimize the inherent risks for contamination and streamline the process simultaneously to stay economically competitive. With RoSS.FILL, Single Use Support takes on the challenge with a completely scalable design that is able to reach filling speeds up to 300 liters per hour. Single-use bioprocess containers are filled in an aseptically closed system and in a fully automated manner. The process can be controlled via a computerized system. Not only can additional racks be added via plug & play to the aseptic filling and filtration unit, but it is also possible to attach it to other systems and devices, such as RoSS.PADL.  RoSS.FILL | Fill-Filtration RoSS.FILL is a fully automated single-use bag filling system. It is possible to fill unlimited volumes per batch with a speed of up to 300 liters per hour. The entire filling process is fully disposable, thus warranting an absolutely sterile fill & drain process. For further productivity improvements check out our pinch valve innovation. More information RoSS® Shell: Advanced protection for single-use bags Protecting single-use containers during transport and storage is essential to prevent damage and product loss. With RoSS® Shell, Single Use Support has developed a robust protective case for single-use bags. The resilient shell protects 2D single-use bags of different sizes and all vendors and is not only optimized for transport situations but also for freezing biosimilars – another critical step for manufacturers. The durable and compact protective shell also offers enough space for tubing and sterile connectors and maximizes storage density. This leads to a reduction of required space in freezers once advanced plate freezing has been performed, which is also enabled by RoSS® Shell. RoSS® Shell | Protecting single-use bags The safest transport solution for all available single-use bioprocess containers. Robust. Scalable. Single-use bag independent. More information   What makes freezing and thawing biosimilars so complex? Freezing and thawing biosimilars pose unique challenges due to the inherent complexity of these molecules. Unlike small-molecule drugs, biosimilars are intricate biological molecules designed to mimic existing biologic drugs. This complexity arises from their large molecular size, three-dimensional structure, and post-translational modifications. Maintaining the integrity and efficacy of biosimilars during freeze-thaw processes is critical for ensuring their therapeutic effectiveness. Any deviation from the optimal temperature range or handling procedure can lead to changes of protein stability. These changes can compromise the safety, efficacy, and quality of the final product. Furthermore, biosimilars and biologics are often more sensitive to temperature fluctuations compared to small-molecule drugs. Even minor variations in temperature or storage conditions can result in protein denaturation, aggregation, or degradation. These alterations may impact the stability and bioactivity of the biosimilar, rendering it less effective or even potentially harmful to patients. In order to master the complexities revolving around freezing and thawing biosimilars, several approaches have emerged – some of which will be discussed below. Uncontrolled slow freezing Uncontrolled slow freezing due to cooling with air (e.g. with conventional lab freezers, either upright or chest static freezers) may pose significant risks to the integrity and efficacy of biosimilars during the manufacturing process. Slow freezing refers to the gradual reduction of temperature over an extended period. This process can result in several detrimental effects, including cryoconcentration. Static freezers are designed to hold low temperatures which is why it cannot fully control the impact of the cooling process on biosimilars. As a consequence, the slow uncontrolled freezing process may not adequately preserve the biological activity of the biosimilar, compromising its therapeutic effectiveness. This is due to a lack of control over freezing rates and the risk for cryoconcentration. [[4]] Evolving Methods of Bulk Freezing Lyophilization Lyophilization, also known as freeze-drying, is a commonly used method for preserving the stability and extending the shelf life of biosimilars. This process involves freezing the biosimilar at low temperatures and then subjecting it to vacuum conditions to remove water by sublimation. However, lyophilization can be an overall time-consuming and expensive process, requiring specialized equipment, larger footprint and higher risk of product loss. It may come with an elevated potential for microbial contamination and longer reconstitution times, leading to inconveniences in certain formulations. Additionally, it may not be eligible for all kinds of biosimilars, as it brings significant stress to protein structures. While, under certain circumstances, this approach may be eligible for some types of monoclonal antibodies. LNP-based mRNA vaccines and cell therapies using living cells, for instance, are usually not freeze-dried. Despite its challenges, lyophilization remains a technique for ensuring the stability of biosimilar products. [[5]] [[6]] Plate freezing in biosimilar production Plate freezing is a method used in the freezing of biosimilars that offers precise temperature control and uniform freezing rates. In this process, biosimilar solutions, filled into bags or other bioprocess containers, are placed on metal plates that are cooled to the desired temperature using a refrigeration system. The plates provide a large surface area for efficient heat transfer, ensuring rapid and uniform freezing of the biosimilar solution. Plate freezing prevents the formation of undesired ice crystals, minimizing damage to the biosimilar molecules and preserving their integrity and activity. Furthermore, it is a scalable and cost-effective alternative to conventional methods, offering improved product quality and consistency. Cryogenic freezing Cryogenic freezing is an advanced method used in the preservation of biosimilars that involves ultra-low temperatures below -150° celsius. This technique utilizes pressured gases, such as liquid nitrogen or liquid helium, that has the capability to rapidly freeze the biosimilar solution. The extremely low temperatures achieved during cryogenic freezing are necessary for the storage of biologics and biosimilars like certain cell therapies, including gene-modified cell therapies. Cryogenic freezing is recommended when preserving the biological activity and stability of biosimilars over long periods. However, cryogenic freezing has often been “too effective”, meaning that the cooling process occurred too fast and with insufficient control over freezing rates, resulting in intracellular ice formation and hence higher occurrences of cell death. In recent years, though, novel cryogenic freezers have entered the market that address this issue and provide enhanced control during cryogenic freezing. [[7]]   Controlling cryogenic freezing What about thawing biosimilars? Thawing biosimilars means reverting them to their liquid state, which is just as important as freezing them in the first place. And just as intricate, since control over the thawing process is equally vital for the freezing outcome. In order to meet the individual cold chain requirements of protein substances, it is necessary to provide greater control over thawing rates. Controlled thawing of drug substances ensures standardized processes, as opposed to uncontrolled thawing, where items are simply removed from the fridge and brought to a warmer environment, such as water baths. Facing freeze-thaw challenges with single-use solutions A great deal of the challenges in manufacturing biosimilars, especially revolving around freezing and thawing them, comes from the sensitivity of the proteins they are composed of. However, there are also technological limitations to stand in the way of maximum efficiency in biomanufacturing. Conventional freezing technologies are often either not as scalable or as precise as necessary. Furthermore, widespread needs for human intervention may increase the risks of human error, ultimately leading to product loss. Still, there are solutions based on single-use technology on the market that address these very problems. Product loss in biomanufacturing – a bitter pill to swallow? Product loss in biomanufacturing is a significant concern, impacting both the efficiency and profitability of the process. It can occur either due to loss of product quality, as mentioned before, and therefore limited vaccine production yield. But a loss can also occur due to various other factors, including breakage or leakage of single-use bioprocess containers during freezing, shipping, and storage. Excessive manual handling and a missing secondary packaging may be reasons for single-use bags to break. Such vulnerabilities can lead to a loss of valuable drug substances, causing financial setbacks and delaying production timelines. To address this challenge, innovative solutions like the RoSS® Shell offer a robust secondary packaging option. By providing a protective shell around single-use bags, RoSS® Shell minimizes the risk of breakage or leakage significantly. This solution not only safeguards the integrity of the bioprocess containers but also ensures the preservation of valuable drug substances throughout the biomanufacturing process. Freeze-thaw solutions for biosimilar production Achieving precise control over freezing processes presents a significant challenge in biomanufacturing. The delicate nature of biological substances, such as monoclonal antibodies (mAbs) (mAbs) and other biopharmaceuticals, demands meticulous handling to maintain their efficacy and integrity. Traditional freezing methods often lack the necessary precision and consistency, leading to potential product loss and compromised quality. To address this challenge, advanced freezing technologies like the plate freezing platform RoSS.pFTU and the cryogenic freezer RoSS.LN2F offer robust solutions. The RoSS.pFTU leverages plate-based freezing to ensure uniform and controlled freezing of drug substances, maintaining their original quality throughout the process. Similarly, the RoSS.LN2F cryogenic freezer provides an innovative approach to achieve extremely low temperatures. By utilizing an enclosed LN2 system, this freezer ensures safe and efficient freezing down to temperatures as low as -180°C. With precise temperature control of exposure to liquid nitrogen, the RoSS.LN2F offers unmatched reliability and stability for freezing high-value biopharmaceuticals.  Freeze & Thaw platform The Single Use Support freeze-thaw platforms provide insular solutions for the freeze/thaw processes of each clinical phase. Our new freeze-thaw units are fully scalable and compatible with all batch sizes and bags from all established manufacturers – you will only require one single system from the lab to blockbuster production. More information  RoSS.LN2F | Cryogenic Freezer RoSS.LN2F is a powerful cryogenic controlled rate freeze for temperatures down to -170°C. An enclosed LN2 system and our innovative direct injection system ensure no direct exposure and no mechanical compressors are needed. This ensures a safe, low-maintenance and energy-saving handling. More information Freezing pharmaceutical bulk: Preparing for scale-up Scalability is another critical consideration for freezing processes in biosimilar production – but one that, at some point, is inevitable for many manufacturers. There are numerous reasons why these considerations are best made early on in process development, as the necessary equipment requires significant investments. Modular and scalable solutions have therefore entered the market, being able to smoothly transition from small to large scale. Scaling pharmaceutical freezing, though, does not only refer to an increasing number of individual items to be processed, but also to their respective volumes. Freezing pharmaceutical bulk comes with its own set of challenges, such as achieving homogeneous freezing results. Single Use Support has made these considerations while developing its freeze-thaw platform based on single-use technologies. Their modular platform design allows for flexible expansion, accommodating varying batch sizes and production volumes with ease, while transferring freezing protocols to larger units. By using the plate freezing platform RoSS.pFTU, for instance, the direct contact between cooling plates and the packaging surface allows controlled and even freezing processes for various volumes – from 1 ml up to 500 L, depending on the chosen system. This scalability ensures that freezing processes can evolve in tandem with production demands, minimizing disruptions and maximizing productivity. Scalability was not only a core idea at the conception of plate and cryogenic freezers, but rather for all process solutions developed by Single Use Support – such as fluid management solutions for biosimilar production, storage and transport systems. This enables manufacturers to establish highly automated biomanufacturing processes with minimal need for human intervention, enhanced safety and cost efficiency.  [[download-1-email-detailed]] References The process defines the product: what really matters in biosimilar design and production?, http://dx.doi.org/10.1093/rheumatology/kex278, Published 2017-07-03 A Single-use Strategy to Enable Manufacturing of Affordable Biologics, http://dx.doi.org/10.1016/j.csbj.2016.06.007, Published 2016-07-06 A Single-use Strategy to Enable Manufacturing of Affordable Biologics, http://dx.doi.org/10.1016/j.csbj.2016.06.007, Published 2016-07-06 Impact of Freeze/Thaw Process on Drug Substance Storage of Therapeutics, http://dx.doi.org/10.1016/j.xphs.2017.03.019, Published 2017-03-24 Strategies to Reduce Reconstitution Time of Lyophilized Biotherapeutics, http://dx.doi.org/10.1016/j.xphs.2020.02.019, Published 2020-03-02 Lyophilization considerations: Comparing freeze-drying to freezing for biopharmaceutical products, https://www.susupport.com/blogs/manufacturing-processes/lyophilization-considerations-comparing-freeze-drying-to-freezing-for-biopharmaceutical-products, Published 07/2023 Cryopreservation as a Key Element in the Successful Delivery of Cell-Based Therapies—A Review, http://dx.doi.org/10.3389/fmed.2020.592242, Published 2020-11-26