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市場調查報告書
商品編碼
1454741
體外毒理學測試市場 - 產品和服務、終點和測試、技術、方法、產業 - 全球預測,2024 年 - 2032 年In-vitro Toxicology Testing Market - Product and Services, Endpoint and Test, Technology, Method, Industry - Global Forecast, 2024 - 2032 |
預計從 2024 年到 2032 年,體外毒理學測試市場規模將以超過 7.7% 的CAGR成長,這主要是由於出於倫理問題和監管壓力,擴大採用體外方法而不是動物測試。人們越來越認知到化學物質對人類健康的不利影響,以及細胞培養技術的發展,正在加速體外測試的吸引力。
近年來,藥品、化妝品和化學品等各行業的藥物開發和化學品風險評估過程中的安全性評估越來越受到重視。毒理學研究資金的可用性和高通量篩選分析的開發將進一步提高體外毒理學測試解決方案的使用率。例如,2023 年 8 月,Altis Biosystems 推出了 RepliGut(R) Planar InflammaScreen(TM) 服務,利用人源體外結腸發炎模型來增強發炎性腸道疾病 (IBD) 的藥物發現。
體外毒理學測試產業分為產品和服務、終點和測試、技術、方法、產業和地區。
在產品和服務方面,由於對高通量篩選分析的需求不斷增加,從2024年到2032年,分析領域的市場規模將以8%的成長率成長。檢測技術的不斷進步使得結果更加準確可靠。人們越來越關注開發針對特定毒理學終點的專門測定方法,這將增加體外測試的滲透率。針對不同應用客製化的各種檢測試劑盒和服務的可用性也將推動該細分市場的成長。
在終點和測試方面,預計從 2024 年到 2032 年,基因毒性領域的體外毒理學測試行業將以 8% 的CAGR成長。這是由於基因毒性測試方法的進步、各個領域對基因毒性化合物的監管審查力度加大。行業,以及人們對與遺傳毒性物質相關的潛在危害的認知不斷增強。用於評估遺傳毒性的新測定方法和測試策略的開發也將增加對遺傳毒性測試中體外測試的需求。
從地區來看,亞太地區體外毒理學測試市場在預計時間內將呈現 8.2% 的成長率。這可以歸因於工業化程度的不斷提高、人們對毒性測試在藥物開發和化學品安全評估中的重要性的認知不斷提高,以及嚴格的產品安全監管指南。製藥和生物技術領域不斷成長的研發活動以及不斷擴大的醫療基礎設施將刺激該地區體外毒理學測試解決方案的採用。
In-vitro Toxicology Testing Market size is predicted to expand at over 7.7% CAGR from 2024 to 2032, mainly led by the increasing adoption of in-vitro methods over animal testing due to ethical concerns and regulatory pressures. The rising awareness about the adverse effects of chemicals on human health and the developments in cell culture technologies are accelerating the appeal of in-vitro testing.
Lately, there has been growing emphasis on safety assessment during drug development and chemical risk assessment in various industries, such as pharmaceuticals, cosmetics, and chemicals. The availability of funding for research in toxicology and the development of high-throughput screening assays will further increase the utilization of in-vitro toxicology testing solutions. For instance, in August 2023, Altis Biosystems launched RepliGut(R) Planar InflammaScreen(TM) Services to enhance drug discovery for inflammatory bowel diseases (IBD) using a human-derived in vitro model of colon inflammation.
The in-vitro toxicology testing industry is segregated into product and services, endpoint and test, technology, method, industry, and region.
With respect to product and services, the market size from the assays segment will rise at 8% growth rate from 2024 to 2032, on account of the increasing demand for high-throughput screening assays. Rising advancements in assay technologies are allowing for more accurate and reliable results. The growing focus on developing specialized assays for specific toxicological endpoints will increase the penetration of in-vitro testing. The availability of a wide range of assay kits and services tailored to different applications will also drive the segment growth.
In terms of endpoint and test, the in-vitro toxicology testing industry from the genotoxicity segment is anticipated to rise at 8% CAGR from 2024 to 2032. This is due to the advancements in genotoxicity testing methods, increased regulatory scrutiny on genotoxic compounds in various industries, and the growing awareness about the potential hazards associated with genotoxic substances. The development of novel assays and testing strategies for assessing genotoxicity will also increase the demand for in-vitro testing in genotoxicity testing.
Regionally, the Asia Pacific in-vitro toxicology testing market will depict 8.2% growth rate during the projected timeframe. This can be attributed to the increasing industrialization, rising awareness about the importance of toxicity testing in drug development and chemical safety assessment, as well as stringent regulatory guidelines for product safety. The growing R&D activities in pharmaceutical and biotechnology sectors along with the expanding healthcare infrastructure will stimulate the adoption for in-vitro toxicology testing solutions in the region.