Fluorescence Correlation Spectroscopy as a Quantitative Tool Applied to Drug Delivery Model Systems

The delivery of drugs to cells is a very active area of research. Drugs are commonly believed to ameliorate illnesses. The targeted, controlled and/or enhanced uptake of the drug into cells is facilitated by loading the drug into carrier vehicles (nanoparticles, e.g.. micelles).The distribution of a drug over the nanoparticles used to deliver the drug to the targeted cells is of vital importance. It makes a difference, whether all nanoparticles carry the same amount of drug or whether a little amount of the nanoparticles carries a high proportion of the drug material and most nanoparticles carry no material. This depends on the method used to load the drugs into the carriers. Furthermore, the absolute amount of drug present in the nanoparticles and the absolute number of nanoparticles loaded with drug molecules is very important, because "dosis venum facit" [Paracelsus]. We present an approach to resolve these issues by optical means.If the drug is fluorescent or labeled with a fluorescent label, fluorescence correlation spectroscopy (FCS) can be used to determine quantitative size distributions with a (confocal) microscope. In order to determine absolute concentrations the spatial dimensions of the confocal observation volume have to be known. These can be obtained from numerical simulations using vectorial diffraction theory. The theoretical results have been compared with experimental results from FCS using the calibration dye Rhodamine 6G. In a straightforward procedure the results were corrected for adsorption effects and excellent agreement to the theory was foun

Thermoresponsive Colloidal Molecules

We fabricated thermoresponsive colloidal molecules of ca. 250 nm size. Electron- and scanning force microscopy reveal the dumbbell-shaped morphology. The temperature dependence of the size and aspect ratio (ca. 1.4 to 1.6) is analyzed by depolarized dynamic light scattering and found to be in good agreement with microscopic evidence

Enzyme-triggered model self-assembly in surfactant-cyclodextrin systems

We present here a host-guest approach to construct enzyme-triggered assembly systems on the basis of surfactant-cyclodextrin complexes and alpha-amylase. We realized enzyme-responsive model self-assembly systems including monolayers, micelles, and vesicles. The host-guest approach is expected to be extended to more complicated assembly systems with widespread applications.http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000305792800003&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=8e1609b174ce4e31116a60747a720701Chemistry, MultidisciplinarySCI(E)PubMed37ARTICLE597347-73494

Nanoemulsions as vehicles for topical administration of glycyrrhetic acid: characterization and in vitro and in vivo evaluation.

Nano-emulsions are innovative colloidal systems characterized by high kinetic stability, low viscosity, and optical transparency, which make them very attractive in many dermatological applications. Furthermore their small size seems to favor the topical administration of actives which scarcely cross the skin. In the light of these interesting features, the present study was aimed to the evaluation, in vitro and in vivo, of glycyrrhetic acid (GA) release through the skin from the nanoemulsion system. GA-loaded nanoemulsion (GA(N)) was prepared by phase inversion temperature (PIT) method, and was characterized in order to determine mean droplet size and its stability during a well-defined storage period. Further Cryo-TEM studies were performed to obtain information regarding nanoemulsion structure. The GA release pattern from nanoemulsion was evaluated in vitro, to determine its percutaneous absorption through excised human skin (stratum corneum and epidermis, SCE), and in vivo evaluating GA topical anti-inflammatory activity on healthy human volunteers by the UVB-induced erythema model. Nanoemulsions prepared by PIT method showed a mean droplet diameter of 210 nm that drastically changed during a storage of 5 weeks at room temperature. In vitro and in vivo evidence showed that the nanoemulsion system significantly increased the transdermal permeability of GA in comparison to a control O/W emulsion (GA(O/W)) containing the same amount of active compound

Development of intimate contact during processing of carbon fiber reinforced Polyamide-6 tapes

Contact development between the surfaces of two tapes is considered as a critical step in processing carbon fiber reinforced thermoplastic composites. In this study, the development of intimate contact between carbon fiber reinforced Polyamide-6 (PA-6) tapes is investigated experimentally using consolidation experiments and X-ray computed tomography for quantitative contact characterization. The experimental results indicate that the development of intimate contact occurs in the range of seconds even when temperatures are only slightly above the melting temperature and applied pressures is in the range of 1-4 kPa. Experimental data are compared with the results of the two analytical models proposed by Lee and Springer as well as Yang and Pitchumani. Both models overestimate the time needed to reach full contact for the PA-6 tape. In comparison to previously investigated PEEK materials, PA-6 has a relatively low viscosity and the tapes possess a resin-rich layer near the surface, which seems to influence the contact development process. Besides the assumptions made for viscosity, the sensitivity to input parameters describing the surface topology strongly influence the model results and the accuracy of predictions. </jats:p