Shape, membrane morphology, and morphodynamic response of metabolically active human mitochondria revealed by scanning ion conductance microscopy

• Eric Lieberwirth,
• Anja Schaeper,
• Regina Lange,
• Ingo Barke,
• Simone Baltrusch and
• Sylvia Speller

Beilstein J. Nanotechnol. 2025, 16, 951–967, doi:10.3762/bjnano.16.73

• . Consequently, the outer membrane, which separates the mitochondrion from the cytoplasm, has become a focus of investigation. We analysed metabolically active mitochondria from HeLa cells using scanning ion conductance microscopy to generate nanoscopically resolved, three-dimensional topographies. Our

• local environment. The similarities between the nanopipette in the measurement setup and the microtubules in the cellular context are discussed as the basis for the hypothesis. Keywords: HeLa; metabolically active; mitochondria; morphodynamics; scanning ion conductance microscopy; Introduction

• study of metabolically active organelles [26]. Scanning ion conductance microscopy (SICM) enables three-dimensional visualisation of living cells in their native state [27]. Pioneered by Hansma et al. [28], the method has been continuously refined since the 1990s [27][29][30]. SICM utilises a

Mechanistic insights into endosomal escape by sodium oleate-modified liposomes

• Ebrahim Sadaqa,
• Satrialdi,
• Fransiska Kurniawan and
• Diky Mudhakir

Beilstein J. Nanotechnol. 2024, 15, 1667–1685, doi:10.3762/bjnano.15.131

• reduction of resazurin to resorufin by metabolically active cells. The data reveal that Unmodified-Lipo exhibited minimal cytotoxicity at lower lipid concentrations (15.625 to 250 µM), with no statistically significant differences compared to untreated control cells (p > 0.05). However, at a concentration

• transformation of resazurin (initially blue and non-fluorescent) into resorufin (pink and fluorescent) by metabolically active cells, facilitating the measurement of cell viability [35][36]. Briefly, 4T1 cells were cultured in DMEM supplemented with 10% FBS and 1% penicillin–streptomycin in a humidified

Synthesis, characterization and anticancer effect of doxorubicin-loaded dual stimuli-responsive smart nanopolymers

• Ömür Acet,
• Pavel Kirsanov,
• Burcu Önal Acet,
• Inessa Halets-Bui,
• Dzmitry Shcharbin,
• Şeyda Ceylan Cömert and
• Mehmet Odabaşı

Beilstein J. Nanotechnol. 2024, 15, 1189–1196, doi:10.3762/bjnano.15.96

• ). Cytotoxicity test Cell viability was assessed using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT). The method is based on the ability of NADPH-dependent cellular oxidoreductase in living, metabolically active cells to reduce MTT to water-insoluble crystals of formazan. Cells were seeded

Curcumin-loaded albumin submicron particles with potential as a cancer therapy: an in vitro study

• Nittiya Suwannasom,
• Netsai Sriaksorn,
• Chutamas Thepmalee,
• Krissana Khoothiam,
• Ausanai Prapan,
• Hans Bäumler and
• Chonthida Thephinlap

Beilstein J. Nanotechnol. 2023, 14, 1127–1140, doi:10.3762/bjnano.14.93

• the tetrazolium dye MTT to water-insoluble purple formazan crystals, indicating mitochondrial function and metabolically active cells. After medium removal, the dark blue crystals were dissolved in 100 μL of DMSO; then, the absorption was measured at wavelengths of 570 nm with a Cytation™ 5 Cell

Characterization, bio-uptake and toxicity of polymer-coated silver nanoparticles and their interaction with human peripheral blood mononuclear cells

• Sahar Pourhoseini,
• Reilly T. Enos,
• Angela E. Murphy,
• Bo Cai and
• Jamie R. Lead

Beilstein J. Nanotechnol. 2021, 12, 282–294, doi:10.3762/bjnano.12.23

• measures the insoluble formazan that is accumulated in the metabolically active cells. The MTS assay was performed according to the manufacturer’s protocol. Briefly, isolated PBMCs were exposed to 0, 10, 100, 500, and 1000 µg·L−1 of PVP-AgNPs, AgNO3, AgNO3-PVP and PVP in 96-well plates in six replicates

Toxicity and safety study of silver and gold nanoparticles functionalized with cysteine and glutathione

• Barbara Pem,
• Igor M. Pongrac,
• Lea Ulm,
• Ivan Pavičić,
• Valerije Vrček,
• Darija Domazet Jurašin,
• Marija Ljubojević,
• Adela Krivohlavek and
• Ivana Vinković Vrček

Beilstein J. Nanotechnol. 2019, 10, 1802–1817, doi:10.3762/bjnano.10.175

• bromide) to a purple MTT-formazan crystal by metabolically active cells, was used to determine cell viability after 24 h exposure. The assay was performed according to the manufacturer’s instructions. Briefly, the cells were seeded in 96-well tissue culture plates (5 × 104 cells/mL growth medium, i.e

Optical techniques for cervical neoplasia detection

• Tatiana Novikova

Beilstein J. Nanotechnol. 2017, 8, 1844–1862, doi:10.3762/bjnano.8.186

• precancerous modifications of cervical epithelium [31]. The differences in fluorescence spectra of normal and precancerous cervical tissue are explained by the concomitance of two phenomena linked with the CIN progression. An increase in number of metabolically active mitochondria in epithelial cells with CIN

Calcium fluoride based multifunctional nanoparticles for multimodal imaging

• Marion Straßer,
• Joachim H. X. Schrauth,
• Sofia Dembski,
• Daniel Haddad,
• Bernd Ahrens,
• Stefan Schweizer,
• Bastian Christ,
• Alevtina Cubukova,
• Marco Metzger,
• Heike Walles,
• Peter M. Jakob and
• Gerhard Sextl

Beilstein J. Nanotechnol. 2017, 8, 1484–1493, doi:10.3762/bjnano.8.148

• (hdF) after treatment with the NPs stabilized with Melpers®2450 for 24 h was evaluated. Therefore, the CellTiter-Glo assay was used [44], a method that is based on the quantification of adenosine-5′-triphosphate (ATP), which signals the presence of metabolically active cells. Adding the CellTiter-Glo

Facile fabrication of luminescent organic dots by thermolysis of citric acid in urea melt, and their use for cell staining and polyelectrolyte microcapsule labelling

• Nadezhda M. Zholobak,
• Anton L. Popov,
• Alexander B. Shcherbakov,
• Nelly R. Popova,
• Mykhailo M. Guzyk,
• Valeriy P. Antonovich,
• Alla V. Yegorova,
• Yuliya V. Scrypynets,
• Inna I. Leonenko,
• Alexander Ye. Baranchikov and
• Vladimir K. Ivanov

Beilstein J. Nanotechnol. 2016, 7, 1905–1917, doi:10.3762/bjnano.7.182

• also known that the MTT assay is typically used for quantifying metabolically active cells, independently of proliferation [63]. Therefore, the highest concentration of sample that caused, in the treated cells, the activation of NADP-H-dependent oxidoreductases, not more than in the intact cells, was