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

Entry of nanoparticles into cells and tissues: status and challenges

• Kirsten Sandvig,
• Tore Geir Iversen and
• Tore Skotland

Beilstein J. Nanotechnol. 2024, 15, 1017–1029, doi:10.3762/bjnano.15.83

• ) are important tools to diagnose and treat diseases, and have proven useful in basic mechanistic studies of cells and animals. Thus, knowledge about cellular uptake, intracellular transport, and metabolism of NPs in cells, as well as their biodistribution, degradation, and excretion following

• of new types of NPs, there is a knowledge gap when it comes to our understanding of the interaction of NPs with both cells and tissues. However, it is well known that NP properties, such as surface charge, size, and the material they are composed of can affect cellular uptake, biodistribution, and

• studies, and transport in vivo also holds true for these particles. We will start by describing the status and challenges when it comes to cellular uptake mechanisms, and in the last part discuss interactions of NPs with tissues and biodistribution of these particles. Endocytic Pathways Involved in

Identification of structural features of surface modifiers in engineered nanostructured metal oxides regarding cell uptake through ML-based classification

• Indrasis Dasgupta,
• Totan Das,
• Biplab Das and
• Shovanlal Gayen

Beilstein J. Nanotechnol. 2024, 15, 909–924, doi:10.3762/bjnano.15.75

• medicine, electronics, and environmental science. Understanding the structural aspects of surface modifiers in nanoparticles that govern their cellular uptake is crucial for optimizing their efficacy and minimizing potential cytotoxicity. The cellular uptake is influenced by multiple factors, namely, size

• significantly contribute to the cellular uptake of ENMOs in multiple cell types, including pancreatic cancer cells (PaCa2), human endothelial cells (HUVEC), and human macrophage cells (U937). The best models have been identified for each cell type and analyzed to detect the structural fingerprints/features

• governing the cellular uptake of ENMOs. The study will direct scientists in the design of ENMOs of higher cellular uptake efficiency for better therapeutic response. Keywords: Bayesian classification; cellular uptake; machine learning; nanoparticles (NPs); Introduction In recent years, the rapid

Radiofrequency enhances drug release from responsive nanoflowers for hepatocellular carcinoma therapy

• Yanyan Wen,
• Ningning Song,
• Yueyou Peng,
• Weiwei Wu,
• Qixiong Lin,
• Minjie Cui,
• Rongrong Li,
• Qiufeng Yu,
• Sixue Wu,
• Yongkang Liang,
• Wei Tian and
• Yanfeng Meng

Beilstein J. Nanotechnol. 2024, 15, 569–579, doi:10.3762/bjnano.15.49

• with the release of CUR-Fe NPs and is in accordance with the Fick diffusion (Table 2). Cellular uptake study Prussian blue staining was performed to detect the ability of Huh-7 cells to uptake NFs, as shown in Figure 5. Compared with those in the control group, blue particles were observed in the

• = kHt1/2, where Qt is the amount of CUR in NFs released after time t, and kH is the Higuchi dissolution constant. Ritger–Peppas Model: Mt/M∞ = ktn, where Mt/M∞ is the fraction of CUR in NFs released at time t, k is the rate constant, and n is the diffusional release exponent. Cellular uptake of CUR-Fe

Multiscale modelling of biomolecular corona formation on metallic surfaces

• Parinaz Mosaddeghi Amini,
• Ian Rouse,
• Julia Subbotina and
• Vladimir Lobaskin

Beilstein J. Nanotechnol. 2024, 15, 215–229, doi:10.3762/bjnano.15.21

• reactivity, sensitivity of NPs, as well as their cellular uptake and systemic transfer [21]. However, in order to develop predictive models, a deeper understanding of the interactions at the bionano interface and their relationship to material and protein properties is necessary. Gathering more information

Nanocarrier systems loaded with IR780, iron oxide nanoparticles and chlorambucil for cancer theragnostics

• Phuong-Thao Dang-Luong,
• Hong-Phuc Nguyen,
• Loc Le-Tuan,
• Xuan-Thang Cao,
• Vy Tran-Anh and
• Hieu Vu Quang

Beilstein J. Nanotechnol. 2024, 15, 180–189, doi:10.3762/bjnano.15.17

• and F127@NP had the same impact. However, both NPs produced superior outcomes than those for PVA@NP control. It has been demonstrated that F127 can enhance the cellular uptake of NPs in vitro via clathrin-mediated endocytosis and caveolae-mediated endocytosis [31][40]. The absorption of F127 onto

Curcumin-loaded nanostructured systems for treatment of leishmaniasis: a review

• Douglas Dourado,
• Thayse Silva Medeiros,
• Éverton do Nascimento Alencar,
• Edijane Matos Sales and
• Fábio Rocha Formiga

Beilstein J. Nanotechnol. 2024, 15, 37–50, doi:10.3762/bjnano.15.4

• context, we could observe that the studies failed to correlate consecutive intra-macrophage and intra-amastigote cellular uptake kinetics, once it appears to greatly interfere with the proposed biochemical triggers of Leishmania spp. cell death. In addition, the work could also summarize that lipid-based

Elasticity, an often-overseen parameter in the development of nanoscale drug delivery systems

• Agnes-Valencia Weiss and
• Marc Schneider

Beilstein J. Nanotechnol. 2023, 14, 1149–1156, doi:10.3762/bjnano.14.95

• examining the characteristics of nanoparticles used for drug delivery, one can see that some are better understood then others. The size of nanoparticles, for example, is shown to play an important role in tissue or mucus penetration [8] and in cellular uptake [9]. Also surface charge and chemical

• properties are well investigated regarding their effect on cellular uptake and the influence on in vivo performance [3][10]. Only since the first decade of the 2000s, mechanical properties have been investigated in the development of nanoparticulate drug delivery systems. A well-known example in biology

• particles showed better cellular uptake if no mucus layer was present. In contrast to this, the cellular uptake for semielastic particles was not significantly affected by the presence of a mucus layer [38]. Liposomes with PLGA cores were used by Yu et al. to increase the stiffness in combination with

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

• silk core–shell nanoparticles show high cytotoxicity and cellular uptake regarding breast cancer cells [14]. However, the effectiveness of zein nanoparticles as a delivery vehicle is limited by their poor stability, as they tend to aggregate when suspended in water [15]. Lyophilizing the particles

• cellular uptake of HSA-MPs and CUR-HSA-MPs. The intrinsic fluorescence of both particle types excited at 488 nm allowed for their visualization, as the fluorescence properties were preserved upon encapsulation (Figure 2E). Quantitative analysis of cellular uptake, performed through flow cytometry, revealed

• -MPs by MCF-7 cells is challenging. Cellular uptake was measured in MCF-7 cells as these cells have a high affinity for albumins. Figure 8C shows a z-stack section for FITC-CUR-HSA-MPs, exhibiting green fluorescence due to the uptake of CUR. This demonstrates that CUR-HSA-MPs were readily taken up by

Antibody-conjugated nanoparticles for target-specific drug delivery of chemotherapeutics

• Mamta Kumari,
• Amitabha Acharya and
• Praveen Thaggikuppe Krishnamurthy

Beilstein J. Nanotechnol. 2023, 14, 912–926, doi:10.3762/bjnano.14.75

• fragment antigen-binding (Fab) region of mAbs are chemically conjugated to NP surfaces to recognize protein targets that are overexpressed on the surface of tumor cells. Conjugation of mAbs to NP surfaces improves targeting capacity, cellular uptake, and intracellular stability [12]. The mAb-functionalized

• Herceptin® to improve cellular uptake and cytotoxicity in breast cancer cells [41]. Similarly, Rayavarapu et al. conjugated HER2 antibodies on the surface of gold nanoparticles using a noncovalent conjugation method in order to increase intracellular uptake into cancer cells [42]. The adsorption results

• of the specific nature of the targeting antibody. ACNPs are expected to accumulate at the target site and to improve the tumor uptake. ACNPs receptor binding efficacies were determined using in vitro studies including cellular uptake and internalization studies [71]. Multivalent effect of antibody

Nanostructured lipid carriers containing benznidazole: physicochemical, biopharmaceutical and cellular in vitro studies

• Giuliana Muraca,
• María Esperanza Ruiz,
• Rocío C. Gambaro,
• Sebastián Scioli-Montoto,
• María Laura Sbaraglini,
• Gisel Padula,
• José Sebastián Cisneros,
• Cecilia Yamil Chain,
• Vera A. Álvarez,
• Cristián Huck-Iriart,
• Guillermo R. Castro,
• María Belén Piñero,
• Matias Ildebrando Marchetto,
• Catalina Alba Soto,
• Germán A. Islan and
• Alan Talevi

Beilstein J. Nanotechnol. 2023, 14, 804–818, doi:10.3762/bjnano.14.66

• high-negative ζ values may impede cellular uptake [40]. On the other hand, it was observed that the nanoparticulated systems remained stable after six months with no precipitation. This suggests that in this case the stabilization is not achieved by means of surface charge alone, but also by the steric

Carboxylic acids and light interact to affect nanoceria stability and dissolution in acidic aqueous environments

• Matthew L. Hancock,
• Eric A. Grulke and
• Robert A. Yokel

Beilstein J. Nanotechnol. 2023, 14, 762–780, doi:10.3762/bjnano.14.63

• , distribution, and toxicity of nanoceria within biological systems. Cellular uptake studies of nanoceria in lung adenocarcinoma (A549) cells favored particles with a negative zeta potential. However, positively charged particles resulted in greater bovine serum albumin adsorption. This suggests that surface

The steep road to nonviral nanomedicines: Frequent challenges and culprits in designing nanoparticles for gene therapy

• Yao Yao,
• Yeongun Ko,
• Grant Grasman,
• Jeffery E. Raymond and
• Joerg Lahann

Beilstein J. Nanotechnol. 2023, 14, 351–361, doi:10.3762/bjnano.14.30

• Need for Multimodal Characterization of Nanoparticles The methods chosen to investigate NP uptake and transfection can be biased towards particular properties and may provide limited insights into the efficiency of NP internalization and efficacy. Typically, cellular uptake and transfection efficiency

• ]. This technology measures the mean fluorescence intensity and percent positive value of cells, while also capturing an image of each individual event; this provides information, such as cellular distribution patterns of NPs [22], while also allowing for investigating cellular uptake pathways and

• 50 nanoparticle (NP)-mediated plasmid DNA (pDNA) delivery experiments published in 2017–2022. (a) 5-year prevalence of reporting imaging, imaging quantification, and 3D imaging capture for investigating NP cellular uptake and (or) transfection. (b) 5-year prevalence of reporting flow cytometry for

Polymer nanoparticles from low-energy nanoemulsions for biomedical applications

• Santiago Grijalvo and
• Carlos Rodriguez-Abreu

Beilstein J. Nanotechnol. 2023, 14, 339–350, doi:10.3762/bjnano.14.29

• corona formation (upon incubation in FBS). The nanoparticles showed low cytotoxicity for SH-SY5Y cells (viabilities of ca. 100% for nanoparticle concentrations equal or lower than 0.23 mg/mL), high cellular uptake (in SH-SY5Y cells), and dose-dependent antioxidant activity. The properties of the PIC

Structural, optical, and bioimaging characterization of carbon quantum dots solvothermally synthesized from o-phenylenediamine

• Zoran M. Marković,
• Milica D. Budimir,
• Martin Danko,
• Dušan D. Milivojević,
• Pavel Kubat,
• Danica Z. Zmejkoski,
• Vladimir B. Pavlović,
• Marija M. Mojsin,
• Milena J. Stevanović and
• Biljana M. Todorović Marković

Beilstein J. Nanotechnol. 2023, 14, 165–174, doi:10.3762/bjnano.14.17

• oxygen species production, and showed low dark cytotoxicity. By investigating the cellular uptake, it was established that these dots penetrated the HeLa cells and could be used as probes for bioimaging. Keywords: antibacterial; bioimaging; carbon quantum dots; precursor; reactive oxygen species

• composites has a crucial effect on the properties of CQDs/PU composites. Cellular uptake Photobleaching limits the use of hydrophobic probes (e.g., Nile red) [50]. CQDs can be used as probes for bioimaging because of the tuneable strong photoluminescence and high resistance to photobleaching. In order to

Facile preparation of Au- and BODIPY-grafted lipid nanoparticles for synergized photothermal therapy

• Yuran Wang,
• Xudong Li,
• Haijun Chen and
• Yu Gao

Beilstein J. Nanotechnol. 2022, 13, 1432–1444, doi:10.3762/bjnano.13.118

• could be associated stably to Au-LNPs, and the release of BODIPY from AB-LNPs could be accelerated by laser irradiation. AB-LNPs are scalable and showed excellent photothermal effects. AB-LNPs showed enhanced cellular uptake efficiency compared to free BODIPY in 4T1 breast cancer cells. Under laser

• -LNPs with optimized particle size and polydispersity index (PDI), and then mixed BDP with Au-LNPs to obtain both Au- and BDP-grafted LNPs (AB-LNPs). The physiochemical characteristics, the photothermal properties, and the stabilities of AB-LNPs were studied in detail. The cellular uptake efficiency and

• 10% FBS. The cells were cultured in a humidified incubator with atmosphere of 5% CO2 at 37 °C. Cellular uptake studies 4T1 cells were grown in 12-well plates and cultured for 24 h. The cells were incubated with free BDP (30 μM) and AB-LNPs (with a BDP concentration of 30 μM and a Au concentration of