RESUMO
Chirality is one of the hallmarks of biomolecules. Herein, we utilize heparin, a chiral biomolecule and potent drug, to induce chiral organization into the assembly of an achiral molecule. Polyanionic heparin binds with a dicationic perylenediimide derivative to induce supramolecular helical organization in aqueous medium as well as in a highly competitive cell culture medium.
Assuntos
Heparina , Imidas , Perileno , Heparina/química , Imidas/química , Perileno/química , Perileno/análogos & derivados , Estereoisomerismo , Humanos , Estrutura Molecular , Substâncias Macromoleculares/química , Substâncias Macromoleculares/síntese químicaRESUMO
Supramolecular systems chemistry has been an area of active research to develop nanomaterials with life-like functions. Progress in systems chemistry relies on our ability to probe the nanostructure formation in solution. Often visualizing the dynamics of nanostructures which transform over time is a formidable challenge. This necessitates a paradigm shift from dry sample imaging towards solution-based techniques. We review the application of state-of-the-art techniques for real-time, in situ visualization of dynamic self-assembly processes. We present how solution-based techniques namely optical super-resolution microscopy, solution-state atomic force microscopy, liquid-phase transmission electron microscopy, molecular dynamics simulations and other emerging techniques are revolutionizing our understanding of active and adaptive nanomaterials with life-like functions. This Review provides the visualization toolbox and futuristic vision to tap the potential of dynamic nanomaterials.
RESUMO
Bioceramics have emerged as a hopeful remedy for site-specific drug delivery in orthopaedic complications, especially in chronic osteomyelitis. The bioresorbable nature of bioceramic materials shaped them into a versatile class of local antibiotic delivery systems in the treatment of chronic osteomyelitis. Hydroxyapatite (HA) based bioceramics with natural bone mimicking chemical composition are of particular interest due to their excellent biocompatibility, better osteoconductive and osteointegrative properties. Although HA has been widely recognized as an efficient tool for local delivery of antibiotics, information regarding its subchronic systemic toxicity have not been explored yet. Moreover, a detailed investigation of in vivo subchronic systemic toxicity of HA is critical for understanding its biocompatibility and futuristic clinical applications of these materials as novel therapeutic system in its long haul. Evaluation of biocompatibility and sub-chronic systemic toxicity are significant determinants in ensuring biomedical device's long-term functionality and success. Sub-chronic systemic toxicity allows assessing the potential adverse effects caused by leachable and nanosized wear particles from the device materials under permissible human exposure to the distant organs that are not in direct contact with the devices. In this context, the present study evaluates the sub-chronic systemic toxicity of in-house developed Hydroxyapatite porous beads (HAPB), gentamicin-loaded HAPB (HAPB + G) and vancomycin- loaded HAPB (HAPB + V) through 4 and 26-week muscle implantation in New Zealand white rabbits, as per ISO 10993-6 and ISO 10993-11. Analysis of cellular responses of HAPB towards Human Osteosarcoma (HOS) cell line through MTT assay, direct contact cytotoxicity, live/dead assay based on Imaging Flow Cytometry (IFC) showed its non-cytotoxic behaviour. Histopathological analysis of muscle tissue, organs like heart, lungs, liver, kidney, spleen, adrenals, intestine, testes, ovaries, and uterus did not reveal any abnormal biological responses. Our study concludes that the HAPB, gentamicin-loaded HAPB (HAPB + G) and vancomycin-loaded HAPB (HAPB + V) are biocompatible and did not induce sub-chronic systemic toxicity and hence satisfies the criteria for regulatory approval of HAs as a plausible candidate for clinical applications.
Assuntos
Durapatita , Osteomielite , Animais , Antibacterianos/química , Materiais Biocompatíveis/química , Durapatita/química , Durapatita/toxicidade , Feminino , Osteomielite/tratamento farmacológico , Porosidade , CoelhosRESUMO
Synthesis of supramolecular block co-polymers (BCP) with small monomers and predictive sequence requires elegant molecular design and synthetic strategies. Herein we report the unparalleled synthesis of tri-component supramolecular BCPs with tunable microstructure by a kinetically controlled sequential seeded supramolecular polymerization of fluorescent π-conjugated monomers. Core-substituted naphthalene diimide (cNDI) derivatives with different core substitutions and appended with ß-sheet forming peptide side chains provide perfect monomer design with spectral complementarity, pathway complexity and minimal structural mismatch to synthesize and characterize the multi-component BCPs. The distinct fluorescent nature of various cNDI monomers aids the spectroscopic probing of the seeded growth process and the microscopic visualization of resultant supramolecular BCPs using Structured Illumination Microscopy (SIM). Kinetically controlled sequential seeded supramolecular polymerization presented here is reminiscent of the multi-step synthesis of covalent BCPs via living chain polymerization. These findings provide a promising platform for constructing unique functional organic heterostructures for various optoelectronic and catalytic applications.
RESUMO
Herein, we report the catalytic potential of short peptide based cross-ß amyloid nanotubes with surface exposed histidine capable of binding hemin and showing facile cascade reactions, playing the dual roles of hydrolases and peroxidases, two of the most important classes of enzymes in extant biology. The activity of these simple systems exceeded those of modern and larger proteins like cytochrome C and hemoglobin. Further, evidence suggested that these self-assembled nanotubes foreshadow the process of intermediate channeling, a feature seen in the case of advanced enzymes.
Assuntos
Peptídeos beta-Amiloides/metabolismo , Hidrolases/metabolismo , Nanotubos/química , Peroxidases/metabolismo , Peptídeos beta-Amiloides/química , Citocromos c/química , Citocromos c/metabolismo , Hemina/química , Hemina/metabolismo , Hemoglobinas/química , Hemoglobinas/metabolismo , Histidina/química , Histidina/metabolismo , Hidrolases/química , Estrutura Molecular , Tamanho da Partícula , Peroxidases/química , Propriedades de SuperfícieRESUMO
The pH-responsive nature of two self-assembled NDI-peptide amphiphile conjugates is reported. The diethoxy substituted NDI showed a pH-dependent assembly behaviour, as expected. In contrast, the isopropylamino- and ethoxy-substituted NDI based supramolecular polymer was stable at acidic and basic aqueous conditions. This finding highlights how subtle changes in the molecular design of π-stacked chromophore-peptide conjugates have a drastic impact on their equilibrium structure and ultimately functional properties.
RESUMO
Key to the 22 species of genus Pheropsophus Solier 1833 of Indian subcontinent with diagnostic characters, notes, new synonyms, distribution patterns and record of two new species-Pheropsophus devagiriensis sp. nov. and P. indicus sp. nov.-from south west India are provided. Synonymisation of Pheropsophus discicollis (Dejean 1826) with Pheropsophus hilaris (Fabricius 1798) syn. nov., clearing the complications regarding the taxonomy of P. hilaris and P. sobrinus by tracking down the type series of P. hilaris, and reinstating the species status of Pheropsophus sobrinus (Dejean 1826) are the other outcomes of the present study. Out of the 22 species recorded in India, 14 species are confined to Oriental realm and rest of the eight species penetrates into the Palearctics also; 10 (of the 22) are endemic to Indian subcontinent with P. indicus sp. nov. endemic to south western India; P. devagiriensis sp. nov. endemic to the Western Ghats; P. andrewesi, P. krichna and P. prophylax are endemic to the Indo-Burma; and P. nanodes and P. scythropus are endemic to the Eastern Himalayas.