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Markus Drechsler

Publications and source records attributed to Markus Drechsler.

14 recordsLinked to original sources
PubMed2006

Rheology and phase behavior of poly(n-butyl acrylate)-block-poly(acrylic acid) in aqueous solution.

The surface activity and the rheological properties of aqueous solutions of the amphiphilic block copolymer poly(n-butyl acrylate)-block-poly(acrylic acid) (PnBA-b-PAA) were studied as a function of the degree of neutralization, alpha, of the poly(acrylic acid) block. Although the block copolymer spontaneously forms spherical micelles having a stretched PAA corona and a collapsed PnBA core in water for alpha > 0.1, the solutions do not exhibit any surface activity at this degree of neutralization. Cryo-TEM micrographs show that the radii of the hydrophobic core of the largest micelles are as long as the length of the hydrophobic chain. The micelles, however, have a broad size distribution, and on average, as shown by SANS, the micelles are only about half as long. At concentrations as low as 1 wt %, the solutions exhibit highly viscoelastic behavior and have a yield stress value depending on alpha. The globular micelles are highly ordered in the bulk phase, and the viscoelastic properties are a result of the dense packing of the micelles. The addition of salt or cationic surfactants dramatically decreases the viscosity of the solution. The observed properties seem to be due to electrostatic interactions between the PAA chains of the micelles.

Journal Article↗
PubMed2006

Influence of hydrocarbon surfactant on the aggregation behavior of silicone surfactant: observation of intermediate structures in the vesicle-micelle transition.

Intermediate structures of the aggregates in the aqueous solution of an ABA-type silicone surfactant and in the process of an SDS-induced vesicle-micelle transition are reported. In single ABA silicone surfactant aqueous solutions, large multilamellar vesicles (MLV), small single lamellar vesicles (SLV), threadlike micelles (TLM), and spheroidal micelles were observed. Interestingly, a large amount of TLMs were found entrapped into the large MLVs, but not in SLVs. Disintegration of the small vesicles inside the MLVs indicates that the entrapped TLM are from the disintegrated membrane of the entrapped small vesicles. Addition of SDS induced a transition from vesicles or threadlike micelles to spheroidal micelles. The intermediate structures, such as the appearance of small holes in the vesicle membrane, the budding of threadlike micelles from the membrane fracture, and the clusters of spheroidal micelles, were observed with increase of the SDS concentration. The electrical conductivity measurements indicated that complex micelles of SDS and silicone surfactant were formed in the solution due to the interaction between the SDS and PEO part of the silicone surfactant.

Journal Article↗
PubMed2006

Imaging the volume transition in thermosensitive core-shell particles by cryo-transmission electron microscopy.

We report a study of colloidal thermosensitive core-shell particles by cryo-transmission electron microscopy (cryo-TEM). The particles consist of a solid core of poly(styrene), onto which a network of cross-linked poly(N-isopropylacrylamide) (PNIPAM) is affixed. In water, the shell of these particles swells when the temperature is low. Raising the temperature above 32 degrees C leads to a marked shrinking of the shell. In this letter, we present the first study of these core-shell particles by cryo-TEM in situ, that is, in aqueous solution. We demonstrate that the core-shell particles are well-defined and exhibit a narrow size distribution. In particular, the PNIPAM shell is compact and has a defined outer surface of a slightly irregular shape. The micrographs show that there are density fluctuations within the network. Cryo-TEM of the system above and below the transition temperature furnishes information about the thermosensitive particles that had not been available through other methods employed in previous investigations.

Journal Article↗
PubMed2006

Thermosensitive core-shell particles as carrier systems for metallic nanoparticles.

We present a new system that allows us to modulate the catalytic activity of metal nanoparticles (Ag) by a thermodynamic transition that takes place within the carrier system. Thermosensitive core-shell particles have been used as the carrier system in which the core consists of poly(styrene) (PS), whereas the shell consists of a poly(N-isopropylacrylamide) (PNIPA) network cross-linked by N,N'-methylenebisacrylamide (BIS). Immersed in water, the shell of these particles is swollen. Heating the suspension above 32 degrees C leads to a volume transition within the shell that is followed by a marked shrinking of the network of the shell. The maximum degree of swelling can be adjusted by the degree of cross-linking. Silver nanoparticles with diameters ranging from 6.5 to 8.5 nm have been embedded into thermosensitive PNIPA networks with different cross-linking densities. The Ag nanoparticles do not influence the swelling and the shrinking of the network in the shell. The surface plasmon absorption band of the nanoparticles is shifted to higher wavelengths with temperature. This is traced back to the varying distance of the nanoparticles caused by the swelling and the shrinking of the shell. The catalytic activity is investigated by monitoring photometrically the reduction of 4-nitrophenol by an excess of NaBH4 in the presence of the silver nanocomposite particles. The rate constant kapp was found to be strictly proportional to the total surface of the nanoparticles in the system. Moreover, kapp is first decreasing with increasing temperature when approaching the volume transition. This is due to the strong shrinking of the network. Only at temperatures above the volume transition is the normal Arrhenius-type dependence of kapp found again. In this way, catalytic activity of the metal nanoparticles enclosed in a "nanoreactor" can be modulated by volume transition over a wide range.

Journal Article↗
PubMed2005

High catalytic activity of platinum nanoparticles immobilized on spherical polyelectrolyte brushes.

We present a study on the catalytic activity of platinum nanoparticles immobilized on spherical polyelectrolyte brushes that act as carriers. The spherical polyelectrolyte brushes consist of a solid core of poly(styrene) onto which long chains of poly(2-methylpropenoyloxyethyl) trimethylammonium chloride are grafted. These positively charged chains form a dense layer of polyelectrolytes on the surface of the core particles ("spherical polyelectrolyte brush") that tightly binds divalent PtCl6-(2) ions. The reduction of these ions within the brush layer leads to nearly monodisperse nanoparticles of metallic platinum. The average size of the particles is approximately 2 nm. The composite particles exhibit excellent colloidal stability. The catalytic activity is investigated by photometrically monitoring the reduction of p-nitrophenol by an excess of NaBH4 in the presence of the nanoparticles. The kinetic data could be explained by the assumption of a pseudo-first-order reaction with regard to p-nitrophenol. In all cases, a delay time t0 has been observed, after which the reactions start. This time is shorter when the catalyst has already been used. All data demonstrate that spherical polyelectrolyte brushes present an ideal carrier system for metallic nanoparticles.

Journal Article↗
PubMed2005

High elongation of polyelectrolyte chains in the osmotic limit of spherical polyelectrolyte brushes: a study by cryogenic transmission electron microscopy.

We investigate the conformation of long polyelectrolyte chains attached to colloidal latex particles by cryogenic transmission electron microscopy (cryo-TEM). The dense grafting of the polyelectrolyte chains ("polyelectrolyte brush") leads to a confinement of the counterions and a concomitantly high osmotic pressure within the polyelectrolyte layer attached to the core particles. Cryo-TEM has provided first model-independent direct proof for the strong stretching of the polyelectrolyte chains by direct visualization. If salt is added, cryo-TEM clearly shows how chains collapse because of the strong screening of the electrostatic interaction. Moreover, the analysis of interacting particles by cryo-TEM shows that the polyelectrolyte chains retract at close contact. Hence, we demonstrate how cryo-TEM can be used to analyze directly the spatial structure of polyelectrolyte brushes in situ.

Journal Article↗
PubMed2005

Cubosome dispersions as delivery systems for percutaneous administration of indomethacin.

PURPOSE: The present study concerns the production and characterization of monooleine (MO) dispersions as drug delivery systems for indomethacin, taken as model anti-inflammatory drug. METHODS: Dispersions were produced by emulsification and homogenization of MO and poloxamer in water. Morphology and dimensional distribution of the disperse phase have been characterized by cryo-transmission electron microscopy and photon correlation spectroscopy, respectively. X-ray diffraction has been performed to determine the structural organization of the disperse phase. Sedimentation field flow fractionation (SdFFF) has been performed to investigate drug distribution in the dispersion. An in vitro diffusion study was conducted by Franz cell associated to stratum corneum epidermis membrane on cubosome dispersions viscosized by carbomer. In vivo studies based on skin reflectance spectrophotometry and tape stripping were performed to better investigate the performance of cubosome as indomethacin delivery system. RESULTS: Microscopy studies showed the coexistence of vesicles and cubosomes. X-ray diffraction revealed the presence of a bicontinuous cubic phase of spatial symmetry Im3m (Q229). SdFFF demonstrated that no free drug was present in the dispersion. Indomethacin incorporated in viscosized MO dispersions exhibited a lower flux with respect to the analogous formulation containing the free drug in the aqueous phase and to the control formulation based on carbomer gel. Reflectance spectroscopy demonstrated that indomethacin incorporated into MO dispersions can be released in a prolonged fashion. Tape-stripping experiments corroborated this finding. CONCLUSIONS: MO dispersions can be proposed as nanoparticulate systems able to control the percutaneous absorption of indomethacin.

Adult↗
PubMed2004

Temperature-dependent behavior of a symmetric long-chain bolaamphiphile with phosphocholine headgroups in water: from hydrogel to nanoparticles.

The temperature-dependent self-assembly of the single-chain bolaamphiphile dotriacontan-1,1'-diyl-bis[2-(trimethylammonio)ethyl phosphate] (PC-C32-PC) was investigated by transmission electron microscopy (TEM), differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FT-IR), X-ray scattering, rheological measurements, and dynamic light scattering (DLS). At room temperature this compound, in which two phosphocholine headgroups are connected by a C(32) alkyl chain, proved to be capable of gelling water very efficiently by forming a dense network of nanofibers (Kohler et al. Angew. Chem., Int. Ed. 2004, 43, 245). A specific feature of this self-assembly process is that it is not driven by hydrogen bonds but solely by hydrophobic interactions of the long alkyl chains. The nanofibers have a thickness of roughly the molecular length and show a helical superstructure. A model for the molecular structure of the fibrils which considers the extreme constitution of the bolaamphiphile is proposed. Upon heating the suspensions three different phase transitions can be detected. Above 49 degrees C, the temperature of the main transition where the alkyl chains become "fluid", a clear low-viscosity solution is obtained due to a breakdown of the fibrils into smaller aggregates. Through mechanical stress the gel structure can be destroyed as well, indicating a low stability of these fibers. The gel formation is reversible, but as a drastic rearrangement of the molecules takes place, metastable states occur.

Antifungal Agents↗
PubMed2004

Investigations on the structure of solid lipid nanoparticles (SLN) and oil-loaded solid lipid nanoparticles by photon correlation spectroscopy, field-flow fractionation and transmission electron microscopy.

Recently, colloidal dispersions made from mixtures of solid and liquid lipids were described to combine controlled release characteristics with higher drug loading capacities than solid lipid nanoparticles (SLN). It has been proposed that these nanostructured lipid carriers (NLC) are composed of oily droplets which solubilize the drug and which are embedded in a solid lipid matrix. The structures of SLN and NLC based on glyceryl behenate and medium chain triglycerides were characterized by photon correlation spectroscopy (PCS) and laser diffraction (LD), field-flow fractionation (FFF) with multi-angle light scattering detection (MALS), and cryo transmission electron microscopy (cryo TEM). PCS indicates that SLN and NLC differ from a nanoemulsion with respect to Brownian motion due to asymmetric particle shapes. Non-spherical particles, in case of SLN and NLC, lead to higher polydispersity indices compared to the nanoemulsion. In FFF, the nanodroplets elute much earlier than SLN- and NLC-platelets although their PCS and LD data show similar particle sizes. In TEM platelet (for SLN), oil loaded platelet ("nanospoons"; for NLC) and droplet (for nanoemulsion) structures were observed. In contrast to literature reports, the investigated SLN appear as thin platelets. NLC are found to be lipid platelets with oil spots sticking on the surface. Very short diffusion pathways in platelets, increased water-lipid interfaces and low drug incorporation in crystalline lipids are the drawback of SLN and NLC compared to conventional nanoemulsions.

Chemical Phenomena↗
PubMed2003

Lipid-based supramolecular systems for topical application: a preformulatory study.

This article describes the production and characterization of monoglyceride-based supramolecular systems by a simple processing technique, avoiding time-consuming procedures, high energy input, and the use of organic solvents. A preformulatory study was performed to study the influence of the experimental parameters on the production of monoglyceride-based disperse systems. In particular the effects of (1) stirring speed, (2) type and concentration of monoglyceride mixture, and (3) type and concentration of surfactant were investigated on the recovery, fraction of larger particles, mean diameter, and shape of smaller particles (so called nanosomes). Dispersions were first characterized by optical microscopy and freeze-fracture electron microscopy. The mean diameter of standard nanosomes, analyzed by photon correlation spectroscopy (PCS) after elimination of larger particles by filtration, was 193.5 nm. Cryotransmission electron microscopy studies, conducted in order to investigate the structure of dispersions, showed the coexistence of vesicles and particles characterized by a cubic organization. X-ray diffraction data revealed the coexistence of 2 different cubic phases, the first being a bicontinuous cubic phase of spatial symmetry Im3m (Q229) and the second belonging to the Pn3m spatial symmetry. A study on the stability of monoglyceride-based dispersions based on macroscopical analysis of organoleptic properties and dimensional analysis by time was performed after elimination of larger particles by filtration. Organoleptic and morphological features do not change by time, appearing free from phase-separation phenomena for almost 1 year from production. PCS studies showed that nanosomes undergo an initial increase in mean diameter within the first month following production; afterwards they generally maintain their dimensions for the next 4 months.

Chemistry, Pharmaceutical↗