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Use and comparison of MTT, XTT and iCELLigence methods in the evaluation of drug toxicity

Yıl 2025, Cilt: 6 Sayı: 1, 66 - 71, 14.02.2025
https://doi.org/10.47582/jompac.1605042

Öz

Toxicology tests are one of the fundamental methods used in biological and pharmaceutical research. These tests are used to evaluate the viability, proliferation and toxic responses of cells. The study of biological activities of cells plays a critical role in drug development, cancer research, toxicology and various biotechnological applications. Drug toxicology is an important field of research to determine the harmful effects of drugs on cellular and biological systems. In vitro tests are widely used for accurate evaluation of drugs and their toxic effects. These tests examine the effects of drugs on cell cultures, rapidly revealing their potential harmful effects in terms of time and resources. This review discusses the advantages of the MTT (3-(4,5-dimethylthiazol-2-yl)2,5-diphenyltetrazolium bromide) and XTT (sodium 3'-[1-(phenylamino)-carbonyl]-3,4-tetrazolium]-bis (4 methoxy-6-nitro) benzene-sulfonic acid hydrate) tests, which are widely used as cytotoxicity tests, as well as the newer method iCELLigence. MTT and XTT are widely used and reliable tests that measure cell metabolism; both methods are very effective in assessing cell viability, but provide limited dynamic data. In contrast, iCELLigence is a newer technology and provides more in-depth data by monitoring the real-time responses of cells. iCELLigence continuously monitors the growth rate and morphological changes of cells, allowing for more comprehensive and sensitive results compared to traditional methods. Comparison of these methods allows determining which methodology provides more appropriate results according to different research needs.These tests are also used to define the concentration range over which more comprehensive and detailed in vitro testing can be performed to obtain meaningful data on parameters such as genotoxicity, mutation induction or programmed cell death. This review aims to compare these three methods and discuss their advantages and limitations in the assessment of drug toxicity

Etik Beyan

This study is a compilation and is considered a research that does not require ethics committee approval. Referee Evaluation Process Externally peer-reviewed. Conflict of Interest Statement The authors have no conflicts of interest to declare.

Destekleyen Kurum

Financial Disclosure: The authors declared that this study has received no financial support.

Kaynakça

  • Broadhead CL, Combes RD. The current status of food additives toxicity testing and the potential for application of the three Rs. ATLA. 2001; 29(4):471-485. doi:10.1177/026119290102900403
  • Çinarli M, Ataol ÇY, Zeyrek CT, Kiray E, Demirkalp ANC. Synthesis, single crystal investigations, DFT studies, biological activities, DNA cytotoxicity and molecular docking studies of copper (II) complex derived from the new o-vanillin Schiff base ligand. Polyhedron. 2024; 117315:1-15. doi:10.1016/j.poly.2024.117315
  • Gribaldo L, Casati S, Figliuzzi L, Marafante E. In vitro myelotoxicity of environmental contaminants. Environ Toxicol Pharmacol. 1995;6(2): 135-141. doi:10.1016/S1382-6689(98)00029-5
  • Bácskay I, Nemes D, Fenyvesi, F, et al. Role of cytotoxicity experiments in pharmaceutical development. Cytotoxicity. 2018; 8:131-146. doi:10.5772/intechopen.72539
  • Gutiérrez AC, Hoyos CG, Cock, JV, et.al. Health and toxicological effects of nanocellulose when used as a food ingredient: a review. Carbohydr Polym. 2024;323:121382. doi:10.1016/j.carbpol.2023.121382
  • Ali A, Banerjee S, Kamaal S, et al. Ligand substituent effect on the cytotoxicity activity of two new copper (ii) complexes bearing 8-hydroxyquinoline derivatives: validated by MTT assay and apoptosis in MCF-7 cancer cell line (human breast cancer). RSC Adv. 2021;11(24): 14362-14373. doi:10.1039/D1RA00172H
  • Terr AI. The cytotoxic test. West J Med. 1983;139(5):702.
  • Fenech M, Crott J, Turner J, Brown S. Necrosis, apoptosis, cytostasis and DNA damage in human lymphocytes measured simultaneously within the cytokinesis-block micronucleus assay: description of the method and results for hydrogen peroxide. Mutagenesis. 1999;14(6):605-612. doi:10.1093/mutage/14.6.605
  • Riss TL, Moravec RA, Niles AL. Cytotoxicity testing: measuring viable cells, dead cells, and detecting mechanism of cell death. In: Stoddart MJ. Eds. Mammalian cell viability: methods and protocols. Humana Press. 2011. doi:10.1007/978-1-61779-108-6_12
  • Wang K, Shindoh H, Inoue T, Horii I. Advantages of in vitro cytotoxicity testing by using primary rat hepatocytes in comparison with established cell lines. J Toxicol Sci. 2002;27(3):229-237. doi:10.2131/jts.27.229
  • Kumar P, Nagarajan A, Uchil PD. Analysis of cell viability by the MTT assay. Cold Spring Harb Protoc. 2018;2018(6):469-471. doi:10.1101/pdb.prot095505
  • Zegers J, Peters M, Albada B. DNA G-quadruplex-stabilizing metal complexes as anticancer drugs. J Biol Inorg Chem. 2023;28(2):117-138. doi:10.1007/s00775-022-01973-0
  • Scudiero DA, Shoemaker RH, Paull KD, et al. Evaluation of a soluble tetrazolium/formazan assay for cell growth and drug sensitivity in culture using human and other tumor cell lines. Cancer Res. 1988;48(17): 4827-4833.
  • Aslantürk ÖS. In vitro cytotoxicity and cell viability assays: principles, advantages, and disadvantages. In: Larramendy ML, Soloneski S. eds. Genotoxicity-A predictable risk to our actual world. 2018. doi:10. 5772/intechopen.71923
  • Ghasemi M, Turnbull T, Sebastian S, Kempson I. The MTT assay: utility, limitations, pitfalls, and interpretation in bulk and single-cell analysis. Int J Mol Sci. 2021;22(23):12827. doi:10.3390/ijms222312827
  • Şener LT, Albeni z G, Dinç B, Albeniz I. iCELLigence real time cell analysis system for examining the cytotoxicity of drugs to cancer cell lines. Exp Ther Med. 2017;14(3):1866-1870. doi:10.3892/etm.2017.4781
  • Teng Z, Kuang X, Wang J, Zhang X. Real-time cell analysis–a new method for dynamic, quantitative measurement of infectious viruses and antiserum neutralizing activity. J Virol Methods. 2013;193(2):364-370. doi:10.1016/j.jviromet.2013.06.034
  • Berg K, Hansen MB, Nielsen SE. A new sensitive bioassay for precise quantification of interferon activity as measured via the mitochondrial dehydrogenase function in cells (MTT-method). Apmis. 1990;98(1-6): 156-162. doi:10.1111/j.1699-0463.1990.tb01016.x
  • Supino R. MTT assays, In: O’Hare S, Atterwil CK eds. In vitro toxicity testing protocols. Methods in Molecular Biology™, Humana Press, New Jersey, 1995.
  • Stockert JC, Blázquez-Castro A, Cañete M, Horobin RW, Villanueva Á. MTT assay for cell viability: intracellular localization of the formazan product is in lipid droplets. Acta Histochem. 2012;114(8):785-796. doi:10. 1016/j.acthis.2012.01.006
  • Huet O, Petit JM, Ratinaud MH, Julien R. NADH-dependent dehydrogenase activity estimation by flow cytometric analysis of 3-(4, 5-dimethylthiazolyl-2-yl)-2, 5-diphenyltetrazolium bromide (MTT) reduction. Cytometry A. 1992;13(5):532-539. doi:10.1002/cyto.990130513
  • Wang X, Ge J, Wang K, Qian J, Zou Y. Evaluation of MTT assay for measurement of emodin-induced cytotoxicity. Assay Drug Dev Technol. 2006;4(2):203-207. doi:10.1089/adt.2006.4.203
  • Mosmann, T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Methods. 1983;65(1-2):55-63. doi:10.1016/0022-1759(83)90303-4
  • Wang S, Yu H, Wickliffe JK. Limitation of the MTT and XTT assays for measuring cell viability due to superoxide formation induced by nano-scale TiO2. ToxicolIn Vitro. 2011;25(8):2147-2151. doi:10.1016/j.tiv.2011. 07.007
  • Goodwin CJ, Holt SJ, Downes S, Marshall NJ. Microculture tetrazolium assays: a comparison between two new tetrazolium salts, XTT and MTS. J Immunol Methods. 1995;179(1):95-103. doi:10.1016/0022-1759 (94)00277-4
  • Zhang W, Zhu M, Wang F, et al. Mono-sulfonated tetrazolium salt based NAD (P) H detection reagents suitable for dehydrogenase and real-time cell viability assays. Anal Biochem. 2016;509:33-40. doi:10.1016/j.ab. 2016.06.026
  • Hawser S. Adhesion of different Candida spp. to plastic: XTT formazan determinations. J Med Vet Mycol. 1996;34(6):407-410. doi:10. 1080/02681219680000721
  • Hawser S. Comparisons of the susceptibilities of planktonic and adherent Candida albicans to antifungal agents: a modified XTT tetrazolium assay using synchronised C. albicans cells. J Med Vet Mycol. 1996;34(2):149-152. doi:10.1080/02681219680000231
  • Skehan P., Storeng R., Scudiero D., et al. New colorimetric cytotoxicity assay for anticancer-drug screening. JNCI:J Natl Cancer Inst. 1990; 82(13):1107-1112. doi:10.1093/jnci/82.13.1107
  • Ke N, Wang X, Xu X, Abassi YA. The xCELLigence system for real time and label free monitoring of cell viability. Methods Mol Biol. 2011;740: 33 43. doi:10.1007/978-1-61779-108-6_6
  • Giaever I and Keese CR: A morphological biosensor for mamma­lian cells. Nat. 1993;366(6455):591-592. doi:10.1038/366591a0
  • Lee RC. Cell injury by electric forces. Ann N Y Acad Sci. 2006;1066(1):85-91. doi:10.1196/annals.1363.007
  • Unwin N. The structure of ion channels in membranes of excitable cells. Neuron. 1989;3(6):665-676. doi:10.1016/0896-6273(89)90235-3
  • Wang T, Hu N, Cao J, Wu J, Su K, Wang P. A cardiomyocyte-based biosensor for antiarrhythmic drug evaluation by simultaneously monitoring cell growth and beating. Biosens Bioelectron. 2013;49:9-13. doi:10.1016/j.bios.2013.04.039
  • Schröterová L, Králová V, Voráčová A, Hašková P, Rudolf E, Červinka, M. Antiproliferative effects of selenium compounds in colon cancer cells: comparison of different cytotoxicity assays. Toxicol in vitro. 2009; 23(7):1406-1411. doi:10.1016/j.tiv.2009.07.013
  • Atmaca H, Bozkurt E, Kısım A, Uslu R. Comparative analysis of XTT assay and xCELLigence system by measuring cytotoxicity of resveratrol in human cancer cell lines. Turk Biyokim Derg. 2016;41(6):413-421. doi: 10.1515/tjb-2016-0128
  • Garcia SN, Gutierrez L, McNulty A. Real-time cellular analysis as a novel approach for in vitro cytotoxicity testing of medical device extracts. J Biomed Mater Res A. 2013;101(7):2097-2106. doi:10.1002/jbm.a.34507
  • Türker Şener L, Albeniz G, Dinç B, Albeniz I. iCELLigence real time cell analysis system for examining the cytotoxicity of drugs to cancer cell lines. Exp Ther Med. 2017;14(3):1866-1870. doi:10.3892/etm.2017.4781
  • Burton JD. The MTT assay to evaluate chemosensitivity. In: Blumenthal RD. eds. Chemosensitivity: Volume 1 In Vitro Assays. 2005. doi:10. 1385/1-59259-869-2:069
  • Mahto SK, Chandra P, Rhee SW. In vitro models, endpoints and assessment methods for the measurement of cytotoxicity. J Toxicol Environ Health Sci. 2010;2(2):87-93. doi:10.1007/BF03216487
  • Lundstrom K. Cell-impedance-based label-free technology for the identification of new drugs. Expert Opin Drug Discov. 2017;12(4):335-343. doi:10.1080/17460441.2017.1297419

İlaç toksisitesinin değerlendirilmesinde MTT, XTT ve iCELLigence yöntemlerinin kullanımı ve karşılaştırılması

Yıl 2025, Cilt: 6 Sayı: 1, 66 - 71, 14.02.2025
https://doi.org/10.47582/jompac.1605042

Öz

Toksikoloji testleri biyolojik ve farmasötik araştırmalarda kullanılan temel yöntemlerden biridir. Bu testler hücrelerin canlılığını, çoğalmasını ve toksik tepkilerini değerlendirmek için kullanılır. Hücrelerin biyolojik aktivitelerinin incelenmesi ilaç geliştirme, kanser araştırması, toksikoloji ve çeşitli biyoteknolojik uygulamalarda kritik bir rol oynar. İlaç toksikolojisi, ilaçların hücresel ve biyolojik sistemler üzerindeki zararlı etkilerini belirlemek için önemli bir araştırma alanıdır. İn vitro testler ilaçların ve toksik etkilerinin doğru değerlendirilmesi için yaygın olarak kullanılır. Bu testler ilaçların hücre kültürleri üzerindeki etkilerini inceler ve zaman ve kaynak açısından potansiyel zararlı etkilerini hızla ortaya çıkarır. MTT (3-(4,5-dimetiltiazol-2-il)-2,5-difeniltetrazolium bromür), XTT (sodyum 3'-[1-(fenilamino)-karbonil]-3,4-tetrazolium]-bis(4 metoksi-6-nitro)benzen-sülfonik asit hidrat) ve iCELLigence gibi hücresel canlılık testleri ilaç toksisitesini belirlemede kullanılan yaygın yöntemlerdir. Bu testler ayrıca genotoksisite, mutasyon indüksiyonu veya programlanmış hücre ölümü gibi parametreler hakkında anlamlı veriler elde etmek için daha kapsamlı ve ayrıntılı in vitro testlerin yapılabileceği konsantrasyon aralığını tanımlamak için kullanılır. Bu derleme, bu üç yöntemi karşılaştırmayı ve ilaç toksisitesinin değerlendirilmesindeki avantajlarını ve sınırlamalarını tartışmayı amaçlamaktadır.

Kaynakça

  • Broadhead CL, Combes RD. The current status of food additives toxicity testing and the potential for application of the three Rs. ATLA. 2001; 29(4):471-485. doi:10.1177/026119290102900403
  • Çinarli M, Ataol ÇY, Zeyrek CT, Kiray E, Demirkalp ANC. Synthesis, single crystal investigations, DFT studies, biological activities, DNA cytotoxicity and molecular docking studies of copper (II) complex derived from the new o-vanillin Schiff base ligand. Polyhedron. 2024; 117315:1-15. doi:10.1016/j.poly.2024.117315
  • Gribaldo L, Casati S, Figliuzzi L, Marafante E. In vitro myelotoxicity of environmental contaminants. Environ Toxicol Pharmacol. 1995;6(2): 135-141. doi:10.1016/S1382-6689(98)00029-5
  • Bácskay I, Nemes D, Fenyvesi, F, et al. Role of cytotoxicity experiments in pharmaceutical development. Cytotoxicity. 2018; 8:131-146. doi:10.5772/intechopen.72539
  • Gutiérrez AC, Hoyos CG, Cock, JV, et.al. Health and toxicological effects of nanocellulose when used as a food ingredient: a review. Carbohydr Polym. 2024;323:121382. doi:10.1016/j.carbpol.2023.121382
  • Ali A, Banerjee S, Kamaal S, et al. Ligand substituent effect on the cytotoxicity activity of two new copper (ii) complexes bearing 8-hydroxyquinoline derivatives: validated by MTT assay and apoptosis in MCF-7 cancer cell line (human breast cancer). RSC Adv. 2021;11(24): 14362-14373. doi:10.1039/D1RA00172H
  • Terr AI. The cytotoxic test. West J Med. 1983;139(5):702.
  • Fenech M, Crott J, Turner J, Brown S. Necrosis, apoptosis, cytostasis and DNA damage in human lymphocytes measured simultaneously within the cytokinesis-block micronucleus assay: description of the method and results for hydrogen peroxide. Mutagenesis. 1999;14(6):605-612. doi:10.1093/mutage/14.6.605
  • Riss TL, Moravec RA, Niles AL. Cytotoxicity testing: measuring viable cells, dead cells, and detecting mechanism of cell death. In: Stoddart MJ. Eds. Mammalian cell viability: methods and protocols. Humana Press. 2011. doi:10.1007/978-1-61779-108-6_12
  • Wang K, Shindoh H, Inoue T, Horii I. Advantages of in vitro cytotoxicity testing by using primary rat hepatocytes in comparison with established cell lines. J Toxicol Sci. 2002;27(3):229-237. doi:10.2131/jts.27.229
  • Kumar P, Nagarajan A, Uchil PD. Analysis of cell viability by the MTT assay. Cold Spring Harb Protoc. 2018;2018(6):469-471. doi:10.1101/pdb.prot095505
  • Zegers J, Peters M, Albada B. DNA G-quadruplex-stabilizing metal complexes as anticancer drugs. J Biol Inorg Chem. 2023;28(2):117-138. doi:10.1007/s00775-022-01973-0
  • Scudiero DA, Shoemaker RH, Paull KD, et al. Evaluation of a soluble tetrazolium/formazan assay for cell growth and drug sensitivity in culture using human and other tumor cell lines. Cancer Res. 1988;48(17): 4827-4833.
  • Aslantürk ÖS. In vitro cytotoxicity and cell viability assays: principles, advantages, and disadvantages. In: Larramendy ML, Soloneski S. eds. Genotoxicity-A predictable risk to our actual world. 2018. doi:10. 5772/intechopen.71923
  • Ghasemi M, Turnbull T, Sebastian S, Kempson I. The MTT assay: utility, limitations, pitfalls, and interpretation in bulk and single-cell analysis. Int J Mol Sci. 2021;22(23):12827. doi:10.3390/ijms222312827
  • Şener LT, Albeni z G, Dinç B, Albeniz I. iCELLigence real time cell analysis system for examining the cytotoxicity of drugs to cancer cell lines. Exp Ther Med. 2017;14(3):1866-1870. doi:10.3892/etm.2017.4781
  • Teng Z, Kuang X, Wang J, Zhang X. Real-time cell analysis–a new method for dynamic, quantitative measurement of infectious viruses and antiserum neutralizing activity. J Virol Methods. 2013;193(2):364-370. doi:10.1016/j.jviromet.2013.06.034
  • Berg K, Hansen MB, Nielsen SE. A new sensitive bioassay for precise quantification of interferon activity as measured via the mitochondrial dehydrogenase function in cells (MTT-method). Apmis. 1990;98(1-6): 156-162. doi:10.1111/j.1699-0463.1990.tb01016.x
  • Supino R. MTT assays, In: O’Hare S, Atterwil CK eds. In vitro toxicity testing protocols. Methods in Molecular Biology™, Humana Press, New Jersey, 1995.
  • Stockert JC, Blázquez-Castro A, Cañete M, Horobin RW, Villanueva Á. MTT assay for cell viability: intracellular localization of the formazan product is in lipid droplets. Acta Histochem. 2012;114(8):785-796. doi:10. 1016/j.acthis.2012.01.006
  • Huet O, Petit JM, Ratinaud MH, Julien R. NADH-dependent dehydrogenase activity estimation by flow cytometric analysis of 3-(4, 5-dimethylthiazolyl-2-yl)-2, 5-diphenyltetrazolium bromide (MTT) reduction. Cytometry A. 1992;13(5):532-539. doi:10.1002/cyto.990130513
  • Wang X, Ge J, Wang K, Qian J, Zou Y. Evaluation of MTT assay for measurement of emodin-induced cytotoxicity. Assay Drug Dev Technol. 2006;4(2):203-207. doi:10.1089/adt.2006.4.203
  • Mosmann, T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Methods. 1983;65(1-2):55-63. doi:10.1016/0022-1759(83)90303-4
  • Wang S, Yu H, Wickliffe JK. Limitation of the MTT and XTT assays for measuring cell viability due to superoxide formation induced by nano-scale TiO2. ToxicolIn Vitro. 2011;25(8):2147-2151. doi:10.1016/j.tiv.2011. 07.007
  • Goodwin CJ, Holt SJ, Downes S, Marshall NJ. Microculture tetrazolium assays: a comparison between two new tetrazolium salts, XTT and MTS. J Immunol Methods. 1995;179(1):95-103. doi:10.1016/0022-1759 (94)00277-4
  • Zhang W, Zhu M, Wang F, et al. Mono-sulfonated tetrazolium salt based NAD (P) H detection reagents suitable for dehydrogenase and real-time cell viability assays. Anal Biochem. 2016;509:33-40. doi:10.1016/j.ab. 2016.06.026
  • Hawser S. Adhesion of different Candida spp. to plastic: XTT formazan determinations. J Med Vet Mycol. 1996;34(6):407-410. doi:10. 1080/02681219680000721
  • Hawser S. Comparisons of the susceptibilities of planktonic and adherent Candida albicans to antifungal agents: a modified XTT tetrazolium assay using synchronised C. albicans cells. J Med Vet Mycol. 1996;34(2):149-152. doi:10.1080/02681219680000231
  • Skehan P., Storeng R., Scudiero D., et al. New colorimetric cytotoxicity assay for anticancer-drug screening. JNCI:J Natl Cancer Inst. 1990; 82(13):1107-1112. doi:10.1093/jnci/82.13.1107
  • Ke N, Wang X, Xu X, Abassi YA. The xCELLigence system for real time and label free monitoring of cell viability. Methods Mol Biol. 2011;740: 33 43. doi:10.1007/978-1-61779-108-6_6
  • Giaever I and Keese CR: A morphological biosensor for mamma­lian cells. Nat. 1993;366(6455):591-592. doi:10.1038/366591a0
  • Lee RC. Cell injury by electric forces. Ann N Y Acad Sci. 2006;1066(1):85-91. doi:10.1196/annals.1363.007
  • Unwin N. The structure of ion channels in membranes of excitable cells. Neuron. 1989;3(6):665-676. doi:10.1016/0896-6273(89)90235-3
  • Wang T, Hu N, Cao J, Wu J, Su K, Wang P. A cardiomyocyte-based biosensor for antiarrhythmic drug evaluation by simultaneously monitoring cell growth and beating. Biosens Bioelectron. 2013;49:9-13. doi:10.1016/j.bios.2013.04.039
  • Schröterová L, Králová V, Voráčová A, Hašková P, Rudolf E, Červinka, M. Antiproliferative effects of selenium compounds in colon cancer cells: comparison of different cytotoxicity assays. Toxicol in vitro. 2009; 23(7):1406-1411. doi:10.1016/j.tiv.2009.07.013
  • Atmaca H, Bozkurt E, Kısım A, Uslu R. Comparative analysis of XTT assay and xCELLigence system by measuring cytotoxicity of resveratrol in human cancer cell lines. Turk Biyokim Derg. 2016;41(6):413-421. doi: 10.1515/tjb-2016-0128
  • Garcia SN, Gutierrez L, McNulty A. Real-time cellular analysis as a novel approach for in vitro cytotoxicity testing of medical device extracts. J Biomed Mater Res A. 2013;101(7):2097-2106. doi:10.1002/jbm.a.34507
  • Türker Şener L, Albeniz G, Dinç B, Albeniz I. iCELLigence real time cell analysis system for examining the cytotoxicity of drugs to cancer cell lines. Exp Ther Med. 2017;14(3):1866-1870. doi:10.3892/etm.2017.4781
  • Burton JD. The MTT assay to evaluate chemosensitivity. In: Blumenthal RD. eds. Chemosensitivity: Volume 1 In Vitro Assays. 2005. doi:10. 1385/1-59259-869-2:069
  • Mahto SK, Chandra P, Rhee SW. In vitro models, endpoints and assessment methods for the measurement of cytotoxicity. J Toxicol Environ Health Sci. 2010;2(2):87-93. doi:10.1007/BF03216487
  • Lundstrom K. Cell-impedance-based label-free technology for the identification of new drugs. Expert Opin Drug Discov. 2017;12(4):335-343. doi:10.1080/17460441.2017.1297419
Toplam 41 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Kanser Hücre Biyolojisi
Bölüm Review [en] Derleme [tr]
Yazarlar

Ayşe Nur Coşkun Demirkalp 0000-0002-8125-7670

Yayımlanma Tarihi 14 Şubat 2025
Gönderilme Tarihi 21 Aralık 2024
Kabul Tarihi 14 Ocak 2025
Yayımlandığı Sayı Yıl 2025 Cilt: 6 Sayı: 1

Kaynak Göster

AMA Coşkun Demirkalp AN. Use and comparison of MTT, XTT and iCELLigence methods in the evaluation of drug toxicity. J Med Palliat Care / JOMPAC / Jompac. Şubat 2025;6(1):66-71. doi:10.47582/jompac.1605042

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