A biomimetic approach towards a universal slippery liquid infused surface coating

• Ryan A. Faase,
• Madeleine H. Hummel,
• AnneMarie V. Hasbrook,
• Andrew P. Carpenter and
• Joe E. Baio

Beilstein J. Nanotechnol. 2024, 15, 1376–1389, doi:10.3762/bjnano.15.111

• reducing the thrombogenicity of a material lies in addressing the intricate layer of protein within blood that adsorbs to any surface it comes into contact with. This layer is responsible for the initiation of host responses such as coagulation or inflammation. To address the body’s reaction to these

• removal and or repulsion of these important molecules that control the clotting cascade. The most prominent of the methods are ones that aim to reduce non-specific protein adsorption, increase adhesion resistance, use biomolecules to remove targets of interest, and enhance endothelial cell attachment. One

• was added to each well of a 96-well plate blocked with BSA. After incubation for 60 min, 90 μL of protein solution was removed and added to a new plate containing 5 μL 4.7mM soybean trypsin inhibitor (Sigma). 5 μL of chromogenic substrate S-2302 (Chromogenix) was added to each well and the absorbance

Interaction of graphene oxide with tannic acid: computational modeling and toxicity mitigation in C. elegans

• Romana Petry,
• James M. de Almeida,
• Francine Côa,
• Felipe Crasto de Lima,
• Diego Stéfani T. Martinez and
• Adalberto Fazzio

Beilstein J. Nanotechnol. 2024, 15, 1297–1311, doi:10.3762/bjnano.15.105

• C. elegans [35][54]. Oxidative stress is one of the central mechanisms and, in fact, the main cause of the toxicity outcomes discussed above. It is associated to changes in the function or expression of superoxide dismutase, “Rieske” iron-sulfur protein, mitochondrial complex I, and the ubiquinone

• biosynthesis protein COQ7 [51][53][54][55]. The co-exposure of GO with antioxidant molecules, such as ʟ-cysteine and ascorbate, can mitigate the oxidative effects of the material and minimize GO’s toxicity [35][53]. Moreover, GO also shows important neuronal effects; for example, it influences protein–protein

Functional morphology of cleaning devices in the damselfly Ischnura elegans (Odonata, Coenagrionidae)

• Silvana Piersanti,
• Gianandrea Salerno,
• Wencke Krings,
• Stanislav Gorb and
• Manuela Rebora

Beilstein J. Nanotechnol. 2024, 15, 1260–1272, doi:10.3762/bjnano.15.102

• , situated on the foreleg tibiae, were observed using scanning electron microscopy, and the presence and distribution of resilin, an elastomeric protein that enhances cuticle flexibility, were analyzed using confocal laser scanning microscopy. Eye and antennal grooming behavior were analyzed to evaluate the

• used to clean the head and, especially, the eyes and the antennae. The microstructures were observed using scanning electron microscopy (SEM), and the presence and distribution of resilin, an elastomeric protein that enhances cuticle deformability and flexibility (review in [36]), were analyzed using

• exoskeleton structures, green color indicates chitinous and non- or weakly sclerotized exoskeleton structures, and blue color indicates exoskeleton structures that either contain large proportions of the elastic protein resilin or are unsclerotized. (a) Dorsal view of the tibial grooming devices, revealing

Dual-functionalized architecture enables stable and tumor cell-specific SiO₂NPs in complex biological fluids

• Iris Renata Sousa Ribeiro,
• Raquel Frenedoso da Silva,
• Romênia Ramos Domingues,
• Adriana Franco Paes Leme and
• Mateus Borba Cardoso

Beilstein J. Nanotechnol. 2024, 15, 1238–1252, doi:10.3762/bjnano.15.100

• -depth studies in complex environments to evaluate nanoparticle stability, protein corona formation, hemolytic activity, and targeting capabilities. To address this issue, fluorescent silica nanoparticles (SiO2NPs) are here functionalized with zwitterionic (kinetic stabilizer) and folate groups

• biological identity of these particles, impairing their therapeutic efficiency [12][13][14][15]. Proteins and other biomolecules can be adsorbed on the surface of NPs (protein corona formation), masking their original functionality and hiding their target ability [16][17][18]. Protein corona can further lead

• and (ii) targeting peptide for targeted delivery aimed at increasing efficiency against cancer. Although valuable, these systems have not been able to provide reduced protein corona formation and targeting ability, or they have not been scrutinized in complex biological environments. In fact, there is

Realizing active targeting in cancer nanomedicine with ultrasmall nanoparticles

• André F. Lima,
• Giselle Z. Justo and
• Alioscka A. Sousa

Beilstein J. Nanotechnol. 2024, 15, 1208–1226, doi:10.3762/bjnano.15.98

• globular proteins, usNPs exhibit unique physicochemical properties and physiological behavior distinct from larger particles, including lack of protein corona formation, efficient renal clearance, and reduced recognition and sequestration by the reticuloendothelial system. In cancer treatment, usNPs

• reliance on passive targeting, the more complex designs of targeted NPs, the potential for attached functional ligands to increase phagocytic capture and shorten blood circulation time, and the formation of a protein corona that may block the targeting ligand on the particle surface [15][16][17]. Over the

• , iron oxide, copper sulfide), and rare earth-based usNPs (cerium oxide, gadolinium oxide) [22]. Ultrasmall NPs have dimensions comparable to those of a typical globular protein of 3 to 6 nm in diameter [22][25], although the precise size criteria can vary among researchers. For the purpose of this

AI-assisted models to predict chemotherapy drugs modified with C₆₀ fullerene derivatives

• Jonathan-Siu-Loong Robles-Hernández,
• Dora Iliana Medina,
• Katerin Aguirre-Hurtado,
• Marlene Bosquez,
• Roberto Salcedo and
• Alan Miralrio

Beilstein J. Nanotechnol. 2024, 15, 1170–1188, doi:10.3762/bjnano.15.95

• –COOH) were investigated with the protein CXCR7 as the molecular docking target. The research involved over 30 drugs and employed Pearson’s hard–soft acid–base theory and common QSAR/QSPR descriptors to build predictive models for the docking scores. Energetic descriptors were computed using quantum

• ][17]. This G-protein is targeted because studies show a possible positive effect on inhibiting the metastasis of cervical cancer cells [18]. However, more clinical and preclinical studies on CXCR7 and its co-player CXCR4 are required since alterations have been detected in diseases such as cancer

• descriptors for predictive models. Besides, Pearson’s hard–soft acid–base (HSAB) theory suggests other descriptors to describe and predict the interactions between chemical species, such as those between a drug molecule as a ligand and a protein [32]. These quantitative values are based on the vertical

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

• to the trans-differentiation of hepatic stellate cells (HSCs) into collagen-producing myofibroblasts, resulting in the progressive accumulation of extracellular matrix (ECM) protein [12]. The condition may be caused by various etiologies, including viral hepatitis infection, alcohol abuse, and

• targeting activated HSCs. The presence of HSA on the surface of the nanocrystals may facilitate active targeting to activated HSCs via secreted protein acidic and rich in cysteine (SPRAC)-mediated endocytosis. It was reported that the activated HSCs overexpressed SPRAC, which is known as classic albumin

• binding protein. This protein is not available in hepatocytes, thus enabling specific targeting to activated HSCs in liver fibrosis [72]. Tan and co-workers also constructed albumin–mannose 6-phosphate-modified solid lipid NPs to deliver matrine to HSCs [73]. The active substance matrine was first loaded

Interface properties of nanostructured carbon-coated biological implants: an overview

• Mattia Bartoli,
• Francesca Cardano,
• Erik Piatti,
• Stefania Lettieri,
• Andrea Fin and
• Alberto Tagliaferro

Beilstein J. Nanotechnol. 2024, 15, 1041–1053, doi:10.3762/bjnano.15.85

• response. The mechanisms involved in inflammation related to NDs are not yet clear, but authors suggest that the process is started by serum protein deposition triggering the inflammatory cascade. Moreover, polymeric films containing NDs were optimum substrates for osteoblast proliferation as reported by

• roughness, inducing macrophage polarization to the pro-inflammatory state without producing a great excess of pro-inflammatory factors. Furthermore, GO-coated implants showed a reduction of the expression of the fibrosis-related protein α-SMA and collagen deposition in the presence of both fibroblasts and

• the FimH protein complex involved in bladder infection. CNTs also prevent the formation of biofilm as reported by Sivaraj et al. [126], who obtained zones of inhibition of up to 12 mm. Morco et al. [127] suggested that the biofilm inhibition by CNTs is mainly due to the increase of surface

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

• involved in macropinocytosis, the CLIC/GEEC (clathrin-independent carrier/glycosylphosphatidylinositol (GPI)-anchored protein-enriched endosomal compartments) pathway, as well as in FEME (fast endophilin-mediated endocytosis) and phagocytosis (an uptake mechanism for large particles mostly found in

• , it was recently published that globular particles with regularly spaced green fluorescent protein (GFP) and a diameter of 40 nm could induce membrane curvature and be internalized when binding to glycosylphosphatidyl-anchored GFP nanobodies [19]. Vesicle formation was energy dependent and dynamin

• stimulation of protein kinase A [7]. To which extent this is a general phenomenon is still unknown. In contrast, in endothelial cells caveolae can be seen on both sides of the endothelial cell layer, and caveolae have been reported to be involved in transcytosis across the cell layer [23]. It should, however

Therapeutic effect of F127-folate@PLGA/CHL/IR780 nanoparticles on folate receptor-expressing cancer cells

• Thi Ngoc Han Pham,
• Phuong-Thao Dang-Luong,
• Hong-Phuc Nguyen,
• Loc Le-Tuan,
• Xuan Thang Cao,
• Thanh-Danh Nguyen,
• Vy Tran Anh and
• Hieu Vu_Quang

Beilstein J. Nanotechnol. 2024, 15, 954–964, doi:10.3762/bjnano.15.78

• . The outer PEO corona prevents aggregation, protein adsorption, and recognition by the reticuloendothelial system, while the hydrophobic PPO core may be modified to contain hydrophobic anticancer drugs, fluorophores, or even anchor to the hydrophobic layer of the nanoparticles [8][9]. The F127

• increased, respectively, to 372 nm and 0.486 for F127-folate@PLGA/CHL/IR780, and, respectively, to 288 nm and 0.663 for F127@PLGA/CHL/IR780. The increase in nanoparticle size could be the result of protein absorption the nanoparticle surface [38]. However, the absorption of protein from the cell culture

• than the negative ones [42]. Preventing protein absorption by nanoparticles might enhance the systemic half-life of nanoparticles. According to reports, nanoparticles with a stealth surface have a longer half-life [39]. Typically, hydrophilic substances, such as PVA and PEG, serve as stealth surface

Electrospun nanofibers: building blocks for the repair of bone tissue

• Tuğrul Mert Serim,
• Gülin Amasya,
• Tuğba Eren-Böncü,
• Ceyda Tuba Şengel-Türk and
• Ayşe Nurten Özdemir

Beilstein J. Nanotechnol. 2024, 15, 941–953, doi:10.3762/bjnano.15.77

• bone [16]. The most dominant component of the organic matrix is collagen, which is synthesized by osteoblasts and performs many mechanical functions. Collagen is a protein found abundantly not only in bones but also in almost every tissue of mammals. One third of all body proteins are collagens [20

• ]. Type-I collagen constitutes approximately 90–95% of the organic matrix in bone tissue, and smaller amounts of other collagen types (i.e., III, V, X, and XII) are included in the bone composition [12][21]. It has been emphasized that type-I collagen is the most important protein structure that carries

• responsible for bone remodeling. Osteoblasts are tightly bound to each other and they cover the bone surface. They are also known as protein-synthesizing cells and responsible for bone formation because they secrete organic bone matrix. Following the formation of this unmineralized cell matrix called osteoid

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

• “protein corona”, which dictates the biological characteristics of the nanoparticles [10][11]. The composition of this corona is variable and relies on the concentrations and affinities of its different components to the nanoparticle surface. Cellular uptake of NPs happens through receptor-mediated active

The effect of age on the attachment ability of stick insects (Phasmatodea)

• Marie Grote,
• Stanislav N. Gorb and
• Thies H. Büscher

Beilstein J. Nanotechnol. 2024, 15, 867–883, doi:10.3762/bjnano.15.72

• . aeta. Some arthropod claws, such as those in ticks [69], have been shown to contain small amounts of resilin, an elastomeric protein providing flexibility in cuticle composites [70]. Voigt and Gorb [69] also suspect resilin to occur in other arthropod claws as well, but melanization impedes

Functional fibrillar interfaces: Biological hair as inspiration across scales

• Guillermo J. Amador,
• Brett Klaassen van Oorschot,
• Caiying Liao,
• Jianing Wu and
• Da Wei

Beilstein J. Nanotechnol. 2024, 15, 664–677, doi:10.3762/bjnano.15.55

• cells (bacteria) should not be confused. Eukaryotic flagella are essentially the same organelles as cilia, consisting of a well-organized microtubular backbone and orchestrated internal protein motors, whereas bacterial flagella are simply passive, stiff filaments. The passive nature of the hairs does

• still made of the protein complex keratin. Plants also make use of fibrillar structures to provide defense against predators. These structures are known as trichomes and vary in morphology and density. While trichomes may also secrete chemicals to warn predators, they can impale insects and their larvae

• generation. The flagella of archaea and bacteria are themselves passive hairs and are driven by protein motors at the base. Hair-like ultrastructures, or mastigonemes, on eukaryotic flagella/cilia comprise helical glycoproteins (≈10–20 nm thick) and lack a membrane [106]. They can be either stiff or flexible

Comparative analysis of the ultrastructure and adhesive secretion pathways of different smooth attachment pads of the stick insect Medauroidea extradentata (Phasmatodea)

• Julian Thomas,
• Stanislav N. Gorb and
• Thies H. Büscher

Beilstein J. Nanotechnol. 2024, 15, 612–630, doi:10.3762/bjnano.15.52

• both layers emit a blue signal, indicative of the presence of resin (rubber-like protein) with relatively soft properties (Figure 3C). The morphological details of these layers are also apparent in longitudinal microtome sections (Figure 3B) and SEM sections (Figure 3D). The primary rod layer is

On the additive artificial intelligence-based discovery of nanoparticle neurodegenerative disease drug delivery systems

• Shan He,
• Julen Segura Abarrategi,
• Harbil Bediaga,
• Sonia Arrasate and
• Humberto González-Díaz

Beilstein J. Nanotechnol. 2024, 15, 535–555, doi:10.3762/bjnano.15.47

• , protein targeting, the prediction of coated-NP drug release systems [41][42][43][44][45][46][47][48][49], multitarget networks of neuroprotective compounds for a theoretical study of new asymmetric 1,2-rasagiline carbamates [50], a TOPS-MODE model of multiplexing neuroprotective effects of drugs, an

• biological activity parameter, cd1, the target protein involved in NDs, cd2, the cell line for NDD assays, and cd3, the model organism. Each one of these assays included one out of n(cd0) = 46 possible biological activity parameters (e.g., EC50 or Ki (nM)). They also involved some of the n(cd1) = 21 target

• included another set of discrete variables used to codify the nature/quality of data. These variables are cd4, the type of target, cd5, the type of assay, cd6, the data curation, cd7, the confidence score, and cd8, the target mapping. Specifically, the target types are n(cd4) = 6 (single protein, organism

Cholesterol nanoarchaeosomes for alendronate targeted delivery as an anti-endothelial dysfunction agent

• Horacio Emanuel Jerez,
• Yamila Roxana Simioni,
• Kajal Ghosal,
• Maria Jose Morilla and
• Eder Lilia Romero

Beilstein J. Nanotechnol. 2024, 15, 517–534, doi:10.3762/bjnano.15.46

• have lately been described [30][31][32]. Endothelial cells express a diversity of innate immune receptors including Toll-like receptors (TLRs) and NOD-like receptors (NLRs), which activate intracellular inflammatory pathways mediated by nuclear factor kappa B (NF-kB) and the mitogen-activated protein

• -fraction V were obtained from Sigma-Aldrich (MO, USA). Lissamine™ rhodamine B 1,2-dihexadecanoyl-sn-glycero-3-phosphoethanolamine triethylammonium salt (RhPE), Hoechst 33342, Pierce™ BCA Protein Assay Kit, and CM-H2DCFDA (general oxidative stress indicator) were purchased from Thermo Fisher Scientific (MA

Classification and application of metal-based nanoantioxidants in medicine and healthcare

• Nguyen Nhat Nam,
• Nguyen Khoi Song Tran,
• Tan Tai Nguyen,
• Nguyen Ngoc Trai,
• Nguyen Phuong Thuy,
• Hoang Dang Khoa Do,
• Nhu Hoa Thi Tran and
• Kieu The Loan Trinh

Beilstein J. Nanotechnol. 2024, 15, 396–415, doi:10.3762/bjnano.15.36

• than copper content and size. The enzyme activity of natural CAT highly depends on the three-dimensional (3D) structure of the protein. A significant decrease or even loss of CAT activity can be caused already by small changes in the protein conformation and structure. As a matter of fact, cellular

• is caused by protein denaturation at high temperatures. Impressively, Co3O4 nanomaterials with different morphologies (nanoplates, nanorods, and nanocubes) exhibited the highest relative activity at very high pH (pH 9) and temperature (90 °C) [39]. Similar results were also reported for platinum

• lipoprotein receptor-related protein overexpressed on cells that comprise the BBB. Figure 3 illustrates the biodistribution and ROS scavenging activity of edaravone-encapsulated nanospherical albumin (EeNA) [91]. Alzheimer’s disease is a neurological disease that slowly destroys thinking skills and memory

Nanomedicines against Chagas disease: a critical review

• Maria Jose Morilla,
• Kajal Ghosal and
• Eder Lilia Romero

Beilstein J. Nanotechnol. 2024, 15, 333–349, doi:10.3762/bjnano.15.30

• , resulting in its fast killing. Lately, it was suggested that the major metabolic impact of BNZ is on the glutathione (and trypanothione) pathway so that covalent binding of BNZ with low-molecular-weight thiols and with protein thiols is the drug’s primary mode of action against T. cruzi [15]. In mammalian

• Loncastuximab tesirine, launched in 2021 to treat B-cell lymphoma [84]. Nearly 10% are polymer–drug/protein conjugates such as polyethylene glycol-ʟ-asparaginase (Calaspargase pegol, Asparlas), launched in 2019 in the USA to treat acute lymphoblastic leukemia [85]. Another 10% are protein-based nanoparticles

• including Abraxane, the first formulation based on protein nanotechnology launched in 2005 [86]. Nearly 10% are inorganic nanoparticles such as the radiosensitizer Hensify, which in 2019 obtained CE Mark approval in the European Union for the treatment of locally advanced soft tissue sarcoma. This category

Exploring the relationships between physiochemical properties of nanoparticles and cell damage to combat cancer growth using simple periodic table-based descriptors

• Joyita Roy and
• Kunal Roy

Beilstein J. Nanotechnol. 2024, 15, 297–309, doi:10.3762/bjnano.15.27

• protein corona. The formation of a protein corona on the surface of NPs, which influences the interaction with cell membranes or proteins, is also associated with zeta potential and surface charge. Very limited studies have reported the influence of zeta potential, surface charge, hydrophobicity, and

• hydroxyl radicals, resulting in oxidative damage to proteins. Moreover, they can bind non-specifically to amino acid residues and replace existing metal ions at active sites of enzymes, leading to abnormal protein folding. Protein aggregation diseases are a type of neurodegenerative diseases that occur

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

• modelling of the interaction between various surfaces, that is (100), (110), and (111), of fcc aluminum with the most abundant milk proteins and lactose. Our approach combines atomistic molecular dynamics, a coarse-grained model of protein adsorption, and kinetic Monte Carlo simulations to predict the

• protein corona composition in the deposited milk layer on aluminum surfaces. We consider a simplified model of milk, which is composed of the six most abundant milk proteins found in natural cow milk and lactose, which is the most abundant sugar found in dairy. Through our study, we ranked selected

• provide valuable insights into the mechanisms of lactose and protein deposition on aluminum surfaces, which can aid in the general understanding of protein corona formation. Keywords: all atomistic; aluminum; bionano interface; coarse grained model; lactose; milk protein; multiscale modelling; protein

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 target efficacy. To increase the blood half-life, stealth materials have been attached to the nanoparticle surface to prevent protein adsorption and immune cell phagocytosis [4]. Most sheath materials are hydrophilic polymers such as poly(vinyl alcohol), poly(ethylene glycol), and poly(ethylene

• cytoskeleton and chlorambucil (CHL) inhibits DNA synthesis. These drugs can be encapsulated inside nanoparticles for administration to increase the stability of the medication in circulation and therapeutic efficacy. For example, doxorubicin can be inserted into liposomes and paclitaxel attaches to the protein

• NPs also helps to maintain its stability. Poly(ethylene glycol) (PEG) on the surface of NPs would serve as a brush to inhibit serum protein adsorption [4]. The PEO block of F127 shares the same core structure as PEG; hence, the emergence of a form of PEG would likewise improve the pharmacokinetics of

Assessing phytotoxicity and tolerance levels of ZnO nanoparticles on Raphanus sativus: implications for widespread adoptions

• Pathirannahalage Sahan Samuditha,
• Nadeesh Madusanka Adassooriya and
• Nazeera Salim

Beilstein J. Nanotechnol. 2024, 15, 115–125, doi:10.3762/bjnano.15.11

• light scattering (DLS), and scanning electron microscopy (SEM). The effect of ZnO NPs (70 nm) on R. sativus grown in coir was evaluated. The application of 1,000 mg/L of ZnO NPs resulted in a significant increase (p < 0.05) in soluble protein content, carbohydrates, chlorophyll a (Chl-a), chlorophyll b

• (p < 0.05) in soluble protein content by 23.1%, accompanied by a notable increase in IAA by 31.1%, indicating potential toxicity. The use of atomic absorption spectroscopy confirmed the internalization of zinc in seedlings, with a statistically significant increase (p < 0.05). In control plants

• at higher doses was investigated against R. sativus to determine its tolerance. Further, this study also attempted to assess the accumulation of Zn in R. sativus seedlings by determining the effect of ZnO NPs on the soluble protein content, indole acetic acid (IAA) content, total carbohydrate content

Study of the reusability and stability of nylon nanofibres as an antibody immobilisation surface

• Inés Peraile,
• Matilde Gil-García,
• Laura González-López,
• Nushin A. Dabbagh-Escalante,
• Juan C. Cabria-Ramos and
• Paloma Lorenzo-Lozano

Beilstein J. Nanotechnol. 2024, 15, 83–94, doi:10.3762/bjnano.15.8

• nanofibres with well-oriented antibodies anchored by protein A/G. Our study shows that stripping with glycine buffer pH 2.5 allows the nanofibres to be reused as long as protein A/G has been previously anchored, leaving both nanofibre and protein A/G unchanged. On the other hand, we investigated the

• stability of the nylon nanofibres. To achieve this, we analysed any loss of immunocapture ability of well-oriented antibodies anchored both to the nylon nanofibres and to a specialised surface with high protein binding capacity. The nanofibre immunocapture system maintained an unchanged immunocapture

• reusability study”. Ricin has been chosen as a representative biotoxin because it has been used in biological warfare attacks because of its high toxicity, stability, and availability. It belongs to the ribosome-inactivating protein family and causes cell death by disrupting protein synthesis [20]. Results

Nanotechnological approaches in the treatment of schistosomiasis: an overview

• Lucas Carvalho,
• Michelle Sarcinelli and
• Beatriz Patrício

Beilstein J. Nanotechnol. 2024, 15, 13–25, doi:10.3762/bjnano.15.2

• , Adekiya et al. [40] produced PZQ encapsulated in nanoliposomes whose surface was modified with an antibody against calpain, a protein found in the tegument of the parasite and is upregulated in the regions where host–parasite interaction occurs [41]. The modified nanoparticles orally administered two or