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市場調査レポート
商品コード
1626599
マイクロ流体市場:製品、用途、エンドユーザー、地域別、2024~2031年Microfluidics Market By Product (Device, Component Chip Sensor), Application (IVD, POC), End-User (Pharmaceutical, Hospital), & Region for 2024-2031 |
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マイクロ流体市場:製品、用途、エンドユーザー、地域別、2024~2031年 |
出版日: 2024年11月09日
発行: Verified Market Research
ページ情報: 英文 202 Pages
納期: 2~3営業日
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ポイントオブケア検査に対する需要の高まりが、マイクロ流体工学の採用を促進しています。精密な流体操作による創薬・市場開拓プロセスの強化が、2024年の市場規模を416億3,000万米ドルから2031年には約1,994億2,000万米ドルに押し上げます。
これに加えて、個別化医療に対するニーズの高まりが、マイクロ流体工学の採用に拍車をかけています。マイクロ流体システムは、検査室や臨床現場での試薬消費量と運用コストを削減するため、2024年から2031年にかけてCAGR 23.86%で市場成長を可能にしています。
マイクロ流体市場定義/概要
マイクロ流体工学とは、マイクロメートル単位で流体を操作・制御する科学技術を指します。この分野では、マイクロリットルやナノリットルといった非常に少量の液体を扱うことができる装置の設計と製造が行われます。マイクロ流体システムは、流体の流れを正確に管理するために流路、バルブ、ポンプを利用するもので、さまざまな産業における幅広い応用を可能にしています。
マイクロ流体工学の最も重要な用途のひとつは、バイオメディカル分野、特に診断とドラッグデリバリーです。マイクロ流体デバイスは、血液や唾液などの生体サンプルの迅速かつ効率的な分析を促進し、病気の早期発見や個別化医療を可能にします。さらに、複数の検査機能を1つのチップに統合するラボオンチップシステムにも使用され、医療検査のスピードと精度を大幅に向上させています。
ポイントオブケア(POC)診断に対する需要の高まりは、マイクロ流体市場の重要な促進要因となっています。マイクロ流体技術は、迅速でポータブル、かつコスト効率の高い診断ソリューションを可能にし、ヘルスケア環境におけるPOCアプリケーションに理想的なものとなっています。米国国立衛生研究所によると、世界のPOC診断市場は2022年に293億米ドルと評価され、急成長が見込まれています。この成長には、特に資源が限られた環境において、迅速かつ正確な診断ツールが必要とされていることが背景にあります。最近、Abbott Laboratoriesは、マイクロ流体技術を利用して最短5分で結果を出す新しいID NOW(TM)COVID-19検査の発売を発表し、迅速診断におけるマイクロ流体の可能性を実証しました。
製薬業界の個別化医療へのシフトがマイクロ流体市場を押し上げています。マイクロ流体デバイスは、少量の流体を正確に制御できるため、創薬、開発、検査に非常に有用です。米国食品医薬品局(FDA)は2022年に34の個別化医薬品を承認し、その年の新薬承認全体の34%を占めました。この統計は、オーダーメイド治療薬の重要性が高まっていることを強調しています。この動向に合わせて、Danaher Corporationの子会社であるMolecular Devicesは、創薬プロセスを強化するマイクロ流体技術を組み込んだQPix(TM)Microbial Colony Pickerを最近発表しました。
臓器オンチップ技術の進歩がマイクロ流体市場を前進させています。これらのマイクロ流体デバイスは、ヒト臓器の生理的状態を模倣し、従来の細胞培養や動物実験に代わるより正確な代替手段を提供します。National Center for Advancing Translational Sciencesは、2012年以来組織チップ研究に2億米ドル以上を投資してきたと報告しており、この技術の重要性を強調しています。Emulate, Inc.は最近、この最近の動向に対応するため、ヒトの血液脳関門をモデル化したマイクロ流体デバイスであるブレイン・チップを発表しました。
マイクロ流体市場は、複雑なデバイスの設計・製造に伴う開発コストの高さが課題となっています。精密なマイクロ流体システムを作るには、高度な材料や製造技術が必要になることが多く、高価になる可能性があります。こうしたコストは、中小企業や新興企業の市場参入を阻み、競争とイノベーションの低下を招きます。
規制上のハードルも、特に医療・製薬分野では大きな足かせとなります。診断やドラッグデリバリーに使用されるマイクロ流体デバイスは、保健当局が定める厳しい規制や基準に準拠しなければなりません。承認手続きに時間がかかるため、製品の上市が遅れ、メーカーにとってはコスト増となり、急速な技術進歩に対応することが難しくなります。
また、エンドユーザー産業からの需要の変動は、マイクロ流体市場の成長に影響を与える可能性があります。研究資金、ヘルスケアニーズ、産業用途の変動は、マイクロ流体製品に対する需要の一貫性の欠如につながる可能性があります。経済不況や優先順位のシフトは投資の減少を招き、この分野のメーカーや開発者にとって市場の安定性をさらに複雑にします。
Increasing demand for point-of-care testing is propelling the adoption of microfluidics. Enhanced drug discovery and development processes benefit from precise fluid manipulation is driving the market size surpass USD 41.63 Billion valued in 2024 to reach a valuation of around USD 199.42 Billion by 2031.
In addition to this, rising need for personalized medicine is spurring up the adoption of microfluidics. Microfluidic systems reduce reagent consumption and operational costs in laboratories and clinical settings, this is enabling the market grow at a CAGR of 23.86% from 2024 to 2031.
Microfluidics Market: Definition/ Overview
Microfluidics refers to the science and technology of manipulating and controlling fluids at the micrometer scale. This field involves the design and fabrication of devices that can handle very small volumes of liquids, often in the range of microliters or nanoliters. Microfluidic systems utilize channels, valves, and pumps to precisely manage fluid flow, enabling a wide range of applications across various industries.
One of the most significant applications of microfluidics is in the biomedical field, particularly for diagnostics and drug delivery. Microfluidic devices can facilitate rapid and efficient analysis of biological samples, such as blood or saliva, allowing for early disease detection and personalized medicine. Additionally, they are used in laboratory-on-a-chip systems that integrate multiple laboratory functions into a single chip, greatly enhancing the speed and accuracy of medical testing.
The growing demand for point-of-care (POC) diagnostics has been a significant driver of the Microfluidics Market. Microfluidic technologies enable rapid, portable, and cost-effective diagnostic solutions, making them ideal for POC applications in healthcare settings. According to the National Institutes of Health, the global POC diagnostics market was valued at $29.3 billion in 2022 and is expected to grow rapidly. This growth is fueled by the need for quick and accurate diagnostic tools, especially in resource-limited settings. Recently, Abbott Laboratories announced the launch of their new ID NOW(TM) COVID-19 test, which utilizes microfluidic technology to deliver results in as little as 5 minutes, demonstrating the potential of microfluidics in rapid diagnostics.
The pharmaceutical industry's shift towards personalized medicine has boosted the Microfluidics Market. Microfluidic devices enable precise control over small volumes of fluids, making them invaluable for drug discovery, development, and testing. The U.S. Food and Drug Administration (FDA) approved 34 personalized medicines in 2022, accounting for 34% of all new drug approvals that year. This statistic underscores the growing importance of tailored therapeutics. In line with this trend, Danaher Corporation's subsidiary, Molecular Devices, recently introduced the QPix(TM) Microbial Colony Picker, which incorporates microfluidic technology to enhance drug discovery processes.
Advancements in organ-on-a-chip technology have propelled the Microfluidics Market forward. These microfluidic devices mimic the physiological conditions of human organs, offering a more accurate alternative to traditional cell cultures and animal testing. The National Center for Advancing Translational Sciences reported that it has invested over USD 200 Million in tissue chip research since 2012, highlighting the significance of this technology. Responding to this growing field, Emulate, Inc. recently launched their Brain-Chip, a microfluidic device that models the human blood-brain barrier, potentially revolutionizing drug development for neurological disorders.
The microfluidics market encounters challenges due to high development costs associated with designing and fabricating complex devices. Creating precise microfluidic systems often requires advanced materials and manufacturing techniques, which can be expensive. These costs can deter smaller companies and startups from entering the market, leading to reduced competition and innovation.
Regulatory hurdles also present a significant restraint, particularly in the medical and pharmaceutical sectors. Microfluidic devices used for diagnostics and drug delivery must comply with stringent regulations and standards set by health authorities. The lengthy approval processes can delay product launches and increase costs for manufacturers, making it difficult for them to keep pace with rapid technological advancements.
Also, fluctuating demand from end-user industries can impact the growth of the microfluidics market. Variations in research funding, healthcare needs, and industrial applications can lead to inconsistent demand for microfluidic products. Economic downturns or shifts in priorities can result in decreased investments, further complicating market stability for manufacturers and developers in this field.
The device segment has emerged as the dominant force in the microfluidics market, driven by the increasing adoption of point-of-care diagnostic devices and lab-on-a-chip systems. These microfluidic devices offer rapid, portable, and cost-effective solutions for various applications in healthcare, research, and environmental monitoring. According to the National Institutes of Health, the global market for microfluidic devices in healthcare was valued at $15.7 billion in 2022 and is projected to grow significantly. Recently, Danaher Corporation's subsidiary, Cepheid, announced the launch of their new GeneXpert Omni system, a portable molecular diagnostics platform utilizing microfluidic technology for rapid testing in remote settings.
In the pharmaceutical industry, microfluidic devices are revolutionizing drug discovery and development processes. These devices enable high-throughput screening, precise drug delivery, and personalized medicine applications. The U.S. Food and Drug Administration reported that in 2023, approximately 25% of all new drug approvals utilized microfluidic technologies in their development process. Addressing this trend, Thermo Fisher Scientific recently introduced their new Gibco CTS Rotea Counterflow Centrifugation System, which incorporates microfluidic technology for cell therapy manufacturing, demonstrating the growing importance of microfluidic devices in advanced therapeutic development.
The in vitro diagnostics (IVD) segment is a dominant force in the microfluidics market, driven by the increasing demand for rapid, accurate, and cost-effective diagnostic solutions. Microfluidic technologies enable the miniaturization and automation of complex diagnostic procedures, leading to improved efficiency and reduced sample volumes. According to the U.S. Food and Drug Administration, the number of approved IVD devices utilizing microfluidic technology increased by 35% between 2020 and 2023, highlighting the growing adoption of this technology in diagnostics. Recently, Roche Diagnostics announced the launch of their cobas(R) pure integrated solutions system, which incorporates microfluidic technology to provide high-speed, compact clinical chemistry and immunoassay testing.
The COVID-19 pandemic has significantly accelerated the growth of the IVD segment in the Microfluidics Market, with a particular focus on rapid point-of-care testing. Microfluidic-based diagnostic devices have played a crucial role in the global response to the pandemic by enabling quick and accurate detection of SARS-CoV-2. The World Health Organization reported that as of December 2023, over 60% of approved rapid COVID-19 tests utilized microfluidic technologies. In response to this demand, Abbott Laboratories expanded their ID NOW(TM) platform, introducing new tests for influenza A & B, strep A, and RSV, all leveraging microfluidic technology for rapid results at the point of care.
The North American microfluidics market has been experiencing rapid growth in recent years, driven by advancements in healthcare technology and increasing demand for point-of-care diagnostics. According to the National Institutes of Health (NIH), as of 2022, the U.S. government has invested over USD 500 Million in microfluidics research and development over the past decade. This substantial funding has fueled innovation and accelerated the adoption of microfluidic technologies across various industries, including pharmaceuticals, biotechnology, and environmental monitoring.
The market's expansion is further propelled by the rising prevalence of chronic diseases and the need for more efficient and cost-effective diagnostic solutions. A report from the U.S. Food and Drug Administration (FDA) in 2023 revealed that microfluidic-based diagnostic devices have shown a 30% reduction in time-to-result compared to traditional methods. This improved efficiency has led to increased interest from both healthcare providers and patients, driving market growth. Additionally, the COVID-19 pandemic has heightened awareness of the importance of rapid, accurate diagnostic tools, further boosting the adoption of microfluidic technologies.
The Asia-Pacific region is emerging as a dominant force in the microfluidics market, driven by rapid technological advancements, increasing healthcare expenditure, and growing research activities. Countries like China, Japan, and South Korea are at the forefront of microfluidics adoption in various applications, including diagnostics, drug discovery, and environmental monitoring. According to the World Health Organization, healthcare spending in the Asia-Pacific region increased by 6.3% annually between 2018 and 2022, outpacing global averages. Recently, Danaher Corporation announced the expansion of its microfluidics research and development center in Singapore, highlighting the region's growing importance in the global microfluidics landscape.
The burgeoning pharmaceutical and biotechnology industries in Asia-Pacific have significantly contributed to the region's dominance in the microfluidics market. Microfluidic technologies are increasingly being utilized in drug discovery processes and personalized medicine applications. The China National Medical Products Administration reported that the number of innovative drug approvals in China increased by 40% from 2020 to 2023, with a significant portion utilizing microfluidic technologies in their development. Addressing this trend, Thermo Fisher Scientific recently launched a new microfluidic-based single-cell sequencing platform in collaboration with Chinese researchers, aimed at accelerating genomic studies and drug discovery efforts in the region.
The microfluidics market is a dynamic and competitive space, characterized by a diverse range of players vying for market share. These players are on the run for solidifying their presence through the adoption of strategic plans such as collaborations, mergers, acquisitions, and political support.
The organizations are focusing on innovating their product line to serve the vast population in diverse regions. Some of the prominent players operating in the microfluidics market include: