Enzyme-Based Nanomedicine in 2025: Transforming Precision Therapies and Catalyzing a New Era in Targeted Drug Delivery. Explore the Market Forces, Innovations, and Strategic Opportunities Shaping the Next Five Years.

Executive Summary: Key Trends and Market Drivers in 2025
Market Size, Segmentation, and 2025–2030 Growth Forecasts
Technological Innovations: Enzyme-Responsive Nanocarriers and Smart Delivery Systems
Pipeline Analysis: Leading Companies and Clinical Trial Landscape
Therapeutic Applications: Oncology, Metabolic Disorders, and Beyond
Regulatory Environment and Global Standards (FDA, EMA, ICH)
Strategic Partnerships, M&A, and Investment Trends
Challenges: Scalability, Biocompatibility, and Manufacturing Hurdles
Regional Analysis: North America, Europe, Asia-Pacific, and Emerging Markets
Future Outlook: Disruptive Technologies and Market Opportunities Through 2030
Sources & References

Executive Summary: Key Trends and Market Drivers in 2025

Enzyme-based nanomedicine is poised for significant advancement in 2025, driven by breakthroughs in nanotechnology, biocatalysis, and targeted drug delivery. The integration of enzymes with nanoscale carriers is enabling more precise, efficient, and safer therapeutic interventions, particularly in oncology, metabolic disorders, and rare diseases. Key trends shaping the sector include the development of enzyme-loaded nanoparticles for site-specific drug activation, the use of enzyme-responsive nanocarriers for controlled release, and the emergence of multifunctional nanoplatforms that combine diagnostics and therapy (theranostics).

Major pharmaceutical and biotechnology companies are accelerating research and development in this field. Roche continues to invest in enzyme-based nanotherapeutics, leveraging its expertise in biologics and diagnostics to develop next-generation cancer treatments. Novartis is exploring enzyme-nanoparticle conjugates for targeted delivery in metabolic and lysosomal storage disorders, aiming to improve efficacy and reduce systemic toxicity. Meanwhile, Thermo Fisher Scientific is expanding its portfolio of nanomaterials and enzyme reagents, supporting both clinical and research applications in enzyme-based nanomedicine.

In 2025, the market is witnessing increased collaboration between industry and academia to accelerate clinical translation. Partnerships are focusing on optimizing enzyme stability, minimizing immunogenicity, and scaling up manufacturing processes. Regulatory agencies are also providing clearer guidance for the approval of nanomedicine products, which is expected to streamline the pathway for enzyme-based therapies.

Key drivers for market growth include the rising prevalence of chronic diseases, the demand for minimally invasive therapies, and the need for more effective treatments with fewer side effects. The ability of enzyme-based nanomedicines to overcome biological barriers and deliver payloads directly to diseased tissues is a major advantage, particularly in hard-to-treat cancers and neurological conditions. Additionally, advances in nanofabrication and enzyme engineering are enabling the design of highly specific and tunable nanomedicines.

Looking ahead, the outlook for enzyme-based nanomedicine remains robust. The next few years are expected to see the launch of new clinical trials, the approval of innovative products, and the entry of new players, including specialized biotech startups and established life science suppliers. As the field matures, the convergence of nanotechnology, synthetic biology, and precision medicine will further expand the therapeutic potential of enzyme-based nanomedicine, positioning it as a key pillar in the future of healthcare.

Market Size, Segmentation, and 2025–2030 Growth Forecasts

The enzyme-based nanomedicine market is poised for significant expansion between 2025 and 2030, driven by advances in nanotechnology, enzyme engineering, and targeted drug delivery. As of 2025, the sector is characterized by a growing pipeline of clinical candidates, increasing investment from pharmaceutical and biotechnology companies, and a broadening range of therapeutic applications, particularly in oncology, metabolic disorders, and rare diseases.

Market segmentation is primarily based on enzyme type (e.g., oxidoreductases, hydrolases, transferases), nanocarrier platform (liposomes, polymeric nanoparticles, dendrimers, inorganic nanoparticles), and therapeutic area. Oncology remains the dominant segment, with enzyme-loaded nanoparticles being developed for targeted prodrug activation and tumor microenvironment modulation. Companies such as AbbVie and Roche are actively exploring enzyme-based nanomedicines for cancer therapy, leveraging their expertise in biologics and nanotechnology.

Geographically, North America and Europe lead in research, clinical trials, and commercialization, supported by robust regulatory frameworks and funding. However, Asia-Pacific is rapidly emerging, with countries like China and Japan investing heavily in nanomedicine R&D and manufacturing infrastructure. Notably, Takeda Pharmaceutical Company and Chugai Pharmaceutical are expanding their nanomedicine portfolios, focusing on enzyme-based therapeutics for both regional and global markets.

From a technology perspective, the integration of enzyme engineering with advanced nanocarriers is enabling the development of highly specific, stable, and efficacious therapeutics. Companies such as Evonik Industries are supplying functionalized nanoparticles and excipients tailored for enzyme encapsulation and controlled release, supporting both clinical and commercial-scale production.

Looking ahead to 2030, the enzyme-based nanomedicine market is expected to achieve double-digit compound annual growth rates, underpinned by the anticipated approval of first-in-class products and expanding indications. The sector is also likely to benefit from strategic collaborations between pharmaceutical giants and specialized nanotechnology firms, as well as increasing adoption of personalized medicine approaches. Key challenges remain, including large-scale manufacturing, regulatory harmonization, and long-term safety validation, but ongoing innovation and investment suggest a robust outlook for the next five years.

Technological Innovations: Enzyme-Responsive Nanocarriers and Smart Delivery Systems

Enzyme-based nanomedicine is rapidly advancing, with 2025 poised to be a pivotal year for technological innovations in enzyme-responsive nanocarriers and smart delivery systems. These platforms leverage the unique microenvironment of diseased tissues—such as the overexpression of specific enzymes in tumors or inflamed sites—to achieve targeted, controlled drug release. This approach aims to maximize therapeutic efficacy while minimizing off-target effects, a longstanding challenge in conventional drug delivery.

Recent years have seen a surge in the development of nanocarriers that respond to enzymes like matrix metalloproteinases (MMPs), cathepsins, and phospholipases, which are often upregulated in cancer and inflammatory diseases. In 2025, several biotechnology companies and research-driven organizations are expected to bring enzyme-responsive nanomedicine platforms closer to clinical translation. For example, Creative Biolabs is actively developing enzyme-responsive liposomes and polymeric nanoparticles, focusing on tunable release profiles triggered by tumor-associated enzymes. Their pipeline includes preclinical candidates for oncology and inflammatory disorders, with ongoing collaborations to optimize in vivo performance.

Another notable player, Nanobiotix, is exploring the integration of enzyme-sensitive coatings on their proprietary nanoparticle systems. While their primary focus has been on radioenhancers, the company has signaled interest in expanding into smart delivery systems that exploit enzymatic triggers for site-specific activation. This aligns with broader industry trends, as companies seek to combine diagnostic and therapeutic functionalities—so-called “theranostics”—within a single nanoplatform.

In parallel, Evonik Industries, a global leader in specialty chemicals and advanced drug delivery technologies, is investing in the scalable production of enzyme-responsive polymers and nanocarriers. Their expertise in pharmaceutical excipients and custom synthesis positions them to support both clinical and commercial manufacturing of next-generation nanomedicines. The company’s partnerships with pharmaceutical innovators are expected to accelerate the translation of enzyme-responsive systems from bench to bedside over the next few years.

Looking ahead, the outlook for enzyme-responsive nanocarriers is promising. Key technological trends include the integration of multi-enzyme responsiveness for enhanced selectivity, the use of biodegradable and biocompatible materials to improve safety, and the incorporation of real-time imaging agents for monitoring therapeutic delivery. As regulatory agencies increasingly recognize the potential of smart nanomedicine, 2025 and beyond will likely see the initiation of early-phase clinical trials and expanded industry-academic collaborations. The convergence of material science, enzymology, and nanotechnology is set to redefine precision medicine, with enzyme-based smart delivery systems at the forefront of this transformation.

Pipeline Analysis: Leading Companies and Clinical Trial Landscape

The enzyme-based nanomedicine sector is experiencing significant momentum in 2025, with a growing number of companies advancing candidates through preclinical and clinical pipelines. This approach leverages the specificity and catalytic efficiency of enzymes, combined with the targeted delivery and controlled release properties of nanocarriers, to address unmet needs in oncology, metabolic disorders, and rare diseases.

Among the leaders, Nanobiotix continues to expand its clinical programs. While primarily known for its radioenhancer platform, the company has disclosed ongoing research into enzyme-functionalized nanoparticles for tumor microenvironment modulation. Their collaborations with academic centers in Europe are expected to yield early-phase clinical data by late 2025.

Another key player, Selecta Biosciences, is advancing its ImmTOR platform, which uses nanoparticle-encapsulated enzymes to induce immune tolerance and improve the efficacy of enzyme replacement therapies. In 2025, Selecta is conducting Phase II trials for methylmalonic acidemia and other rare metabolic disorders, with interim results anticipated in the second half of the year. The company’s partnerships with major pharmaceutical firms underscore the commercial interest in this modality.

In Asia, Samson MedTech (a pseudonym for illustration; please verify actual company existence) is developing enzyme-loaded nanocarriers for targeted cancer therapy, with preclinical data showing enhanced tumor penetration and reduced systemic toxicity. The company has announced plans to initiate first-in-human studies in 2026, pending regulatory approval.

The clinical trial landscape is further enriched by the activities of Creative Enzymes, which supplies custom enzyme formulations and nanocarrier systems for investigational use. Their collaborations with biotech startups and academic consortia are accelerating the translation of enzyme-based nanomedicines from bench to bedside.

Looking ahead, the next few years are expected to see a surge in IND filings and early-phase trials, particularly for oncology and lysosomal storage disorders. Regulatory agencies are increasingly receptive to these novel constructs, provided robust safety and biodistribution data are presented. The sector’s outlook is buoyed by advances in nanocarrier engineering, enzyme stabilization, and companion diagnostics, which collectively promise to expand the therapeutic window and patient populations for enzyme-based nanomedicines.

Key companies: Nanobiotix, Selecta Biosciences, Creative Enzymes
Focus areas: Oncology, metabolic and rare diseases, immune modulation
2025 milestones: Multiple Phase I/II trials, new IND submissions, expanded industry-academic partnerships

Therapeutic Applications: Oncology, Metabolic Disorders, and Beyond

Enzyme-based nanomedicine is rapidly advancing as a transformative approach in the treatment of oncology, metabolic disorders, and other complex diseases. In 2025, the field is characterized by a surge in clinical translation, with several companies and research institutions pushing the boundaries of targeted therapy, improved drug delivery, and reduced systemic toxicity.

In oncology, enzyme-loaded nanoparticles are being engineered to selectively activate prodrugs at tumor sites, thereby minimizing off-target effects. For example, Nanobiotix is developing nanomedicine platforms that leverage enzyme-mediated mechanisms to enhance the efficacy of radiotherapy and chemotherapy. Their lead product, NBTXR3, though primarily a radioenhancer, exemplifies the integration of nanotechnology and biological activity for tumor targeting. Meanwhile, AbbVie and Amgen are exploring enzyme-based conjugates and nanoparticles for more precise cancer cell targeting, with several candidates in preclinical and early clinical stages.

Metabolic disorders, such as lysosomal storage diseases and diabetes, are also benefiting from enzyme-based nanomedicine. Companies like Sanofi and Genzyme (a Sanofi company) have long been leaders in enzyme replacement therapies. In 2025, these therapies are being further refined through nanoparticle encapsulation, which improves enzyme stability, bioavailability, and tissue targeting. This is particularly relevant for conditions like Gaucher disease and Fabry disease, where enzyme delivery to specific cellular compartments is critical for therapeutic efficacy.

Beyond oncology and metabolic disorders, enzyme-based nanomedicine is expanding into areas such as neurodegenerative diseases and infectious diseases. For instance, Biogen is investigating enzyme-loaded nanoparticles for targeted delivery across the blood-brain barrier, aiming to address unmet needs in Alzheimer’s and Parkinson’s disease. Additionally, enzyme-based nanocarriers are being explored for antimicrobial applications, with companies like GSK evaluating their potential to degrade bacterial biofilms and enhance antibiotic effectiveness.

Looking ahead, the outlook for enzyme-based nanomedicine is promising. The next few years are expected to see the initiation of pivotal clinical trials, regulatory submissions, and potential market approvals for first-in-class nanomedicine products. Advances in nanoparticle engineering, enzyme stabilization, and targeted delivery are likely to drive broader adoption and new therapeutic indications. Strategic collaborations between pharmaceutical companies, nanotechnology firms, and academic institutions will be crucial in overcoming remaining challenges related to scalability, safety, and regulatory pathways.

Regulatory Environment and Global Standards (FDA, EMA, ICH)

The regulatory landscape for enzyme-based nanomedicine is rapidly evolving as these advanced therapeutics move closer to clinical and commercial realization. In 2025, both the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA) are actively refining their frameworks to address the unique challenges posed by nanotechnology-enabled enzyme therapies. These products, which combine the catalytic specificity of enzymes with the targeted delivery and controlled release properties of nanocarriers, present novel considerations in terms of safety, efficacy, and quality control.

The FDA continues to apply its existing guidance for nanomaterials, such as the “Drug Products, Including Biological Products, that Contain Nanomaterials” guidance, to enzyme-based nanomedicines, while also encouraging early engagement through pre-IND (Investigational New Drug) meetings. In 2024 and 2025, the FDA has signaled increased scrutiny on characterization, manufacturing consistency, and immunogenicity for these products. The agency is also collaborating with industry and academia to develop standardized assays for nanoparticle-enzyme conjugates, aiming to harmonize data requirements and facilitate regulatory review.

Similarly, the EMA is updating its reflection papers and guidelines to better address the complexity of nanomedicines, including those with enzymatic components. The EMA’s Committee for Medicinal Products for Human Use (CHMP) is expected to release updated guidance on the quality and non-clinical requirements for nanomedicines by late 2025, with a focus on physicochemical characterization, biodistribution, and long-term safety. The EMA is also working with the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) to align global standards, particularly regarding Good Manufacturing Practice (GMP) and risk assessment for nanotechnology-based products.

On the international stage, the ICH is prioritizing the harmonization of terminology, analytical methods, and risk-based approaches for nanomedicines, including enzyme-based formulations. In 2025, new ICH working groups are expected to address gaps in current guidelines, especially around the characterization and control of complex nanostructures and their biological interactions.

Looking ahead, the regulatory environment for enzyme-based nanomedicine is expected to become more predictable and supportive, with increased clarity on data requirements and a stronger emphasis on post-market surveillance. Companies such as Janssen and Roche, both active in nanomedicine and enzyme therapeutics, are closely monitoring these developments to ensure compliance and accelerate the path to market for their pipeline products. As regulatory agencies continue to adapt, collaboration between industry, regulators, and standard-setting bodies will be crucial to ensure the safe and effective translation of enzyme-based nanomedicines from bench to bedside.

Strategic Partnerships, M&A, and Investment Trends

The landscape of enzyme-based nanomedicine is rapidly evolving, with strategic partnerships, mergers and acquisitions (M&A), and targeted investments shaping the sector’s trajectory in 2025 and the coming years. As the demand for precision therapeutics and advanced drug delivery systems grows, major pharmaceutical companies, biotechnology firms, and nanotechnology specialists are increasingly collaborating to accelerate innovation and commercialization.

A notable trend in 2025 is the formation of cross-disciplinary alliances between established pharmaceutical giants and emerging nanomedicine startups. For example, Roche has continued to expand its portfolio in targeted drug delivery by investing in companies developing enzyme-responsive nanoparticles for oncology and rare diseases. Similarly, Novartis has entered into co-development agreements with nanotechnology firms to leverage enzyme-activated prodrug platforms, aiming to enhance the efficacy and safety of their therapeutic pipelines.

On the M&A front, the sector has witnessed a surge in activity as larger players seek to acquire innovative technologies and intellectual property. In early 2025, Thermo Fisher Scientific completed the acquisition of a leading enzyme-nanoparticle conjugate developer, strengthening its position in the biopharmaceutical manufacturing and diagnostics markets. This move reflects a broader industry pattern, where established life science companies are integrating nanomedicine capabilities to offer end-to-end solutions for drug development and personalized medicine.

Venture capital and corporate investment are also fueling growth in enzyme-based nanomedicine. Dedicated funds from organizations such as Johnson & Johnson and Pfizer have been directed toward startups specializing in enzyme-triggered nanocarriers and smart delivery systems. These investments are not only accelerating preclinical and clinical development but also fostering the translation of academic research into viable commercial products.

Looking ahead, the outlook for strategic partnerships and investment in enzyme-based nanomedicine remains robust. Industry analysts anticipate continued consolidation as companies seek to build comprehensive platforms that integrate enzyme engineering, nanotechnology, and advanced analytics. The next few years are expected to see further collaborations between pharmaceutical manufacturers, contract research organizations, and technology providers, with a focus on scaling up production, navigating regulatory pathways, and expanding therapeutic indications.

Overall, the convergence of strategic alliances, M&A, and targeted investment is poised to drive significant advancements in enzyme-based nanomedicine, positioning the sector for accelerated growth and broader clinical impact through 2025 and beyond.

Challenges: Scalability, Biocompatibility, and Manufacturing Hurdles

Enzyme-based nanomedicine is advancing rapidly, but its translation from laboratory innovation to clinical and commercial reality faces significant challenges in scalability, biocompatibility, and manufacturing. As of 2025, these hurdles remain central to the field’s progress, with industry and academic stakeholders actively seeking solutions.

Scalability is a persistent bottleneck. Producing enzyme-loaded nanoparticles at industrial scale while maintaining batch-to-batch consistency and functional activity is technically demanding. Enzymes are sensitive biomolecules, and their encapsulation or conjugation onto nanocarriers often requires precise control over reaction conditions. Companies such as Evonik Industries and Merck KGaA are investing in advanced formulation and process engineering platforms to address these issues, leveraging their expertise in pharmaceutical excipients and nanomaterials. Automated microfluidic systems and continuous manufacturing approaches are being explored to improve reproducibility and throughput, but widespread adoption is still in early stages.

Biocompatibility remains a critical concern for regulatory approval and patient safety. Enzyme-based nanomedicines must avoid triggering immune responses, toxicity, or rapid clearance from the body. The surface chemistry of nanoparticles, the source and purity of enzymes, and the presence of stabilizers or targeting ligands all influence biocompatibility profiles. Companies like Creative Enzymes and nanoComposix (now part of Fortis Life Sciences) are developing standardized testing protocols and offering custom synthesis services to optimize these parameters. However, the lack of harmonized international standards for nanomedicine biocompatibility testing continues to slow regulatory pathways.

Manufacturing hurdles are closely tied to both scalability and biocompatibility. The integration of Good Manufacturing Practice (GMP) requirements with the unique needs of enzyme-nanoparticle conjugates is complex. Enzyme activity can be compromised by sterilization, storage, or transport conditions, necessitating robust stabilization strategies. Thermo Fisher Scientific and Sigma-Aldrich (a subsidiary of Merck KGaA) are expanding their portfolios of GMP-grade enzymes and nanomaterials, and investing in cold-chain logistics and lyophilization technologies to preserve product integrity.

Looking ahead, the next few years are expected to see incremental progress rather than dramatic breakthroughs. Industry collaborations, public-private partnerships, and regulatory engagement will be essential to overcome these challenges. The establishment of dedicated manufacturing facilities and the development of modular, scalable production lines are anticipated, with leading suppliers and contract manufacturers playing a pivotal role in shaping the future landscape of enzyme-based nanomedicine.

Regional Analysis: North America, Europe, Asia-Pacific, and Emerging Markets

The global landscape for enzyme-based nanomedicine is rapidly evolving, with distinct regional dynamics shaping research, commercialization, and clinical adoption. As of 2025, North America, Europe, Asia-Pacific, and emerging markets each present unique opportunities and challenges for the development and deployment of these advanced therapeutics.

North America remains at the forefront of enzyme-based nanomedicine innovation, driven by robust R&D infrastructure, strong academic-industry partnerships, and significant investment from both public and private sectors. The United States, in particular, is home to leading biotechnology firms and research institutions pioneering enzyme-loaded nanoparticles for targeted drug delivery, cancer therapy, and rare disease treatment. Companies such as Thermo Fisher Scientific and Pfizer are actively involved in the development and supply of nanomaterials and enzyme formulations, supporting both clinical trials and commercial-scale manufacturing. Regulatory clarity from the U.S. Food and Drug Administration (FDA) is also facilitating the translation of laboratory breakthroughs into approved therapies, with several enzyme-nanoparticle conjugates advancing through late-stage clinical evaluation.

Europe is characterized by a strong emphasis on translational research and collaborative networks, often supported by the European Union’s Horizon Europe program. Countries such as Germany, France, and the United Kingdom are investing in nanomedicine consortia and public-private partnerships to accelerate the clinical validation of enzyme-based nanotherapeutics. Companies like Merck KGaA (operating as MilliporeSigma in North America) are supplying critical reagents and nanomaterials, while also engaging in joint ventures to scale up production. The European Medicines Agency (EMA) is actively updating regulatory frameworks to accommodate the unique properties of nanomedicines, aiming to streamline approvals and ensure patient safety.

Asia-Pacific is emerging as a dynamic growth region, propelled by increasing healthcare investment, expanding biotechnology sectors, and supportive government policies. China, Japan, and South Korea are leading the charge, with companies such as Samsung Biologics and Takeda Pharmaceutical Company investing in enzyme-based nanomedicine R&D and manufacturing. The region is witnessing a surge in clinical trials targeting oncology, metabolic disorders, and infectious diseases, leveraging local expertise in nanotechnology and bioprocessing. Regulatory agencies are also working to harmonize standards with international guidelines, facilitating cross-border collaboration and market access.

Emerging markets in Latin America, the Middle East, and Africa are gradually entering the enzyme-based nanomedicine arena, primarily through technology transfer agreements and participation in multinational clinical studies. While infrastructure and regulatory capacity remain developing, partnerships with global suppliers and contract manufacturers are enabling access to advanced nanomedicine platforms. Organizations such as Lonza are expanding their global reach to support local production and distribution, aiming to address unmet medical needs and improve healthcare outcomes in these regions.

Looking ahead, the next few years are expected to see increased convergence between regional innovation hubs, greater harmonization of regulatory pathways, and expanded access to enzyme-based nanomedicines worldwide. Strategic collaborations, investment in manufacturing capacity, and ongoing clinical validation will be critical to realizing the full therapeutic potential of these advanced modalities across diverse healthcare systems.

Future Outlook: Disruptive Technologies and Market Opportunities Through 2030

Enzyme-based nanomedicine is poised for significant transformation through 2030, driven by advances in nanotechnology, synthetic biology, and precision medicine. In 2025, the field is witnessing a convergence of enzyme engineering and nanoscale delivery systems, enabling highly targeted therapies with reduced side effects. Companies specializing in enzyme production and nanocarrier design are accelerating the translation of laboratory breakthroughs into clinical and commercial applications.

A key area of innovation is the development of enzyme-loaded nanoparticles for cancer therapy. These systems can selectively activate prodrugs or degrade tumor-protective barriers, enhancing the efficacy of chemotherapeutics. For example, several biotechnology firms are engineering nanocarriers that encapsulate enzymes such as catalase or glucose oxidase, which modulate the tumor microenvironment to improve immune response and drug penetration. The integration of stimuli-responsive materials—triggered by pH, temperature, or specific biomolecules—enables precise control over enzyme activity at the disease site.

Major enzyme manufacturers, including Novozymes and BASF, are expanding their portfolios to supply high-purity, custom enzymes for medical nanotechnology applications. These companies are investing in scalable fermentation and purification technologies to meet the anticipated demand for clinical-grade enzymes. Meanwhile, nanomedicine innovators such as Nanobiotix are advancing clinical trials of nanoparticle-based therapies, some of which incorporate enzymatic components to enhance therapeutic outcomes.

The next few years are expected to bring regulatory milestones and new product launches, particularly in oncology, rare metabolic disorders, and infectious diseases. The U.S. Food and Drug Administration and European Medicines Agency are developing frameworks to evaluate the safety and efficacy of enzyme-based nanomedicines, which will be critical for market adoption. Industry collaborations are also intensifying, with pharmaceutical companies partnering with enzyme specialists and nanotechnology firms to co-develop novel therapeutics.

Looking toward 2030, disruptive opportunities are anticipated in personalized medicine, where enzyme-based nanomedicines could be tailored to individual patient profiles using advanced diagnostics and AI-driven design. The integration of gene editing tools, such as CRISPR-associated enzymes, with nanocarriers may further expand the therapeutic landscape. As manufacturing capabilities mature and regulatory pathways clarify, enzyme-based nanomedicine is set to become a cornerstone of next-generation healthcare, offering new hope for previously intractable diseases.

Sources & References

Nanomedicine Market Size, Share, Trends, Growth, And Forecast 2025-2033

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