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Pharmaceutics. 2019 Apr 1;11(4). pii: E151. doi: 10.3390/pharmaceutics11040151.

Synthesis and Biological Evaluation of RGD⁻Cryptophycin Conjugates for Targeted Drug Delivery.

Author information

1
Organic and Bioorganic Chemistry, Department of Chemistry, Bielefeld University, Universitätsstraße 25, DE-33615 Bielefeld, Germany. adina.borbely@uni-bielefeld.de.
2
Organic and Bioorganic Chemistry, Department of Chemistry, Bielefeld University, Universitätsstraße 25, DE-33615 Bielefeld, Germany. eduard.figueras@uni-bielefeld.de.
3
Organic and Bioorganic Chemistry, Department of Chemistry, Bielefeld University, Universitätsstraße 25, DE-33615 Bielefeld, Germany. ana_martins@exiris.it.
4
Exiris s.r.l., Via di Castel Romano 100, IT-00128 Rome, Italy. ana_martins@exiris.it.
5
IRBM S.p.A, Via Pontina km. 30,600, IT-00071 Pomezia (Rome), Italy. s.esposito@irbm.com.
6
IRBM S.p.A, Via Pontina km. 30,600, IT-00071 Pomezia (Rome), Italy. g.auciello@irbm.com.
7
IRBM S.p.A, Via Pontina km. 30,600, IT-00071 Pomezia (Rome), Italy. e.monteagudo@irbm.com.
8
IRBM S.p.A, Via Pontina km. 30,600, IT-00071 Pomezia (Rome), Italy. a.dimarco@irbm.com.
9
IRBM S.p.A, Via Pontina km. 30,600, IT-00071 Pomezia (Rome), Italy. v.summa@irbm.com.
10
Italfarmaco S.p.A., Via dei Lavoratori, 54, IT-20092 Cinisello Balsamo (Milano), Italy. p.cordella@italfarmaco.com.
11
Italfarmaco S.p.A., Via dei Lavoratori, 54, IT-20092 Cinisello Balsamo (Milano), Italy. r.perego@italfarmaco.com.
12
Organic and Bioorganic Chemistry, Department of Chemistry, Bielefeld University, Universitätsstraße 25, DE-33615 Bielefeld, Germany. isabell.kemker@uni-bielefeld.de.
13
Organic and Bioorganic Chemistry, Department of Chemistry, Bielefeld University, Universitätsstraße 25, DE-33615 Bielefeld, Germany. marcel.frese@uni-bielefeld.de.
14
Exiris s.r.l., Via di Castel Romano 100, IT-00128 Rome, Italy. paola_gallinari@exiris.it.
15
Exiris s.r.l., Via di Castel Romano 100, IT-00128 Rome, Italy. christian_steinkuhler@exiris.it.
16
Italfarmaco S.p.A., Via dei Lavoratori, 54, IT-20092 Cinisello Balsamo (Milano), Italy. christian_steinkuhler@exiris.it.
17
Organic and Bioorganic Chemistry, Department of Chemistry, Bielefeld University, Universitätsstraße 25, DE-33615 Bielefeld, Germany. norbert.sewald@uni-bielefeld.de.

Abstract

Cryptophycins are potent tubulin polymerization inhibitors with picomolar antiproliferative potency in vitro and activity against multidrug-resistant (MDR) cancer cells. Because of neurotoxic side effects and limited efficacy in vivo, cryptophycin-52 failed as a clinical candidate in cancer treatment. However, this class of compounds has emerged as attractive payloads for tumor-targeting applications. In this study, cryptophycin was conjugated to the cyclopeptide c(RGDfK), targeting integrin αvβ₃, across the protease-cleavable Val-Cit linker and two different self-immolative spacers. Plasma metabolic stability studies in vitro showed that our selected payload displays an improved stability compared to the parent compound, while the stability of the conjugates is strongly influenced by the self-immolative moiety. Cathepsin B cleavage assays revealed that modifications in the linker lead to different drug release profiles. Antiproliferative effects of Arg-Gly-Asp (RGD)⁻cryptophycin conjugates were evaluated on M21 and M21-L human melanoma cell lines. The low nanomolar in vitro activity of the novel conjugates was associated with inferior selectivity for cell lines with different integrin αvβ₃ expression levels. To elucidate the drug delivery process, cryptophycin was replaced by an infrared dye and the obtained conjugates were studied by confocal microscopy.

KEYWORDS:

RGD peptides; antitumor agents; drug delivery; small molecule–drug conjugates

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