Frequency-dependent nanomechanical profiling for medical diagnosis

• Santiago D. Solares and
• Alexander X. Cartagena-Rivera

Beilstein J. Nanotechnol. 2022, 13, 1483–1489, doi:10.3762/bjnano.13.122

• . Similar considerations exist for the development of soft wearable sensors or hydrogels for wound healing or drug delivery, among others. In all cases, it is of prime importance to create project teams with the appropriate make-up of expertise and within a well-designed strategy, such that ideas can be

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

• are hydrophobic PTAs with rigid structure and poor water solubility [11][12]. Therefore, several lipid nanoparticulate drug delivery systems have been reported to encapsulate BODIPYs to improve their water solubility and photostability while retaining their original photothermal effects [13][14

• mean particle size and zeta potential of the samples in phosphate-buffered saline (PBS) or in RPMI-1640 medium with 10% FBS over a period of 7 days. Samples were collected at specific time points to monitor the changes in particle size and zeta potential. In vitro drug release properties of AB-LNPs The

• taken out to measure the amount of the released drug by UV–vis spectroscopy, and an equal volume of fresh release medium was added to keep the volume constant. Photothermal measurement for AB-LNPs To study the photothermal properties of AB-LNPs, different concentrations of AB-LNPs with BDP

Orally administered docetaxel-loaded chitosan-decorated cationic PLGA nanoparticles for intestinal tumors: formulation, comprehensive in vitro characterization, and release kinetics

• Sedat Ünal,
• Osman Doğan and
• Yeşim Aktaş

Beilstein J. Nanotechnol. 2022, 13, 1393–1407, doi:10.3762/bjnano.13.115

• . Pharmaceutically, clinical failure due to a drug’s wide biodistribution and non-selective toxicity is one of the major challenges of chemotherapy. In addition, parenteral drug administration in chronic diseases that require long-term drug use, such as intestinal tumors, is challenging in terms of patient

• orally applicable nanodrug formulations that can act against diseases seen in the distant region of the gastrointestinal tract (GIT), such as intestinal tumor, brings with it a series of difficulties depending on the drug and/or GIT physiology. The aim of this study is to develop an oral nanoparticle

• drug delivery system loaded with docetaxel (DCX) as an anticancer drug, using poly(lactic-co-glycolic acid) (PLGA) as nanoparticle material, and modified with chitosan (CS) to gain mucoadhesive properties. In this context, an innovative nanoparticle formulation that can protect orally administered DCX

LED-light-activated photocatalytic performance of metal-free carbon-modified hexagonal boron nitride towards degradation of methylene blue and phenol

• Nirmalendu S. Mishra and
• Pichiah Saravanan

Beilstein J. Nanotechnol. 2022, 13, 1380–1392, doi:10.3762/bjnano.13.114

• of electrons in the HBN lattice. This results in photoinactivity due to a wider bandgap (5.5 eV) and limits its applicability to adsorption, drug delivery, insulators, flame retardants, hydrogen storage, among others [3][4][5][6][7][8][9]. This dictates the development of various innovative

Supramolecular assembly of pentamidine and polymeric cyclodextrin bimetallic core–shell nanoarchitectures

• Alexandru-Milentie Hada,
• Nina Burduja,
• Marco Abbate,
• Claudio Stagno,
• Guy Caljon,
• Louis Maes,
• Nicola Micale,
• Massimiliano Cordaro,
• Angela Scala,
• Antonino Mazzaglia and
• Anna Piperno

Beilstein J. Nanotechnol. 2022, 13, 1361–1369, doi:10.3762/bjnano.13.112

• monometallic (nanoG) structures or core–shell bimetallic (nanoGS) architectures with an external silver layer. Here, we describe the preparation of a supramolecular assembly between nanoGS and pentamidine, an antileishmanial drug endowed with a wide range of therapeutic properties (i.e., antimicrobial, anti

• , antileishmanial drugs which are currently available on the market showed several drawbacks including irreversible toxic effects, high costs, prolonged treatment, need for adequate medical care, emergence of drug resistance, and parenteral administration [20][21]. Recently, nanoantimicrobials based on biogenic

• , Figure 1) achieved by supramolecular assembly of the components as well as their physicochemical characterization in terms of size and colloidal stability. The drug binding ability of nanoGS with Pent has been investigated by complementary spectroscopic techniques such as UV–vis, zeta potential (ζ

Studies of probe tip materials by atomic force microscopy: a review

• Ke Xu and
• Yuzhe Liu

Beilstein J. Nanotechnol. 2022, 13, 1256–1267, doi:10.3762/bjnano.13.104

• ]. In particular, metal nanoclusters exhibit excellent photostability, large Stokes shifts, and low toxicity compared to quantum dots and organic dyes. Researchers increasingly use them in analytical detection fields such as metal ions, small biological molecules, drug delivery, and bioimaging [22][23

• nanotubes and functional nanomaterials, will significantly improve the performance of probes and further promote the broader and deeper application of SPM. It will significantly impact society in life science, drug discovery, and medical diagnosis. Sharpening of a blunt tip and study of its stability after

Microneedle-based ocular drug delivery systems – recent advances and challenges

• Piotr Gadziński,
• Anna Froelich,
• Monika Wojtyłko,
• Antoni Białek,
• Julia Krysztofiak and
• Tomasz Osmałek

Beilstein J. Nanotechnol. 2022, 13, 1167–1184, doi:10.3762/bjnano.13.98

• used. Unfortunately, they are usually not well tolerated by patients due to the need for frequent use as well as the discomfort during application. Therefore, novel drug delivery systems with improved biopharmaceutical properties are a subject of ongoing scientific investigations. Due to the

• physiology of the eye are summarized and discussed. Keywords: eye; microneedles; ocular drug delivery; ophthalmic drugs; Review 1 Introduction Since its first appearance in biomedicine, microtechnology is rapidly entering the world of pharmaceutical sciences, including pharmaceutical technology [1][2][3][4

• ]. Due to the impressive evolution of new manufacturing techniques, it offers completely new opportunities to develop very sophisticated and precise drug delivery tools [5][6]. A large number of concepts and implemented projects, which is reflected in a large number of scientific papers, consistently

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

• sensing, bioimaging, catalysis, medicine, optoelectronics, and drug delivery due to their unique properties, that is, low cytotoxicity, cytocompatibility, water-solubility, multicolor wavelength tuned emission, photo-stability, easy modification, strong chemical inertness, etc. This review article

• nanomaterials has proved to be useful for applications in a variety of disciplines, including chemical or biological sensing, bioimaging, drug delivery, photodynamic therapy, electrocatalysis, and photocatalysis, with advantages over commonly used semiconductor dots or conventional fluorescent probes such as

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

• tissue engineering, drug delivery, diagnostic, and bioimaging applications due to its biocompatibility, tuneable size, and ability to cover different kinds of therapeutic agents. Gold nanoparticles control osteoclastic differentiation [113][114][115]. Osteogenic properties of AuNPs were proven by in

• fluids [117][118]. A recent study has proven that synthetic changes made to the surface of titanium oxide (TiO2) nanotubes can influence their characteristics, substantially impacting cell contacts and antibacterial activity. As a result, antibiotic drugs combined with a surface-modified TiO2-based drug

• delivery system in synthetic bone implants can stimulate bone regeneration while preventing bacterial infection. Furthermore, coating materials containing TiO2 can help drug stabilisation producing a long-term drug release profile [119]. The electrochemical anodization process was used by Lai et al. (2018

Spindle-like MIL101(Fe) decorated with Bi₂O₃ nanoparticles for enhanced degradation of chlortetracycline under visible-light irradiation

• Chen-chen Hao,
• Fang-yan Chen,
• Kun Bian,
• Yu-bin Tang and
• Wei-long Shi

Beilstein J. Nanotechnol. 2022, 13, 1038–1050, doi:10.3762/bjnano.13.91

• cavities, and excellent thermal stability [20][21]. These advantages make it appalling to adsorption [22], gaseous capture/separation [23], sensing [24], and drug release applications [25]. Moreover, some MOFs can be excited under UV or visible light and exhibit light harvesting properties due to ligand

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

• of bio-inspired selective surface modifications The increasing knowledge on natural receptor–ligand binding mechanisms led to various approaches in the last years to increase both cellular adhesion on surfaces of biomaterials and biosensors, as well as for therapeutic drug carrier systems against

Solar-light-driven LaFe_xNi_1−xO₃ perovskite oxides for photocatalytic Fenton-like reaction to degrade organic pollutants

• Chao-Wei Huang,
• Shu-Yu Hsu,
• Jun-Han Lin,
• Yun Jhou,
• Wei-Yu Chen,
• Kun-Yi Andrew Lin,
• Yu-Tang Lin and
• Van-Huy Nguyen

Beilstein J. Nanotechnol. 2022, 13, 882–895, doi:10.3762/bjnano.13.79

• industry often contains biological drugs, such as antibiotics and pesticides. These drug residues in various industries would enter the drinking water source. It threatens human health and makes bacteria and viruses resistant to drugs, significantly impacting the environment [5]. Notably, wastewater

Gelatin nanoparticles with tunable mechanical properties: effect of crosslinking time and loading

• Agnes-Valencia Weiss,
• Daniel Schorr,
• Julia K. Metz,
• Metin Yildirim,
• Saeed Ahmad Khan and
• Marc Schneider

Beilstein J. Nanotechnol. 2022, 13, 778–787, doi:10.3762/bjnano.13.68

• Agnes-Valencia Weiss Daniel Schorr Julia K. Metz Metin Yildirim Saeed Ahmad Khan Marc Schneider Department of Pharmacy, Biopharmaceutics and Pharmaceutical Technology, Saarland University, Campus C4 1, Saarbruecken, Germany Department, Drug Delivery, PharmBioTec Research and Development GmbH

• nanoparticles intended to be used in drug delivery is of great interest. To this end, different potential formulations are developed since the particle elasticity is affecting the in vitro and in vivo performance of the nanoparticles. Here we present a method to determine the elasticity of single gelatin

• revealed the influence of loading a macromolecular model drug (FITC-dextran) on the mechanical properties, which decreased with raising amounts of loaded drug. Loaded particles were significantly softer, with Young’s moduli between 1.06 and 5.79 MPa for the same crosslinking time, than the blank GNPs. In

Recent advances in nanoarchitectures of monocrystalline coordination polymers through confined assembly

• Lingling Xia,
• Qinyue Wang and
• Ming Hu

Beilstein J. Nanotechnol. 2022, 13, 763–777, doi:10.3762/bjnano.13.67

• ]. This is applicable to monocrystalline coordination polymers as well. For instance, poly(ethyleneglycol) (PEG) molecular chains show an affinity to Zn2+ ions, and can, thus, trigger mineralization of ZIF-8 crystals around. Doxorubicin, a kind of antitumor drug, could be dissolved in the parent solution

• acidic environment. Enhanced cell toxicity was found by encapsulating the doxorubicin drug into ZIF-8 crystals because intracellular uptake was facilitated. When multiple cargos were required, this strategy showed good feasibility. Multiple molecules could be simultaneously encapsulated during formation

Design and selection of peptides to block the SARS-CoV-2 receptor binding domain by molecular docking

• Kendra Ramirez-Acosta,
• Ivan A. Rosales-Fuerte,
• J. Eduardo Perez-Sanchez,
• Alfredo Nuñez-Rivera,
• Josue Juarez and
• Ruben D. Cadena-Nava

Beilstein J. Nanotechnol. 2022, 13, 699–711, doi:10.3762/bjnano.13.62

• residues of the RBD, and a peptide with 20 amino acid binds to the Gln493 and Asn501 residues of the RBD. However, neither of these peptides was able to block the three regions of the RBD [8]. The results reported herein suggest that OAPs have a great potential as drug inhibitors of SAR-CoV2 and can block

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

• solubility of a drug leads to low drug absorption. Thus, a sufficient drug concentration in plasma is not achieved, and a high therapeutic effect is not reached. As a result, high dose requirements and more adverse side effects limit the development of phytochemicals in the pharmaceutical industry. BBR

• nanoparticles produced by EPN and ASP techniques have notably increased solubility and dissolution rate due to their semicrystalline form. The small size of the nanoparticles can be obtained by adjusting the drug concentration, flow rate, stirring rate, and antisolvent volume in EPN and ASP methods [28]. Many

• : (1) Almost all drug-carrying nanomaterials have high cost, (2) the drug concentration of the encapsulated form is usually low, and (3) the toxicity risk of nanomaterials must be strictly controlled [32][33][34]. Most nanoformulations have relatively low drug loading (typically a few weight percent

Fabrication and testing of polymer microneedles for transdermal drug delivery

• Vahid Ebrahiminejad,
• Zahra Faraji Rad,
• Philip D. Prewett and
• Graham J. Davies

Beilstein J. Nanotechnol. 2022, 13, 629–640, doi:10.3762/bjnano.13.55

• considerable potential for medical applications such as transdermal drug delivery, point-of-care diagnostics, and vaccination. These miniature microdevices should successfully pierce the skin tissues while having enough stiffness to withstand the forces imposed by penetration. Developing low-cost and simple

• safety for the current MN design demonstrated its potential for transdermal drug delivery and fluid sampling. Experimental results indicated significant penetration improvements using the prototype applicator, which produced array penetration efficiencies as high as >92%, depending on the impact velocity

• setting. Keywords: hot embossing; microneedles; penetration efficiency; thermoplastic polymers; two-photon polymerization; Introduction During the past two decades, MN devices have become a promising tool for transdermal drug delivery, vaccination, and point-of-care diagnostics [1][2]. MNs are a

A new method for obtaining the magnetic shape anisotropy directly from electron tomography images

• Cristian Radu,
• Ioana D. Vlaicu and
• Andrei C. Kuncser

Beilstein J. Nanotechnol. 2022, 13, 590–598, doi:10.3762/bjnano.13.51

• advancements in medical fields (hyperthermia and drug delivery), permanent magnet industry, sensoristics, and spintronics. The program has been tested not only on simulated tomograms but also on tomograms obtained on real-life systems of magnetite MNPs, obtained in-house by co-precipitation methods. Starting

Effects of substrate stiffness on the viscoelasticity and migration of prostate cancer cells examined by atomic force microscopy

• Xiaoqiong Tang,
• Yan Zhang,
• Jiangbing Mao,
• Yuhua Wang,
• Zhenghong Zhang,
• Zhengchao Wang and
• Hongqin Yang

Beilstein J. Nanotechnol. 2022, 13, 560–569, doi:10.3762/bjnano.13.47

• study may provide a new approach to investigate the migration mechanism of PCa cells in addition to cytoskeleton-mediated migration of PCa cells, which can be useful for cancer therapeutic drug screening and development. Experimental Cell culture PZ-HPV-7 normal human prostate epithelial cells and PC-3

Detection and imaging of Hg(II) in vivo using glutathione-functionalized gold nanoparticles

• Gufeng Li,
• Shaoqing Li,
• Rui Wang,
• Min Yang,
• Lizhu Zhang,
• Yanli Zhang,
• Wenrong Yang and
• Hongbin Wang

Beilstein J. Nanotechnol. 2022, 13, 549–559, doi:10.3762/bjnano.13.46

• the fluorescent “ON” form. Keywords: cell imaging; fluorescence probes; glutathione; gold nanoparticles; mercury ions; rhodamine 6G derivatives; Introduction Metal nanoparticles have been widely used in the development and construction of sensor systems and drug carriers due to their excellent

• biocompatibility, large specific surface area, and remarkable photoelectric properties [1][2][3]. Among them, gold nanoparticles (GNPs) have been frequently employed for drug delivery, sensing, imaging, and photodynamic therapy owing to their high extinction coefficient, distinct optical properties, excellent

• conjugate with drug molecules and fluorescent dyes [24]. Recently, we developed a novel Cu(II)-triggered release system with gold nanoparticles surface-modified with ʟ-cysteine for molecular delivery and imaging in cells [31]. Well dispersed GNP–ʟ-cysteine was conjugated with Rh6G2 (GNP–ʟ-Cys–Rh6G2) for a

Ciprofloxacin-loaded dissolving polymeric microneedles as a potential therapeutic for the treatment of S. aureus skin infections

• Sharif Abdelghany,
• Walhan Alshaer,
• Yazan Al Thaher,
• Maram Al Fawares,
• Amal G. Al-Bakri,
• Saja Zuriekat and
• Randa SH. Mansour

Beilstein J. Nanotechnol. 2022, 13, 517–527, doi:10.3762/bjnano.13.43

• results suggest that CIP_MN1 can be a potential delivery system for the treatment of S. aureus skin infections. Keywords: dissolving microneedles; microneedles; polyvinyl alcohol (PVA); polyvinylpyrrolidone (PVP); skin infection; Introduction Topical and transdermal drug delivery is a major route for

• the administration of antimicrobials to the infected parts of the skin and to the systemic circulation. The main limitation to dermal drug delivery is skin barriers. This is mainly due the uppermost dead keratinized skin layer known as the stratum corneum [1]. Microneedles of different shapes and

• sizes have been utilized to overcome this limitation since they can painlessly penetrate the upper skin layers [2]. Patients can self-administer microneedles and, thus, overcome the pain associated with conventional parenteral injections. Moreover, this drug delivery system can potentially overcome the

Design and characterization of polymeric microneedles containing extracts of Brazilian green propolis

• Camila Felix Vecchi,
• Rafaela Said dos Santos,
• Jéssica Bassi da Silva and
• Marcos Luciano Bruschi

Beilstein J. Nanotechnol. 2022, 13, 503–516, doi:10.3762/bjnano.13.42

• Camila Felix Vecchi Rafaela Said dos Santos Jessica Bassi da Silva Marcos Luciano Bruschi Laboratory of Research and Development of Drug Delivery Systems, Postgraduate Program in Pharmaceutical Sciences, Department of Pharmacy, State University of Maringa, Maringa, Brazil 10.3762/bjnano.13.42

• permeation mechanism [6][9][10]. Nanocarriers can be used together with polymeric MNs in a synergistic therapy. The nanocarriers can immediately come into contact with the stratum corneum with the help of polymeric MNs, enhancing the transdermal drug delivery of the drugs. Furthermore, these polymeric MNs

• can encapsulate several types of nanocarriers, making it a unique system with different activities [11]. Solid MNs are used for pre-treatment of the skin. They serve only to create micropores, increasing permeability and facilitating the administration of the drug. The drug will be inserted over the

Ethosomal (−)-epigallocatechin-3-gallate as a novel approach to enhance antioxidant, anti-collagenase and anti-elastase effects

• Çiğdem Yücel,
• Gökçe Şeker Karatoprak,
• Sena Yalçıntaş and
• Tuğba Eren Böncü

Beilstein J. Nanotechnol. 2022, 13, 491–502, doi:10.3762/bjnano.13.41

• Cigdem Yucel Gokce Seker Karatoprak Sena Yalcintas Tugba Eren Boncu Faculty of Pharmacy, Department of Pharmaceutical Technology, Erciyes University, 38280 Kayseri, Turkey Faculty of Pharmacy, Department of Pharmacognosy, Erciyes University, 38280 Kayseri, Turkey Erciyes University, Ziya Eren Drug

• neurodegenerative disorders [7][8][9]. However, there are some difficulties in the formulation of EGCG such as the first pass metabolism effect, enzymatic degradation, and low bioavailability [8][10]. Skin delivery, besides being painless and noninvasive, has many advantages such as controlled drug delivery

• , reduced dose frequency, avoidance of first pass metabolism by the liver, and it can be self-administered. It includes the concept of topical drug delivery aimed at treating a local dermatological disorder without the need to target the systemic circulation by using transdermal drug delivery for systemic

Zinc oxide nanostructures for fluorescence and Raman signal enhancement: a review

• Ioana Marica,
• Fran Nekvapil,
• Maria Ștefan,
• Cosmin Farcău and
• Alexandra Falamaș

Beilstein J. Nanotechnol. 2022, 13, 472–490, doi:10.3762/bjnano.13.40

• diagnosis, therapeutic monitoring, and drug discovery [51]. Several examples of fluorescence enhancement using ZnO nanostructures are given in Table 1. Fewer studies investigated the enhancement of fluorescence in ZnO–metal nanocomposites and further research is still needed to explore this direction. Core

Micro- and nanotechnology in biomedical engineering for cartilage tissue regeneration in osteoarthritis

• Zahra Nabizadeh,
• Mahmoud Nasrollahzadeh,
• Hamed Daemi,
• Mohamadreza Baghaban Eslaminejad,
• Ali Akbar Shabani,
• Mehdi Dadashpour,
• Majid Mirmohammadkhani and
• Davood Nasrabadi

Beilstein J. Nanotechnol. 2022, 13, 363–389, doi:10.3762/bjnano.13.31

• engineering cartilage tissue structures. 3.1.1 Application of microspheres in chondrogenic differentiation. Microspheres are used in drug delivery systems because of their spatiotemporally controlled release capabilities (see Table 2 below). They are small spherical particles from organic or inorganic

• 19 days [28]. In another study, researchers developed PLGA-based microspheres to control the release of rapamycin in the joint [29]. The microspheres provided sustained and controlled release of rapamycin for several weeks, retained drug potency, and prevented OA-like changes in chondrocytes cultured

• biomimetic nanocomposites to imitate pseudostratified features of the ECM to develop bioinspired scaffolds [47][48][49]. 3.1.2.1 Nanoparticles (NPs). In recent years, NPs have been increasingly used in regenerative medicine (Table 1) and other medical areas. NPs have been successfully developed for drug