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Sreevidya Thekku Veedu

Publications and source records attributed to Sreevidya Thekku Veedu.

3 recordsLinked to original sources

Molecular-Size Control of Properties of Therapeutic Nano-Paper Allows for Selective Drug Storage in Small Doses

A novel concept of nano-scaled interwoven templates for drug delivery with alternating hydro- and lipophilicity properties is introduced. They are built from cellulose and peptide hydrogel in tandem, and characterized by a nano-stacked interwoven design, thus enabling for tuning the lipophilicity in the mesh nano-domains in which drug candidates of complementary lipophilicities can be embedded. This allows for low-dose-controlled consumption and therapeutic applications. Time-resolved and in-situ grazing incidence X-ray scattering studies confirm the design of the therapeutic nano-paper and create conditions suitable for the drug storage of complementary properties. The molecular design has the potential of a locally controlled, site-specific drug release on a beyond-nanomolar scale. Generalized, the design may contribute to facile developments of personalized medicine.

physics.med-ph↗

3D atomic structure determination with ultrashort-pulse MeV electron diffraction

Understanding structure at the atomic scale is fundamental for the development of materials with improved properties. Compared to other probes providing atomic resolution, electrons offer the strongest interaction in combination with minimal radiation damage. Here, we report the successful implementation of MeV electron diffraction for ab initio 3D structure determination at atomic resolution. Using ultrashort electron pulses from the REGAE accelerator, we obtained high-quality diffraction data from muscovite and $1T-TaS_2$, enabling structure refinements according to the dynamical scattering theory and the accurate determination of hydrogen atom positions. The increased penetration depth of MeV electrons allows for structure determination from samples significantly thicker than those typically applicable in electron diffraction. These findings establish MeV electron diffraction as a viable approach for investigating a broad range of materials, including nanostructures and radiation-sensitive compounds, and open up new opportunities for in-situ and time-resolved experiments.

cond-mat.mtrl-sci↗

Ultrafast Processes in Isomeric Pyrene-N-methylacetamides: Formation of Hydrogen Bond Induced Static Excimers with Varied Coupling Strength

Pyrene based molecules are inclined to form excimers through self-association upon photoexcitation. In this work, the pyrene core is functionalized with N-methylacetamide group at the position 1 or 2, to develop pyren-1-methylacetamide (PyMA1) and pyren-2-methylacetamide (PyMA2), respectively. Upon photoexcitation, PyMA1 and PyMA2, at 1.0mM, in toluene, have formed predominantly static excimers. The steady state spectroscopic studies have showed that the excitonic coupling of PyMA1 dimers are much stronger in solution than its isomeric counterpart, PyMA2. The transient absorption (TA) measurements over fs-ps regime (fs-TA) showed that the formation of static excimers with the strongly-coupled pre-associated dimers, in PyMA1, happens in approx. 560fs, whereas, the excimers for the weakly-coupled pre-associated dimers in PyMA2 have formed in much slower time scale (approx. 65ps). The introduction of methylacetamide group at the position 1 or 2 on pyrene ring, was believed to have allowed forming hydrogen bonded excimers with different degrees of excitonic coupling.

cond-mat.mtrl-sci↗