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市場調查報告書
商品編碼
1473809
支原體測試市場 - 按產品類型(儀器、試劑盒和試劑、服務)、按技術(PCR、ELISA、微生物培養技術、酶法)、按應用(細胞株測試、病毒測試)、按最終用途和預測, 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 |
由於細胞培養研究中支原體污染的流行以及對生物製藥和疫苗的強烈需求,支原體測試市場規模預計在 2024 年至 2032 年期間將以超過 11.9% 的複合年成長率成長。對生物製藥和疫苗不斷成長的需求是推動市場擴張的重要驅動力。生物製藥,包括單株抗體、重組蛋白和基因療法,正成為現代醫學的基石。根據世界衛生組織統計,光是2021年,全球疫苗供應量就達160億劑,價值約1,410億美元。
由於生物製藥和疫苗是使用複雜的細胞培養過程製造的,因此確保其安全性和有效性變得至關重要。支原體污染對這些產品的品質和安全構成嚴重風險。受污染的生物藥品和疫苗可能會對患者造成不利影響、監管問題以及製造商的財務損失。為了滿足監管要求並維持產品質量,生物製藥和疫苗製造商擴大投資先進的支原體檢測解決方案。這些解決方案能夠快速且準確地檢測支原體污染,同時有助於維護生物製藥和疫苗生產過程的完整性。
支原體檢測市場根據產品類型、應用、技術、最終用途和地區進行分類。
2024年至2032年,儀器產品類型細分市場的市場規模預計將以11.8%的複合年成長率大幅成長。 、準確的支原體檢測細胞培養物和生物製藥產品中的污染。這些儀器可實現高通量篩選和自動化,進而提高支原體檢測實驗室的效率和生產力。此外,創新攜帶式儀器的出現促進了現場測試,進一步縮短了周轉時間並實現了污染風險的即時監控。
從技術角度來看,酵素連結免疫吸附測定(ELISA) 領域的支原體檢測產業預計到2032 年複合年成長率將達到11.8%。製品中的支原體抗原或抗體。憑藉其高靈敏度和可擴展性,ELISA 還為研究實驗室和生物製藥生產設施中的常規支原體篩檢提供了經濟高效的解決方案。
在快速工業化、生物製藥研發投資增加以及對產品安全和品質標準意識不斷增強的推動下,亞太地區支原體檢測行業預計到 2032 年將以 12.3% 的複合年成長率成長。在政府有利措施、基礎設施發展和技術進步的推動下,中國、印度和日本等國家的生物製藥生產活動激增。此外,大量熟練勞動力和具有成本效益的製造能力的存在將進一步擴大區域市場的擴張。
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.