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

• demonstrated that no additional steps for conjugation were required, such as antibody modification or NP surface group activation. However, there are several drawbacks of this method. The method is the least stable and requires high concentrations of antibodies for adsorption. Hydrophobic interaction can also

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

• attraction, and hydrophobic interaction free energies of surface-bound hydrophilic polyethylene oxide (PEO) polymer [67]. Greater surface density and chain length of terminally attached PEO chains were reported to correlate to a lower van der Waals attractive component. In turn, steric repulsion of the

Stimuli-responsive polypeptide nanogels for trypsin inhibition

• Petr Šálek,
• Jana Dvořáková,
• Sviatoslav Hladysh,
• Diana Oleshchuk,
• Ewa Pavlova,
• Jan Kučka and
• Vladimír Proks

Beilstein J. Nanotechnol. 2022, 13, 538–548, doi:10.3762/bjnano.13.45

• interaction [35][36]. Our observation indicates that the adsorption of 125I-radiolabeled BSA onto Nα-Lys-NG is mainly driven by hydrophobic interaction. At higher initial concentrations of 125I-radiolabeled BSA, both polypeptide nanogels, Nα-Lys-NG and PHEG-Tyr, are quickly saturated and unable to adsorb

Alcohol-perturbed self-assembly of the tobacco mosaic virus coat protein

• Ismael Abu-Baker and
• Amy Szuchmacher Blum

Beilstein J. Nanotechnol. 2022, 13, 355–362, doi:10.3762/bjnano.13.30

• hydrophobic interaction strength in the presence of alcohol and reduced particle–particle repulsion near the isoelectric point (5.09) of TMV-cp. This is very similar to what was previously observed in water–alcohol–LiCl solutions [33]. To further investigate the effect of alcohols on the protein self-assembly

• rods. This could be the result of increased hydrophobic interaction strength, as determined by Lee and co-workers [33]. If disks interact with each other too strongly in the initial non-helical conformation, the energy barrier to rearrange into a helical conformation may become prohibitive. Potential

Self-assembly of amino acids toward functional biomaterials

• Huan Ren,
• Lifang Wu,
• Lina Tan,
• Yanni Bao,
• Yuchen Ma,
• Yong Jin and
• Qianli Zou

Beilstein J. Nanotechnol. 2021, 12, 1140–1150, doi:10.3762/bjnano.12.85

• combinations suggest that all assembled ultrastructures formed from various metabolites exhibit amyloidosis. These metabolites not only self-assemble into supramolecular amyloid fiber structures, but also have significant apoptotic effects on neuron model cells. Singh et al. [36] showed that the hydrophobic

• interaction between phenylalanine (Phe) rings may play a major role in the self-assembly process. Interestingly, their study also revealed that ᴅ-Phe changes ʟ-Phe fibrous state to flakes, which do not propagate further and do not seed ʟ-Phe, suggesting that ᴅ-Phe may be a potential therapeutic molecule for

Adsorptive removal of bulky dye molecules from water with mesoporous polyaniline-derived carbon

• Hyung Jun An,
• Jong Min Park,
• Nazmul Abedin Khan and
• Sung Hwa Jhung

Beilstein J. Nanotechnol. 2020, 11, 597–605, doi:10.3762/bjnano.11.47

• other adsorbent, KOH-900 showed the highest performance in AR1 adsorption, as shown in Figure 3. Therefore, hydrophobic interaction can be suggested as a plausible mechanism for AR1 and JGB adsorption. This mechanism, which has been suggested earlier in adsorption of malachite green [52], aromatics [64

Identification of physicochemical properties that modulate nanoparticle aggregation in blood

• Ludovica Soddu,
• Duong N. Trinh,
• Eimear Dunne,
• Dermot Kenny,
• Giorgia Bernardini,
• Ida Kokalari,
• Arianna Marucco,
• Marco P. Monopoli and
• Ivana Fenoglio

Beilstein J. Nanotechnol. 2020, 11, 550–567, doi:10.3762/bjnano.11.44

• groups/nm2 [31][32]. Both surfaces exhibit surface sites able to form hydrogen bonds or hydrophobic interaction with proteins. However, such tendency may be different since hydrogen bond formation obeys geometrical constraints due to the directional character of this bond. On the other hand, both silica

Multilayer capsules made of weak polyelectrolytes: a review on the preparation, functionalization and applications in drug delivery

• Varsha Sharma and
• Anandhakumar Sundaramurthy

Beilstein J. Nanotechnol. 2020, 11, 508–532, doi:10.3762/bjnano.11.41

• calixarene units covalently bound in various ways. Although there are many reports on calixerene [59], cyclodextrins offer a wide scope for such interactions in biological applications. They could act as a host for many biomolecules or drugs via hydrogen bonding, hydrophobic interaction or van der Waals

• responsive to external stimuli such as temperature, light and chemical environment. They might also have the capability to self-assemble into functional materials via hydrogen bonding, hydrophobic interaction, metal–ligand interaction and van der Waals forces. Among them, the major driving force of such

Internalization mechanisms of cell-penetrating peptides

• Ivana Ruseska and
• Andreas Zimmer

Beilstein J. Nanotechnol. 2020, 11, 101–123, doi:10.3762/bjnano.11.10

• the CPP. Since the hydrophobic interaction is necessary for this model, it seems unlikely that it is being used for the internalization of strongly cationic peptides such as TAT. According to this, it is logical that this mechanism was first proposed for dermaseptin, which is an antimicrobial

• lipid core. It is assumed that there is hydrophobic interaction between the less hydrophilic peptide backbone and the lipid core involved in this process. The aforementioned translocation processes have been observed for octa-arginine (R8) and the HIV TAT peptide [44]. Studies conducted on the

Multiwalled carbon nanotube based aromatic volatile organic compound sensor: sensitivity enhancement through 1-hexadecanethiol functionalisation

• Nadra Bohli,
• Meryem Belkilani,
• Juan Casanova-Chafer,
• Eduard Llobet and
• Adnane Abdelghani

Beilstein J. Nanotechnol. 2019, 10, 2364–2373, doi:10.3762/bjnano.10.227

• of operation/storage. The weak interaction of the toluene molecule with the surface of both functionalised and non-functionalised sensors can be explained by the hydrophobic–hydrophobic interaction between the functional groups of the monolayer (CH3 groups) and the CH3 group of the toluene molecule

Tailoring the stability/aggregation of one-dimensional TiO₂(B)/titanate nanowires using surfactants

• Atiđa Selmani,
• Johannes Lützenkirchen,
• Kristina Kučanda,
• Dario Dabić,
• Engelbert Redel,
• Ida Delač Marion,
• Damir Kralj,
• Darija Domazet Jurašin and
• Maja Dutour Sikirić

Beilstein J. Nanotechnol. 2019, 10, 1024–1037, doi:10.3762/bjnano.10.103

• affinity and stronger hydrophobic interaction in systems with dimeric surfactant due to the presence of two dodecyl chains. The presence of DTAB and 12-2-12 affects the surface charge of the TNWs. Both surfactants showed a shifted pHiep of TNWs to higher pH values, indicating the adsorption of the DTAB and

Development of polycationic amphiphilic cyclodextrin nanoparticles for anticancer drug delivery

• Gamze Varan,
• Juan M. Benito,
• Carmen Ortiz Mellet and
• Erem Bilensoy

Beilstein J. Nanotechnol. 2017, 8, 1457–1468, doi:10.3762/bjnano.8.145

• -loaded nanoparticles maintained their stability for 30 days in ultrapure water. This data shows that PCX crystals are not formed in aqueous dilution, which is believed to improve the safety of the drug delivery system. PCX exists in a crystal form in aqueous media due to hydrophobic interaction between

A novel electrochemical nanobiosensor for the ultrasensitive and specific detection of femtomolar-level gastric cancer biomarker miRNA-106a

• Maryam Daneshpour,
• Kobra Omidfar and
• Hossein Ghanbarian

Beilstein J. Nanotechnol. 2016, 7, 2023–2036, doi:10.3762/bjnano.7.193

• hydrophobic interaction between streptavidin and gold-magnetic NPs was used, the covalent binding methods provided more stable chemical bonds and higher binding efficacy. The main parameters that should be carefully controlled when using EDC/NHS are the pH value, the EDC/NHS ratio, and the amount of EDC that

Fabrication and characterization of novel multilayered structures by stereocomplexion of poly(D-lactic acid)/poly(L-lactic acid) and self-assembly of polyelectrolytes

• Elena Dellacasa,
• Li Zhao,
• Gesheng Yang,
• Laura Pastorino and
• Gleb B. Sukhorukov

Beilstein J. Nanotechnol. 2016, 7, 81–90, doi:10.3762/bjnano.7.10

• [12][13][14], hydrogen bonding [15][16][17] and hydrophobic interaction [18][19][20] have been investigated, and also non-water-soluble polymers, viruses [21], proteins [22][23][24][25][26], and amphiphiles [27][28][29] have been used in LBL multilayers. Among the non-water-soluble polymers, the

Hydrophobic interaction governs unspecific adhesion of staphylococci: a single cell force spectroscopy study

• Nicolas Thewes,
• Peter Loskill,
• Philipp Jung,
• Henrik Peisker,
• Markus Bischoff,
• Mathias Herrmann and
• Karin Jacobs

Beilstein J. Nanotechnol. 2014, 5, 1501–1512, doi:10.3762/bjnano.5.163

• , yet it is unclear up to now which forces are governing this process. Alongside long-ranged van der Waals and electrostatic forces, short-ranged hydrophobic interaction plays an important role. To characterize the forces involved during approach and retraction of an individual bacterium to and from a

• hydrophobic interaction of the involved surfaces is mainly responsible for adhesion. The ostensibly long range of the attraction is a result of the large size of the cell wall proteins, searching for contact via hydrophobic interaction. The model also explains the strong (weak) adhesion of S. carnosus to

• hydrophobic (hydrophilic) surfaces. Keywords: atomic force microscopy (AFM); force spectroscopy; hydrophobic interaction; single cell; Staphylococcus carnosus; Introduction Members of the genus Staphylococcus are known to form extremely resistant biofilms, some of which can cause severe infectious diseases

In vitro interaction of colloidal nanoparticles with mammalian cells: What have we learned thus far?

• Moritz Nazarenus,
• Qian Zhang,
• Mahmoud G. Soliman,
• Pablo del Pino,
• Beatriz Pelaz,
• Susana Carregal-Romero,
• Joanna Rejman,
• Barbara Rothen-Rutishauser,
• Martin J. D. Clift,
• Reinhard Zellner,
• G. Ulrich Nienhaus,
• James B. Delehanty,
• Igor L. Medintz and
• Wolfgang J. Parak

Beilstein J. Nanotechnol. 2014, 5, 1477–1490, doi:10.3762/bjnano.5.161

• to positively charged NPs [121][122]. iii) Lipids present in membranes or second-messenger lipids wrap around NPs driven by hydrophilic/hydrophobic interaction and often result in formation of micelles [123][124]. iv) Thiols, present in glutathione or reduced proteins bind to the surface of noble

Nanoscopic surfactant behavior of the porin MspA in aqueous media

• Ayomi S. Perera,
• Hongwang Wang,
• Tej B. Shrestha,
• Deryl L. Troyer and
• Stefan H. Bossmann

Beilstein J. Nanotechnol. 2013, 4, 278–284, doi:10.3762/bjnano.4.30

• ; hydrophobic interaction; liposome-type cluster; protein cluster; supramolecular; temperature influence; zeta potential; Introduction The homo-octameric porin MspA from Mycobacterium smegmatis is one of the most stable proteins known to date [1]. Due to its size and unique structure [2], its resistance to

Review and outlook: from single nanoparticles to self-assembled monolayers and granular GMR sensors

• Alexander Weddemann,
• Inga Ennen,
• Anna Regtmeier,
• Camelia Albon,
• Annalena Wolff,
• Katrin Eckstädt,
• Nadine Mill,
• Michael K.-H. Peter,
• Jochen Mattay,
• Carolin Plattner,
• Norbert Sewald and
• Andreas Hütten

Beilstein J. Nanotechnol. 2010, 1, 75–93, doi:10.3762/bjnano.1.10

• arrangement [15][51] and the size distribution along the chains [51]. Bao et al. explained the formation of disk rows by a hydrophobic interaction between the ligand tails, thus, minimizing exposure to air by maximizing the contact between the ligand tails [60]. Due to the magnetic nature of the Co disks, a