20 research outputs found
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Polyelectrolyte nanocontainers: controlled binding and release of indomethacin
Herein, polyelectrolyte capsules containing anti-inflammatory drug indomethacin were formed using layer-by-layer strategy, which involves alternative deposition of oppositely charged polyelectrolytes, such as poly(acrylic acid) and poly(ethyleneimine) (or chitosan) onto the drug substrate. Two variants of encapsulation have been implemented: direct deposition of polyelectrolytes onto indomethacin dispersed in water at рН 6, and preliminary formation of soft matrix by solubilization of indomethacin in micellar solutions of cationic surfactants. The inclusion of indomethacin into nanosized polyelectrolyte capsules (hydrodynamic diameter of three- and five-layer capsules is 90–180 nm) has given a new form of indomethacin with the drug content of 0.20–0.25%, which exceeds its limiting solubility in water nearly by the factor of 40. The choice of materials and procedures used for preparation of capsules, as well as the number of polyelectrolyte layers that form shell has provided the control of the drug release from capsule and resulted in the design of pharmaceutical dosage forms with long-lasting effect
Platinum Nanoscale Lattice on a Graphite Surface Using Cetyltrimethylammonium Bromide Hemi- and Precylindrical Micelle Templates
One-dimentional (1-D) thin-layer (2–5 nm) parallel
strips
of Pt on a graphite surface have been synthesized via a template-directed
chemical deposition of Pt. The templates are a surface micellar strip
of cetyltrimethylammonium bromide (CTAB) at highly ordered pyrolytic
graphite (HOPG). The concentration- and temperature-dependent morphology
of surface micellar strips of CTAB at the graphite/aqueous solution
is elucidated by using the atomic force microscopy (AFM) soft-contacting
techniques. The dimentions and repeat period of the Pt strips can
be widely controlled by the temperature: the width is from 47 to 169
nm and the period from 134 to 233 nm in the temperature range 25–33
°C. The morphological characteristics of the Pt strips depend
on those of the original surface micellar strips. The fact that the
strips are composed of metallic platinum was confirmed by testing
the membrane electrode assembly with the strips in a special fuel
cell. This approach could be extended to fabricate a wide range of
1-D self-assembling metallic nanostructures on surfaces using micelle-like
self-assemblies carrying metal ions at interfaces
Adsorption and Premicellar Aggregation of CTAB Molecules and Fabrication of Nanosized Platinum Lattice on the Glass Surface
Premicellar
aggregation processes were investigated in a wide range of concentrations
and temperatures of cetyltrimethylammonium bromide (CTAB) aqueous
solutions. Two independent techniques were involved to study adsorption
and aggregation of CTAB molecules at the glass/solution interface.
Electronic spin resonance (ESR) was used to estimate microviscosity
properties through the reorientation correlation time Ď„<sub><i>c</i></sub> of (2,2,6,6-tetramethylpiperidin-1-oxyl),
while atomic force microscopy (AFM) was involved to evaluate the CTAB
molecule morphology at the glass/solution interface. In the dependence
of Ď„<sub><i>c</i></sub> vs the CTAB concentration
three discontinuities were revealed within 0.2–0.5, 0.5–1.02,
and 1.02–1.1 mM narrow concentration ranges, which are probably
connected with the formation of bilayer and hemispherical, hemicylindrical,
cylindrical, and spherical admicelles. The images of some of them
at the glass surface have been independently obtained by AFM. One-dimensional
thin layer (2 nm) of Pt parallel strips on a glass surface have been
synthesized by chemical vapor deposition of the Pt on the surface
micellar CTAB linear templates followed by washing of the latter
Closed polymer containers based on phenylboronic esters of resorcinarenes
Novel polymer nanospheres (p(SRA-B)) were prepared by cross-linking a sulfonated resorcinarene (SRA) with phenylboronic acid. p(SRA-B) shows good stability in water and can be used as a nanocontainer for the pH- and glucose-controlled substrate release. Fluorescent dyes (fluorescein, pyrene and 1,3,6,8-pyrenetetrasulfonic acid tetrasodium salt) were successfully loaded into p(SRA-B). The release of dye is achieved by lowering the pH value to 3 or by adding glucose
Complexes of Sodium Pectate with Nickel for Hydrogen Oxidation and Oxygen Reduction in Proton-Exchange Membrane Fuel Cells
A number of nickel complexes of sodium pectate with varied Ni2+ content have been synthesized and characterized. The presence of the proton conductivity, the possibility of the formation of a dense spatial network of transition metals in these coordination biopolymers, and the immobilization of transition ions in the catalytic sites of this class of compounds make them promising for proton-exchange membrane fuel cells. It has been established that the catalytic system composed of a coordination biopolymer with 20% substitution of sodium ions for divalent nickel ions, Ni (20%)-NaPG, is the leading catalyst in the series of 5, 15, 20, 25, 35% substituted pectates. Among the possible reasons for the improvement in performance the larger specific surface area of this sample compared to the other studied materials and the narrowest distribution of the vertical size of metal arrays were registered. The highest activity during CV and proximity to four-electron transfer during the catalytic cycle have also been observed for this compound
Nanoscale isoindigo-carriers: self-assembly and tunable properties
Over the last decade isoindigo derivatives have attracted much attention due to their high potential in pharmacy and in the chemistry of materials. In addition, isoindigo derivatives can be modified to form supramolecular structures with tunable morphologies for the use in drug delivery. Amphiphilic long-chain dialkylated isoindigos have the ability to form stable solid nanoparticles via a simple nanoprecipitation technique. Their self-assembly was investigated using tensiometry, dynamic light scattering, spectrophotometry, and fluorometry. The critical association concentrations and aggregate sizes were measured. The hydrophilic–lipophilic balance of alkylated isoindigo derivatives strongly influences aggregate morphology. In the case of short-chain dialkylated isoindigo derivatives, supramolecular polymers of 200 to 700 nm were formed. For long-chain dialkylated isoindigo derivatives, micellar aggregates of 100 to 200 nm were observed. Using micellar surfactant water-soluble forms of monosubstituted 1-hexadecylisoindigo as well as 1,1′-dimethylisoindigo were prepared for the first time. The formation of mixed micellar structures of different types in micellar anionic surfactant solutions (sodium dodecyl sulfate) was determined. These findings are of practical importance and are of potential interest for the design of drug delivery systems and new nanomaterials
Thymine-Modified Nanocarrier for Doxorubicin Delivery in Glioblastoma Cells
Brain tumor glioblastoma is one of the worst types of cancer. The blood–brain barrier prevents drugs from reaching brain cells and shields glioblastoma from treatment. The creation of nanocarriers to improve drug delivery and internalization effectiveness may be the solution to this issue. In this paper, we report on a new nanocarrier that was developed to deliver the anticancer drug doxorubicin to glioblastoma cells. The nanocarrier was obtained by nanoemulsion polymerization of diallyl disulfide with 1-allylthymine. Diallyl disulfide is a redox-sensitive molecule involved in redox cell activities, and thymine is a uracil derivative and one of the well-known bioactive compounds that can enhance the pharmacological activity of doxorubicin. Doxorubicin was successfully introduced into the nanocarrier with a load capacity of about 4.6%. Biological studies showed that the doxorubicin nanocarrier composition is far more cytotoxic to glioblastoma cells (T98G) than it is to cancer cells (M-HeLa) and healthy cells (Chang liver). The nanocarrier improves the penetration of doxorubicin into T98G cells and accelerates the cells’ demise, as is evident from flow cytometry and fluorescence microscopy data. The obtained nanocarrier, in our opinion, is a promising candidate for further research in glioblastoma therapy
Langmuir Monolayers and Thin Films of Amphifilic Thiacalix[4]arenes. Properties and Matrix for the Immobilization of Cytochrome <i>c</i>
Formation and properties
of Langmuir films of thiacalix[4]Âarene
(TCA) derivatives containing N-donor groups on the lower rim (Yî—»OÂ(CH<sub>2</sub>)<sub>3</sub>CN; OCH<sub>2</sub>CN; NH<sub>2</sub>; OCH<sub>2</sub>ArCN-<i>p</i>) in <i>1</i>,<i>3</i>-<i>alternate</i> conformation on aqueous subphase and
solid substrates have been studied. Only <i>tetra</i>-cyanopropoxy-<i>p</i>-<i>tert</i>-butylthiacalixÂ[4]Âarene <b>1</b> forms a typical monomolecular layer with perpendicular orientation
of the macrocycle relative to the water–air interface that
is able to immobilize cytochrome <i>c</i> in the entire
range of the surface pressure. Obtained monolayers were transferred
by Langmuir–Schaefer technique onto quartz, indium–tin
oxide (ITO), and silicon. It was demonstrated that protein activity
is retained after immobilization on the substrate