Rapid synthesis of highly monodisperse AgSbS₂ nanocrystals: unveiling multifaceted activities in cancer therapy, antibacterial strategies, and antioxidant defense

• Funda Ulusu,
• Adem Sarilmaz,
• Yakup Ulusu,
• Faruk Ozel and
• Mahmut Kus

Beilstein J. Nanotechnol. 2025, 16, 2105–2115, doi:10.3762/bjnano.16.145

• direct ROS measurement and apoptosis marker assays (e.g., Annexin V/PI staining, caspase-3 activation) will be crucial for validating and further elucidating these mechanistic pathways. The surface charge and zeta potential of AgSbS2 NCs, which strongly influence their colloidal stability and cellular

• uptake, are expected to be within the range typically reported for Ag-based chalcogenides exhibiting stable dispersions. Antioxidant activity of AgSbS2 NCs The DPPH radical scavenging activity of AgSbS2 NCs in the assay using ascorbic acid as a positive control is revealed in Figure 5. The synthesized

Toward clinical translation of carbon nanomaterials in anticancer drug delivery: the need for standardisation

• Michał Bartkowski,
• Francesco Calzaferri and
• Silvia Giordani

Beilstein J. Nanotechnol. 2025, 16, 2092–2104, doi:10.3762/bjnano.16.144

• coupled with systematic biological evaluation to ensure reliable assessment of safety and performance. Physicochemical evaluation of CNMs Size and shape are critical parameters that influence the biological behaviour of CNMs. These factors affect biodistribution, clearance, and cellular uptake. For

• atomic force microscopy. Surface charge plays a significant role in determining how CNMs interact with biological membranes and intracellular environments. It influences processes such as cellular uptake, cytotoxicity, and inflammatory signalling. For example, BSA-derived negatively charged CDs exhibited

• enhanced cellular uptake, whereas positively charged CDs elicited stronger cytokine responses [41]. Zeta potential measurements are routinely used to quantify surface charge, which can be tuned through appropriate surface functionalisation strategies. Stability is another essential aspect of NM evaluation

PEGylated lipids in lipid nanoparticle delivery dynamics and therapeutic innovation

• Peiyang Gao

Beilstein J. Nanotechnol. 2025, 16, 1914–1930, doi:10.3762/bjnano.16.133

• chains arrange on the nanoparticle surface and the potential impacts on LNPs’ physicochemical properties by varying surface PEG density or PEG chemistry. Subsequently, PEG conformations are discussed in terms of their modulation of protein corona formation, cellular uptake, and immunogenic responses

• properties of LNPs including particle size, surface charge, and encapsulation efficiency. Subsequent sections explore the roles of PEG lipids in modulating protein corona formation and cellular uptake. The latter parts highlight the potential of functionalized PEG lipids for targeted delivery and the

• shell of LNPs plays a pivotal role. As hydrophilic and protective shield during LNP circulation and in vivo activities, the conformation and binding kinetics of PEG layer are both important, particularly in modulating protein adsorption and subsequent interactions with cellular uptake pathways [23

Phytol-loaded soybean oil nanoemulsion as a promising alternative against Leishmania amazonensis

• Victória Louise Pinto Freire,
• Mariana Farias Alves-Silva,
• Johny W. de Freitas Oliveira,
• Matheus de Freitas Fernandes-Pedrosa,
• Alianda Maira Cornélio,
• Marcelo de Souza-Silva,
• Thayse Silva Medeiros and
• Arnóbio Antônio da Silva Junior

Beilstein J. Nanotechnol. 2025, 16, 1826–1836, doi:10.3762/bjnano.16.126

• can improve the cellular uptake of various drugs and can facilitate targeted delivery to the intracellular parasites [50][51]. Since the amastigote forms of Leishmania spp. reside within the phagolysosomes of macrophages, the phagocytic uptake of nanodroplets significantly increases the intracellular

Exploring the potential of polymers: advancements in oral nanocarrier technology

• Rousilândia de Araujo Silva,
• Igor Eduardo Silva Arruda,
• Luise Lopes Chaves,
• Mônica Felts de La Roca Soares and
• Jose Lamartine Soares Sobrinho

Beilstein J. Nanotechnol. 2025, 16, 1751–1793, doi:10.3762/bjnano.16.122

Advances of aptamers in esophageal cancer diagnosis, treatment and drug delivery

• Yang Fei,
• Hui Xu,
• Chunwei Zhang,
• Jingjing Wang and
• Yong Jin

Beilstein J. Nanotechnol. 2025, 16, 1734–1750, doi:10.3762/bjnano.16.121

• cellular uptake, poor stability due to tumor microenvironment, and inadequate drug release due to inadequate drug release mechanisms. Two years later, a novel bivalent aptamer-DNA-Dox conjugate (BADD) [117], was developed, and the A2 aptamer was truncated to A2 (35) to reduce steric hindrance and improve

• cellular uptake. While cationic nanocarriers can effectively mediate delivery, this strategy substantially increases manufacturing complexity and production costs. Regulatory bodies must therefore establish new quality control standards to ensure batch-to-batch consistency. Third, approved aptamer-based

Prospects of nanotechnology and natural products for cancer and immunotherapy

• Jan Filipe Andrade Santos,
• Marcela Bernardes Brasileiro,
• Pamela Danielle Cavalcante Barreto,
• Ligiane Aranha Rocha and
• José Adão Carvalho Nascimento Júnior

Beilstein J. Nanotechnol. 2025, 16, 1644–1667, doi:10.3762/bjnano.16.116

• scattering (DLS), and UV–visible (UV–vis) spectroscopy were used for characterization. The nanoparticles showed increased cellular uptake compared to free PD-L1, suppression of the NF-κB pathway as indicated by reduced PHO-P65 protein expression, and enhanced tumor inhibition due to immune activation and

• spectroscopy, TEM, DLS, X-ray diffraction (XRD), and Fourier-transform infrared (FTIR) spectroscopy, revealing a polygonal or oval morphology. To evaluate the antitumor effects, cytotoxicity assays, cellular uptake assays, apoptosis detection, ROS production, qRT-PCR, and Western blotting for gene and protein

Venom-loaded cationic-functionalized poly(lactic acid) nanoparticles for serum production against Tityus serrulatus scorpion

• Philippe de Castro Mesquita,
• Karla Samara Rocha Soares,
• Manoela Torres-Rêgo,
• Emanuell dos Santos-Silva,
• Mariana Farias Alves-Silva,
• Alianda Maira Cornélio,
• Matheus de Freitas Fernandes-Pedrosa and
• Arnóbio Antônio da Silva-Júnior

Beilstein J. Nanotechnol. 2025, 16, 1633–1643, doi:10.3762/bjnano.16.115

• nanoparticles can be modified to achieve high protein loading or avoid a rapid cellular uptake. Using different strategies, nanoparticles have been functionalized with a variety of ligands such as small molecules, surfactants, polymers, and biomolecules [21][22]. The use of cationic molecules, as

• nanoparticles was functionalized with PEI, a hydrophilic polymer that provides a positive surface charge. This modification enhances high macromolecule loading or improves the cell interaction and cellular uptake [22][33][34]. The cationic character induces biomolecules with negative charges, such as proteins

Enhancing the therapeutical potential of metalloantibiotics using nano-based delivery systems

• Alejandro Llamedo,
• Marina Cano,
• Raquel G. Soengas and
• Francisco J. García-Alonso

Beilstein J. Nanotechnol. 2025, 16, 1350–1366, doi:10.3762/bjnano.16.98

• receptors and ligands, as well as the number of interactions necessary to overcome the energy barrier for cellular uptake. Properly balancing these factors ensures efficient binding and internalization of the nanoparticles by the target cells [50][51]. For example, nanoparticles can be engineered to

• , such as biocompatibility and drug protection, while avoiding many of their limitations. In comparison to conventional colloidal carriers, SLNs demonstrate reduced toxicity, greater surface area, enhanced biocompatibility, extended drug release, improved cellular uptake, and increased drug solubility

• , which improves cellular uptake and facilitates drug release within the target site [90]. The incorporation of stimuli-responsive agents in the pores also enables MSiNPs to release therapeutic agents upon exposure to specific environmental cues, such as pH or temperature. These interesting features for

Ferroptosis induction by engineered liposomes for enhanced tumor therapy

• Alireza Ghasempour,
• Mohammad Amin Tokallou,
• Mohammad Reza Naderi Allaf,
• Mohsen Moradi,
• Hamideh Dehghan,
• Mahsa Sedighi,
• Mohammad-Ali Shahbazi and
• Fahimeh Lavi Arab

Beilstein J. Nanotechnol. 2025, 16, 1325–1349, doi:10.3762/bjnano.16.97

• a crucial parameter that influences their biodistribution, cellular uptake, and drug release. DLS is a widely used technique to determine the size distribution of liposomes in solution [110][125]. DLS measures the fluctuations in light intensity generated by the Brownian motion of liposome particles

Acrocomia aculeata oil-loaded nanoemulsion: development, anti-inflammatory properties, and cytotoxicity evaluation

• Verónica Bautista-Robles,
• Hady Keita,
• Edgar Julián Paredes Gamero,
• Layna Tayná Brito Leite,
• Jessica de Araújo Isaías Muller,
• Mônica Cristina Toffoli Kadri,
• Ariadna Lafourcade Prada and
• Jesús Rafael Rodríguez Amado

Beilstein J. Nanotechnol. 2025, 16, 1277–1288, doi:10.3762/bjnano.16.93

• counterpart [47]. The superior pharmacological response of the nanoemulsion may be attributed to the nanoscale droplet size, which increases the surface area-to-volume ratio, enhances solubility and stability, and promotes rapid absorption and cellular uptake [56]. The nanometric scale facilitates more

Better together: biomimetic nanomedicines for high performance tumor therapy

• Imran Shair Mohammad,
• Gizem Kursunluoglu,
• Anup Kumar Patel,
• Hafiz Muhammad Ishaq,
• Cansu Umran Tunc,
• Dilek Kanarya,
• Mubashar Rehman,
• Omer Aydin and
• Yin Lifang

Beilstein J. Nanotechnol. 2025, 16, 1246–1276, doi:10.3762/bjnano.16.92

• involving recognition, binding, cellular uptake, and intracellular transport. These steps are specific to different types of target cells and determine the fate of exosomes [107]. Moreover, they offer prolonged circulation, excellent target specificity, and intracellular delivery without degradation

• siRNA and enabled proton sponge-mediated endosomal escape, ensuring cytoplasmic release of the gene cargo. These LC3siRNA-loaded nanoparticles (LC3siRNA-NPs) exhibited pH-responsive behavior, enhanced cellular uptake, and potent suppression of autophagy. In vitro and in vivo experiments demonstrated

Fabrication of metal complex phthalocyanine and porphyrin nanoparticle aqueous colloids by pulsed laser fragmentation in liquid and their potential application to a photosensitizer for photodynamic therapy

• Taisei Himeda,
• Risako Kunitomi,
• Ryosuke Nabeya,
• Tamotsu Zako and
• Tsuyoshi Asahi

Beilstein J. Nanotechnol. 2025, 16, 1088–1096, doi:10.3762/bjnano.16.80

• be properly assessed at this stage of the study. This is because the evaluation of cellular phototoxicity requires consideration of cellular uptake and localization, and further studies must be conducted. Conclusion We successfully fabricated several MPc (M = AlCl, Fe, Co, Zn) and PtOEP nanoparticles

Piezoelectricity of hexagonal boron nitrides improves bone tissue generation as tested on osteoblasts

• Sevin Adiguzel,
• Nilay Cicek,
• Zehra Cobandede,
• Feray B. Misirlioglu,
• Hulya Yilmaz and
• Mustafa Culha

Beilstein J. Nanotechnol. 2025, 16, 1068–1081, doi:10.3762/bjnano.16.78

• osteoblast cell activity, the HOb cell line (cell line no. 406-05a, European Collection of Cell Cultures, UK) was chosen due to its sensitivity to mechanical and electric stimuli. Cell viability, reactive oxygen species (ROS) detection, cellular uptake, scratch, and von Kossa staining assays (Abcam, UK) were

• 45 min. Afterward, fluorescence and absorbance were measured at the 485/535 nm range by a microplate reader (Tecan, Switzerland). Cellular uptake assay According to the logic of the NMs uptake procedure by flow cytometry, an increasing percentage of side scatter (SSC%) shift indicates growth in

• granulation, so that the cellular uptake of NMs and the effect of US exposure on uptake can be determined. HOb cells were seeded in 24-well plates at 5 × 104 cells/well and incubated for 24 h. Then, cells were treated with NMs with increasing concentration values (1, 5, and 10 µg/mL) and left for incubation

A calix[4]arene-based supramolecular nanoassembly targeting cancer cells and triggering the release of nitric oxide with green light

• Cristina Parisi,
• Loredana Ferreri,
• Tassia J. Martins,
• Francesca Laneri,
• Samantha Sollima,
• Antonina Azzolina,
• Antonella Cusimano,
• Nicola D’Antona,
• Grazia M. L. Consoli and
• Salvatore Sortino

Beilstein J. Nanotechnol. 2025, 16, 1003–1013, doi:10.3762/bjnano.16.75

• keeping them inclined to bind specific choline transporter-positive cells overexpressed in tumoral cells [53][65]. To verify if the choline motifs confer to 1 the capability to penetrate selectively choline-positive cells, cellular uptake experiments were performed on tumoral MCF-7 cells and non-malignant

• expressed as a percentage of the absorbance measured in the control cells, and values expressed as mean ± SD of two separate experiments, each performed in triplicate. Cellular uptake of the nanoassembly of 1 HuDe cells (1 × 105) and MCF7 cells (2 × 105) were plated in complete medium on coverslips placed

• effects and cellular uptake of the nanoassembly of 1 (0.5 μM) in HuDe cells (A, C) and MCF7 cells (B, D). Green: nanoassembly of 1; blue: DAPI stain to visualize nuclei. Scale bar = 50 µm. (A) Absorption spectra of NOPD 2 (a) and the non-nitrosated analogue 2b (b) in water. (B) Absorption spectral changes

Serum heat inactivation diminishes ApoE-mediated uptake of D-Lin-MC3-DMA lipid nanoparticles

• Demian van Straten,
• Luuk van de Schepop,
• Rowan Frunt,
• Pieter Vader and
• Raymond M. Schiffelers

Beilstein J. Nanotechnol. 2025, 16, 740–748, doi:10.3762/bjnano.16.57

• ) ionizable lipids. Cellular uptake and siRNA delivery efficiency of the LNPs were determined in media containing untreated or heat-inactivated serum. Mechanistically, we found that apolipoprotein E, a protein corona component that is crucial for MC3 LNP tropism, displayed reduced stability and functionality

• -lipids from the LNP surface, which needs to occur before a protein corona can be established that allows cellular uptake of LNPs [29]. A difference in FCS protein concentration can thus introduce variations in results when performing experiments with different FCS brands or even different lots of the

• media. A similar observation was made by Simon et al. [30], who attributed a difference in cellular uptake of PEGylated polystyrene nanocarriers in untreated or heat-inactivated FCS to the denaturation of important protein corona components. Indeed, heat inactivation did not reduce the amount of protein

Synthetic-polymer-assisted antisense oligonucleotide delivery: targeted approaches for precision disease treatment

• Ana Cubillo Alvarez,
• Dylan Maguire and
• Ruairí P. Brannigan

Beilstein J. Nanotechnol. 2025, 16, 435–463, doi:10.3762/bjnano.16.34

• potential in precision disease treatment. Synthetic polymers have shown significant promise in enhancing the delivery, stability, and therapeutic efficacy of ASOs by addressing key challenges such as cellular uptake, endosomal escape, and reducing cytotoxicity. The review highlights key studies from the

• ) (PLL) is a cationic biopolymer, commonly employed in the delivery of ASOs because of its ability to facilitate enhanced cellular uptake [61]. Depending on desired molecular weight (Mw), molecular architecture, and molar-mass polymer dispersity (ÐM), PLL is traditionally synthesised through three

• played a crucial role in the successful coating of these nanoparticles, significantly increasing their zeta potential and improving cellular uptake. Moreover, εPLL-coated GNPs were found to provide robust protection for the ASOs against nuclease degradation, maintaining over 78% of the oligonucleotides

Development of a mucoadhesive drug delivery system and its interaction with gastric cells

• Ahmet Baki Sahin,
• Serdar Karakurt and
• Deniz Sezlev Bilecen

Beilstein J. Nanotechnol. 2025, 16, 371–384, doi:10.3762/bjnano.16.28

• concluded that EudAlg nanoparticles do not significantly affect the viability of AGS cell (Figure 4A). Internalization of nanoparticles When nanoparticles are designed for biomedical applications, two important properties to be considered are toxicity and cellular uptake. The cellular uptake of

• after 1 and 4 h of treatment to determine the efficiency of acute cellular uptake of nanoparticles. Mucus-secreting AGS cells were incubated with fluorescently labeled EudAlg (F-EudAlg) nanoparticles to track the internalization. The cell nuclei were stained with DAPI, and micrographs were taken with a

Recent advances in photothermal nanomaterials for ophthalmic applications

• Jiayuan Zhuang,
• Linhui Jia,
• Chenghao Li,
• Rui Yang,
• Jiapeng Wang,
• Wen-an Wang,
• Heng Zhou and
• Xiangxia Luo

Beilstein J. Nanotechnol. 2025, 16, 195–215, doi:10.3762/bjnano.16.16

• explanations of material size, structure, dosage, and administration methods [215]. During treatment, processes such as nanoparticle aggregation, material degradation, cellular uptake/excretion, and unintended release of adsorbents require comprehensive safety analysis. In inorganic photothermal nanomaterials

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

• candidate for drug delivery applications. The data support the use of SO as a safe modification in liposomal formulations, particularly in contexts where minimizing cytotoxicity is paramount. Cellular uptake The cellular uptake of DiD-labeled liposomes (Unmodified-Lipo, SO-Lipo, and AUR-Lipo) in 4T1 cells

• ). The plates were incubated for an additional 3 h at 37 °C to facilitate the reduction of resazurin by the cells. Absorbance was subsequently measured at 570 and 600 nm using a microplate reader, providing data on cell viability. Cellular uptake assay 4T1 triple-negative breast cancer cells were seeded

• nuclei. Confocal microscopy (Olympus FV-1200 Tokyo, Japan) was used to capture images of cellular uptake, and the mean fluorescence intensity was quantified using Fiji-ImageJ software for semi-quantitative analysis. Evaluation of endosomal escape efficiency through subcellular colocalization analysis In

The round-robin approach applied to nanoinformatics: consensus prediction of nanomaterials zeta potential

• Dimitra-Danai Varsou,
• Arkaprava Banerjee,
• Joyita Roy,
• Kunal Roy,
• Giannis Savvas,
• Haralambos Sarimveis,
• Ewelina Wyrzykowska,
• Mateusz Balicki,
• Tomasz Puzyn,
• Georgia Melagraki,
• Iseult Lynch and
• Antreas Afantitis

Beilstein J. Nanotechnol. 2024, 15, 1536–1553, doi:10.3762/bjnano.15.121

• of nanoinformatics, various consensus approaches have been proposed over the past years for the prediction of different NM endpoints, such as NMs’ cellular uptake [20], zeta potential (ZP) [16], and electrophoretic mobility [21]. The complexity of predictive models requires the development of

Polymer lipid hybrid nanoparticles for phytochemical delivery: challenges, progress, and future prospects

• Iqra Rahat,
• Pooja Yadav,
• Aditi Singhal,
• Mohammad Fareed,
• Jaganathan Raja Purushothaman,
• Mohammed Aslam,
• Raju Balaji,
• Sonali Patil-Shinde and
• Md. Rizwanullah

Beilstein J. Nanotechnol. 2024, 15, 1473–1497, doi:10.3762/bjnano.15.118

• (i.e., IQN-iRGD-PLHNPs) to enhance anti-BC activity by active tumor targeting [121]. Coumarin-6 was tagged with the nanocarrier to investigate the cellular uptake potential. The developed targeted PLHNPs represented markedly enhanced cell uptake in MDA-MB-231 due to integrin receptor-mediated

• [171]. EDN-PLHNPs revealed much higher cytotoxicity (>2 times higher) against MCF-7 cells by enhancing the cellular uptake of EDN and promoting the apoptosis of MCF-7 cells. Besides

Nanotechnological approaches for efficient N2B delivery: from small-molecule drugs to biopharmaceuticals

• Selin Akpinar Adscheid,
• Akif E. Türeli,
• Nazende Günday-Türeli and
• Marc Schneider

Beilstein J. Nanotechnol. 2024, 15, 1400–1414, doi:10.3762/bjnano.15.113

• delivery. They showed that the transferrin-decorated NPs with the highest amount of targeting ligand exhibited the highest cellular uptake in the RPMI 2650 human epithelium cell line [79]. In another study, the researchers studied the chitosan coating of PLGA NPs regarding the mucosal uptake. Chatzitaki et

• antibody-modified PLGA NPs. The NPs were coated with N-trimethylated chitosan (TMC) to overcome nasal clearance and, thus, increase brain delivery. The TMC-coated NPs showed increased cellular uptake compared to the non-coated NPs in cell uptake studies with C6 cells. Moreover, when glioma-bearing rats

Introducing third-generation periodic table descriptors for nano-qRASTR modeling of zebrafish toxicity of metal oxide nanoparticles

• Supratik Kar and
• Siyun Yang

Beilstein J. Nanotechnol. 2024, 15, 1142–1152, doi:10.3762/bjnano.15.93

• alternative, more detrimental cellular uptake pathways or provoke harmful responses by accumulating on cell surfaces. Such MONPs might also elevate oxidative stress by triggering the production of reactive oxygen species, which damage cellular components. They can obstruct vital biological processes and

Recent updates in applications of nanomedicine for the treatment of hepatic fibrosis

• Damai Ria Setyawati,
• Fransiska Christydira Sekaringtyas,
• Riyona Desvy Pratiwi,
• A’liyatur Rosyidah,
• Rohimmahtunnissa Azhar,
• Nunik Gustini,
• Gita Syahputra,
• Idah Rosidah,
• Etik Mardliyati,
• Tarwadi and
• Sjaikhurrizal El Muttaqien

Beilstein J. Nanotechnol. 2024, 15, 1105–1116, doi:10.3762/bjnano.15.89

• complexation and cholesterol–polyethylene glycol–vitamin A as a helper lipoid. In the in vitro evaluation, the nanocarrier showed enhanced cellular uptake in HSCs-T6 cells, nine times higher than that in macrophages, displaying specific targeting to HSCs that could avoid phagocytosis by macrophages. These

• cellular uptake results accordingly affected the in vitro gene silencing activity as shown in decreased expression of Col1α1 and TIMP-1 after administering the nanocarriers. The in vivo cellular localization of siRNA-VLNPs in the liver tissue was evaluated in CCl4-treated mice. The result shows that the

• peptide-based micelle nanocomplex for delivering Pcbp2 siRNA as gene-silencing agent [74]. The surface of the nanocarrier was modified with a dimeric IGF2R peptide as a M6PR-targeting ligand of the activated HSCs. The use of cholesteryl peptide to construct the nanocarrier facilitated in vitro cellular