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11.
Z. Kalva 《Czechoslovak Journal of Physics》1972,22(12):1330-1331
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Meerja Khalim Amjad Naidu Praveen V. Kalva Sri Rama Krishna 《Mobile Networks and Applications》2019,24(3):1078-1094
Mobile Networks and Applications - Many devices share their data with the online world to derive global knowledge and information that have high business value. Trillions of smart devices are... 相似文献
13.
Pati D Kalva N Das S Kumaraswamy G Sen Gupta S Ambade AV 《Journal of the American Chemical Society》2012,134(18):7796-7802
Glycopolypeptides (GPs) were synthesized by ring-opening polymerization of glycosylated N-carboxyanhydride monomer and attached to hydrophobic dendrons at one chain end by "click" reaction to obtain amphiphilic anisotropic macromolecules. We show that by varying polypeptide chain length and dendron generation, an organogel was obtained in dimethylsulfoxide, while nanorods and micellar aggregates were observed in aqueous solutions. Assemblies in water were characterized by electron microscopy and dye encapsulation. Secondary structure of the GP chain was shown to affect the morphology, whereas the chain length of the poly(ethylene glycol) linker between the GP and dendron did not alter rod-like assemblies. Bioactive surface chemistry of these assemblies displaying carbohydrate groups was demonstrated by interaction of mannose-functionalized nanorods with ConA. 相似文献
14.
It is shown that magnetic dipolar interaction gives rise to a discontinuity in the magnon dispersion relation for antiferromagnetic spiral spin structures. Some numerical results for the magnon energy in dysprosium are presented. 相似文献
15.
Nagendra Kalva Saji Uthaman Rimesh Augustine Su Hyeon Jeon Kang Moo Huh In‐Kyu Park Il Kim 《Macromolecular bioscience》2020,20(8)
Photo/pH dual‐responsive amphiphilic diblock copolymers with alkyne functionalized pendant o‐nitrobenzyl ester group are synthesized using poly(ethylene glycol) as a macroinitiator. The pendant alkynes are functionalized as aldehyde groups by the azide‐alkyne Huisgen cycloaddition. The anticancer drug doxorubicin (DOX) molecules are then covalently conjugated through acid‐sensitive Schiff‐base linkage. The resultant prodrug copolymers self‐assemble into nanomicelles in aqueous solution. The prodrug nanomicelles have a well‐defined morphology with an average size of 20–40 nm. The dual‐stimuli are applied individually or simultaneously to study the release behavior of DOX. Under UV light irradiation, nanomicelles are disassembled due to the ONB ester photocleavage. The light‐controlled DOX release behavior is demonstrated using fluorescence spectroscopy. Due to the pH‐sensitive imine linkage the DOX molecules are released rapidly from the nanomicelles at the acidic pH of 5.0, whereas only minimal amount of DOX molecules is released at the pH of 7.4. The DOX release rate is tunable by applying the dual‐stimuli simultaneously. In vitro studies against colon cancer cells demonstrate that the nanomicelles show the efficient cellular uptake and the intracellular DOX release, indicating that the newly designed copolymers with dual‐stimuli‐response have significant potential applications as a smart nanomedicine against cancer. 相似文献