Literature DB >> 16715394

Biopharmaceutical characterization of the telomerase inhibitor BRACO19.

S Taetz1, C Baldes, T E Mürdter, E Kleideiter, K Piotrowska, U Bock, E Haltner-Ukomadu, J Mueller, H Huwer, U F Schaefer, U Klotz, C-M Lehr.   

Abstract

PURPOSE: To characterize the telomerase inhibitor and G-quadruplex stabilizing substance 9-[4-(N,N-dimethylamino)phenylamino]-3,6-bis (3-pyrrolodino-propionamido) acridine x 3HCl (BRACO19) in terms of biopharmaceutical properties such as solubility, protein binding, interaction with membrane lipids, cytotoxicity, and permeability across pulmonary epithelial cells.
METHODS: Protein binding and interaction with membrane lipids were investigated by two high-performance liquid chromatography methods with immobilized human serum albumin and immobilized phosphatidylcholine, respectively. Cytotoxicity (methyl-thiazolyl-tetrazolium assay) and transport studies were performed with the bronchial cell lines 16HBE14o- and Calu-3, primary human alveolar epithelial cells, and the intestinal cell line Caco-2. Transport experiments were also done in the presence of cyclosporin A (10 microM) and tetraethylammonium chloride (5 mM) and at low temperature (4 degrees C).
RESULTS: BRACO19 has good solubility of at least 2 mg/mL in water and in physiological buffers of pH 7.4 and below. Protein binding to human serum albumin was 38%. No interaction with membrane lipids could be found. Cytotoxicity in 16HBE14o-, Calu-3, and human alveolar epithelial cells was in the range of IC50 = 3.5 to 13.5 microM. Caco-2 cells were not affected at concentrations up to 50 microM. No transport of BRACO19 was detected across either cell monolayer in absorptive direction. In secretory direction, permeability was very low, with P (app) values in the range of 0.25 x 10(-7) to 0.98 x 10(-7) cm/s for all epithelial cell cultures tested. The transport was not influenced by cyclosporin A or tetraethylammonium chloride or at 4 degrees C, indicating that no efflux/influx systems or active transport are involved.
CONCLUSIONS: From these results, we conclude that the very poor permeability of BRACO19 is its main biopharmaceutical limitation. Further applications will require a suitable formulation to warrant adequate delivery across cellular barriers.

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Year:  2006        PMID: 16715394     DOI: 10.1007/s11095-006-0026-y

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.580


  27 in total

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Authors:  K J Elbert; U F Schäfer; H J Schäfers; K J Kim; V H Lee; C M Lehr
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3.  Trisubstituted acridine derivatives as potent and selective telomerase inhibitors.

Authors:  R John Harrison; Javier Cuesta; Gianni Chessari; Martin A Read; Sanji K Basra; Anthony P Reszka; James Morrell; Sharon M Gowan; Christopher M Incles; Farial A Tanious; W David Wilson; Lloyd R Kelland; Stephen Neidle
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4.  Validation of cell culture models for the intestine and the blood-brain barrier and comparison of drug permeation.

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5.  Optimization of the TRAP assay to evaluate specificity of telomerase inhibitors.

Authors:  Kamilla Piotrowska; Elke Kleideiter; Thomas E Mürdter; Sebastian Taetz; Christiane Baldes; Ulrich Schaefer; Claus-Michael Lehr; Ulrich Klotz
Journal:  Lab Invest       Date:  2005-12       Impact factor: 5.662

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7.  Indomethacin enhances the cytotoxicity of VCR and ADR in human pulmonary adenocarcinoma cells.

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8.  The G-quadruplex-interactive molecule BRACO-19 inhibits tumor growth, consistent with telomere targeting and interference with telomerase function.

Authors:  Angelika M Burger; Fangping Dai; Christoph M Schultes; Anthony P Reszka; Michael J Moore; John A Double; Stephen Neidle
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9.  Inhibition of human telomerase enhances the effect of chemotherapeutic agents in lung cancer cells.

Authors:  Masafumi Misawa; Tetsuzo Tauchi; Goro Sashida; Akihiro Nakajima; Kenji Abe; Junko H Ohyashiki; Kazuma Ohyashiki
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10.  CFTR expression and chloride secretion in polarized immortal human bronchial epithelial cells.

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1.  Heterocyclic dications as a new class of telomeric G-quadruplex targeting agents.

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4.  Molecular docking based screening of triterpenoids as potential G-quadruplex stabilizing ligands with anti-cancer activity.

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5.  Identification of G-Quadruplex Inducers Usinga Simple, Inexpensiveand Rapid High Throughput Assay, and TheirInhibition of Human Telomerase.

Authors:  Maria Florencia Sassano; Alexander P Schlesinger; Michael B Jarstfer
Journal:  Open Med Chem J       Date:  2012-10-19

Review 6.  G-quadruplexes and G-quadruplex ligands: targets and tools in antiviral therapy.

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  6 in total

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