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On the use of acridinium indicators for the chemiluminescent determination of the total antioxidant capacity of dietary supplements
Authors: Krzyminski, K. K., Roshal, A. D., Rudnicki-Velasquez, P. B., Zamojc, K.
Journal: Luminescence (2019): ersion="1.0" encoding="UTF-8" ?>26005.enlEndN

A novel chemiluminescent immunoassay based on original acridinium ester labels as better solution for diagnosis of human toxoplasmosis than conventional ELISA test
Authors: Holec-Gasior, L., Ferra, B., Czechowska, J., Serdiuk, I. E., Krzyminski, K.
Journal: Diagn Microbiol Infect Dis (2018): 13-19

Enhancement effect on the chemiluminescence of acridinium esters under neutral conditions
Authors: Nakazono, M., Nanbu, S.
Journal: Luminescence (2018): 345-348

A comparison of chemiluminescent acridinium dimethylphenyl ester labels with different conjugation sites
Authors: Natrajan, A., Wen, D.
Journal: Org Biomol Chem (2015): 2622-33

Chemiluminescence accompanied by the reaction of acridinium ester and manganese (II)
Authors: Ren, L., Cui, H.
Journal: Luminescence (2014): 929-32

Development of a highly sensitive chemiluminescent assay for hydrogen peroxide under neutral conditions using acridinium ester and its application to an enzyme immunoassay
Authors: Arakawa, H., Tsuruoka, K., Ohno, K., Tajima, N., Nagano, H.
Journal: Luminescence (2014): 374-7

Synthesis and properties of chemiluminescent acridinium ester labels with fluorous tags
Authors: Natrajan, A., Wen, D., Sharpe, D.
Journal: Org Biomol Chem (2014): 3887-901

Quenching the chemiluminescence of acridinium ester by graphene oxide for label-free and homogeneous DNA detection
Authors: He, Y., Huang, G., Cui, H.
Journal: ACS Appl Mater Interfaces (2013): 11336-40

An efficient fluorescence sensor for superoxide with an acridinium ion-linked porphyrin triad
Authors: Kotani, H., Ohkubo, K., Crossley, M. J., Fukuzumi, S.
Journal: J Am Chem Soc (2011): 11092-5

Effect of surfactants on the chemiluminescence of acridinium dimethylphenyl ester labels and their conjugates
Authors: Natrajan, A., Sharpe, D., Wen, D.
Journal: Org Biomol Chem (2011): 5092-103

Chemiluminescent reductive acridinium triggering (CRAT)--mechanism and applications
Authors: Zomer, B., Colle, L., Jedynska, A., Pasterkamp, G., Kooter, I., Bloemen, H.
Journal: Anal Bioanal Chem (2011): 2945-54

Superquenching acridinium ester chemiluminescence by gold nanoparticles for DNA detection
Authors: Xu, Q., Liu, J., He, Z., Yang, S.
Journal: Chem Commun (Camb) (2010): 8800-2

Chemiluminogenic properties of 10-methyl-9-(phenoxycarbonyl)acridinium cations in organic environments
Authors: Krzyminski, K., Roshal, A. D., Zadykowicz, B., Bialk-Bielinska, A., Sieradzan, A.
Journal: J Phys Chem A (2010): 10550-62

Development and application of a novel acridinium ester for use as a chemiluminescent emitter in nucleic acid hybridisation assays using chemiluminescence quenching
Authors: Brown, R. C., Li, Z., Rutter, A. J., Mu, X., Weeks, O. H., Smith, K., Weeks, I.
Journal: Org Biomol Chem (2009): 386-94

Acridinium ester conjugated to lectin as chemiluminescent histochemistry marker
Authors: Campos, L. M., Cavalcanti, C. L., Lima-Filho, J. L., Carvalho, L. B., Beltrao, E. I.
Journal: Biomarkers (2006): 480-4

Novel biotinylated acridinium derivatives: new reagents for fluorescence immunoassays and proteomics
Authors: Scorilas, A., Agiamarnioti, K., Papadopoulos, K.
Journal: Clin Chim Acta (2005): 159-67

Chemiluminescence quenching of pteroic acid-N-sulfonyl-acridinium-9-carboxamide conjugates by folate binding protein
Authors: Adamczyk, M., Fino, J. R., Mattingly, P. G., Moore, J. A., Pan, Y.
Journal: Bioorg Med Chem Lett (2004): 2313-7

Intrinsic factor-mediated modulation of cyanocobalamin-N-sulfonyl-acridinium-9-carboxamide chemiluminescence
Authors: Adamczyk, M., Johnson, D. D., Mattingly, P. G., Moore, J. A., Pan, Y.
Journal: Bioorg Med Chem Lett (2004): 3917-21

Regiodependent luminescence quenching of biotinylated N-sulfonyl-acridinium-9-carboxamides by avidin
Authors: Adamczyk, M., Mattingly, P. G., Moore, J. A., Pan, Y.
Journal: Org Lett (2003): 3779-82

High stability and high efficiency chemiluminescent acridinium compounds obtained from 9-acridine carboxylic esters of hydroxamic and sulphohydroxamic acids
Authors: Renotte, R., Sarlet, G., Thunus, L., Lejeune, R.
Journal: Luminescence (2000): 311-20

Stable and versatile active acridinium esters II
Authors: Razavi, Z., McCapra, F.
Journal: Luminescence (2000): 245-9

Selectivity and sensitivity in the measurement of reactive oxygen species (ROS) using chemiluminescent microspheres prepared by the binding of acridinium ester or ABEI to polymer microspheres
Authors: Hosaka, S., Itagaki, T., Kuramitsu, Y.
Journal: Luminescence (1999): 349-54

Acridinium ester labelled cytokines: receptor binding studies with human interleukin-1 alpha, interleukin-1 beta and interferon-gamma
Authors: Joss, U. R., Towbin, H.
Journal: J Biolumin Chemilumin (1994): 21-8

Synthesis and properties of new luminescent acridinium-9-carboxylic acid derivatives and their application in luminescence immunoassays (LIA)
Authors: Kinkel, T., Lubbers, H., Schmidt, E., Molz, P., Skrzipczyk, H. J.
Journal: J Biolumin Chemilumin (1989): 136-9

Chemiluminescence immunoassay of plasma progesterone, with progesterone-acridinium ester used as the labeled antigen
Authors: Richardson, A. P., Kim, J. B., Barnard, G. J., Collins, W. P., McCapra, F.
Journal: Clin Chem (1985): 1664-8

Acridinium esters as high-specific-activity labels in immunoassay
Authors: Weeks, I., Beheshti, I., McCapra, F., Campbell, A. K., Woodhead, J. S.
Journal: Clin Chem (1983): 1474-9