02001nas a2200265 4500008004100000022001400041245008700055210006900142260007100211300001400282490000600296520106100302653003101363653001601394653002001410100002301430700001801453700002401471700002201495700002401517700002001541700002901561700002501590856012001615 2014 eng d a2168-048500aFunctionally engineered egg albumen gel for quasi-solid dye sensitized solar cells0 aFunctionally engineered egg albumen gel for quasisolid dye sensi a1155 16TH ST, NW, WASHINGTON, DC 20036 USAbAMER CHEMICAL SOCcDEC a2707-27140 v23 a

In this report, we demonstrated an interesting application of a bioderived material for the dye sensitized solar cells (DSSCs). Egg white, the clear liquid in a hen's egg, which possesses a remarkable gelling/cross-linking ability, was applied in the form of a gel electrolyte in a DSSC architecture to enhance its durability. A hybrid gel composed of poly(acrylic acid), polyaniline and egg albumen was synthesized, and the cell efficiency, stability and durability of the corresponding DSSC device were studied in detail. The dye sensitized solar cell with the egg albumen based electrolyte demonstrated a conversion energy efficiency of 4.6%. Further, a chemically modified egg albumen with ethylenediaminetetraacetic dianhydride showed improved cross-linking, microstructural and conductivity properties of the gel, and yielded a remarkable 5.75% conversion efficiency. Electrochemical impedance spectroscopy data showed favorable characteristics for charge transport through the modified gel and supported the efficiency observations very well.

10adye sensitized solar cells10aEgg albumen10agel electrolyte1 aKelkar, Sarika, A.1 aPandey, Komal1 aAgarkar, Shruti, A.1 aSaikhedkar, Nidhi1 aTathavadekar, Mukta1 aAgrawal, Ishita1 aGundloori, Rathna, V. N.1 aOgale, Satishchandra uhttps://library.ncl.res.in/content/functionally-engineered-egg-albumen-gel-quasi-solid-dye-sensitized-solar-cells-000791nas a2200145 4500008004100000245006400041210006400105260001300169300001200182520028400194100002900478700002100507700001800528856009900546 2019 eng d00aNanobased intravenous and transdermal drug delivery systems0 aNanobased intravenous and transdermal drug delivery systems bElsevier a551-5943 aIn this chapter we bring in the collective information about intravenous and transdermal nano drug delivery systems (DDSs), which include different kinds of constituents used for the design of nano DDSs, their various forms, methods, and characterization of nanoformulations. 1 aGundloori, Rathna, V. N.1 aSingam, Amarnath1 aKilli, Naresh uhttps://library.ncl.res.in/content/nanobased-intravenous-and-transdermal-drug-delivery-systems01724nas a2200157 4500008004100000245009600041210006900137260000800206300001600214490000600230520114000236100001801376700002501394700002901419856011801448 2019 eng d00aPolyesteramide of neem oil and its blends as an active nanomaterial for tissue regeneration0 aPolyesteramide of neem oil and its blends as an active nanomater cJUL a3341–33510 v23 a

Neem oil gained importance due to its antibacterial properties. Therefore, it is extensively being used for various applications. Oils can be polymerized as a polyesteramide to extend their utility as biomaterials. In our studies, we synthesized polyesteramide from neem oil and various compositions of blends were prepared with the drug, chlorohexidine digluconate (CH) to develop a nanomaterial for tissue regeneration. The studies such as cytotoxicity, biodegradable, antibacterial, in vitro drug release, in vivo wound healing, and histopathological studies were performed to identify their potential for tissue regeneration. In vivo wound healing studies of the nanofiber mats with and without CH recorded a faster healing rate as compared to the commercial cream (povidone–iodine). Most importantly, there was no requirement of repeated application of nanofiber mats during the treatment. The histopathology studies also suggested the re-epithelialization of the wounds. Hence, these nanomaterials are considered to be environmentally safe scaffolds for efficient tissue regeneration applications.

1 aKilli, Naresh1 aPawar, Anil, Tukaram1 aGundloori, Rathna, V. N. uhttps://library.ncl.res.in/content/polyesteramide-neem-oil-and-its-blends-active-nanomaterial-tissue-regeneration02551nas a2200181 4500008004100000245008300041210006900124260000900193300001600202490000700218520191800225100002302143700001802166700002102184700002602205700002902231856010902260 2020 eng d00aBlends of neem oil based polyesteramide as nanofiber mats to control Culicidae0 aBlends of neem oil based polyesteramide as nanofiber mats to con cNOV  a42827-428370 v103 a

Mosquitoes act as vectors for several disease-causing microorganisms and pose a threat to mankind by transmitting various diseases. There are different conventional methods to repel or kill these mosquitoes for avoiding susceptibility against infections. However, to overcome the difficulties with conventional methods, new advanced materials are being studied. For the first time, we report developing a nanofiber mat with a controlled release of insecticide to repel or detain the mosquitoes. Briefly, various blend compositions were prepared by manipulating the ratio of neem oil-based polyesteramide (PEA) and polycaprolactone (PCL) immobilized with insecticide, transfluthrin (Tf). The blend solutions were electrospun to get non-woven nanofiber mats, and these nanomaterials were characterized by various spectroscopic techniques to understand their physicochemical properties. The surface morphology was analyzed using environmental scanning electron microscopy (E-SEM), and the diameter of the nanofibers was in the range of 200 to 450 nm. Further, thermal and mechanical properties were evaluated to understand the stability of nanofiber mats. In vitro drug release studies of nanofiber mat PPT-1335 showed controlled and sustained release of Tf, with similar to 35% of Tf released in 24 h. However, a film of the same composition (PPT-1335) showed similar to 5% of Tf release within 24 h. Moreover, in vivo bio-efficacy studies suggested the mortality of mosquitoes was about 50% with PP-133, which was further increased to 100% within 12 h in the presence of Tf (PPT-1335). However, 60% mortality of mosquitoes was observed with the film of PPT-1335. Hence, the nanofiber mat showed better efficacy against mosquitoes as compared to the film of the same composition. The degradation studies under various conditions revealed biocompatibility of the developed nanofiber mats with the ecosystem.

1 aKonchada, Sravanya1 aKilli, Naresh1 aSayyad, Shahebaz1 aGathalkar, Ganesh, B.1 aGundloori, Rathna, V. N. uhttps://library.ncl.res.in/content/blends-neem-oil-based-polyesteramide-nanofiber-mats-control-culicidae02692nas a2200169 4500008004100000245007400041210006900115260000900184300001600193490000700209520210900216100002102325700001802346700002902364700002902393856010002422 2021 eng d00aPEGylated ethyl cellulose micelles as a nanocarrier for drug delivery0 aPEGylated ethyl cellulose micelles as a nanocarrier for drug del cNOV  a30532-305430 v113 aNatural polymers provide a better alternative to synthetic polymers in the domain of drug delivery systems (DDSs) because of their renewability, biocompatibility, and low immunogenicity; therefore, they are being studied for the development of bulk/nanoformulations. Likewise, current methods for engineering natural polymers into micelles are in their infancy, and in-depth studies are required using natural polymers as controlled DDSs. Accordingly, in our present study, a new micellar DDS was synthesized using ethyl cellulose (EC) grafted with polyethylene glycol (PEG); it was characterized, its properties, cell toxicity, and hemocompatibility were evaluated, and its drug release kinetics were demonstrated using doxorubicin (DOX) as a model drug. Briefly, EC was grafted with PEG to form the amphiphilic copolymers EC-PEG1 and EC-PEG2 with varying PEG concentrations, and nano-micelles were prepared with and without the drug (DOX) via a dialysis method; the critical micelle concentrations (CMCs) were recorded to be 0.03 mg mL(-1) and 0.00193 mg mL(-1) for EC-PEG1 and EC-PEG2, respectively. The physicochemical properties of the respective nano-micelles were evaluated via various characterization techniques. The morphologies of the nano-micelles were analyzed via transmission electron microscopy (TEM), and the average size of the nano-micelles was recorded to be similar to 80 nm. In vitro, drug release studies were done for 48 h, where 100% DOX release was recorded at pH 5.5 and 52% DOX release was recorded at pH 7.4 from the micelles. In addition, cytotoxicity studies suggested that DOX-loaded micelles were potent in killing MDA-MB-231 and MCF-7 cancer cells, and the blank micelles were non-toxic toward cancerous and normal cells. A cellular uptake study via fluorescence microscopy indicated the internalization of DOX-loaded micelles by cancer cells, delivering the DOX into the cellular compartments. Based on these studies, we concluded that the developed material should be studied further via in vivo studies to understand its potential as a controlled DDS to treat cancer.1 aSingam, Amarnath1 aKilli, Naresh1 aPatel, Pratikshkumar, R.1 aGundloori, Rathna, V. N. uhttps://library.ncl.res.in/content/pegylated-ethyl-cellulose-micelles-nanocarrier-drug-delivery02574nas a2200229 4500008004100000022001400041245012000055210006900175260000900244300001200253490000700265520175800272100001802030700002102048700002902069700001802098700002702116700001502143700002902158700002502187856013202212 2022 eng d a2040-336400aCombinatorial therapy using RNAi and curcumin nano-architectures regresses tumors in breast and colon cancer models0 aCombinatorial therapy using RNAi and curcumin nanoarchitectures  cJAN  a492-5050 v143 aCancer is a debilitating disease and one of the leading causes of death in the world. In spite of the current clinical management being dependent on applying robust pathological variables and well-defined therapeutic strategies, there is an imminent need for novel and targeted therapies with least side effects. RNA interference (RNAi) has gained attention due to its precise potential for targeting multiple genes involved in cancer progression. Nanoparticles with their enhanced permeability and retention (EPR) effect have been found to overcome the limitations of RNAi-based therapies. With their high transportation capacity, nanocarriers can target RNAi molecules to tumor tissues and protect them from enzymatic degradation. Accumulating evidence has shown that tyrosine kinase Ephb4 is overexpressed in various cancers. Therefore, we report here the development and pre-clinical validation of curcumin-chitosan-loaded: eudragit-coated nanocomposites conjugated with Ephb4 shRNA as a feasible bio-drug to suppress breast and colon cancers. The proposed bio-drug is non-toxic and bio-compatible with a higher uptake efficiency and through our experimental results we have demonstrated the effective site-specific delivery of this biodrug and the successfull silencing of their respective target genes in vivo in autochthonous knockout models of breast and colon cancer. While mammary tumors showed a considerable decrease in size, oral administration of the biodrug conjugate to Apc knockout colon models prolonged the animal survival period by six months. Hence, this study has provided empirical proof that the combinatorial approach involving RNA interference and nanotechnology is a promising alliance for next-generation cancer therapeutics.1 aKumar, Aviral1 aSingam, Amarnath1 aSwaminathan, Guruprasadh1 aKilli, Naresh1 aTangudu, Naveen, Kumar1 aJose, Jedy1 aGundloori, Rathna, V. N.1 aKumar, Lekha, Dinesh uhttps://library.ncl.res.in/content/combinatorial-therapy-using-rnai-and-curcumin-nano-architectures-regresses-tumors-breast-and02680nas a2200253 4500008004100000022001400041245012900055210006900184260000800253300001100261490000800272520180000280653002302080653001402103653002002117653002102137653002002158653001902178100002702197700002402224700002902248700002002277856012902297 2025 eng d a0926-669000aEthyl cellulose-based controlled-release atrazine nanoformulation for effective and long-term weed management in agriculture0 aEthyl cellulosebased controlledrelease atrazine nanoformulation  cJUL a1209920 v2293 a

Atrazine (ATZ) is the second most widely used herbicide. However, its widespread use is hazardous to the environment. We developed ethyl cellulose-based nanoformulated atrazine (nfATZ) to achieve slow and sustained release of ATZ for long-term weed control in crops such as maize. Maize or corn is used in several industrial applications, including the production of ethanol, corn syrup, adhesives, textiles, biodegradable plastics, etc. As broadleaf weeds significantly impact maize yields, we evaluated the effects of nfATZ and conventional ATZ on tomato as a representative of broadleaf weeds. Various concentrations of ATZ and nfATZ (1-10 mg per kg of soil) were evaluated in pre-emergence, post-emergence, and re-emergence studies. Several morphological, physiological, and biochemical parameters of weeds were assessed, and the efficacy of the herbicide formulations was evaluated. nfATZ outperformed conventional ATZ even at lower concentrations with prolonged herbicidal effectiveness beyond 30 days, while the main crop remained unaffected. The weed mortality in nfATZ treatment was > 80 %, while it was 35 % - 45 % in ATZ treatment. The chlorophyll and carotenoid contents decreased by similar to 65 % in nfATZ-treated weeds, impacting their photosynthesis and overall health. ATZ and nfATZ also significantly impacted the activities of antioxidant enzymes, such as ascorbate peroxidase (similar to 57 %), superoxide dismutase (similar to 67 %), and peroxidase (similar to 77 %) in weeds. Thus, we conclude that nfATZ performed significantly better than ATZ in controlling weeds over the long term and reducing its environmental impact. Therefore, we propose nfATZ for highly effective and long-term weed control in large-scale production of industrial crops like maize.

10aControlled-release10aHerbicide10aNanoformulation10aOxidative stress10aWeed management10aWeed mortality1 aGautam, Tripurari, Rao1 aVasmatkar, Pashupat1 aGundloori, Rathna, V. N.1 aKadoo, Narendra uhttps://library.ncl.res.in/content/ethyl-cellulose-based-controlled-release-atrazine-nanoformulation-effective-and-long-term02793nas a2200301 4500008004100000022001400041245009500055210006900150260000900219300001100228490000800239520180900247653001302056653002202069653003102091653002402122653001402146653001802160100002702178700002902205700002502234700002302259700001802282700002902300700001602329700002302345856012302368 2025 eng d a0378-517300aStimulant immobilized bioactive film of functionalized egg albumin blend for wound healing0 aStimulant immobilized bioactive film of functionalized egg album cSEP  a1258960 v6823 a

Wound healing materials with advanced properties that facilitates higher collagen deposition, improved angiogenesis and quick tissue regeneration are crucial for clinical wound management. To meet the requirement, for the first time, our studies focus on engineering bio-originated natural materials, which are tested in combination with the active agents, ascorbic acid (AA), a stimulant and metronidazole (Mtz), an anti-microbial drug. Accordingly, a dual drug (AA, and Mtz) loaded film of functionalized egg albumin (FEA)-poly(vinyl alcohol) (PVA) was fabricated following the solution casting method. The film was characterized for its morphology and physicochemical properties using various analytical tools. The potential of the film as a wound healing material was evaluated, by in vitro drug release, degradation, cell viability, antimicrobial studies, in vivo wound healing, and histopathological analyses. In vitro degradation studies confirmed their degradability in enzymatic and soil burial conditions. Cytotoxicity studies demonstrated their non-toxicity, and the antimicrobial investigations showcased that the material was antibacterial. On the 14th day, the wound closure percentage of the wound induced control group, GI (without treatment) was notably higher at 95 % compared to the test formulation group, GV [FEA-PVA (30/70 w/w) loaded with Mtz and AA (10 % w/w of the total polymer weight), respectively], which exhibited a wound closure of 83 %. Furthermore, the histopathological examinations revealed that the inner wound healing in GV was comparatively better than in GI in terms of angiogenesis, epidermal remodeling, higher collagen deposition, coherency, and tissue regeneration. Consequently, the formulated film can be deemed a suitable wound dressing material.

10acollagen10aDual drug release10aFunctionalized egg albumin10aPolymer blend films10aStimulant10awound Healing1 aGautam, Tripurari, Rao1 aPatel, Pratikshkumar, R.1 aSingam, Amarnath, R.1 aJagtap, Ashish, S.1 aDesai, Prasad1 aGundloori, Rathna, V. N.1 aPawar, Anil1 aDastager, Syed, G. uhttps://library.ncl.res.in/content/stimulant-immobilized-bioactive-film-functionalized-egg-albumin-blend-wound-healing