市场调查报告书
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1503341
2030 年微射流市场预测:按产品类型、材料、技术、应用、最终用户和地区进行的全球分析Microfluidics Market Forecasts to 2030 - Global Analysis By Product Type (Microfluidic-Based Devices, Microfluidic Components and Other Product Types), Material, Technology, Application, End User and By Geography |
根据 Stratistics MRC 的数据,2024 年全球微射流市场规模将达到 256 亿美元,预计到 2030 年将达到 593 亿美元,预测期内复合年增长率为 15.0%。
微射流工程是一个跨学科领域,涉及微製造设备中微升或纳升规模的少量流体的精确控制和操纵。这些设备有时被称为实验室晶片系统,整合了流道、阀门、泵浦和感测器等各种组件,以实现流体的精确处理、混合和分析。微射流设备在医疗诊断、疾病检测、生物标记监测和药物传递方面也发挥着重要作用。微射流所提供的小型化、自动化和多功能性已经彻底改变了科学研究,并有可能在未来对各种行业产生重大影响。
对照护现场(POC) 诊断的需求不断增长
POC 诊断需要紧凑、高效且经济高效的解决方案,能够在患者所在地提供快速、准确的结果,并减少对密集实验室测试的需求。可以操纵少量液体的微射流技术完美地满足了这些需求。微射流技术提高了诊断测试的灵敏度和速度,同时允许以便携式格式多重分析和整合复杂的测定。这种需求正在推动微射流设备的创新和投资,从而推动实验室晶片技术和整合诊断平台的进步。因此,微射流市场正在经历强劲成长。
微射流设计与操作的复杂性
设计微射流系统需要先进的工程和精密製造技术,这是昂贵且耗时的。这种复杂性通常会导致製造成本增加,使得微射流装置与传统诊断方法相比在经济上没有吸引力。此外,微射流操作的复杂性需要专门的知识和技术,这可能需要大量的培训并限制普及。此外,将微射流系统整合到现有的实验室基础设施中并确保其可靠性和可重复性可能是一项挑战。
科技的进步与应用的扩展
微加工技术、材料科学和数位技术整合的创新提高了微射流的精度、效率和功能。这些进步使得先进的实验室晶片系统的开发成为可能,该系统可以高精度、高速度地执行复杂的生化分析。微射流工程在医疗诊断、药物传输、环境监测和食品安全等领域的广泛应用正在扩大其市场范围。
监管审批流程漫长而复杂
对医疗设备的严格监管要求,尤其是涉及新技术的医疗器械,可能会导致核准时间延长并增加製造商的成本。这种延迟可能会延迟创新微射流解决方案的上市时间,降低竞争力,并阻碍及时获得先进的诊断和治疗方法。此外,应对复杂的监管环境需要大量资源和专业知识,这对于小型企业和新兴企业来说尤其具有挑战性。
COVID-19 的影响
能够有效处理少量液体的微射流设备对于开发快速照护现场COVID-19 测试至关重要。此次疫情加速了微射流技术的创新和投资,以满足对可扩展且经济高效的诊断解决方案的高需求。此外,人们对快速诊断重要性的认识不断增强,微射流技术的应用范围已扩展到 COVID-19 之外,并促进其在感染疾病中的广泛采用。
基于微射流的设备领域预计将在预测期内成为最大的领域
基于微射流的设备预计将在预测期内成长最快,因为它们能够精确控制少量流体,以实现高通量筛检、快速诊断和高效的药物输送系统。将多种实验室功能整合到单一晶片上的能力可以降低成本并提高各种应用的便携性和效率,包括医疗诊断、环境监测和药物研究。实验室晶片技术的兴起,促进了照护现场快速、准确的测试,就体现了这种影响。
预计硅细分市场在预测期间内复合年增长率最高
由于微加工精度高、坚固性和生物相容性等优异的材料特性,硅细分市场预计在预测期内将表现出最高的复合年增长率。在微射流装置的製造中使用硅可以创建对于诊断、药物传输和生物研究应用至关重要的复杂且可靠的结构。硅的导热性和电特性有利于整合感测器和电子元件。然而,基于硅的製造成本高、复杂性高,这会限制可访问性和扩充性。
北美拥有完善的医疗保健系统,一般人群越来越多地采用新疗法,该地区人口中感染疾病和慢性病的患病率预计将在预测期内占据最大的市场占有率。此外,癌症负担的增加预计也将推动对微射流工程的需求。例如,2024年1月,美国癌症协会估计,2024年美国将有超过200万人被诊断出罹患癌症,高于2023年的190万人。因此,该国癌症发病率的上升预计将推动微射流工程的需求并推动市场成长。
由于对可携式和具有成本效益的诊断设备的需求不断增长、微加工技术的进步以及政府支持该地区研发的倡议,预计亚太地区将在预测期内保持最高的复合年增长率。由于强大的製造能力和对医疗基础设施的投资,中国、日本和韩国等国家处于市场成长的前沿。此外,学术机构和产业相关人员之间的合作正在推动微射流技术的创新。
According to Stratistics MRC, the Global Microfluidics Market is accounted for $25.6 billion in 2024 and is expected to reach $59.3 billion by 2030 growing at a CAGR of 15.0% during the forecast period. Microfluidics is a multidisciplinary field that deals with the precise control and manipulation of small volumes of fluids, typically on the microliter or nanoliter scale, within microfabricated devices. These devices, often referred to as lab-on-a-chip systems, integrate various components such as channels, valves, pumps, and sensors, allowing for the precise handling, mixing, and analysis of fluids. Microfluidic devices also play a crucial role in medical diagnostics, enabling the detection of diseases, monitoring of biomarkers, and drug delivery. The miniaturization, automation, and versatility offered by microfluidics have revolutionized scientific research and have the potential to significantly impact various industries in the future.
Rising demand for point-of-care (POC) diagnostics
POC diagnostics require compact, efficient, and cost-effective solutions to deliver quick and accurate results at the patient's location, reducing the need for centralized laboratory testing. Microfluidic technologies, with their capability to manipulate small volumes of fluids, perfectly meet these requirements. They enhance the sensitivity and speed of diagnostic tests while enabling multiplexing and integration of complex assays in portable formats. This demand is driving innovations and investments in microfluidic devices, leading to advancements in lab-on-a-chip technologies and integrated diagnostic platforms. As a result, the microfluidics market is experiencing robust growth.
Complexity of microfluidic design and operation
Designing microfluidic systems requires sophisticated engineering and precise fabrication techniques, which can be costly and time-consuming. These complexities often lead to higher production costs, making microfluidic devices less economically attractive compared to traditional diagnostic methods. Additionally, the intricate nature of microfluidic operations demands specialized knowledge and skills, potentially limiting widespread adoption in clinical and research settings due to the necessity for extensive training. Moreover, integrating microfluidic systems with existing laboratory infrastructure and ensuring their reliability and reproducibility can be challenging.
Technological advancements and expanding applications
Innovations in microfabrication techniques, material sciences, and integration of digital technologies have enhanced the precision, efficiency, and functionality of microfluidic devices. These advancements enable the development of sophisticated lab-on-a-chip systems capable of performing complex biochemical analyses with high accuracy and speed. The expanding applications of microfluidics in areas such as medical diagnostics, drug delivery, environmental monitoring, and food safety are broadening its market scope.
Lengthy and complex regulatory approval process
Stringent regulatory requirements for medical devices, particularly those involving new technologies, can lead to prolonged approval timelines and increased costs for manufacturers. These delays can slow down the time-to-market for innovative microfluidic solutions, reducing their competitive advantage and hindering timely access to advanced diagnostics and treatment options. Additionally, navigating the complex regulatory landscape requires substantial resources and expertise, which can be particularly challenging for smaller companies and startups.
Covid-19 Impact
Microfluidic devices, with their ability to process small fluid volumes efficiently, became crucial for developing quick, point-of-care COVID-19 tests. The pandemic accelerated innovations and investments in microfluidic technologies to meet the high demand for scalable and cost-effective diagnostic solutions. Additionally, the heightened awareness of the importance of quick diagnostics has expanded the applications of microfluidics beyond COVID-19, promoting broader adoption in infectious di
The microfluidic-based devices segment is expected to be the largest during the forecast period
The microfluidic-based devices is expected to be the largest during the forecast period as these devices offer precise control over small fluid volumes, enabling high-throughput screening, rapid diagnostics, and efficient drug delivery systems. Their ability to integrate multiple laboratory functions on a single chip reduces costs and enhances portability and efficiency in various applications, including medical diagnostics, environmental monitoring, and pharmaceutical research. The rise of lab-on-a-chip technologies exemplifies this impact, facilitating quick, accurate testing at the point-of-care.
The silicon segment is expected to have the highest CAGR during the forecast period
The silicon segment is expected to have the highest CAGR during the forecast period due to its excellent material properties, including high precision in microfabrication, robustness, and biocompatibility. Silicon's use in manufacturing microfluidic devices enables the creation of intricate and reliable structures essential for applications in diagnostics, drug delivery, and biological research. Its thermal conductivity and electrical properties are beneficial for integrating sensors and electronic components. However, the high cost and complexity of silicon-based fabrication can limit accessibility and scalability.
North America is projected to hold the largest market share during the forecast period due to factors such as the well-established healthcare system, the higher adoption of novel therapeutics among the general population, and the increasing prevalence of infectious and chronic diseases among the region's population. Moreover the rising burden of cancer is also expected to fuel the demand for microfluidics. For instance, in January 2024, according to the American Cancer Society, it was estimated that more than 2.0 million cancer cases would be diagnosed in the United States in 2024, an increase from 1.9 million cancer cases in 2023. Hence, the country's growing burden of cancer is expected to fuel the demand for microfluidics and favor market growth.
Asia Pacific is projected to hold the highest CAGR over the forecast period owing to rising demand for portable and cost-effective diagnostic devices, advancements in microfabrication technologies, and government initiatives supporting research and development in the region. Countries like China, Japan, and South Korea are at the forefront of market growth, fueled by their strong manufacturing capabilities and investments in healthcare infrastructure. Additionally, collaborations between academic institutions and industry players are fostering innovation in microfluidics technology.
Key players in the market
Some of the key players in Microfluidics market include Illumina, Inc., Agilent Technologies, Inc., Perkinelmer, Inc., Danaher, Life Technologies Corporation, Bio-Rad Laboratories, Inc., Hoffmann-La Roche Ltd, Abbott Laboratories, Fluidigm Corporation, Qiagen N.V., Thermo Fischer Scientific, Biomerieux, Cellix Ltd., Elveflow, Micronit Micro Technologies B.V., Standard BioTools, UFluidix, Emulate Inc., Dolomite Microfluidics and Sphere Fluidics Limited
In June 2024, Illumina launches latest chemistry across most popular mid-throughput sequencers, enabling higher quality and greater speed for customers at lower cost. XLEAP-SBS chemistry is a faster, higher quality, and more robust sequencing-by-synthesis chemistry that delivers approximately 20% faster turnaround times.
In June 2024, Agilent Announces Cutting-Edge Advances in GC/MS and LC/Q-TOF Technology at ASMS 2024. These instruments exemplify Agilent's unwavering commitment to advancing scientific discovery through innovative instrumentation, significantly shaping the landscape of mass spectrometry.
In January 2024, Illumina expands collaboration with Janssen to advance molecular residual disease cancer test This collaboration will be the first relating to the development of Illumina's novel molecular residual disease (MRD) assay, a whole-genome sequencing.
Note: Tables for North America, Europe, APAC, South America, and Middle East & Africa Regions are also represented in the same manner as above.