Structure of Supramers Formed by the Amphiphile Biotin-CMG-DOPE

The synthetic function-spacer-lipid (FSL) amphiphile biotin-CMG-DOPE is widely used for delicate ligation of living cells with biotin residues under physiological conditions. Since this molecule has an “apolar-polar-hydrophobic” gemini structure, the supramolecular organization is expected to differ significantly from the classical micelle. Its organization is investigated with experimental methods and molecular dynamics simulations (MDS). Although the linear length of a single biotin-CMG-DOPE molecule is 9.5 nm, the size of the dominant supramer globule is only 14.6 nm. Investigations found that while the DOPE tails form a hydrophobic core, the polar CMG spacer folds back upon itself and predominantly places the biotin reside inside the globule or planar layer. MDS demonstrates that <10 % of biotin residues on the highly water dispersible globules and only 1 % of biotin residues in layer coatings are in an linear conformation and exposing biotin into the aqueous medium. This explains why in biotin-CMG-DOPE apolar biotin residues both in water dispersible globules and coatings on solid surfaces are still capable of interacting with streptavidin.     

Application of new synthesized zwitterionic surfactants as hair shampoo components

Abstract

The purpose of the study was to applicate new synthesized zwitterionic surfactants as hair shampoo components. Hair shampoos formulated for the study contained newly synthesized sulfobetaines at a concentration of 2%. The above additives were evaluated to determine their effect on shampoo dynamic viscosity, texture, yield stress, foaming properties and surface tension of aqueous shampoo solutions. The viscosity of the sulfobetaine-enriched hair shampoos ranged between 6,000 and 21,000?mPa·s, which ensures the required application properties of the formulated products. The yield stress in three prototypical shampoos was equal to approximately 10?Pa, which represents the minimum value that should characterize cosmetics of this type. The sulfobetaines added to the formulations were not found to significantly affect the parameters of hardness and adhesive force. All the formulations under study, except for the shampoo containing N-dodecyl-N-piperidinium-1-propanesulfonate, exhibited good foaming properties. The incorporation of sulfobetaines into hair shampoos contributes to an effective decrease in the surface tension of their aqueous solutions, which may indicate beneficial washing properties. The use of the proposed sulfobetaines in hair shampoos favorably modifies their physicochemical and functional properties. The findings of the study can provide useful insights for the formulation of hair shampoos containing zwitterionic surfactants.     

Radon concentrations in kindergartens and schools in two cities: Kalisz and Ostrów Wielkopolski in Poland

Plastic PicoRad detectors with activated charcoal have been used for radon monitoring in local kindergartens and schools in two cities, Kalisz and Ostrów Wielkopolski, in the region of Greater Poland. Detectors were exposed for a standard time of 48 h during the autumn and winter of 2011 in 103 rooms (Kalisz) and 55 rooms (Ostrów Wlkp), respectively. The detectors were calibrated in the certified radon chamber of the Central Laboratory for Radiological Protection in Warsaw, Poland. The arithmetic and geometric means of indoor radon concentrations in the examined rooms were 46.0 and 30.3 Bq/m³ for Kalisz and 48.9 and 29.8 Bq/m³ for Ostrów Wlkp, respectively. The measured levels of the indoor radon concentrations were relatively low, since the main source of indoor radon for these low storey (max. three storeys) buildings is radon escaping from the underlying soil with a low ²²⁶Ra concentration (~15 Bq/m³). Therefore, the calculated annual effective doses from that source for the children in Kalisz and Ostrów Wlkp were also low 0.35 mSv.     

Orientational order of guest molecules in aligned liquid crystal as measured by EPR and UV–vis techniques

Orientational order of guest molecules in aligned liquid crystal 4-cyano-4′-pentylbiphenyl (5CB) is studied via optical dichroism and electron paramagnetic resonance (EPR) spectra measurements. The guest molecules used are bifunctional molecules bearing paramagnetic nitroxide group and photochromic azobenzene moiety. The bifunctional probe with rigidly bonded nitroxide and azobenzene moieties was found to align as a whole, while flexible long spacer between the moieties provides independent alignment for the nitroxide and azobenzene parts. Intermolecular interactions responsible for the alignment of azobenzene and nitroxide moieties of the probe molecules are discussed. The molecules with cis-configuration of azobenzene moiety are able to align in the liquid-crystalline medium, but to a lesser extent than the molecules with trans-configuration. Directions of orientational axes and characteristics of rotational mobility of spin probes are determined. Second, fourth and, in some cases, sixth rank order parameter values are found.     

Radon (222Rn) in underground drinking water supplies of the Southern Greater Poland Region

Activity concentration of the ²²²Rn radionuclide was determined in drinking water samples from the Sothern Greater Poland region by liquid scintillation technique. The measured values ranged from 0.42 to 10.52 Bq/dm³ with the geometric mean value of 1.92 Bq/dm³. The calculated average annual effective doses from ingestion with water and inhalation of this radionuclide escaping from water were 1.15 and 11.8 μSv, respectively. Therefore, it should be underlined that, generally, it’s not the ingestion of natural radionuclides with water but inhalation of the radon escaping from water which is a substantial part of the radiological hazard due to the presence of the natural radionuclides from the uranium and thorium series in the drinking water.     

Artificial Iono‐ and Photosensitive Membranes Based on an Amphiphilic Aza‐Crown‐Substituted Hemicyanine

Artificial iono‐ and photosensitive membranes based on an amphiphilic aza‐crown‐substituted hemicyanine are assembled on liquid and solid supports and their aggregation behaviour, which is influenced by the binding of metal cations and surface density, is studied. The photoinduced charge‐transfer properties of an analogous non‐amphiphilic hemicyanine in solution are also demonstrated. An asymmetric sandwich dimer model is proposed and existence of such dimers in solution is evidenced by transient absorption and fluorescence anisotropy experiments. Changes in absorption and emission spectra, as well as compression isotherms of the amphiphile observed in the presence of cations, are discussed in terms of 2D molecular reorganisation. Surface‐pressure‐controlled reversible excimer formation at the air–water interphase and excimer‐type emission of Langmuir–Blodgett films in the presence of cations are demonstrated and are discussed on the basis of fibre‐optic fluorimetry and fluorescence microscopy results.