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Biomimetics
  • Review
  • Open Access

20 September 2023

Artificial Intelligence in Regenerative Medicine: Applications and Implications

and
1
Biosensor Research Center, Isfahan University of Medical Sciences, Isfahan 81746-73461, Iran
2
Department of Computer Science, Iowa State University, Ames, IA 50011, USA
*
Authors to whom correspondence should be addressed.
This article belongs to the Section Bioinspired Sensorics, Information Processing and Control

Abstract

The field of regenerative medicine is constantly advancing and aims to repair, regenerate, or substitute impaired or unhealthy tissues and organs using cutting-edge approaches such as stem cell-based therapies, gene therapy, and tissue engineering. Nevertheless, incorporating artificial intelligence (AI) technologies has opened new doors for research in this field. AI refers to the ability of machines to perform tasks that typically require human intelligence in ways such as learning the patterns in the data and applying that to the new data without being explicitly programmed. AI has the potential to improve and accelerate various aspects of regenerative medicine research and development, particularly, although not exclusively, when complex patterns are involved. This review paper provides an overview of AI in the context of regenerative medicine, discusses its potential applications with a focus on personalized medicine, and highlights the challenges and opportunities in this field.

1. Introduction

Artificial intelligence (AI) refers to the development of computer systems that can perform tasks that would typically require human intelligence. This includes learning, reasoning, perception, and problem-solving. AI systems are designed to mimic human cognition and to work autonomously, learning from data and prior experiences to improve their performance over time [1,2]. The concept of AI has been around for decades. Still, recent advances in machine learning, deep learning, and natural language processing have made it possible to develop more sophisticated AI systems. Machine learning empowers researchers to analyze vast amounts of data, recognize patterns, make predictions based on that data [3,4], and even learn from their mistakes and adjust their behavior accordingly [5] without being explicitly programmed. Machine learning is used in a wide range of applications, including natural language processing [6], image recognition [7], autonomous vehicles [8], and biomedical engineering [9].
Deep learning is a subset of machine learning that uses artificial neural networks to learn from data. These neural networks are designed to mimic the structure and function of the human brain, allowing them to identify more complex patterns and make decisions based on the data they have been trained with [10,11]. Deep learning has revolutionized the field of artificial intelligence, enabling machines to perform tasks that were once thought to be impossible. One of the key advantages of deep learning is its ability to handle large and complex datasets [12]. Traditional machine learning algorithms struggle to make sense of data that is too vast or too complex for humans to process. On the other hand, deep learning algorithms can handle millions of data points and identify patterns that would be impossible for a human to detect [13,14]. Another advantage of deep learning is its ability to learn and improve over time [15]. Traditional machine learning algorithms commonly do not offer memory, requiring humans to manually adjust the parameters and settings to improve their performance. Some deep learning algorithms, such as Long Short-Term Memory [16] and Recurrent Neural Networks [17], can adjust themselves automatically based on the data they are processing. This means that deep learning algorithms can continue improving and evolving as they process more data (Figure 1) [18,19].
Figure 1. Schematic outlining the AI areas. Adapted from [20].
Regenerative medicine is a rapidly evolving field that seeks to restore or replace damaged or diseased tissues and organs through advanced technologies such as stem cell-based therapies, gene therapy, and tissue engineering [21,22]. With the potential to revolutionize medical treatment, regenerative medicine offers hope for patients suffering from a wide range of conditions, including heart disease, diabetes, and neurological disorders [23,24]. However, developing effective regenerative therapies requires the ability to analyze large amounts of complex data, which is where AI comes in.
This paper offers a distinct contribution by synthesizing and analyzing the available literature on AIs applications in regenerative medicine, providing an overview, identifying gaps in the existing literature, and proposing novel research directions. By adopting a holistic perspective, we not only consider empirical studies but also include theoretical perspectives and expert opinions. This approach broadens the scope of our analysis and allows for a more comprehensive understanding of the topic. By incorporating diverse sources of evidence, our manuscript offers a unique perspective that is not limited to a single methodological approach. Thus, our study presents a novel synthesis of the literature, shedding light on the potential of AI to revolutionize regenerative medicine.

2. AI in Regenerative Medicine

AI has become a crucial aspect in performing computational simulations and in silico studies in medical applications and offers several advantages, such as lower costs and faster results compared to other medical investigation approaches, such as clinical and laboratory methods [25,26,27]. Currently, multiple ongoing initiatives are aimed at incorporating AI into a wide range of fields, including but not limited to medicine, pharmaceuticals, and healthcare [28,29,30]. These projects aim to leverage the power of AI to enhance and streamline various processes, such as drug development, disease diagnosis, and medical treatment. By integrating AI, researchers and practitioners hope to achieve more accurate and efficient outcomes, ultimately improving the quality of life for individuals and communities [30,31]. To be more specific, deep learning can help accelerate the development of regenerative therapies by facilitating tasks such as analyzing large datasets of molecular and genetic data and identifying patterns and correlations that may be missed by human researchers. This can help researchers better understand the underlying disease mechanisms and develop more effective therapies to address them. Some of the most important scopes of regenerative medicine for which AI could be useful are discussed in this section.

2.1. Drug Discovery

There are a huge number of molecules in the chemical space, presenting both opportunities and challenges in drug discovery and development. In the context of regenerative medicine, drug discovery involves identifying molecules, biologics, or other therapeutic agents that can promote tissue regeneration and functional recovery. The development of drugs is limited by the lack of advanced technologies. Traditional drug development processes can be time-consuming and expensive, as they involve synthesizing and testing a large number of compounds to identify potential drug candidates. Another major concern in drug discovery is ensuring that the potential drug candidates are safe and effective [32]. To overcome these challenges, AI has emerged as a powerful tool that can analyze large datasets of chemical compounds to predict which treatments work best for certain illnesses. It has become possible to detect patterns and associations by analyzing chemical structures and properties, which can help identify potential drug candidates. This information can be used to prioritize compounds for further testing and development. AI can also assist in validating the drug target, which is the specific biological molecule or pathway a drug aims to interact with. By using AI, researchers can gain insights into the drug target’s function and potential effectiveness, saving time and resources. Additionally, it can predict the toxicity of potential drug candidates by analyzing their chemical structures and properties. This can help to identify potential safety concerns early in the drug discovery process, reducing the risk of adverse events. Moreover, AI can assist in designing new molecules that are optimized for specific therapeutic applications. Moreover, it can facilitate the identification of new molecules that are more likely to be effective treatments for particular diseases. While AI has the potential to enhance the drug discovery process significantly, researchers and clinicians must address challenges related to data quality, transparency, and regulatory issues. By addressing these challenges, they can continue to refine AI technologies and improve the efficiency and effectiveness of drug discovery. There are currently various AI tools used in different aspects of drug discovery and development, including drug design (e.g., target protein structure prediction, drug-protein interactions, and de novo drug design) and drug screening (e.g., prediction of physicochemical properties, bioactivity, and toxicity) [33,34]. Some of these tools are presented in Table 1.
Table 1. Some of the AI tools and platforms used in drug discovery.

2.2. Disease Modeling

Disease modeling involves creating in vitro models of diseases, which can be used to study the underlying mechanisms of the disease and test potential treatments. By employing disease modeling, researchers can gain a comprehensive understanding of disease pathology, identify new therapeutic targets, and gain insights into regenerative processes for restoring normal tissue function. Additionally, disease modeling can also be used to screen potential drugs and identify the most promising candidates for further development [43,44,45]. AI can help researchers analyze data generated from disease models and identify patterns and correlations that may not be immediately apparent. This can help identify new therapeutic targets and potential drug candidates for further development.
One of the key advantages of disease modeling is the ability to create personalized models of diseases using patient-specific cells. This allows researchers to study the disease in a more accurate and relevant context, as each model reflects the unique genetic and environmental factors that contribute to the condition in the patient [46,47]. AI can help identify biomarkers, genetic mutations, and other factors that contribute to the development and progression of diseases. This information can then be used to create more accurate disease models that can be used to identify potential treatments. Furthermore, these models can be used to test the efficacy of personalized treatments, such as gene- or cell-based therapies, which can be tailored to the individual patient’s needs. AI algorithms can be used to identify genetic variations that are associated with specific diseases, allowing researchers to develop personalized treatments based on an individual’s genetic profile. AI could also be considered in the development of gene therapies for rare genetic disorders.

2.3. Predictive Modeling

Predictive modeling involves using data to train machine/deep learning models to predict future outcomes based on unforeseen data. Its connection to regenerative medicine is rooted in their mutual goal of advancing personalized medicine and optimizing treatment strategies. Predictive modeling plays a crucial role by providing insights into diverse areas, such as predicting disease progression, identifying patients at risk of developing certain conditions, and optimizing treatment plans. Predictive modeling is a challenging task in healthcare due to the complexity of healthcare data and the large amounts of data involved [48,49]. AI offers high-accuracy predictive models for analyzing clinical and biological data to identify patterns and associations that can be used to predict future outcomes. Machine learning algorithms can identify factors that contribute to the development and progression of diseases. This information can then be used to create more accurate predictive models to identify patients at risk of developing certain conditions and optimize treatment plans. Additionally, AI allows the development of personalized predictive models by analyzing patient data, such as genomics, proteomics, and metabolomics. It helps identify individual disease process differences that can be used to create personalized predictive models. This information is then used to develop personalized treatment plans tailored to individual patients’ specific needs. Furthermore, AI can identify possibilities for creating new medicines by studying biological data. It can uncover targets and paths linked to particular diseases, enabling the development of drugs that aim for these paths and enhance the effectiveness of existing ones.

2.4. Personalized Medicine

Personalized medicine aims to provide tailored medical treatments to individual patients based on their genetic, environmental, and lifestyle factors. However, accurately predicting a patient’s response to a particular treatment remains a significant challenge due to the system’s complexity [50,51]. AI can help overcome this challenge by analyzing patient information and identifying patterns and associations that can predict treatment outcomes. One way AI can assist in personalized medicine is by analyzing a patient’s genomic data. AI algorithms can identify genetic variations linked to specific diseases or treatment responses, enabling the development of personalized treatment plans based on the patient’s genetic profile. Another way AI can help is by analyzing patient health data, including electronic medical records, imaging data, and patient-reported outcomes. This data can reveal patterns and associations that predict treatment outcomes and inform personalized treatment plans. For instance, AI algorithms can identify patients most likely to benefit from a specific treatment or predict which patients may experience adverse reactions to a treatment. AI can also develop personalized treatment plans based on patient preferences and values. Analyzing patient-reported outcomes and other data can identify treatment options that align with the patient’s values and preferences. AI has the potential to enhance the effectiveness of personalized medicine significantly, providing new tools and insights for clinicians and researchers. However, issues related to data privacy, bias, and regulatory challenges still must be addressed. By working to overcome these challenges, researchers and clinicians can refine AI technologies and improve patient care quality.

2.5. Tissue Engineering

Tissue engineering is an interdisciplinary field that integrates principles of engineering, biology, and medicine to develop novel approaches to repair, replace, or regenerate tissues and organs. This field has emerged as a promising alternative to traditional approaches [52]. However, it faces significant challenges, as summarized in Table 2.
Table 2. Tissue engineering challenges [22].
To tackle these challenges, AI has emerged as a powerful tool that analyzes the physicochemical and biological properties of a wide range of materials to predict the most successful outcomes. AI algorithms can identify patterns and associations in cellular behavior and interactions, thereby enabling the prediction of cell behavior in different environments. This information is crucial in designing and optimizing tissue engineering strategies to develop functional organs and tissues.
Scaffolds are one of the key components of tissue engineering, as they provide a structure for cells to grow and form new tissue. The success of tissue engineering approaches depends largely on their ability to create effective scaffolds that can support the growth and differentiation of cells into functional tissue [53]. Scaffolds can be made from a variety of materials, such as ceramics, synthetic polymers, and natural biopolymers, and can be designed to mimic the properties of natural tissue [54]. AI can optimize material properties for specific applications by analyzing their properties and interactions with biological systems. This information can then be utilized to design and develop scaffolds for specific tissue engineering applications. Scaffolds can be fabricated using a variety of techniques, depending on the type of material being used and the desired properties of the scaffold [55]. AI can play a significant role in choosing an efficient and effective scaffold fabrication method for the intended application. AI algorithms can analyze large amounts of data on different materials and fabrication techniques to identify suitable combinations for a specific tissue engineering application. These algorithms can also simulate the fabrication process and predict the properties of the resulting scaffold, which can help researchers optimize the design and reduce the time and cost of the fabrication process. Additionally, AI can assist in quality control by monitoring the fabrication process in real-time and detecting any deviations from the desired parameters. This can help in ensuring that the scaffold is fabricated according to the desired specifications and quality.

2.6. Cell Therapy

Cell therapy is a promising field in regenerative medicine that involves the use of living cells to replace or repair damaged or diseased tissues and organs. It is based on the concept that cells have the ability to regenerate and differentiate, which makes them ideal candidates for repairing damaged tissues and organs [56]. Cell therapy can potentially revolutionize the treatment of many chronic diseases and injuries that currently have limited or no treatment options [57,58]. One of the most promising areas of cell therapy is the use of stem cells. Stem cells are undifferentiated cells that have the ability to differentiate into different cell types [59]. They can be obtained from various sources, including embryonic tissue, adult tissue, and umbilical cord blood [60]. While cell therapy has shown promising results in clinical trials, it still faces significant challenges in identifying suitable cells, ensuring their safety, and optimizing their effectiveness [61,62]. This is where AI comes in. AI has the potential to revolutionize cell therapy by enabling researchers to analyze vast amounts of data and develop new insights into how cells work. One of the key benefits of using AI in cell therapy is its ability to help identify the best cells for a particular patient. By analyzing a patient’s genetic information and medical history, AI algorithms can predict which cells will most likely be effective in treating their condition. AI can also help researchers identify the optimal conditions for growing cells. In cell therapy, the delivery of cells to the target site is a critical step that can significantly impact the success of the treatment. AI can help improve the delivery of cells by optimizing the route of administration and ensuring the cells reach the target site effectively. AI can also help determine the optimal dose and timing of cell delivery to maximize therapeutic benefits. Additionally, it can assist in tracking the cells after delivery, monitoring their migration and survival, and detecting any adverse effects. This can aid in adjusting the treatment plan and improving patient outcomes. Despite its potential benefits, there are also limitations to the use of AI in cell therapy. One major limitation is the quality and quantity of available data. AI algorithms require large amounts of high-quality data to accurately predict outcomes. However, in the field of cell therapy, patient data are often limited and heterogeneous, making it challenging to train AI models effectively. AI models are only as good as the data they are trained on, and there may be biases or inconsistencies in the data that can affect the accuracy of AI predictions. Another limitation is the complexity of biological systems. Cell therapy involves excessively intricate interactions between cells and tissues, making the analysis difficult for many of the machine and deep learning algorithms to model them accurately.

2.7. Clinical Trial Design

Clinical trial design plays a crucial role in the field of regenerative medicine, as it enables the evaluation of drugs and novel regenerative therapies in terms of their safety and efficacy. Nonetheless, designing clinical trials can be convoluted and time-consuming, with multiple variables to consider, including patient selection, study endpoints, and statistical analysis [63,64]. In this context, AI has emerged as a powerful tool to address these challenges and enhance the accuracy and efficiency of clinical trial design. AI can assist in clinical trials by identifying patients most likely to respond to new treatments. By analyzing datasets of clinical and biological data, AI algorithms can identify biomarkers, genetic mutations, and other factors associated with treatment response, leading to the identification of patient populations that are most likely to benefit from new treatments. This reduces the number of patients needed to achieve statistically significant results, improving the efficiency of clinical trials. AI can also improve the selection of study endpoints by analyzing datasets of clinical trial data to identify endpoints that are more sensitive and specific than traditional endpoints. This ensures clinical trials measure clinically relevant outcomes and provide more meaningful results. Additionally, AI can improve the statistical analysis of clinical trial data by using machine learning algorithms to analyze and interpret complex datasets. This can help to identify patterns and insights that may not be immediately apparent to human analysts, improving the accuracy and efficiency of statistical analysis.

2.8. Patient Monitoring

Patient monitoring is not only essential for assessing the effectiveness, safety, and progress of treatments but also crucial for the identification and management of potential complications. This ensures optimal outcomes through timely interventions and optimized treatment outcomes [65,66]. However, patient monitoring can be complex and time-consuming due to the large amounts of data that must be analyzed and interpreted. This is where AI can significantly help by analyzing large datasets of patient data to identify patterns and anomalies that may indicate a change in patient health. By using machine learning algorithms to analyze data from wearable devices, electronic health records, and other sources, AI can identify changes in patient health that may not be immediately apparent to healthcare providers. This information can then be used to alert healthcare providers to potential problems and enable them to take proactive measures to prevent complications by using AI-generated solutions. Additionally, AI can provide real-time insights into patient health by using natural language processing and other AI technologies. For example, AI algorithms can analyze patient data to identify trends and patterns indicating a need for medication adjustments, lifestyle changes, or other interventions. AI can also improve the accuracy and efficiency of patient monitoring by automating routine tasks such as data entry and analysis, enabling healthcare providers to focus on more complex tasks and enhance the quality of patient care. Furthermore, AI can reduce the time and cost associated with patient monitoring by enabling healthcare providers to monitor more patients simultaneously and identify potential problems earlier.

2.9. Patient Education

Patient education is essential to healthcare, as it enables patients to be actively involved in their health and make informed decisions [67]. However, patient education can be challenging due to the diverse backgrounds, preferences, and levels of health literacy among patients [68]. AI can improve patient education by addressing these challenges. Generative language models such as ChatGPT [69] can help by providing personalized education materials tailored to individual patients’ specific needs and preferences. In this regard, AI algorithms can identify differences in education needs and preferences and generate personalized education materials such as videos, infographics, and interactive tools. AI technologies can also improve the accessibility and usability of educational materials by using natural language processing to present materials in plain language in visually appealing and engaging ways. AI can also identify gaps in patient education and improve education interventions. By analyzing patient outcomes and behavior data, AI algorithms can provide insights into improving education interventions and identify areas where education is lacking or ineffective. Therefore, AI has the potential to improve the effectiveness and efficiency of patient education significantly. However, challenges such as data privacy, ethics, and trust need to be addressed. Researchers and healthcare providers need to work together to refine AI technologies and ensure they are used ethically and in a way that builds patient trust.

2.10. Regulatory Compliance

Regulatory compliance refers to ensuring that an organization or individual complies with the laws, regulations, and standards that apply to their industry or field. Regulatory compliance is particularly crucial in the complex and rapidly evolving field of regenerative medicine. In this regard, AI can improve data collection and analysis by utilizing machine learning algorithms to identify patterns and insights that may be difficult for human analysts to detect. This information can then be used to ensure products and therapies comply with regulatory standards. Additionally, the transparency and traceability of data and processes can be enhanced through blockchain technology and AI-powered tools. This enables tracking the entire lifecycle of products or therapies, from development to patient outcomes, ensuring transparency and the availability of relevant data for analysis and review. Furthermore, personalized treatments can be developed by using AI algorithms to tailor treatments to the specific needs and characteristics of individual patients. This reduces the risk of adverse events and ensures compliance with regulatory standards. While AI has the potential to significantly improve regulatory compliance in regenerative medicine, challenges such as data privacy, ethics, and regulatory oversight need to be addressed. By addressing these challenges, researchers and clinicians can continue to refine and develop AI technologies to enhance the safety and efficacy of products and therapies.

4. Considerations for AI Applications in Regenerative Medicine

Although AI has offered many advantages to regenerative medicine and opened up new research opportunities, it is also accompanied by certain considerations and challenges. The notable ones are listed below.

4.1. Trustworthiness

Probably the most important consideration in medicine is trustworthiness [128], which refers to the validity and reliability of a model. The trustworthiness of AI is closely related to the interpretability of the model and deals with the answer to this question: “How can people trust the AI-generated information when the result is not interpretable?” An example of an interpretable model is a decision tree [129], shown in Figure 2. The top node of the tree represents the entire dataset. It is the starting point for the decision-making process. Internal nodes represent features or attributes from the dataset. Each internal node makes a decision based on a specific feature. The branches that connect nodes represent the decision outcomes or choices based on the feature’s values. Finally, at the lowest level, the leaf nodes are the endpoints of the decision tree. They provide the final output, which can be a class label (for classification problems) or a numerical value (for regression problems). A decision tree algorithm builds such a tree based on the existing data. Once the tree is created, the unforeseen data could be checked against it and decided for the category or the value that should be assigned. In the example of Figure 2, the decision tree algorithm gets the available data of persons A and B and builds the model tree, which can identify the status of unforeseen person C. In terms of interpretability, the decision tree identifies person C as unfit, and the reason for such a classification is that “age < 40” and “eats a lot”. However, this is not the case with Figure 3, where a Multi-Layer Perceptron Neural Network is shown [130]. An MLP consists of many small computational units with an activation function that determines their output. To use the MLP, it should first be trained with the available data. Each data record runs through the network, and each neuron tunes itself so that the network’s final output converges to the right answer. At the end of the training phase, the MLP would be a collection of tuned neurons that were able to classify the unforeseen data. However, in terms of interpretability, it is usually impossible to look at an MLP and understand why it might label a person as fit or unfit since the network might have thousands of neurons organized in several layers. Indeed, many machine learning and deep learning models are like a black box, containing such a large amount of information that they are excessively difficult, if not impossible, to interpret.
Figure 2. Decision tree (interpretable).
Figure 3. Multi-Layer Perceptron (not interpretable).
Some ways to address the interpretability issue include developing simplified models using techniques such as knowledge distillation [131]. Such models retain high performance while also being more interpretable. Another method uses algorithms such as SHAP (SHapley Additive exPlanations) values [132]. These values can indicate the impact of each feature on a model’s prediction, making it easier to understand how different features contribute to the overall result. Additionally, researchers are creating visuals such as Confusion Matrices and Calibration Plots that help scientists explore model decisions. These tools provide visualization of feature importance and relationships, allowing for a better understanding of the factors influencing the model’s output.
Another consideration relevant to trustworthiness is data quality. High-quality and diverse datasets are essential for training effective AI models. Many of the models can inherit biases present in the data used for training. Hence, the result of the model would be negatively affected. Ensuring fairness and mitigating bias in AI algorithms is a significant challenge to avoiding discrimination in decision-making. In some areas of regenerative medicine, obtaining clean and well-distributed data might be difficult, and consequently, the AI results might become invalid.

4.2. Model Application

Not all the models are appropriate for all problems. Selecting a model depends on factors such as the problem’s nature, the data’s size and quality, interpretability requirements, computational resources, and so on. A problem might be of the classification, regression, or clustering type. Moreover, in a different taxonomy, either of the following types of models might be appropriate for a problem:
  • Supervised models: the algorithms learn from labeled data, where the input data are paired with corresponding target or output values. The goal is to predict these target values for new, unseen data. A few examples of supervised models are linear [133] and logistic regressions [134], decision trees [129], random forests [135], support vector machines [136], Convolutional Neural Networks [137], and Recurrent Neural Networks [138]. Some examples, such as linear regression, could be used for classification (finding the category of the data) and regression (finding the numerical value of the data), and some are specific to classification or regression.
  • Unsupervised models: the algorithms work with unlabeled data, seeking to discover patterns, structures, or relationships within the data without explicit guidance on what to look for. They are also known as clustering algorithms. A few examples of unsupervised models are K-Means [139], Hierarchical Clustering [140], and Generative Adversarial Networks [141].
  • Reinforcement learning: an agent learns to make decisions by interacting with an environment. It receives feedback in the form of rewards or penalties based on its actions to maximize cumulative rewards over time. The most well-known example of this category is Q-Learning [142], which is used in tasks such as tic-tac-toe game playing and simple robot control.
Moreover, a specific model is not guaranteed to be better than others. Choosing a model depends on various parameters, as mentioned before. However, algorithm selection is often an iterative process that needs refining as more insights from experiments and data analysis are obtained.

4.3. Multidisciplinary Collaboration

Building an AI system necessitates a solid foundation of technical knowledge. AI, with its complex algorithms, intricate neural networks, and extensive data manipulation, demands a deep understanding of computer science, mathematics, and programming languages. Proficiency in machine learning frameworks, such as TensorFlow [143] or PyTorch [144], and expertise in data preprocessing, feature engineering, and model selection are vital. Additionally, a grasp of software engineering principles is crucial for developing scalable, efficient, and maintainable AI solutions. Demanding a broad range of technical expertise promoted multidisciplinary collaboration. A real-world example of such collaboration is Japan’s national strategy for developing AI technology in the medical field. An early challenge for Japan was having relatively few AI experts compared to countries such as the US and China. To address talent shortages, Japan launched the AI Technology Strategy Council in 2016 to make AI a focus of its Society 5.0 national strategy. The strategy emphasizes using AI to boost productivity, healthcare, and mobility. Japan aims to capitalize on aggregating its population of 125 million citizens’ health data through laws and infrastructure to create one of the largest centralized medical data repositories. The government and private sector in Japan are collaborating to develop AI-enhanced hospitals, make AI/data science courses mandatory in universities, particularly for healthcare students, and provide online medical AI education resources. This aims to cultivate expertise while leveraging Japan’s universal healthcare system and large volumes of standardized health data to lead in medical AI [145]. In this regard, researchers have made progress in recent years. For example, researchers from Osaka University, JST PRESTO, the University of Tokyo, and RIKEN have developed a deep neural network called “MNet” that can classify multiple neurological diseases using resting-state MEG signals with high specificity. This technology has the potential to improve neurological diagnoses and reduce the burden on clinicians in critical care [146]. In the field of oncology, the University of Tokyo, Shimadzu Corporation, and Juntendo University have developed a predictive model that significantly reduces misclassification rates of diseases compared to using a single tumor marker [147]. Additionally, institutes from Japan, Germany, the US, and Chile have collaborated to enhance the classification of breast tumors using subtle differences in the nuclei of microenvironmental myoepithelial cells [148].
It is important to note that regulations require human supervision of AI used for clinical decision support. In addition, challenges such as data privacy, multi-sector collaboration, and developing a robust medical AI workforce should be addressed by bringing together clinicians and data scientists (Figure 4) [145].
Figure 4. An example of a clinical diagnostic database aimed at promoting the development of supplementary AI tools in healthcare. Reprinted from [145].

5. Conclusions and Future Perspective

In conclusion, AI has tremendous potential to revolutionize and accelerate the development of therapies in regenerative medicine. From enhancing drug discovery to optimizing tissue engineering and cellular therapies, AI can provide insights by analyzing vast molecular and genomic datasets that would be impossible for humans to perceive. While AI shows promise to advance regenerative medicine research and development, there are significant technical challenges that must be addressed before these technologies can be widely adopted. One of the significant limitations is the lack of large, high-quality datasets needed to train sophisticated machine-learning models. Regenerative medicine involves complex biological interactions that are difficult to fully capture in data.
Additionally, developing accurate computational models that can simulate and predict cell behavior over time poses immense technical challenges due to our still-limited understanding of cellular and molecular pathways. Validating AI systems and gaining regulatory approval also requires extensive clinical testing, which takes considerable time and resources. Addressing concerns around data privacy, security, and bias and ensuring fair and equitable access to new tools is equally important. Moreover, obtaining clinician buy-in for technologies promising more effective personalized care will require overcoming adoption hurdles. Substantial ongoing research is still needed to overcome these limitations and translate AIs theoretical potential in regenerative medicine into real-world solutions that tangibly improve patient outcomes. Researchers, policymakers, healthcare providers, and AI developers must work together to develop appropriate safeguards, oversight mechanisms, and guidelines for using AI in regenerative medicine. As AI technologies continue to improve and more high-quality data becomes available, the opportunity for refining and customizing AI algorithms specifically for regenerative medicine purposes will increase.
Moving forward, further innovations in areas such as machine learning, natural language processing, computer vision, and robotics have the potential to uncover new insights that could revolutionize how regenerative therapies are developed and delivered. Combining AI with other emerging technologies such as nanotechnology, genome editing, and 3D bioprinting may lead to unprecedented advances in creating personalized regenerative solutions. With the appropriate ethical framework and governance structures in place, the future of AI-driven regenerative medicine seems promising. However, progress will depend on maintaining a human-centric approach that utilizes AI capabilities to serve the best interests of patients and society. Through multidisciplinary collaborations and responsible development and use of these technologies, we may one day realize the full potential of AI to usher in a new era of customized and effective regenerative therapies.

Summary of the Key Points

  • AI can help accelerate drug discovery by analyzing large datasets to identify promising drug candidates and optimize drug properties.
  • AI-enabled disease modeling can provide insights into disease mechanisms and aid in the identification of new therapeutic targets.
  • AI can improve predictive modeling to identify patients who may benefit from regenerative therapies and optimize treatment plans.
  • AI can enable the development of personalized medicine approaches based on a patient’s genetic and health data.
  • AI can optimize materials and fabrication methods for tissue engineering applications.
  • AI can assist in identifying the most suitable cell types for cell therapies and optimizing cell delivery and monitoring.
  • AI can enhance the efficiency and accuracy of clinical trial design.
  • AI can be used to monitor patients in real-time to detect changes and risks early.
  • AI can provide personalized patient education materials tailored to individual needs and preferences.
  • AI can improve regulatory compliance through enhanced data analysis, traceability, and transparency.
  • AI also has roles in related fields such as immunotherapy, genetic engineering, nanotechnology, and microfluidics, which can further advance regenerative medicine.
In summary, AI has the potential to significantly enhance various aspects of regenerative medicine research and development through analyzing large and complex datasets, identifying patterns and trends, and making accurate predictions to optimize processes and therapies. However, challenges related to ethics, data quality, and regulation must be addressed to ensure the safe and effective use of AI in regenerative medicine.

Author Contributions

The authors have contributed equally to this work. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Data Availability Statement

No data were used for the research described in the article.

Acknowledgments

ChatGPT is acknowledged as making some contribution to the writing of this paper. After using this tool, the authors reviewed and edited the content as needed.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Bays, H.E.; Fitch, A.; Cuda, S.; Gonsahn-Bollie, S.; Rickey, E.; Hablutzel, J.; Coy, R.; Censani, M. Artificial intelligence and obesity management: An Obesity Medicine Association (OMA) Clinical Practice Statement (CPS) 2023. Obes. Pillars 2023, 6, 100065. [Google Scholar] [CrossRef]
  2. Nelson, S.D.; Walsh, C.G.; Olsen, C.A.; McLaughlin, A.J.; LeGrand, J.R.; Schutz, N.; Lasko, T.A. Demystifying artificial intelligence in pharmacy. Am. J. Health-Syst. Pharm. 2020, 77, 1556–1570. [Google Scholar] [CrossRef] [PubMed]
  3. Kaul, V.; Enslin, S.; Gross, S.A. History of artificial intelligence in medicine. Gastrointest. Endosc. 2020, 92, 807–812. [Google Scholar] [CrossRef] [PubMed]
  4. Lauriola, I.; Lavelli, A.; Aiolli, F. An introduction to Deep Learning in Natural Language Processing: Models, techniques, and tools. Neurocomputing 2022, 470, 443–456. [Google Scholar] [CrossRef]
  5. Alam, A. Possibilities and apprehensions in the landscape of artificial intelligence in education. In Proceedings of the 2021 International Conference on Computational Intelligence and Computing Applications (ICCICA), Maharashtra, India, 26–27 November 2021; pp. 1–8. [Google Scholar]
  6. Trappey, A.J.C.; Trappey, C.V.; Wu, J.-L.; Wang, J.W.C. Intelligent compilation of patent summaries using machine learning and natural language processing techniques. Adv. Eng. Inform. 2020, 43, 101027. [Google Scholar] [CrossRef]
  7. Liu, L.; Wang, Y.; Chi, W. Image Recognition Technology Based on Machine Learning. IEEE Access 2020, 1. [Google Scholar] [CrossRef]
  8. Qayyum, A.; Usama, M.; Qadir, J.; Al-Fuqaha, A. Securing Connected & Autonomous Vehicles: Challenges Posed by Adversarial Machine Learning and the Way Forward. IEEE Commun. Surv. Tutor. 2020, 22, 998–1026. [Google Scholar] [CrossRef]
  9. Strzelecki, M.; Badura, P. Machine Learning for Biomedical Application. Appl. Sci. 2022, 12, 2022. [Google Scholar] [CrossRef]
  10. Sakshi; Das, P.; Jain, S.; Sharma, C.; Kukreja, V. Deep Learning: An Application Perspective. In Cyber Intelligence and Information Retrieval; Springer: Singapore, 2022; pp. 323–333. [Google Scholar]
  11. Asmika, B.; Mounika, G.; Rani, P.S. Deep learning for vision and decision making in self driving cars-challenges with ethical decision making. In Proceedings of the 2021 International Conference on Intelligent Technologies (CONIT), Hubli, India, 25–27 June 2021; pp. 1–5. [Google Scholar]
  12. Mandalapu, V.; Elluri, L.; Vyas, P.; Roy, N. Crime Prediction Using Machine Learning and Deep Learning: A Systematic Review and Future Directions. IEEE Access 2023, 11, 60153–60170. [Google Scholar] [CrossRef]
  13. Taye, M.M. Understanding of Machine Learning with Deep Learning: Architectures, Workflow, Applications and Future Directions. Computers 2023, 12, 91. [Google Scholar] [CrossRef]
  14. Wan, K.W.; Wong, C.H.; Ip, H.F.; Fan, D.; Yuen, P.L.; Fong, H.Y.; Ying, M. Evaluation of the performance of traditional machine learning algorithms, convolutional neural network and AutoML Vision in ultrasound breast lesions classification: A comparative study. Quant. Imaging Med. Surg. 2021, 11, 1381–1393. [Google Scholar] [CrossRef]
  15. Kaur, G.; Adhikari, N.; Krishnapriya, S.; Wawale, S.G.; Malik, R.Q.; Zamani, A.S.; Perez-Falcon, J.; Osei-Owusu, J. Recent Advancements in Deep Learning Frameworks for Precision Fish Farming Opportunities, Challenges, and Applications. J. Food Qual. 2023, 2023, 4399512. [Google Scholar] [CrossRef]
  16. Graves, A. (Ed.) Long short-term memory. In Supervised Sequence Labelling with Recurrent Neural Networks; Springer: Berlin/Heidelberg, Germany, 2012; pp. 37–45. [Google Scholar] [CrossRef]
  17. Medsker, L.; Jain, L.C. Recurrent Neural Networks: Design and Applications; CRC Press: Boca Raton, FL, USA, 1999. [Google Scholar]
  18. Hongen, C.; Zhenyuan, L.; Weinan, Z. The comparison of traditional machine learning and deep learning methods for malicious website detection. In Proceedings of the International Conference on Electronic Information Engineering and Computer Technology (EIECT 2021), Chiang Mai, Thailand, 14–15 October 2021; p. 120871G. [Google Scholar]
  19. Yang, X.; Zhang, S.; Liu, J.; Gao, Q.; Dong, S.; Zhou, C. Deep learning for smart fish farming: Applications, opportunities and challenges. Rev. Aquac. 2021, 13, 66–90. [Google Scholar] [CrossRef]
  20. de Antonio, M.; Timothy, J.W.D.; James Philip, H.; O’Regan, D.P. Artificial intelligence and the cardiologist: What you need to know for 2020. Heart 2020, 106, 399. [Google Scholar] [CrossRef]
  21. Altyar, A.E.; El-Sayed, A.; Abdeen, A.; Piscopo, M.; Mousa, S.A.; Najda, A.; Abdel-Daim, M.M. Future regenerative medicine developments and their therapeutic applications. Biomed. Pharmacother. 2023, 158, 114131. [Google Scholar] [CrossRef]
  22. Nosrati, H.; Aramideh Khouy, R.; Nosrati, A.; Khodaei, M.; Banitalebi-Dehkordi, M.; Ashrafi-Dehkordi, K.; Sanami, S.; Alizadeh, Z. Nanocomposite scaffolds for accelerating chronic wound healing by enhancing angiogenesis. J. Nanobiotechnol. 2021, 19, 1. [Google Scholar] [CrossRef]
  23. Rajabzadeh, N.; Fathi, E.; Farahzadi, R. Stem cell-based regenerative medicine. Stem Cell Investig. 2019, 6, 19. [Google Scholar] [CrossRef] [PubMed]
  24. Zhong, F.; Jiang, Y. Endogenous Pancreatic β Cell Regeneration: A Potential Strategy for the Recovery of β Cell Deficiency in Diabetes. Front. Endocrinol. 2019, 10, 101. [Google Scholar] [CrossRef]
  25. Tauviqirrahman, M.; Ammarullah, M.I.; Jamari, J.; Saputra, E.; Winarni, T.I.; Kurniawan, F.D.; Shiddiq, S.A.; van der Heide, E. Analysis of contact pressure in a 3D model of dual-mobility hip joint prosthesis under a gait cycle. Sci. Rep. 2023, 13, 3564. [Google Scholar] [CrossRef] [PubMed]
  26. Salaha, Z.F.; Ammarullah, M.I.; Abdullah, N.N.; Aziz, A.U.; Gan, H.-S.; Abdullah, A.H.; Abdul Kadir, M.R.; Ramlee, M.H. Biomechanical Effects of the Porous Structure of Gyroid and Voronoi Hip Implants: A Finite Element Analysis Using an Experimentally Validated Model. Materials 2023, 16, 3298. [Google Scholar] [CrossRef]
  27. Ammarullah, M.I.; Hartono, R.; Supriyono, T.; Santoso, G.; Sugiharto, S.; Permana, M.S. Polycrystalline Diamond as a Potential Material for the Hard-on-Hard Bearing of Total Hip Prosthesis: Von Mises Stress Analysis. Biomedicines 2023, 11, 951. [Google Scholar] [CrossRef]
  28. Thakur, A.; Mishra, A.P.; Panda, B.; Rodríguez, D.C.S.; Gaurav, I.; Majhi, B. Application of Artificial Intelligence in Pharmaceutical and Biomedical Studies. Curr. Pharm. Des. 2020, 26, 3569–3578. [Google Scholar] [CrossRef] [PubMed]
  29. Mak, K.-K.; Pichika, M.R. Artificial intelligence in drug development: Present status and future prospects. Drug Discov. Today 2019, 24, 773–780. [Google Scholar] [CrossRef] [PubMed]
  30. Hamet, P.; Tremblay, J. Artificial intelligence in medicine. Metabolism 2017, 69, S36–S40. [Google Scholar] [CrossRef] [PubMed]
  31. Nsugbe, E. An artificial intelligence-based decision support system for early diagnosis of polycystic ovaries syndrome. Healthc. Anal. 2023, 3, 100164. [Google Scholar] [CrossRef]
  32. Kraljevic, S.; Stambrook, P.J.; Pavelic, K. Accelerating drug discovery. EMBO Rep. 2004, 5, 837–842. [Google Scholar] [CrossRef] [PubMed]
  33. Paul, D.; Sanap, G.; Shenoy, S.; Kalyane, D.; Kalia, K.; Tekade, R.K. Artificial intelligence in drug discovery and development. Drug Discov. Today 2021, 26, 80–93. [Google Scholar] [CrossRef] [PubMed]
  34. Jiménez-Luna, J.; Grisoni, F.; Weskamp, N.; Schneider, G. Artificial intelligence in drug discovery: Recent advances and future perspectives. Expert Opin. Drug Discov. 2021, 16, 949–959. [Google Scholar] [CrossRef] [PubMed]
  35. Korshunova, M.; Ginsburg, B.; Tropsha, A.; Isayev, O. OpenChem: A Deep Learning Toolkit for Computational Chemistry and Drug Design. J. Chem. Inf. Model. 2021, 61, 7–13. [Google Scholar] [CrossRef] [PubMed]
  36. Dobariya, A.; Vaghela, V. Artificial intelligence in drug discovery and development: Current status and future perspectives. Drug Discov. Today 2023, 26, 80. [Google Scholar]
  37. Varadi, M.; Anyango, S.; Deshpande, M.; Nair, S.; Natassia, C.; Yordanova, G.; Yuan, D.; Stroe, O.; Wood, G.; Laydon, A.; et al. AlphaFold Protein Structure Database: Massively expanding the structural coverage of protein-sequence space with high-accuracy models. Nucleic Acids Res. 2022, 50, D439–D444. [Google Scholar] [CrossRef]
  38. David, A.; Islam, S.; Tankhilevich, E.; Sternberg, M.J.E. The AlphaFold Database of Protein Structures: A Biologist’s Guide. J. Mol. Biol. 2022, 434, 167336. [Google Scholar] [CrossRef]
  39. Gromski, P.S.; Granda, J.M.; Cronin, L. Universal Chemical Synthesis and Discovery with ‘The Chemputer’. Trends Chem. 2020, 2, 4–12. [Google Scholar] [CrossRef]
  40. Duvenaud, D.K.; Maclaurin, D.; Iparraguirre, J.; Bombarell, R.; Hirzel, T.; Aspuru-Guzik, A.; Adams, R.P. Convolutional networks on graphs for learning molecular fingerprints. In Proceedings of the Conference on Neural Information Processing Systems, Montreal, QC, Canada, 7–10 December 2015; Volume 28. [Google Scholar]
  41. Mayr, A.; Klambauer, G.; Unterthiner, T.; Hochreiter, S. DeepTox: Toxicity Prediction using Deep Learning. Front. Environ. Sci. 2016, 3, 80. [Google Scholar] [CrossRef]
  42. Wallach, I.; Dzamba, M.; Heifets, A. AtomNet: A deep convolutional neural network for bioactivity prediction in structure-based drug discovery. arXiv 2015, arXiv:1510.02855. [Google Scholar]
  43. Kawaguchi, N.; Nakanishi, T. Animal Disease Models and Patient-iPS-Cell-Derived In Vitro Disease Models for Cardiovascular Biology—How Close to Disease? Biology 2023, 12, 468. [Google Scholar] [CrossRef] [PubMed]
  44. Hasan, M.F. Self-Organization in 3D Neuronal Constructs In Vitro; Lehigh University: Bethlehem, PA, USA, 2020. [Google Scholar]
  45. Chaudhary, S.; Chakraborty, E. Hydrogel based tissue engineering and its future applications in personalized disease modeling and regenerative therapy. Beni-Suef Univ. J. Basic Appl. Sci. 2022, 11, 3. [Google Scholar] [CrossRef]
  46. Nero, C.; Vizzielli, G.; Lorusso, D.; Cesari, E.; Daniele, G.; Loverro, M.; Scambia, G.; Sette, C. Patient-derived organoids and high grade serous ovarian cancer: From disease modeling to personalized medicine. J. Exp. Clin. Cancer Res. 2021, 40, 116. [Google Scholar] [CrossRef] [PubMed]
  47. Vatine, G.D.; Barrile, R.; Workman, M.J.; Sances, S.; Barriga, B.K.; Rahnama, M.; Barthakur, S.; Kasendra, M.; Lucchesi, C.; Kerns, J.; et al. Human iPSC-Derived Blood-Brain Barrier Chips Enable Disease Modeling and Personalized Medicine Applications. Cell Stem Cell 2019, 24, 995–1005.e1006. [Google Scholar] [CrossRef]
  48. Toma, M.; Wei, O.C. Predictive Modeling in Medicine. Encyclopedia 2023, 3, 590–601. [Google Scholar] [CrossRef]
  49. Yang, C.C. Explainable Artificial Intelligence for Predictive Modeling in Healthcare. J. Healthc. Inform. Res. 2022, 6, 228–239. [Google Scholar] [CrossRef]
  50. Mathur, S.; Sutton, J. Personalized medicine could transform healthcare. Biomed. Rep. 2017, 7, 3–5. [Google Scholar] [CrossRef] [PubMed]
  51. Goetz, L.H.; Schork, N.J. Personalized medicine: Motivation, challenges, and progress. Fertil. Steril. 2018, 109, 952–963. [Google Scholar] [CrossRef]
  52. Reis, R.L. Encyclopedia of Tissue Engineering and Regenerative Medicine; Academic Press: Cambridge, MA, USA, 2019. [Google Scholar]
  53. Chan, B.P.; Leong, K.W. Scaffolding in tissue engineering: General approaches and tissue-specific considerations. Eur. Spine J. 2008, 17 (Suppl. S4), 467–479. [Google Scholar] [CrossRef] [PubMed]
  54. O’Brien, F.J. Biomaterials & scaffolds for tissue engineering. Mater. Today 2011, 14, 88–95. [Google Scholar] [CrossRef]
  55. Haider, A.; Haider, S.; Rao Kummara, M.; Kamal, T.; Alghyamah, A.-A.A.; Jan Iftikhar, F.; Bano, B.; Khan, N.; Amjid Afridi, M.; Soo Han, S.; et al. Advances in the scaffolds fabrication techniques using biocompatible polymers and their biomedical application: A technical and statistical review. J. Saudi Chem. Soc. 2020, 24, 186–215. [Google Scholar] [CrossRef]
  56. Gonçalves, A.I.; Costa-Almeida, R.; Gershovich, P.; Rodrigues, M.T.; Reis, R.L.; Gomes, M.E. Chapter 6—Cell-based approaches for tendon regeneration. In Tendon Regeneration; Gomes, M.E., Reis, R.L., Rodrigues, M.T., Eds.; Academic Press: Boston, MA, USA, 2015; pp. 187–203. [Google Scholar] [CrossRef]
  57. Farini, A.; Sitzia, C.; Erratico, S.; Meregalli, M.; Torrente, Y. Clinical Applications of Mesenchymal Stem Cells in Chronic Diseases. Stem Cells Int. 2014, 2014, 306573. [Google Scholar] [CrossRef]
  58. Davatchi, F.; Abdollahi, B.S.; Mohyeddin, M.; Shahram, F.; Nikbin, B. Mesenchymal stem cell therapy for knee osteoarthritis. Preliminary report of four patients. Int. J. Rheum. Dis. 2011, 14, 211–215. [Google Scholar] [CrossRef]
  59. Kolios, G.; Moodley, Y. Introduction to Stem Cells and Regenerative Medicine. Respiration 2012, 85, 3–10. [Google Scholar] [CrossRef]
  60. Nosrati, H.; Alizadeh, Z.; Nosrati, A.; Ashrafi-Dehkordi, K.; Banitalebi-Dehkordi, M.; Sanami, S.; Khodaei, M. Stem cell-based therapeutic strategies for corneal epithelium regeneration. Tissue Cell 2021, 68, 101470. [Google Scholar] [CrossRef]
  61. Loo, S.J.Q.; Wong, N.K. Advantages and challenges of stem cell therapy for osteoarthritis. Biomed. Rep. 2021, 15, 1–12. [Google Scholar]
  62. Munir, H.; McGettrick, H.M. Mesenchymal Stem Cell Therapy for Autoimmune Disease: Risks and Rewards. Stem Cells Dev. 2015, 24, 2091–2100. [Google Scholar] [CrossRef] [PubMed]
  63. Spreafico, A.; Hansen, A.R.; Abdul Razak, A.R.; Bedard, P.L.; Siu, L.L. The Future of Clinical Trial Design in Oncology. Cancer Discov. 2021, 11, 822–837. [Google Scholar] [CrossRef]
  64. Wildiers, H.; Mauer, M.; Pallis, A.; Hurria, A.; Mohile, S.G.; Luciani, A.; Curigliano, G.; Extermann, M.; Lichtman, S.M.; Ballman, K. End points and trial design in geriatric oncology research: A joint European organisation for research and treatment of cancer–Alliance for Clinical Trials in Oncology–International Society of Geriatric Oncology position article. J. Clin. Oncol. 2013, 31, 3711–3718. [Google Scholar] [CrossRef] [PubMed]
  65. Khan, M.A.; Din, I.U.; Kim, B.-S.; Almogren, A. Visualization of Remote Patient Monitoring System Based on Internet of Medical Things. Sustainability 2023, 15, 8120. [Google Scholar] [CrossRef]
  66. Alotaibi, Y.K.; Federico, F. The impact of health information technology on patient safety. Saudi Med. J. 2017, 38, 1173–1180. [Google Scholar] [CrossRef]
  67. Redman, B.K. Advances in Patient Education; Springer: Berlin/Heidelberg, Germany, 2004. [Google Scholar]
  68. Singleton, K.; Krause, E. Understanding cultural and linguistic barriers to health literacy. Online J. Issues Nurs. 2009, 14, 6–9. [Google Scholar] [CrossRef]
  69. OpenAI. ChatGPT (Mar 14 version) [Large language model]. Available online: https://chat.openai.com/chat (accessed on 17 April 2023).
  70. St-Pierre, F.; Bhatia, S.; Chandra, S. Harnessing Natural Killer Cells in Cancer Immunotherapy: A Review of Mechanisms and Novel Therapies. Cancers 2021, 13, 1988. [Google Scholar] [CrossRef]
  71. Till, S.J.; Francis, J.N.; Nouri-Aria, K.; Durham, S.R. Mechanisms of immunotherapy. J. Allergy Clin. Immunol. 2004, 113, 1025–1034. [Google Scholar] [CrossRef]
  72. Spear, T.T.; Nagato, K.; Nishimura, M.I. Strategies to genetically engineer T cells for cancer immunotherapy. Cancer Immunol. Immunother. 2016, 65, 631–649. [Google Scholar] [CrossRef]
  73. Sniecinski, I.; Seghatchian, J. Artificial intelligence: A joint narrative on potential use in pediatric stem and immune cell therapies and regenerative medicine. Transfus. Apher. Sci. 2018, 57, 422–424. [Google Scholar] [CrossRef] [PubMed]
  74. Walker, R.; Enderling, H. From concept to clinic: Mathematically informed immunotherapy. Curr. Probl. Cancer 2016, 40, 68–83. [Google Scholar] [CrossRef]
  75. Khalil, A.M. The genome editing revolution: Review. J. Genet. Eng. Biotechnol. 2020, 18, 68. [Google Scholar] [CrossRef]
  76. Singh, P.; Sharma, D. Playing with Genes: A Pragmatic Approach in Genetic Engineering. In Digital Forensics and Internet of Things; Willey: Hoboken, NJ, USA, 2022; pp. 45–58. [Google Scholar] [CrossRef]
  77. Hassanzadeh, A.; Shamlou, S.; Yousefi, N.; Nikoo, M.; Verdi, J. Genetically-modified Stem Cell in Regenerative Medicine and Cancer Therapy; A New Era. Curr. Gene Ther. 2022, 22, 23–39. [Google Scholar] [CrossRef] [PubMed]
  78. Zhao, C.; Cheng, Y.; Huang, P.; Wang, C.; Wang, W.; Wang, M.; Shan, W.; Deng, H. X-ray-Guided In Situ Genetic Engineering of Macrophages for Sustained Cancer Immunotherapy. Adv. Mater. 2023, 35, 2208059. [Google Scholar] [CrossRef] [PubMed]
  79. Al Abbar, A.; Ngai, S.C.; Nograles, N.; Alhaji, S.Y.; Abdullah, S. Induced Pluripotent Stem Cells: Reprogramming Platforms and Applications in Cell Replacement Therapy. BioRes. Open Access 2020, 9, 121–136. [Google Scholar] [CrossRef] [PubMed]
  80. Kumar, S.R.P.; Markusic, D.M.; Biswas, M.; High, K.A.; Herzog, R.W. Clinical development of gene therapy: Results and lessons from recent successes. Mol. Ther. Methods Clin. Dev. 2016, 3, 16034. [Google Scholar] [CrossRef] [PubMed]
  81. Bansal, A.; Prakash, R.; Agarwal, S.; Advani, U. Gene therapy and its applications. J. Med. Evid. 2023, 4, 46–56. [Google Scholar] [CrossRef]
  82. Doudna, J.A. The promise and challenge of therapeutic genome editing. Nature 2020, 578, 229–236. [Google Scholar] [CrossRef]
  83. Shahcheraghi, N.; Golchin, H.; Sadri, Z.; Tabari, Y.; Borhanifar, F.; Makani, S. Nano-biotechnology, an applicable approach for sustainable future. 3 Biotech 2022, 12, 65. [Google Scholar] [CrossRef]
  84. Bayda, S.; Adeel, M.; Tuccinardi, T.; Cordani, M.; Rizzolio, F. The History of Nanoscience and Nanotechnology: From Chemical-Physical Applications to Nanomedicine. Molecules 2019, 25, 112. [Google Scholar] [CrossRef] [PubMed]
  85. Gonzalez-Rodriguez, R.; Campbell, E.; Naumov, A. Multifunctional graphene oxide/iron oxide nanoparticles for magnetic targeted drug delivery dual magnetic resonance/fluorescence imaging and cancer sensing. PLoS ONE 2019, 14, e0217072. [Google Scholar] [CrossRef]
  86. La Spada, L.; Vegni, L. Electromagnetic Nanoparticles for Sensing and Medical Diagnostic Applications. Materials 2018, 11, 603. [Google Scholar] [CrossRef]
  87. Salvador-Morales, C.; Grodzinski, P. Nanotechnology Tools Enabling Biological Discovery. ACS Nano 2022, 16, 5062–5084. [Google Scholar] [CrossRef]
  88. Jain, K.K. (Ed.) Role of Nanobiotechnology in drug delivery. In Drug Delivery Systems; Springer: New York, NY, USA, 2020; pp. 55–73. [Google Scholar] [CrossRef]
  89. Gehr, P. Interaction of nanoparticles with biological systems. Colloids Surf. B Biointerfaces 2018, 172, 395–399. [Google Scholar] [CrossRef]
  90. Din, F.u.; Rashid, R.; Mustapha, O.; Kim, D.W.; Park, J.H.; Ku, S.K.; Oh, Y.-K.; Kim, J.O.; Youn, Y.S.; Yong, C.S.; et al. Development of a novel solid lipid nanoparticles-loaded dual-reverse thermosensitive nanomicelle for intramuscular administration with sustained release and reduced toxicity. RSC Adv. 2015, 5, 43687–43694. [Google Scholar] [CrossRef]
  91. Lin, J.; Pan, Z.; Song, L.; Zhang, Y.; Li, Y.; Hou, Z.; Lin, C. Design and in vitro evaluation of self-assembled indometacin prodrug nanoparticles for sustained/controlled release and reduced normal cell toxicity. Appl. Surf. Sci. 2017, 425, 674–681. [Google Scholar] [CrossRef]
  92. Nosrati, H.; Heydari, M.; Tootiaei, Z.; Ganjbar, S.; Khodaei, M. Delivery of antibacterial agents for wound healing applications using polysaccharide-based scaffolds. J. Drug Deliv. Sci. Technol. 2023, 84, 104516. [Google Scholar] [CrossRef]
  93. Mohanraj, V.; Chen, Y. Nanoparticles—A review. Trop. J. Pharm. Res. 2006, 5, 561–573. [Google Scholar] [CrossRef]
  94. Shuai, C.; Yang, W.; He, C.; Peng, S.; Gao, C.; Yang, Y.; Qi, F.; Feng, P. A magnetic micro-environment in scaffolds for stimulating bone regeneration. Mater. Des. 2020, 185, 108275. [Google Scholar] [CrossRef]
  95. Han, J.; Xiong, L.; Jiang, X.; Yuan, X.; Zhao, Y.; Yang, D. Bio-functional electrospun nanomaterials: From topology design to biological applications. Prog. Polym. Sci. 2019, 91, 1–28. [Google Scholar] [CrossRef]
  96. Nemati, S.; Kim, S.-j.; Shin, Y.M.; Shin, H. Current progress in application of polymeric nanofibers to tissue engineering. Nano Converg. 2019, 6, 36. [Google Scholar] [CrossRef] [PubMed]
  97. Jhala, D.; Rather, H.A.; Vasita, R. Extracellular matrix mimicking polycaprolactone-chitosan nanofibers promote stemness maintenance of mesenchymal stem cells via spheroid formation. Biomed. Mater. 2020, 15, 035011. [Google Scholar] [CrossRef]
  98. Yeo, L.Y.; Chang, H.-C.; Chan, P.P.Y.; Friend, J.R. Microfluidic Devices for Bioapplications. Small 2011, 7, 12–48. [Google Scholar] [CrossRef]
  99. Ortseifen, V.; Viefhues, M.; Wobbe, L.; Grünberger, A. Microfluidics for Biotechnology: Bridging Gaps to Foster Microfluidic Applications. Front. Bioeng. Biotechnol. 2020, 8, 589074. [Google Scholar] [CrossRef] [PubMed]
  100. Liu, Y.; Jiang, X. Why microfluidics? Merits and trends in chemical synthesis. Lab A Chip 2017, 17, 3960–3978. [Google Scholar] [CrossRef]
  101. Pol, R.; Céspedes, F.; Gabriel, D.; Baeza, M. Microfluidic lab-on-a-chip platforms for environmental monitoring. TrAC Trends Anal. Chem. 2017, 95, 62–68. [Google Scholar] [CrossRef]
  102. Tomazelli Coltro, W.K.; Cheng, C.-M.; Carrilho, E.; de Jesus, D.P. Recent advances in low-cost microfluidic platforms for diagnostic applications. Electrophoresis 2014, 35, 2309–2324. [Google Scholar] [CrossRef] [PubMed]
  103. Cao, S.C.; Jung, J.; Radonjic, M. Application of microfluidic pore models for flow, transport, and reaction in geological porous media: From a single test bed to multifunction real-time analysis tool. Microsyst. Technol. 2019, 25, 4035–4052. [Google Scholar] [CrossRef]
  104. Ye, W.-Q.; Liu, X.-P.; Ma, R.-F.; Yang, C.-G.; Xu, Z.-R. Open-channel microfluidic chip based on shape memory polymer for controllable liquid transport. Lab A Chip 2023, 23, 2068–2074. [Google Scholar] [CrossRef]
  105. Kaminski, T.S.; Garstecki, P. Controlled droplet microfluidic systems for multistep chemical and biological assays. Chem. Soc. Rev. 2017, 46, 6210–6226. [Google Scholar] [CrossRef]
  106. Fair, R.B.; Khlystov, A.; Tailor, T.D.; Ivanov, V.; Evans, R.D.; Srinivasan, V.; Pamula, V.K.; Pollack, M.G.; Griffin, P.B.; Zhou, J. Chemical and Biological Applications of Digital-Microfluidic Devices. IEEE Des. Test Comput. 2007, 24, 10–24. [Google Scholar] [CrossRef]
  107. Harink, B.; Le Gac, S.; Truckenmüller, R.; van Blitterswijk, C.; Habibovic, P. Regeneration-on-a-chip? The perspectives on use of microfluidics in regenerative medicine. Lab A Chip 2013, 13, 3512–3528. [Google Scholar] [CrossRef]
  108. Yoshimitsu, R.; Hattori, K.; Sugiura, S.; Kondo, Y.; Yamada, R.; Tachikawa, S.; Satoh, T.; Kurisaki, A.; Ohnuma, K.; Asashima, M.; et al. Microfluidic perfusion culture of human induced pluripotent stem cells under fully defined culture conditions. Biotechnol. Bioeng. 2014, 111, 937–947. [Google Scholar] [CrossRef] [PubMed]
  109. Filippi, M.; Buchner, T.; Yasa, O.; Weirich, S.; Katzschmann, R.K. Microfluidic Tissue Engineering and Bio-Actuation. Adv. Mater. 2022, 34, 2108427. [Google Scholar] [CrossRef]
  110. Zheng, W.; Xie, R.; Liang, X.; Liang, Q. Fabrication of Biomaterials and Biostructures Based On Microfluidic Manipulation. Small 2022, 18, 2105867. [Google Scholar] [CrossRef]
  111. Wang, Z.; Ahmed, S.; Labib, M.; Wang, H.; Wu, L.; Bavaghar-Zaeimi, F.; Shokri, N.; Blanco, S.; Karim, S.; Czarnecka-Kujawa, K.; et al. Isolation of tumour-reactive lymphocytes from peripheral blood via microfluidic immunomagnetic cell sorting. Nat. Biomed. Eng. 2023, 7, 1188–1203. [Google Scholar] [CrossRef]
  112. Sun, J.; Warden, A.R.; Ding, X. Recent advances in microfluidics for drug screening. Biomicrofluidics 2019, 13, 061503. [Google Scholar] [CrossRef]
  113. Pittman, T.W.; Decsi, D.B.; Punyadeera, C.; Henry, C.S. Saliva-based microfluidic point-of-care diagnostic. Theranostics 2023, 13, 1091–1108. [Google Scholar] [CrossRef] [PubMed]
  114. Agostini, M.; Greco, G.; Cecchini, M. Full-SAW Microfluidics-Based Lab-on-a-Chip for Biosensing. IEEE Access 2019, 7, 70901–70909. [Google Scholar] [CrossRef]
  115. Venugopal Menon, N.; Lim, S.B.; Lim, C.T. Microfluidics for personalized drug screening of cancer. Curr. Opin. Pharmacol. 2019, 48, 155–161. [Google Scholar] [CrossRef]
  116. Mathur, L.; Ballinger, M.; Utharala, R.; Merten, C.A. Microfluidics as an Enabling Technology for Personalized Cancer Therapy. Small 2020, 16, 1904321. [Google Scholar] [CrossRef] [PubMed]
  117. Maurya, R.; Gohil, N.; Bhattacharjee, G.; Khambhati, K.; Alzahrani, K.J.; Ramakrishna, S.; Chu, D.-T.; Singh, V. Chapter Seven—Advances in microfluidics devices and its applications in personalized medicines. In Progress in Molecular Biology and Translational Science; Pandya, A., Singh, V., Eds.; Academic Press: Cambridge, MA, USA, 2022; Volume 186, pp. 191–201. [Google Scholar]
  118. Battat, S.; Weitz, D.A.; Whitesides, G.M. An outlook on microfluidics: The promise and the challenge. Lab Chip 2022, 22, 530–536. [Google Scholar] [CrossRef] [PubMed]
  119. Torres-Alvarez, D.; Aguirre-Soto, A. Polydimethylsiloxane chemistry for the fabrication of microfluidics—Perspective on its uniqueness, limitations and alternatives. Mater. Today: Proc. 2022, 48, 88–95. [Google Scholar] [CrossRef]
  120. Raj, M.K.; Chakraborty, S. PDMS microfluidics: A mini review. J. Appl. Polym. Sci. 2020, 137, 48958. [Google Scholar] [CrossRef]
  121. Lee, J.N.; Park, C.; Whitesides, G.M. Solvent Compatibility of Poly(dimethylsiloxane)-Based Microfluidic Devices. Anal. Chem. 2003, 75, 6544–6554. [Google Scholar] [CrossRef] [PubMed]
  122. Berthier, E.; Young, E.W.; Beebe, D. Engineers are from PDMS-land, Biologists are from Polystyrenia. Lab Chip 2012, 12, 1224–1237. [Google Scholar] [CrossRef]
  123. Carter, S.-S.D.; Atif, A.-R.; Kadekar, S.; Lanekoff, I.; Engqvist, H.; Varghese, O.P.; Tenje, M.; Mestres, G. PDMS leaching and its implications for on-chip studies focusing on bone regeneration applications. Organs Chip 2020, 2, 100004. [Google Scholar] [CrossRef]
  124. Ren, K.; Zhou, J.; Wu, H. Materials for Microfluidic Chip Fabrication. Acc. Chem. Res. 2013, 46, 2396–2406. [Google Scholar] [CrossRef]
  125. Hou, X.; Zhang, Y.S.; Santiago, G.T.-d.; Alvarez, M.M.; Ribas, J.; Jonas, S.J.; Weiss, P.S.; Andrews, A.M.; Aizenberg, J.; Khademhosseini, A. Interplay between materials and microfluidics. Nat. Rev. Mater. 2017, 2, 17016. [Google Scholar] [CrossRef]
  126. Volpatti, L.R.; Yetisen, A.K. Commercialization of microfluidic devices. Trends Biotechnol. 2014, 32, 347–350. [Google Scholar] [CrossRef]
  127. Mosadegh, B.; Bersano-Begey, T.; Park, J.Y.; Burns, M.A.; Takayama, S. Next-generation integrated microfluidic circuits. Lab A Chip 2011, 11, 2813–2818. [Google Scholar] [CrossRef]
  128. Wing, J.M. Trustworthy AI. Commun. ACM 2021, 64, 64–71. [Google Scholar] [CrossRef]
  129. Myles, A.J.; Feudale, R.N.; Liu, Y.; Woody, N.A.; Brown, S.D. An introduction to decision tree modeling. J. Chemom. 2004, 18, 275–285. [Google Scholar] [CrossRef]
  130. Gardner, M.W.; Dorling, S.R. Artificial neural networks (the multilayer perceptron)—A review of applications in the atmospheric sciences. Atmos. Environ. 1998, 32, 2627–2636. [Google Scholar] [CrossRef]
  131. Gou, J.; Yu, B.; Maybank, S.J.; Tao, D. Knowledge Distillation: A Survey. Int. J. Comput. Vis. 2021, 129, 1789–1819. [Google Scholar] [CrossRef]
  132. Vega García, M.; Aznarte, J.L. Shapley additive explanations for NO2 forecasting. Ecol. Inform. 2020, 56, 101039. [Google Scholar] [CrossRef]
  133. Aalen, O.O. A linear regression model for the analysis of life times. Stat. Med. 1989, 8, 907–925. [Google Scholar] [CrossRef]
  134. Daryl, P. Logistic Regression Diagnostics. Ann. Stat. 1981, 9, 705–724. [Google Scholar] [CrossRef]
  135. Tin Kam, H. Random decision forests. In Proceedings of the 3rd International Conference on Document Analysis and Recognition, Montreal, QC, Canada, 14–16 August 1995; Volume 271, pp. 278–282. [Google Scholar]
  136. Hearst, M.A.; Dumais, S.T.; Osuna, E.; Platt, J.; Scholkopf, B. Support vector machines. IEEE Intell. Syst. Their Appl. 1998, 13, 18–28. [Google Scholar] [CrossRef]
  137. Lecun, Y.; Bottou, L.; Bengio, Y.; Haffner, P. Gradient-based learning applied to document recognition. Proc. IEEE 1998, 86, 2278–2324. [Google Scholar] [CrossRef]
  138. McCulloch, W.S.; Pitts, W. A logical calculus of the ideas immanent in nervous activity. Bull. Math. Biophys. 1943, 5, 115–133. [Google Scholar] [CrossRef]
  139. Hartigan, J.A.; Wong, M.A. Algorithm AS 136: A K-Means Clustering Algorithm. J. R. Stat. Society. Ser. C 1979, 28, 100–108. [Google Scholar] [CrossRef]
  140. Johnson, S.C. Hierarchical clustering schemes. Psychometrika 1967, 32, 241–254. [Google Scholar] [CrossRef] [PubMed]
  141. Goodfellow, I.; Pouget-Abadie, J.; Mirza, M.; Xu, B.; Warde-Farley, D.; Ozair, S.; Courville, A.; Bengio, Y. Generative adversarial networks. Commun. ACM 2020, 63, 139–144. [Google Scholar] [CrossRef]
  142. Watkins, C.J.C.H.; Dayan, P. Q-learning. Mach. Learn. 1992, 8, 279–292. [Google Scholar] [CrossRef]
  143. Abadi, M.; Agarwal, A.; Barham, P.; Brevdo, E.; Chen, Z.; Citro, C.; Corrado, G.S.; Davis, A.; Dean, J.; Devin, M. Tensorflow: Large-scale machine learning on heterogeneous distributed systems. arXiv 2016, arXiv:1603.04467. [Google Scholar]
  144. Paszke, A.; Gross, S.; Massa, F.; Lerer, A.; Bradbury, J.; Chanan, G.; Killeen, T.; Lin, Z.; Gimelshein, N.; Antiga, L. Pytorch: An imperative style, high-performance deep learning library. Adv. Neural Inf. Process. Syst. 2019, 32, 1–12. [Google Scholar]
  145. Ishii, E.; Ebner, D.K.; Kimura, S.; Agha-Mir-Salim, L.; Uchimido, R.; Celi, L.A. The advent of medical artificial intelligence: Lessons from the Japanese approach. J. Intensive Care 2020, 8, 35. [Google Scholar] [CrossRef] [PubMed]
  146. Aoe, J.; Fukuma, R.; Yanagisawa, T.; Harada, T.; Tanaka, M.; Kobayashi, M.; Inoue, Y.; Yamamoto, S.; Ohnishi, Y.; Kishima, H. Automatic diagnosis of neurological diseases using MEG signals with a deep neural network. Sci. Rep. 2019, 9, 5057. [Google Scholar] [CrossRef]
  147. Sato, M.; Morimoto, K.; Kajihara, S.; Tateishi, R.; Shiina, S.; Koike, K.; Yatomi, Y. Machine-learning Approach for the Development of a Novel Predictive Model for the Diagnosis of Hepatocellular Carcinoma. Sci. Rep. 2019, 9, 7704. [Google Scholar] [CrossRef] [PubMed]
  148. Yamamoto, Y.; Saito, A.; Tateishi, A.; Shimojo, H.; Kanno, H.; Tsuchiya, S.; Ito, K.-i.; Cosatto, E.; Graf, H.P.; Moraleda, R.R.; et al. Quantitative diagnosis of breast tumors by morphometric classification of microenvironmental myoepithelial cells using a machine learning approach. Sci. Rep. 2017, 7, 46732. [Google Scholar] [CrossRef] [PubMed]
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