Deep learning for continuous manufacturing of pharmaceutical solid dosage form

This report with recommendations is the result of an expert panel meeting on PAT applications in food industry that was organized by the M3C Section of the European Society of Biochemical Engineering Science (ESBES) at the 10th ESBES Symposium. The aim of the panel was to provide an update on the present status of the subject and to identify critical needs and issues for wider applications of PAT in food industry. A brief description of the current state-of-the-art and industrial uptake of the methodology is provided in this report. It concludes with a number of recommendations to facilitate further developments and a wider application of PAT in food industry. Process Analytical Technologies (PAT) [1] (European Medicines Agency EMA-FDA pilot program for parallel assessment of Quality by Design applications; Document EMA/172347/2011) have been extensively discussed in literature, particularly with respect to (bio)pharmaceutical process modelling, monitoring and control [2]. Table 1 provides an historic overview of the PAT development in the context of food applications. Although successful applications within food industry are increasingly being reported [3, 4], the session on PAT in food industries at the ESBES-IFIBiop 2014 in Lille highlighted significant challenges and opportunities for further development in this area. This position paper briefly reviews the current state-of-the-art, industrial needs and opportunities as well as scientific challenges to be addressed in order to extend the use of PAT methodology in the food industries. Currently, quality and safety control are still based mainly on discontinuous analysis with traditional analytical methods in the lab or, at best, at-line measurements. This is no longer sufficient to fulfill the needs of the food industry. Due to higher safety and quality standards and demands and high throughput of production facilities, the number of samples to be analyzed is increasing. Rapid analysis methods and PAT are required to address these needs along the complete production chain leading to a better understanding and control of raw materials, intermediate products in the production process as well as the final products to be packaged and delivered. The goal is to achieve real time analysis in order: • to avoid usage of any out-of-specification raw material and to detect adulteration, substitution, tampering and counterfeiting leading to non-authentic products; • to be able to intervene and stop/change processes in order to secure the target quality; • to assess the final quality to avoid out-of-specification products being packaged and shipped, thus leading to undesirable customer dissatisfaction and costs associated with the resolution of complaints. Over a hundred years ago (on May 22nd, 1913) the first patent on a PAT device ("Pfeiffenanalysator" for measuring the ratio of H2 and N2 gas for ammonia synthesis) was granted to Paul Gmelin from Badische Anilin- und Soda-Fabrik, BASF (Patentschrift Nr. 281157, Klasse 42/. Gruppe 4). Since then, PAT found broad application in chemical industry, which is dominated by highly automated, continuous processes. Today in chemical processes, such as the synthesis of isocyanates, e.g. hexamethylendiisocyanate (HDI), typically 60-130 PAT measurements are collected. In contrast, in sectors like (bio)pharmaceutical or food industry, the application of PAT is significantly less frequent today, especially, in terms of on-line analytics, where the measurement takes place in or close to the production step (or unit operation). One reason for this is the reduced degree of automation of the processes in these industries, which are dominated by unit operations, single production steps consecutively executed after each other, resulting in production batches. Analytics of a production batch takes place mostly off-line in analytical laboratories during hold-up times of the process intermediate between the different unit operations. Regulatory requirements represent an equally important driver for extensive online analytics. With the 2004 FDA's Quality by Design initiative, regulatory agencies demand systematic risk based process development and understanding of the processing space. This also allows for flexible process adjustments within the explored space for producing the desired product quality. In order to achieve the required understanding, more extensive analytical data is required, ideally obtained in-time on raw materials, process intermediates and ideally also on product quality attributes. In food industry, where typically high product titers are obtained, product analytics is sometimes possible by in-line measurements, such as spectroscopy (section 4). In biopharmaceutical processes, product titers are usually very low, the products are proteins with high molecular weight, and quality attributes are challenging to analyse. In these situations, online sampling with automated sample preparation and analytics may open up a solution [5]. But, identifying and implementing analytical methods, which are fast enough for delivering results on product quality attributes (e.g. protein glycosylation) in time, during the unit operation for allowing process modulation, remains a challenge. The overall typical goals in industry are high safety, high and stable product quality, high yield, low consumption of resources (materials, energy, room, time, and people), reduced influence of variability in raw materials as well as an increased shelf life of products which holds also in food processes. However, compared to the chemical and biopharmaceutical industries, food industry has to deal with certain characteristics, which renders PAT a formidable challenge in this context. The characteristic features in food industry are: • Raw materials are not pure substances: they are complex combinations of pure substances with varying compositions • Raw materials are soft, variable size, fragile and slippery • Physical properties of raw materials depend heavily on temperature, pressure, moisture and harvesting, and storage conditions • Raw materials undergo usually a phase transformation during processing and hence change their physical properties during processing • Micro processes (physical, (bio)-chemical, microbiological) are frequently not known • Highly perishable products. Here the challenge is to produce good quality, which maintains for a long time (shelf life) • High demand for hygiene These characteristics lead to a challenge for the application of sensors in the food industry. For important quality and process variables, such as sensory assessment, micro flora or spoilage, reliable and robust sensors are not yet available. Moreover, the sensors which are available are typically used only in isolated applications and frequently provide insufficient reliability. They are often not integrated in a common data management infrastructure. The materials of construction do not always consider suitability of contact with food and the solutions developed within advanced research projects frequently demand high care and maintenance. One reason why PAT is not as common as in other areas is that in food industry knowledge from various subject areas is necessary (such as physics, chemistry, biology, mathematics, informatics, engineering, nutritional science). For unit operations mathematical models are available in principle, but frequently they are too complicated to adapt. One of the biggest challenges in food industries is the dynamic nature of the processes. Changes in geometry, porosity, microstructure, solubility as well as mass and energy transfer coefficients must be addressed. Mostly gradients of temperature and moisture have to be considered as well as changes in kinetic parameters during process run. End product qualities like color, smell and 'brokens' also strongly influence the process. Therefore, food processes can be considered to be significantly more complex then chemical and bio-pharmaceutical processes. To achieve more stable processes PAT applications are necessary to check the quality of the raw and processed materials and their relationship to each other. If the quality is changing, then control actions resulting in online parameter changes are required in order to maintain constant product quality. Measurement systems are required, which guarantee that the process is in accordance with recipe and formulation. Furthermore, disturbances must be compensated for using control actions to reduce process variability and to conform to food regulations. As Glassey [6] argues, PAT methodology can aid in product design and testing as well as in ensuring full compliance with the HACCP and ISO 22000:2005 requirements during processing. As demonstrated below, PAT methodologies have the potential to aid the identification of critical control points and their critical limits, their effective monitoring and control, but also effective communication with suppliers and customers. Documentation which requires measurements of important variables is especially important so that traceability can be guaranteed. Here PAT has to deliver the corresponding measurement systems. Clearly a high demand for PAT in food industry is evident as is the need for further developments in the science and technology that help address the specific challenges posed by the characteristics of the food industry highlighted above. The complexity of raw materials that are typically soft and easily damageable is arguably one of the major scientific and technological challenges in food industry. During storage and processing the quality of such raw materials can decline due to oxidation processes, pressure and temperature effects. In addition, the visual impression of the final product (i.e. its appearance) is much more important than in other industries due to the fact that this will influence the purchase decision of the consumer. During the whole processing from raw material to the storage of the final product, hygiene is of utmost importance. Therefore non-invasive sensor systems are required in these applications. Measurement systems based on optical principles are particularly suitable from this perspective. Such measurement systems, including near infrared (NIR), Raman and fluorescence spectroscopy as well as computer-assisted image-based systems, potentially have a number of advantages in food process supervision and automation. Spectroscopic methods and imaging devices are well suited for PAT purposes because they are fast, non-destructive, provide multiple chemical information, allowing remote in-process analysis via fiber optics or instruments mounted directly on-line. Fluorescence spectroscopy is the most sensitive spectroscopic technique. Recently, many applications have been developed using fluorescence techniques [3, 7, 8]. Raw materials, the supervision of processing as well as product quality and the contamination of the equipment can be monitored by fluorescence. For example, Everard et al. [3] presented a method for detection of fecal contamination on spinach leaves. They coupled three hyperspectral imaging (HSI) configurations with two multivariate image analysis techniques and compared fluorescence imaging in the visible region with ultra violet and violet excitation sources, and reflectance imaging in the visible to near-infrared regions. They showed, that both fluorescence configurations had 100% detection rates for fecal contamination up to 1:10 dilution level and violet HSI had 99% and 87% detection rates for 1:20 and 1:30 levels, respectively. Everard et al. emphasized that on-line detection of fecal contamination on leaves has the potential to reduce the cases of food borne illnesses and their associated costs. A similar approach is presented by Lee et al. [7] where bovine faeces on Romaine lettuce and baby spinach leaves were investigated. They pointed out that two-band ratios using bands at 665.6 nm and 680.0 nm for lettuce and at 660.8 nm and 680.0 nm for spinach effectively differentiated all contamination spots applied. Grote et al. [8] described a fluorescence measurement technique to monitor a sourdough fermentation process. For the prediction of pH value and acidity during rye sourdough fermentations they applied partial least squares regression and principal component regression models for prediction and compared them with an evaluation where principal component analysis was combined with artificial neural networks. Depending on process operation and evaluation technique the average percentage root mean square errors of prediction for pH values were between 2.5 and 5.1%. For the prediction of the acidity level, the best results were between 6.0 and 8.1%. Liu et al. [9] used the Hoffman reaction to convert acrylamide to a compound which shows strong fluorescence emission at 480 nm. They showed good correlation of acrylamide in the range of 0.015 μg/mL to 20 μg/mL. Using this technique the food security will be increased. A fluorescence imaging device to detect deli residues on deli slicers were used by Beck et al. [10] processing four cheeses and four processed meats. The authors suggested that a fluorescence imaging device can be applied for routine use even in delicatessens. Fig. 1 clearly shows that the application of fluorescence for the monitoring of food processes increased from less than 10 before 2003 to more than 60 a year since 2013. This figure includes all papers from a search containing the key words "Food" and "Fluorescence". Although most of these papers describe laboratory applications rather than industrial PAT applications, they indicate potential future applications in this technology in food industry. Number of published papers obtained from the Scopus database searching for the words "Food" and "Image analysis" or "Raman" or "Near infrared spectroscopy" or "Fluorescence spectroscopy". Raman spectroscopy can only be applied if no fluorescence occurs in the corresponding excitation range. He et al. [11] applied the surface enhanced Raman scattering spectroscopy to detect banned food additives, such as Sudan I dye and Rhodamine B in food, Malachite green residues in aquaculture fish. They concluded, that Raman spectroscopy and chemometric evaluation techniques can be used to identify banned food additives to ensure food safety. Ilaslan et al. [12] presented a method based on Raman spectroscopy to provide a rapid method for evaluating the quantitative analysis of glucose, fructose, and sucrose in soft drinks. Wang et al. [13] applied a Raman spectrometer as a process analyzer to monitor the wine fermentation. They demonstrated that sugar, ethanol and glycerol can be measured on-line with high correlation (higher than 0.98) to the HPLC reference measurements. Nache et al. [14] investigated Raman spectra from pork meat to monitor the early postmortem lactate accumulation and pH decline. They suggested that the locally weighted regression applied to the standard normal variate (SNV) normalized Raman spectra provide one of the most accurate and robust models with a cross-validated coefficient of determination (r2cv) of 0.97 for pH and lactate, a cross-validated root mean square error (RMSECV) of 4.5 mmol/kg for the lactate prediction and 0.06 pH-units for the pH prediction. These results demonstrate significant potential of combining chemometrics and Raman spectroscopy for on-line meat quality control applications. Fig. 1 shows the number of papers recorded in Scopus (search words "Food" and "Raman"). Compared to fluorescence, the number of papers describing Raman spectroscopy is twice as high in recent years with a significant rate of increase, demonstrating the increasing interest in this method for food process monitoring. Computer vision systems enable one of the main aspects of consumer preference – the appearance of a product – to be inherently considered. Therefore, computer vision systems for the supervision of food processing also gained importance over the years. An overview of several examples is given by Sun [15]. Especially the supervision of food drying processes is discussed by Aghbashlo at al. [16]. They pointed out that there is a large unexploited potential in the image data captured during various food processing operations. More informative feature extraction algorithms or novel pattern recognition procedures have to be developed. Paquet-Durand et al. [4] described a system for the supervision of the baking process. They demonstrated, by using the Viola–Jones-algorithm as well as neural networks, that the pastry can be identified and the volume increase as well as color development can be monitored. To detect defective apples Zhang et al. [17] used a computer vision system, which was combined with an automatic lightness correction system. For 160 samples they showed a 95% overall detection accuracy. For the evaluation they used a weighted relevance vector machine classifier. Fig. 1 shows the number of papers over time from Scopus searching for "Food" and "Image analysis". Here the applications start earlier compared to the spectroscopic methods, the number of applications per year is higher than in the case of spectroscopic applications; except in the year 2014, where more reports of Raman applications were published. Moreover imaging systems using visible and NIR region are available to perform quality checks based on the spectroscopic information derived from each point in the image. One example is the on-line analysis of the widely varying fat distribution in salmon for sorting purposes [18]. Near infrared (NIR) is a well-established method for rapid analysis of food raw materials and products [18], either on-/in-line, at-line or off-line. In the lab or at-line multiple components such as fat, protein, moisture and many more, can be analyzed without any sample preparation in all kinds of liquid, solid and semi-solid samples. Raw materials can be verified for identity and further characterized regarding composition already in the goods reception. The composition, freshness and adulteration of edible oils [19], e.g. olive oil [20], can be analyzed rapidly before a truck is unloaded. Many other sample types like meat, grains, flour, dairy products [21] and others can be analyzed. Even mixtures like vitamin premixes can be analyzed to make sure that the correct material was delivered and can be used in production. There are several approaches and technologies for PAT available, ranging from simple filter based devices over dispersive diode array spectrometers to Fourier-Transform (FT)-NIR instruments. Samples can be analyzed in-line by fiber optic probes or by contactless systems (Fig. 2). Smaller instruments can be directly attached to pipes, chutes or in other installations. A) NIR reflection probe in a fluid bed dryer. (B) Probe head for contactless measurement of grain and other solids. Applications cover a broad range from a simple monitoring of moisture content of a product on a conveyor belt to more complex control situations. In dairy industry there are demands to control milk powder production by monitoring the feed of the spray tower and the powder after fluid bed drying. Other important production steps to control are the standardization of milk, cream, whey and concentrates [22]. In frying processes with big volumes of oil an in-line monitoring of the oil quality with regards to acid value, anisidine value and the content of polar and polymerized components [23] are of particular interest. Another example of high volume processes where monitoring of protein, moisture and ash is important is the milling of grain to flour and the production of cereals of any kind. Finally there are more and more fermentation processes controlled by in-line NIR to optimize the conditions and follow the feeding and consumption cycles during biomass buildup [24]. In 2013 roughly 120 papers were published, however the recent increase is not as steep as in the case of Raman spectroscopy (Fig. 1). The economic benefits due to PAT can be attributed to higher product quality and yield as well as decreased product variation. This will reduce the overall production costs significantly and increase competitiveness. Furthermore, the knowledge and understanding of the process will increase. However, the level of automation in industrial food processes is significantly lower compared to the chemical and pharmaceutical processes. This is partly due to the complexity of food processes. On the other hand, the lack of reliable sensor systems to determine important process parameters and variables contributed to this in the past. Sensors represent a fundamentalpart of all automation systems, although they only represent a part of the requirements for wider application of PAT in food industry. The areas of further development and recommendations enabling more extensive use of the PAT within this industry also include: • Further industrial case studies and wider dissemination of the positive impact of reliable sensor technology in raw material and product quality as well as process monitoring. • Operational and maintenance requirements of sensor technologies will remain a significant aspect of future sensor technology uptake in this industry. • Data management and analysis software will play a significant role in extending the PAT application within the food industry. Platform solutions, preferably supporting wireless data transfer, at competitive pricing levels are required. • Cost benefit analysis studies are particularly important given the business drivers of this industry. • The impact of PAT is likely to be more pronounced in the new processes, although it is important to continue to encourage the application of PAT approaches within established food processes to enhance the process economics and compliance with the standards ensuring safe food supply chains. • PAT can significantly contribute to the stringent traceability and documentation requirements, although issues of compatibility and data standardization will impact upon data management systems employed by the companies within the supply chain. The authors declare no financial or commercial conflict of interest.

On the influence of raw material attributes on process behaviour and product quality in a continuous WET granulation tableting line

A hybrid NIR-soft sensor method for real time in-process control during continuous direct compression manufacturing operations

Development and Application of Control Concepts for Twin-Screw Wet Granulation in the ConsiGmaTM-25: Part 2 Granule Size

Binder selection is a crucial step in continuous twin-screw wet granulation (TSWG), as the material experiences a much shorter residence time (2–40 s) in the granulator barrel compared to batch-wise granulation processes. Polyvinyl alcohol (PVA) 4-88 was identified as an effective binder during TSWG, but the potential of other PVA grades—differing in polymerization and hydrolysis degree—has not yet been studied. Therefore, the aim of the current study was to evaluate the potential of different PVA grades as a binder during TSWG. The breakage and drying behavior during the fluidized bed drying of drug-loaded granules containing the PVA grades was also studied. Three PVA grades (4-88, 18-88, and 40-88) were characterized and their attributes were compared to previously investigated binders by Vandevivere et al. through principal component analysis. Three binder clusters could be distinguished according to their attributes, whereby each cluster contained a PVA grade and a previously investigated binder. PVA 4-88 was the most effective binder of the PVA grades for both a good water-soluble and water-insoluble formulation. This could be attributed to its high total surface energy, low viscosity, good wettability of hydrophilic and hydrophobic surfaces, and good wettability by water of the binder. Compared to the previously investigated binders, all PVA grades were more effective in the water-insoluble formulation, as they yielded strong granules (friability below 30%) at lower L/S-ratios. This was linked to the high dispersive surface energy of the high-energy sites on the surface of PVA grades and their low surface tension. During fluidized bed drying, PVA grades proved suitable binders, as the acetaminophen (APAP) granules were dried within a short time due to the low L/S-ratio, at which high-quality granules could be produced. In addition, no attrition occurred, and strong tablets were obtained. Based on this study, PVA could be the preferred binder during twin screw granulation due to its high binder effectiveness at a low L/S-ratio, allowing efficient downstream processing. However, process robustness must be controlled by the included excipients, as PVA grades are operating in a narrow L/S-ratio range.

What is process analytical technology (PAT), why is it important, and where is it going? Basically, PAT originated by applying measurement technologies to industrial processes. Some of the first examples of using measurement to monitor a process were performed within the German chemical industry more than 60 years ago [personal discussion with Dr. Jochen Rudolph, Director of Process Control of BASF, in Ludwigshafen, Germany, 30 September 1999]. The ability to monitor processes with measurement technology is not new [1], but the recognition that it will enhance productivity, quality, and environmental impact has grown increasingly over the past 30 years. PAT is now a field of measurement science that involves a number of contributions from the disciplines of chemistry, engineering, biology, data handling, and control strategies, applied in order to gain knowledge about the process being performed. The traditional approach to implementing PAT was to transport laboratory analytical instrumentation to the production plant and modify the instrumentation to accept a process sample. This traditional approach was valuable to the chemical and petrochemical industries for a number of years, as it was able to provide a window into the process, giving information on real-time composition, reaction pathways and kinetics, as well as environmental and hazard evaluation issues. Having instrumentation that could provide a profile of the process under production conditions enables the capabilities of the process to be defined, and to gather data needed to locate critical process parameters. Once these critical process parameters are monitored, process models can be developed or improved, ultimately improving process control. PAT therefore becomes a combination of applying process analytical tools and developing feedback process control strategies based on information management tools or process optimization studies for the purpose of achieving process understanding. Developments in measurement science are influenced by advances in the fields of computation and communication, driven by the needs of the military and computer-related industries. This results in better miniaturization techniques, new materials for heat transfer, new electro-optical materials, and new advanced data handling tools. With the large amount of new technology being developed within analytical sciences, it is important to ask the question: what type of measurement is appropriate for PAT? The answer is probably ‘‘anything that gives more data than you are presently obtaining’’. The constraints of cost and the reliability of the data must be recognized, but more measurement points usually lead to better models, resulting in better control strategies. The fact that more measurement data leads to better models also creates an opportunity to depart from the tradition of basing PAT solely upon traditional laboratory analytical instrumentation.

In-depth experimental analysis of pharmaceutical twin-screw wet granulation in view of detailed process understanding

The pursuit of continuous manufacturing (CM) prompts the use of novel manufacturing equipment to accomplish traditional batch manufacturing unit operations in a continuous fashion. Process development is a critical step in advancing novel equipment applications in CM lines. Wet granulation, accomplished continuously via twin-screw wet granulation, is often evaluated for its ability to increase granule size compared to raw material particle size. The information provided by granule size data analysis drives the depth of relationships between process parameters and granule size, summarized as process development. Granule size data is often presented as a granule size distribution (GSD) and quantified by d-values or size fractions. These numerical descriptors are well-recognized for their simplicity and translatability, but the complexity of granule size data presents the potential for missing information. Treating GSDs as a multivariate dataset facilitates the use of principal component analysis (PCA) as a means for increasing the depth of information derived from granule size data. Decomposition by PCA was deployed in two datasets as a complementary approach to the numerical descriptors, demonstrating the increase in process understanding achieved with PCA of GSDs. Enriching process understanding is a foundational component of the development and adoption of novel CM equipment.

After the Food and Drug Association in the USA published guidelines on the enhanced use of process analytical technology (PAT) and continuous manufacturing, many studies regarding PAT and continuous manufacturing have been published. This paper describes a case study involving granulation and coating steps with ethenzamide to investigate interference for PAT model construction and model management. We investigated what factors should be considered and addressed when PAT is implemented for continuous manufacturing and how predictive models should be constructed. The product qualities that were monitored were moisture content and particle size in the granulation step and tablet weight and moisture content in the coating step. We have constructed models for the granulation step and validated the predictive capability of the models against an external dataset. A partial least squares (PLS) model with manual wavelength selection had the best predictive accuracy for loss on drying against the external validation set. We found that the prediction of loss on drying was accurate, but the prediction of particle size was not sufficiently accurate. In the coating step, because of the small amount of data, we performed three-fold cross-validation and y-scrambling 10 times, to select the optimal hyper-parameters and to check if the models were fitted to chance correlations. We confirmed that the coating agent weights, tablet weights, and water content could be accurately predicted based on the mean of the R2 score for cross-validation. Addition of other variables, as well as the absorbance, slightly improved the predictive accuracy.

Continuous twin screw wet granulation (TSWG) systems are possible pathways for oral solid dosage manufacturing in the pharmaceutical industry. TSWG requires a drying step after granulation before the tableting process. Typically, semi-continuous fluidized bed dryers (FBDs) are used for this purpose. At the same time, the pharmaceutical sector is interested in mathematical prediction models to save resources during the early drug product development (DPD) stage or to control manufacturing. Several authors have already developed prediction models for semi-continuous drying processes. However, these model structures reported systematic prediction offsets, which could be related to the incomplete implementation of fluidization and granule segregation phenomena. This study evaluates the complex fluidization behavior of wet granules in industrially relevant semi-continuous FBDs. A transparent perspex version of the dryer was used for the analysis of bed height, pressure drop, porosity, segregation, and spatial heating patterns at varying process settings. The investigated behaviors of the fluidizing bed will be helpful to derive phenomenological (sub)models for the detailed description of segregation in the semi-continuous fluidized bed system. In this study, it was found that semi-continuous FBDs are characterized by a change in fluidization regime from plug flow to a bubbling bed at the moment that the granule bed slumps. Secondly, the presence of size-based vertical segregation phenomena as well as spatial temperature differences were proven. The experimental results suggest that larger granules are dried under more intense drying conditions than smaller granules.

Adoption of Quality by Design (QbD) principles, regulatory support of QbD, process analytical technology (PAT), and continuous manufacturing are major factors effecting new approaches to pharmaceutical manufacturing and bioprocessing. In this review, we highlight new technology developments, data analysis models, and applications of Raman spectroscopy, which have expanded the scope of Raman spectroscopy as a process analytical technology. Emerging technologies such as transmission and enhanced reflection Raman, and new approaches to using available technologies, expand the scope of Raman spectroscopy in pharmaceutical manufacturing, and now Raman spectroscopy is successfully integrated into real-time release testing, continuous manufacturing, and statistical process control. Since the last major review of Raman as a pharmaceutical PAT in 2010, many new Raman applications in bioprocessing have emerged. Exciting reports of in situ Raman spectroscopy in bioprocesses complement a growing scientific field of biological and biomedical Raman spectroscopy. Raman spectroscopy has made a positive impact as a process analytical and control tool for pharmaceutical manufacturing and bioprocessing, with demonstrated scientific and financial benefits throughout a product’s lifecycle.

Introduction. The production of solid dosage forms from hygroscopic substances is a complex technological task. The addition of hygroscopic substances into a polymer matrix allows to reduce their moisture absorption capacity.Aim. Reducing the hygroscopicity of deliquescent substances and obtaining sustained release solid dosage forms by using solid dispersion systems.Materials and methods. Substance: DEAE; excipients: Kollidon® VA 64, Soluplus®, PEG 1500, PEG 6000, PEG 8000, Poloxamer Kolliphor® P 188 and Kolliphor® P 407; reagents: hydrochloric acid, sodium dihydrogen phosphate, potassium hydrogen phosphate. The melt of the components was obtained on a twin-screw laboratory extruder and cast into silicone molds. The resulting solid dosage forms were studied for disintegration in three environments corresponding to the sections of the human gastrointestinal tract.Results and discussion. The active pharmaceutical substance DEAE is characterized as deliquescent substance. The introduction of DEAE into PEG-polymer matrices made it possible to reduce the hygroscopicity of solid dosage forms in the form of bars. The introduction of solubilizers into the melt made it possible to obtain bars with the appropriate organoleptic properties. The release of DEAE from bear- or toroid-shaped bars occurs on average 29–47 % faster than from heart-shaped bars.Conclusion. Compositions based on Soluplus® and Kolliphor® P 407 have proven promising for further development of tiles containing DEAE. In order to create tiles with a slow release, it is recommended to use heart-shaped forms, as they have a smaller surface area.

Continuous bioprocesses have become a significant technological change in regulated industries, with process analytical technology (PAT) and quality-by-design (QbD) being essential for enabling continuous biomanufacturing. PAT and QbD are associated with process automation and control, providing real-time key process information. Continuous manufacturing eliminates hold times and reduces processing times, providing benefits such as improved product quality, reduced waste, lower costs, and increased manufacturing flexibility and agility. Over the past decade, advancements in science and engineering, along with the adoption of QbD and the advancement of PAT, have progressed the scientific and regulatory readiness for continuous manufacturing. Regulatory authorities support the implementation of continuous manufacturing using science- and risk-based approaches, providing a great deal of potential to address issues of agility, flexibility, cost, and robustness in the development of pharmaceutical manufacturing processes.

Background/Objectives: Quality by Design (QbD) has revolutionized pharmaceutical development by transitioning from reactive quality testing to proactive, science-driven methodologies. Rooted in ICH Q8-Q11 guidelines, QbD emphasizes defining Critical Quality Attributes (CQAs), establishing design spaces, and integrating risk management to enhance product robustness and regulatory flexibility. This review critically examines QbD's theoretical frameworks, implementation workflows, and industrial applications, aiming to bridge academic research and commercial practices while addressing emerging challenges in biologics, advanced therapies, and personalized medicine. Methods: The review synthesizes regulatory guidelines, case studies, and multidisciplinary tools, including Design of Experiments (DoE), Failure Mode Effects Analysis (FMEA), Process Analytical Technology (PAT), and multivariate modeling. It evaluates QbD workflows-from Quality Target Product Profile (QTPP) definition to control strategies-and explores advanced technologies like AI-driven predictive modeling, digital twins, and continuous manufacturing. Results: QbD implementation reduces batch failures by 40%, optimizes dissolution profiles, and enhances process robustness through real-time monitoring (PAT) and adaptive control. However, technical barriers, such as nonlinear parameter interactions in complex systems, and regulatory disparities between agencies hinder broader adoption. Conclusions: QbD significantly advances pharmaceutical quality and efficiency, yet requires harmonized regulatory standards, lifecycle validation protocols, and cultural shifts toward interdisciplinary collaboration. Emerging trends, including AI-integrated design space exploration and 3D-printed personalized medicines, promise to address scalability and patient-centric needs. By fostering innovation and compliance, QbD remains pivotal in achieving sustainable, patient-focused drug development.

ABSTRACTProtein‐based therapeutics have revolutionized modern medicine, addressing complex diseases with unprecedented specificity and efficacy. The rising demand for biologics has driven the evolution of biomanufacturing practices to ensure consistent quality and operational efficiency. Traditional batch testing, with its inherent limitations, is being replaced by quality by design (QbD) frameworks and process analytical technology (PAT). PAT facilitates real‐time monitoring and control by integrating advanced analytical tools and data‐driven methodologies to optimize downstream processing (DSP). This review highlights the recent advancements in PAT tools, including spectroscopy, chromatography and biosensors. Spectroscopic techniques provide rapid, non‐invasive measurements, while biosensors offer high specificity for monitoring critical quality attributes. Additionally, the integration of chemometric modelling and digital twins enables predictive analytics and enhances process control, paving the way for real‐time release (RTR) of the product. Despite challenges in regulatory compliance and technology integration, innovations in automation and machine learning are bridging these gaps, accelerating the transition to intelligent manufacturing systems. This article provides a comprehensive evaluation of emerging analytical technologies and strategic insights into their integration, aiming to support the biopharmaceutical industry's shift towards robust, continuous and adaptive manufacturing paradigms.