市场调查报告书
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1473809
支原体测试市场 - 按产品类型(仪器、试剂盒和试剂、服务)、按技术(PCR、ELISA、微生物培养技术、酶法)、按应用(细胞株测试、病毒测试)、按最终用途和预测, 2024 - 2032Mycoplasma Testing Market - By Product Type (Instruments, Kits & Reagents, Services), By Technique (PCR, ELISA, Microbial Culturing Techniques, Enzymatic Methods), By Application (Cell Line Testing, Virus Testing), By End-use & Forecast, 2024 - 2032 |
由于细胞培养研究中支原体污染的流行以及对生物製药和疫苗的强烈需求,支原体测试市场规模预计在 2024 年至 2032 年期间将以超过 11.9% 的复合年增长率增长。对生物製药和疫苗不断增长的需求是推动市场扩张的重要驱动力。生物製药,包括单株抗体、重组蛋白和基因疗法,正成为现代医学的基石。根据世界卫生组织统计,光是2021年,全球疫苗供应量就达160亿剂,价值约1,410亿美元。
由于生物製药和疫苗是使用复杂的细胞培养过程製造的,因此确保其安全性和有效性变得至关重要。支原体污染对这些产品的品质和安全构成严重风险。受污染的生物药品和疫苗可能会对患者造成不利影响、监管问题以及製造商的财务损失。为了满足监管要求并维持产品质量,生物製药和疫苗製造商越来越多地投资先进的支原体检测解决方案。这些解决方案能够快速且准确地检测支原体污染,同时有助于维护生物製药和疫苗生产过程的完整性。
支原体检测市场根据产品类型、应用、技术、最终用途和地区进行分类。
2024年至2032年,仪器产品类型细分市场的市场规模预计将以11.8%的复合年增长率大幅增长。 、准确的支原体检测细胞培养物和生物製药产品中的污染。这些仪器可实现高通量筛选和自动化,进而提高支原体检测实验室的效率和生产力。此外,创新便携式仪器的出现促进了现场测试,进一步缩短了周转时间并实现了污染风险的即时监控。
从技术角度来看,酵素连结免疫吸附测定(ELISA) 领域的支原体检测产业预计到2032 年复合年增长率将达到11.8%。製品中的支原体抗原或抗体。凭藉其高灵敏度和可扩展性,ELISA 还为研究实验室和生物製药生产设施中的常规支原体筛检提供了经济高效的解决方案。
在快速工业化、生物製药研发投资增加以及对产品安全和品质标准意识不断增强的推动下,亚太地区支原体检测行业预计到 2032 年将以 12.3% 的复合年增长率增长。在政府有利措施、基础设施发展和技术进步的推动下,中国、印度和日本等国家的生物製药生产活动激增。此外,大量熟练劳动力和具有成本效益的製造能力的存在将进一步扩大区域市场的扩张。
Mycoplasma Testing Market size is expected to grow at over 11.9% CAGR during 2024-2032, driven by increasing prevalence of mycoplasma contamination in cell culture-based research and the strong need for biopharmaceuticals and vaccines. The growing demand for biopharmaceuticals and vaccines is a significant driver propelling the market expansion. Biopharmaceuticals, including monoclonal antibodies, recombinant proteins, and gene therapies, are becoming the cornerstone of modern medicine. As per WHO, in 2021 alone, the global supply of vaccines amounted to 16 billion doses, valued at approximately US$ 141 billion.
As biopharmaceuticals and vaccines are manufactured using complex cell culture processes, ensuring their safety and efficacy has turned paramount. Mycoplasma contamination poses a serious risk to the quality and safety of these products. Contaminated biopharmaceuticals and vaccines can lead to adverse effects on patients, regulatory issues, and financial losses for manufacturers. To meet regulatory requirements and maintain product quality, biopharmaceutical and vaccine manufacturers are increasingly investing in advanced mycoplasma testing solutions. These solutions enable rapid and accurate detection of mycoplasma contamination while helping to safeguard the integrity of biopharmaceutical and vaccine production processes.
The mycoplasma testing market is classified based on product type, application, technique, end-use and region.
The market size from the instruments product type segment is expected to grow substantially at 11.8% CAGR from 2024 to 2032. Advanced instrumentation technologies, such as polymerase chain reaction (PCR) and nucleic acid amplification tests (NAATs) offer rapid and accurate detection of mycoplasma contamination in cell cultures and biopharmaceutical products. These instruments enable high-throughput screening and automation, enhancing efficiency and productivity in mycoplasma testing laboratories. Additionally, the advent of innovative portable instruments facilitates on-site testing, further reducing turnaround times and enabling real-time monitoring of contamination risks.
By technique, the mycoplasma testing industry from the enzyme-linked immunosorbent assay (ELISA) segment is poised to record 11.8% CAGR through 2032. ELISA-based assays leverage the specificity of antigen-antibody interactions to detect and quantify mycoplasma antigens or antibodies in biological samples. With its high sensitivity and scalability, ELISA also offers a cost-effective solution for routine mycoplasma screening in research laboratories and biopharmaceutical manufacturing facilities.
Asia Pacific mycoplasma testing industry is set to expand at 12.3% CAGR till 2032, driven by rapid industrialization, increasing investments in biopharmaceutical R&D, and the growing awareness about product safety and quality standards. Countries, such as China, India, and Japan are witnessing a surge in biopharmaceutical manufacturing activities, fueled by favorable government initiatives, infrastructure development, and technological advancements. Moreover, the presence of a large pool of skilled labor and cost-effective manufacturing capabilities will further augment the regional market expansion.