Fabrication of nanocrystal forms of ᴅ-cycloserine and their application for transdermal and enteric drug delivery systems

• Hsuan-Ang Tsai,
• Tsai-Miao Shih,
• Theodore Tsai,
• Jhe-Wei Hu,
• Yi-An Lai,
• Jui-Fu Hsiao and
• Guochuan Emil Tsai

Beilstein J. Nanotechnol. 2024, 15, 465–474, doi:10.3762/bjnano.15.42

• absorber [20]. In addition, silver (Ag) nanoparticles were synthesized from cotton fabrics and exhibited strong inhibition activity against some bacteria [21]. Recently, pure active pharmaceutical ingredient (API) composed of nanocrystals was investigated, as opposed to drug nanocarrier platforms [22

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

• % DPPH inhibition and exhibit in vivo hepatoprotective properties in laboratory mice [12]. The combination of copper and cerium in nanoparticle structures enhances antioxidant activity through a synergistic effect. CuCe nanoparticles have been demonstrated for therapeutic effects in ischemic vascular

• ]. Antioxidants contribute to cancer inhibition and cancer treatment by several mechanisms. First, nanoantioxidants reduce cancer initiation by protecting DNA molecules from oxidative stress and stimulating DNA repair. For example, platinum nanoparticles inhibited the growth of epithelial lung cancer cells by

• between cerium(IV) and cerium(III). SOD activity immobilized through cross-linking on a Zr framework (SOD-ZrMOF) demonstrates effective scavenging of ROS and inhibition of oxidative stress. A prolonged investigation using an animal model of acute myocardial infarction revealed that SOD-ZrMOF has the

Controllable physicochemical properties of WO_x thin films grown under glancing angle

• Rupam Mandal,
• Aparajita Mandal,
• Alapan Dutta,
• Rengasamy Sivakumar,
• Sanjeev Kumar Srivastava and
• Tapobrata Som

Beilstein J. Nanotechnol. 2024, 15, 350–359, doi:10.3762/bjnano.15.31

• inhibition of crystallization at lower thicknesses arises mainly because of a considerable contribution of the surface energy to the total Gibbs free energy of crystallization, resulting in a higher crystallization temperature and/or time [47][48]. It can be concluded that the annealing condition (i.e., 673

Vinorelbine-loaded multifunctional magnetic nanoparticles as anticancer drug delivery systems: synthesis, characterization, and in vitro release study

• Zeynep Özcan and
• Afife Binnaz Hazar Yoruç

Beilstein J. Nanotechnol. 2024, 15, 256–269, doi:10.3762/bjnano.15.24

• cancer cell growth, slowing their proliferation and disrupting mitotic regulation, leading to the stimulation of the tumor suppressor gene p53 and the inhibition or inactivation of various signaling pathways [31][32]. Its widespread adoption in medicine can be attributed to its strong therapeutic

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

• ]. High concentrations of Zn are implicated in the shifting of soil microbial communities and inhibition of microbial enzymes, thereby affecting soil fertility [1]. The excess levels of Zn, disrupting soil homeostasis, negatively affects plants and human health by inducing acute toxicity due to the

• coir without displaying chlorosis, necrosis, or strong growth inhibition, indicating its tolerance to elevated Zn levels [47]. Its resilience may have implications not only for the plant but also for the surrounding soil environment, microflora, and potentially human health. Metal-based engineered

• noteworthy internalization of Zn by R. sativus at 10,000 mg/L exceeded the healthy level of Zn by 340%. Despite this, R. sativus demonstrated survival at 1000 mg/L without signs of chlorosis, necrosis, or growth inhibition, suggesting its Zn-tolerant nature. This study emphasized the need for proactive

Berberine-loaded polylactic acid nanofiber scaffold as a drug delivery system: The relationship between chemical characteristics, drug-release behavior, and antibacterial efficiency

• Le Thi Le,
• Hue Thi Nguyen,
• Liem Thanh Nguyen,
• Huy Quang Tran and
• Thuy Thi Thu Nguyen

Beilstein J. Nanotechnol. 2024, 15, 71–82, doi:10.3762/bjnano.15.7

• inhibition concentration for MRSA. The release of BBR from PLA nanofiber scaffolds was best fit with Ritger–Peppas models, suggesting that BBR release was mainly controlled by a diffusion mechanism. Additionally, the BBR NPs/PLA nanofiber scaffold did not exhibit cytotoxic activity against MA-104 monolayer

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

• model of visceral leishmaniasis. Percentages of inhibition in the liver and spleen were 82.4 ± 3.8% and 77.6 ± 5.5%, respectively [75]. The results of the studies highlighted in this topic confirm the relevance of the use of nanostructured formulations for the delivery of bioactive compounds and uptake

Fluorescent bioinspired albumin/polydopamine nanoparticles and their interactions with Escherichia coli cells

• Eloïse Equy,
• Jordana Hirtzel,
• Sophie Hellé,
• Béatrice Heurtault,
• Eric Mathieu,
• Morgane Rabineau,
• Vincent Ball and
• Lydie Ploux

Beilstein J. Nanotechnol. 2023, 14, 1208–1224, doi:10.3762/bjnano.14.100

• progressive inhibition of the deposition of a PDA film on the wall of the reaction beaker, which was mentioned above and observed above a certain amount of BSA (Figure 3a). This allowed us to assume that BSA molecules below a critical amount cannot surround all DA molecules (some DA molecules thus form a thin

• of pristine and fluorescent BSA/PDA NPs. This effect, which is not elucidated so far, was also observed regarding the growth of S. aureus populations (Supporting Information File 1, Figure S9). Especially the absence of E. coli growth inhibition by RhBITC-BSA/PDA NPs allows us to envisage the use of

• -BSA/PDA NPs with a BSA/DA ratio of 10 was determined by calculating the bacterial growth inhibition from absorption measurements at 620 nm. Measurements were acquired with a Multiskan spectrophotometer (Fisher Scientific, Illkich, France). One colony of E. coli or S. aureus was transferred from the

Low temperature atomic layer deposition of cobalt using dicobalt hexacarbonyl-1-heptyne as precursor

• Mathias Franz,
• Mahnaz Safian Jouzdani,
• Lysann Kaßner,
• Marcus Daniel,
• Frank Stahr and
• Stefan E. Schulz

Beilstein J. Nanotechnol. 2023, 14, 951–963, doi:10.3762/bjnano.14.78

• growth trend of these CVD experiments at 150, 125, 100, and 90 °C. The films grow with linear rates. We assume a linear dependency of type d = r·(t − t0) with film thickness d, deposition rate r, deposition time t, and the inhibition time t0, that is, the time where no CVD-like growth may occur. At

• deposition mechanism has changed. The thickness trend shows that the deposition seems to be inhibited in the initial phase as t0 rises significantly above 0. The assumed linear relationship has been plotted in Figure 3 for each deposition temperature. The calculated inhibition times are 13.2 min for 100 °C

• and 35.8 min for 90 °C. The slopes of the linear dependency on the temperature are plotted in Figure 4. This plot also includes the calculated inhibition times according to the assumed linear fit. This simplified assumption shows that the inhibition time in CVD mode rises significantly at temperatures

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

• , complement activation, complement-dependent cytotoxicity, or by inhibition of signal transduction [20][21]. Molecular cancer targets Cancer is a highly heterogeneous condition that arises from several mutations in transforming and tumor suppressor genes. High rates of metastasis, invasion, relapse, and drug

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

• (Figure 12B), and the corresponding EC50 were calculated. Benznidazole and NLC-BNZ presented inhibition of the intracellular growth of the parasites even at the lowest concentration, with no significant differences observed between the treatments. Benznidazole and NLC-BNZ EC50 values were 3.15 and 3.33 µM

Silver nanoparticles loaded on lactose/alginate: in situ synthesis, catalytic degradation, and pH-dependent antibacterial activity

• Nguyen Thi Thanh Tu,
• T. Lan-Anh Vo,
• T. Thu-Trang Ho,
• Kim-Phuong T. Dang,
• Van-Dung Le,
• Phan Nhat Minh,
• Chi-Hien Dang,
• Vinh-Thien Tran,
• Van-Su Dang,
• Tran Thi Kim Chi,
• Hieu Vu-Quang,
• Radek Fajgar,
• Thi-Lan-Huong Nguyen,
• Van-Dat Doan and
• Thanh-Danh Nguyen

Beilstein J. Nanotechnol. 2023, 14, 781–792, doi:10.3762/bjnano.14.64

• cytoplasm and cell wall, leading to increased permeability and, eventually, disruption of the bacterial cell wall [26]. This disruption can deactivate respiratory enzymes, resulting in the generation of reactive oxygen species [27] and the inhibition of adenosine triphosphate release [26]. The antibacterial

• bioactivity against either of the strains, indicating that the observed bioactivity was due to the nanocomposite alone (Supporting Information File 1, Figure S1). Inhibition images and inhibition zone plots of AgNPs@Lac/Alg at different pH values are presented in Figure 9. The results show that the

• , with the highest inhibition zone diameters recorded at pH 6 against S. aureus (10.8 ± 0.57 mm) and S. typhi (9.3 ± 1.34 mm). In contrast, the nanocomposite showed no inhibition in highly basic media (pH 11 and 12) because of the aggregation of nanoparticles, which hindered the leaching of silver into

Quercetin- and caffeic acid-functionalized chitosan-capped colloidal silver nanoparticles: one-pot synthesis, characterization, and anticancer and antibacterial activities

• Akif Hakan Kurt,
• Elif Berna Olutas,
• Fatma Avcioglu,
• Hamza Karakuş,
• Mehmet Ali Sungur,
• Cansu Kara Oztabag and
• Muhammet Yıldırım

Beilstein J. Nanotechnol. 2023, 14, 362–376, doi:10.3762/bjnano.14.31

• antibacterial activity of NPs was compared to the inhibition zone diameters of control antibiotics. Amikacin antibiotic was used as a positive control for P. aeruginosa, and ampicillin antibiotic was used as a positive control for E. coli, S. aureus, and S. epidermidis. The susceptibility zone diameters were S

• bacterial strain. Then the inoculated plates were kept in an oven at 35 ± 2 °C for 18–24 h. The diameters of the inhibition zones formed around the discs in the medium were measured with millimetric rulers. This process was repeated three times for each antibacterial solution. A statistically average value

• studied against Gram-negative (P. aeruginosa and E. coli) and Gram-positive (S. aureus and S. epidermidis) bacteria using the disc diffusion method. The inhibition zone diameters obtained after adding Ch/Q- and Ch/CA-Ag NPs in three different concentrations (1/1, 1/3, and 1/5 dilutions) are presented in

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

• proteins [33][34]. Overall, there is still a strong tendency for researchers to select pharmacological inhibition over genetic studies. This is due to several considerations, namely (i) rapid action in blocking the uptake route, (ii) equal inhibition of the overall cell population, and (iii) time- and

• should be closely monitored, as cell death can be misinterpreted as efficient inhibition, especially in metabolism-based assays. For these inhibitors that involve the permeablization of plasma membranes, such as filipin III, appropriate controls for plasma membrane integrity during the inhibition

• exposure should be included [35]. In order to overcome the poor specificity of pharmacological inhibitors, genetic approaches can be implemented to change the expression of specific proteins [29]. However, the complexity and care with which these studies must be undertaken are higher than an inhibition

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

• targeting Renilla luciferase mRNA. Gene inhibition showed an optimum efficiency (40%) at a given nanoparticle/antisense oligonucleotide ratio, which is promising for in vitro cell transfection. When water was replaced with PBS (0.16 M) for the PIC preparation of nanoemulsions starting from

• cells incubated with the loaded nanoparticles were close to 100% for GAL concentrations of 0.3 mg/mL. The pharmacological activity of GAL was preserved after encapsulation (as measured by the acetylcholinesterase inhibition test). PLGA nanoparticles prepared from a 0.16 M PBS (W)/Polysorbate 80 (S)/(4

• content is not subject to CC BY 4.0. Luciferase activity inhibition (%) for complexes formulated with PLGA nanoparticles from nanoemulsions and a second-generation dendron at a nanoparticle/antisense oligonucleotide ratio of 0.75. Lipofectamine 2000 was used as the positive control and a scrambled

Recent progress in cancer cell membrane-based nanoparticles for biomedical applications

• Qixiong Lin,
• Yueyou Peng,
• Yanyan Wen,
• Xiaoqiong Li,
• Donglian Du,
• Weibin Dai,
• Wei Tian and
• Yanfeng Meng

Beilstein J. Nanotechnol. 2023, 14, 262–279, doi:10.3762/bjnano.14.24

• tumor tissues. This effective inhibition of the TME improves antitumor efficiency by depleting GSH and generating ROS [39]. Similarly, chemodynamic therapy (CDT) can utilize the Fenton reaction to convert endogenous H2O2 into ROS, resulting in a toxic effect on cancer cells [108]. Biomimetic NPs of

Nanotechnology – a robust tool for fighting the challenges of drug resistance in non-small cell lung cancer

• Filip Gorachinov,
• Fatima Mraiche,
• Diala Alhaj Moustafa,
• Ola Hishari,
• Yomna Ismail,
• Jensa Joseph,
• Maja Simonoska Crcarevska,
• Marija Glavas Dodov,
• Nikola Geskovski and
• Katerina Goracinova

Beilstein J. Nanotechnol. 2023, 14, 240–261, doi:10.3762/bjnano.14.23

• pathways to prevent cross talk between multiple growth factor receptors have emerged as valid approaches that could be used to tackle cancer resistance and maximize the efficacy of EGFR inhibition. Presently, a combinatorial therapeutic strategy is believed to be a rational approach to combat the

• the adverse effects. Inhibitors of multiple targets within a single pathway exerting synergistic effects Amplification, overexpression, and mutation of MET and HER2 are heavily involved in EGFR TKI resistance development, and the cross talk of these receptors is a way to avoid TK inhibition in many

• , erlotinib, and afatinib) and EGFR-specific siRNA. The authors noted that combined therapy with the potent irreversible EGFR/HER TKI afatinib and EGFR-specific siRNA resulted in enhanced growth inhibition and apoptosis due to the inhibitory effect of the EGFR-specific siRNA on the overall EGFR oncogenic

Cyclodextrins as eminent constituents in nanoarchitectonics for drug delivery systems

• Makoto Komiyama

Beilstein J. Nanotechnol. 2023, 14, 218–232, doi:10.3762/bjnano.14.21

• transferrin (tumor-targeting protein) which bears poly(ʟ-lysine), mitochondrion-targeting peptide, poly(ethylene glycol), and arylazopyrazole (trans isomer) [89]. Under irradiation with NIR light (808 nm), the photothermal effect disrupted mitochondrial function, leading to inhibition of tumor growth. 6 Some

Antimicrobial and mechanical properties of functionalized textile by nanoarchitectured photoinduced Ag@polymer coating

• Jessica Plé,
• Marine Dabert,
• Helene Lecoq,
• Sophie Hellé,
• Lydie Ploux and
• Lavinia Balan

Beilstein J. Nanotechnol. 2023, 14, 95–109, doi:10.3762/bjnano.14.11

• activity of the functionalized textiles was quantified via a liquid diffusion assay, while a plate diffusion assay was used to visualize the microbial growth inhibition. Preliminary tests showed that the Ag@PEG600DA-coated textile does not stay flat during immersion into microbial suspensions, despite

• fungicidal effect. This is similar to the efficacy of acetic acid and can be classified as slightly fungicidal [53][54]. The inhibition rate of microorganism growth was determined from the OD600nm measurements, for suspensions in contact with 3 wt % and 5 wt % AgNO3-loaded samples. The results are presented

• in Figure 11a for E. coli and remarkably a total inhibition of growth was reached within 24 hours. The silver concentration has no significant impact on antibacterial activity, which indicates that a mere 3 wt % Ag-loaded sample is sufficient to obtain complete elimination of bacteria. The released

Green synthesis of zinc oxide nanoparticles toward highly efficient photocatalysis and antibacterial application

• Vo Thi Thu Nhu,
• Nguyen Duy Dat,
• Le-Minh Tam and
• Nguyen Hoang Phuong

Beilstein J. Nanotechnol. 2022, 13, 1108–1119, doi:10.3762/bjnano.13.94

• the amount of E. coli that survived (i.e., by counting colonies). Each experiment was repeated three times. The E. coli inhibition percentage was calculated via Equation 4: where c0 is the initial number of E. coli cells and ci is the average number of E. coli cells/plate. Results and Discussion

• synthesized ZnO NPs The experimental results on antibacterial performance of synthesized materials are presented in Table 2, the E. coli inhibition percentage was calculated via Equation 4. Figure 10a shows the results of inhibition efficiency of E. coli at an initial concentration of 5·104 CFU/mL by ZnO NPs

• reached 99.83 and 100%, respectively. When the dose of the photocatalyst increased to 10 mg/mL, the E. coli inhibition efficiency reached 99.35% with a contact time of 1 h and the efficiency was 100% when the contact time was 3 h. The results of E. coli bacteria inhibition by ZnO NPs synthesized by the

Recent advances in green carbon dots (2015–2022): synthesis, metal ion sensing, and biological applications

• Aisha Kanwal,
• Naheed Bibi,
• Sajjad Hyder,
• Arif Muhammad,
• Hao Ren,
• Jiangtao Liu and
• Zhongli Lei

Beilstein J. Nanotechnol. 2022, 13, 1068–1107, doi:10.3762/bjnano.13.93

Biomimetic chitosan with biocomposite nanomaterials for bone tissue repair and regeneration

• Se-Kwon Kim,
• Sesha Subramanian Murugan,
• Pandurang Appana Dalavi,
• Sebanti Gupta,
• Sukumaran Anil,
• Gi Hun Seong and
• Jayachandran Venkatesan

Beilstein J. Nanotechnol. 2022, 13, 1051–1067, doi:10.3762/bjnano.13.92

• and coated with different quantities of chitosan (0.125 and 0.25 g) to achieve higher compressive strength and toughness. The antibacterial activity of the composites was tested against Gram-negative bacteria (Pseudomonas aeruginosa) and the results show excellent activity and inhibition of bacterial

• composites was 36.4 ± 0.7 MPa. The antibacterial activity of chitosan/polyvinyl alcohol/graphene oxide/hydroxyapatite/gold was investigated against Escherichia coli and Staphylococcus aureus with a zone of inhibition of 3–7 mm as compared to Pseudomonas aeruginosa and Enterococcus faecalis. The alkaline

• osteoblasts and inhibition of the development of osteosarcoma cancer cells in the work by Sumathra et al. (2018). The in vitro experiment was carried out by using the osteosarcoma MG-63 cell line. The MTT assay for the composites showed cell expansion and growth. The anticancer activity of cisplatin-loaded

Bioselectivity of silk protein-based materials and their bio-inspired applications

• Hendrik Bargel,
• Vanessa T. Trossmann,
• Christoph Sommer and
• Thomas Scheibel

Beilstein J. Nanotechnol. 2022, 13, 902–921, doi:10.3762/bjnano.13.81

• . Biofouling can be defined as the undesired attachment and growth of life on artificial surfaces [49]. One general strategy to inhibit biofilm formation and microbial colonialization is microbial repellence since it targets a direct inhibition of bacterial adherence on a surface. Various approaches can be

• through direct antimicrobial activity, (2) inhibiting biofilm-specific signalling pathways, and (3) modulating the innate immune responses resulting in the inhibition of potentially harmful inflammation reactions [85][86][88]. In order to highlight the multifaceted nature of AMPs, the term host defense

• in the context of microbial defense is a matter of debate in the scientific community [137][138]. While some of the inconsistencies seem to be related to methodological aspects of the reports in doubt, a misunderstanding of the distinction between the three mechanisms of biofilm inhibition, namely

A nonenzymatic reduced graphene oxide-based nanosensor for parathion

• Sarani Sen,
• Anurag Roy,
• Ambarish Sanyal and
• Parukuttyamma Sujatha Devi

Beilstein J. Nanotechnol. 2022, 13, 730–744, doi:10.3762/bjnano.13.65

• , ethyl parathion, fenitrothion, chlorpyrifos, paraoxon, ethion, and acephate) are based on the inhibition of acetylcholinesterase (AChE) activity (an indirect method) [8][9][10]. Some organic molecules and metal cations also act as an inhibitor of AChE. Thus, interference-free detection of OP in

Antibacterial activity of a berberine nanoformulation

• Hue Thi Nguyen,
• Tuyet Nhung Pham,
• Anh-Tuan Le,
• Nguyen Thanh Thuy,
• Tran Quang Huy and
• Thuy Thi Thu Nguyen

Beilstein J. Nanotechnol. 2022, 13, 641–652, doi:10.3762/bjnano.13.56

• bacterial cell membrane and inhibiting the synthesis of proteins and DNA [15]. Chu et al. [16] reported that BBR showed no antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA) in the range of concentrations from 1 to 64 µg/mL. However, inhibition of MRSA biofilm formation was

• least 2.0 mg/mL. Higher concentrations of BBR could be obtained due to the nanoformulation. Thus, the antibacterial activity could be enhanced. In contrast, determining the inhibition zones against E. coli O157:H7 at different concentrations was very difficult (Figure 4b). Therefore, this method is