NANO-GOLD AND NANO-ZINC OXIDE: EFFECT ON GUSTATORY RECEPTOR GENES IN FLIES

2011 ◽  
Vol 10 (01n02) ◽  
pp. 217-221
Author(s):  
SUMISTHA DAS ◽  
NITAI DEBNATH ◽  
R. L. BRAHMACHARY ◽  
RAMESH CHANDRA ◽  
BISWAJIT ROY ◽  
...  
Keyword(s):  
Drug Delivery ◽  
Particle Size ◽  
Colloidal Gold ◽  
Average Particle Size ◽  
Oral Drug ◽  
Average Particle ◽  
Nano Zno ◽  
Nano Gold ◽  
Custom Made ◽  
Sugar Receptors

Drinking colloidal gold as elixir of life is an age-old practice worldwide. A large body of data containing patients' experiences after intake of colloidal gold for long duration would be available in the medical records of hospitals. ZnO has been approved by FDA for topical use and not for oral intake. Drosophila melanogaster (wild type) strains were fed with physiologically relevant concentrations of nano-gold and nano- ZnO along with appropriate controls. Citrate-capped nano-gold (average particle size is 15–20 nm) synthesized by reducing hydrogen tetrachloroaurate with 1% trisodium citrate and custom-made nano- ZnO , purchased from M K Implex, Canada (average particle size 50 nm) were used as treatments. Microarray studies revealed that fly trehalose receptor genes, Tre and Tre1, are both unaffected after nano-gold and nano- ZnO treatment. Gr64 subfamily members (encoding sugar receptors like glucose, sucrose, and maltose), for example, Gr64a-b become downregulated, but Gr64c, Gr64d, Gr64f remain unaltered in case of both the treatments. Among bitter receptor genes, Gr66a is the most well studied and shows significant downregulation by nano-gold and not by nano- ZnO . Ppk11 and Ppk19 are gustatory ion channel genes which modulate salt perception. Ppk11 was found to be downregulated by both nano-gold and nano- ZnO , while ppk19 expression is suppressed by nano-gold treatment but not by nano- ZnO . The effects of these two nanoparticles on pheromone receptors (Gr32a, Gr39a, and Gr68a) and CO 2 receptors (Gr21a and Gr63a) are presented. To the best of our knowledge, this is the first report on the effect of pure nanoparticles on gustation. Data has been analyzed in the light of the age-old tradition of oral administration of the nano-gold viz-a-viz topical use of nano- ZnO . These results would have far reaching implications in the design of nano-gold mediated oral drug delivery of cancer and other drugs as well as nano- ZnO coated drugs/cosmetics and nano- ZnO carrier based drug delivery in skins and in other topical applications.

Formulating SLN and NLC as Innovative Drug Delivery Systems for Non-Invasive Routes of Drug Administration

2020 ◽  
Vol 27 (22) ◽  
pp. 3623-3656 ◽  
Author(s):  
Bruno Fonseca-Santos ◽  
Patrícia Bento Silva ◽  
Roberta Balansin Rigon ◽  
Mariana Rillo Sato ◽  
Marlus Chorilli
Keyword(s):  
Drug Delivery ◽  
Particle Size ◽  
Drug Release ◽  
Drug Loading ◽  
Average Particle Size ◽  
Delivery Systems ◽  
Average Particle ◽  
Minor Importance ◽  
Routes Of Administration ◽  
Non Invasive

Colloidal carriers diverge depending on their composition, ability to incorporate drugs and applicability, but the common feature is the small average particle size. Among the carriers with the potential nanostructured drug delivery application there are SLN and NLC. These nanostructured systems consist of complex lipids and highly purified mixtures of glycerides having varying particle size. Also, these systems have shown physical stability, protection capacity of unstable drugs, release control ability, excellent tolerability, possibility of vectorization, and no reported production problems related to large-scale. Several production procedures can be applied to achieve high association efficiency between the bioactive and the carrier, depending on the physicochemical properties of both, as well as on the production procedure applied. The whole set of unique advantages such as enhanced drug loading capacity, prevention of drug expulsion, leads to more flexibility for modulation of drug release and makes Lipid-based nanocarriers (LNCs) versatile delivery system for various routes of administration. The route of administration has a significant impact on the therapeutic outcome of a drug. Thus, the non-invasive routes, which were of minor importance as parts of drug delivery in the past, have assumed added importance drugs, proteins, peptides and biopharmaceuticals drug delivery and these include nasal, buccal, vaginal and transdermal routes. The objective of this paper is to present the state of the art concerning the application of the lipid nanocarriers designated for non-invasive routes of administration. In this manner, this review presents an innovative technological platform to develop nanostructured delivery systems with great versatility of application in non-invasive routes of administration and targeting drug release.

Formulation of Vanillin Cross-Linked Chitosan Nanoparticles and its Characterization

2011 ◽  
Vol 335-336 ◽  
pp. 474-477 ◽  
Author(s):  
Guang Wang ◽  
Pu Wang Li ◽  
Zheng Peng ◽  
Mao Fang Huang ◽  
Ling Xue Kong
Keyword(s):  
Drug Delivery ◽  
Particle Size ◽  
Smooth Surface ◽  
Average Particle Size ◽  
Chitosan Nanoparticles ◽  
Aldehyde Group ◽  
Cross Linking ◽  
Average Particle ◽  
Amino Group ◽  
Chemical Cross Linking

Chitosan nanoparticles were successfully prepared by chemical cross-linking with vanillin. The nanoparticles were spherical in shape with smooth surface, and the average particle size of chitosan nanoparticles was 141 nm. The formulation of chitosan nanoparticles is based on Shiff reaction between aldehyde group of vanillin and amino group of chitosan. Chitosan nanoparticles prepared by crosslinking with vanillin are promising vehicle for the drug delivery of various anticancer drugs in the chemotherapy of cancers.

scholarly journals Triple conjugated carbon dots as a nano-drug delivery model for glioblastoma brain tumors

Nanoscale ◽  
2019 ◽  
Vol 11 (13) ◽  
pp. 6192-6205 ◽  
Author(s):  
Sajini D. Hettiarachchi ◽  
Regina M. Graham ◽  
Keenan J. Mintz ◽  
Yiqun Zhou ◽  
Steven Vanni ◽  
...  
Keyword(s):  
Drug Delivery ◽  
Particle Size ◽  
Brain Tumors ◽  
Carbon Dots ◽  
Drug Delivery Systems ◽  
Average Particle Size ◽  
Average Particle ◽  
Delivery Model ◽  
Drug Conjugation ◽  
Nano Drug Delivery

Most of the dual nano drug delivery systems fail to enter malignant brain tumors due to a lack of proper targeting systems and the size increase of the nanoparticles after drug conjugation. Therefore, a triple conjugated system was developed with carbon dots (C-dots) which has an average particle size of 1.5–1.7 nm.

The Performance of Precipitated Calcium Carbonate Fillers in Fine Quality Printing and Writing Papers

1990 ◽  
Vol 197 ◽  
Author(s):  
Robert A. Gill
Keyword(s):  
Particle Size ◽  
Calcium Carbonate ◽  
Surface Area ◽  
Average Particle Size ◽  
Filler Materials ◽  
Average Particle ◽  
Strong Correlations ◽  
Precipitated Calcium Carbonate ◽  
Paper Properties ◽  
Custom Made

ABSTRACTThe trend toward alkaline papermaking has accelerated over the past four years due to the availability of inexpensive, high quality precipitated calcium carbonate. This movement has been largely brought about through on-site production of precipitated calcium carbonate (PCC). Over ten facilities exist in North America providing the host mills with custom-made PCC products to provide specific properties for the paper grades being manufactured.Laboratory studies were recently conducted to investigate the performance of paper-grade PCC fillers in fine quality printing papers. This investigation focused on the effect of changes in PCC particle size, size distribution, surface area, and morphology on paper properties. The PCC fillers were also compared to other filler materials such as ground limestone and kaolin.In general, the results show that sheet properties are greatly influenced by the size and shape of the PCC product used. The data reveal strong correlations between average particle size and/or surface area, and sheet properties such as opacity, porosity, tensile strength, bulk, and sizing within certain filler morphologies.

Indinavir-Loaded Nanostructured Lipid Carriers to Brain Drug Delivery: Optimization, Characterization and Neuropharmacokinetic Evaluation

2019 ◽  
Vol 16 (4) ◽  
pp. 341-354 ◽  
Author(s):  
Mohammad Nasiri ◽  
Amir Azadi ◽  
Mohammad Reza Saghatchi Zanjani ◽  
Mehrdad Hamidi
Keyword(s):  
Drug Delivery ◽  
Particle Size ◽  
Zeta Potential ◽  
Average Particle Size ◽  
In Vitro Release ◽  
Free Drug ◽  
Average Particle ◽  
The Brain

Purpose: As an anti-retroviral Protease Inhibitor (PI), Indinavir (IDV) is part of the regimen known as Highly Active Anti-Retroviral Therapy (HAART) widely used for Human Immunodeficiency Virus (HIV) infection. The drug efficiency in treatment of the brain manifestations of HIV is, however, limited which is mainly due to the efflux by P-glycoprotein (P-gp) expressed at the Blood-Brain Barrier (BBB). Methods: To overcome the BBB obstacle, NLCs were used in this study as carriers for IDV, which were optimized through two steps: a “one-factor-at-a-time” screening followed by a systematic multiobjective optimization. Spherical smooth-surfaced Nanoparticles (NPs), average particle size of 161.02±4.8 nm, Poly-Dispersity Index (PDI) of 0.293±0.07, zeta potential of -40.62±2.21 mV, entrapment efficiency of 93±1.58%, and loading capacity of 9.15±0.15% were obtained after optimization which were, collectively, appropriate in terms of the objective of this study. Result: The surface of the optimized NPs was, then, modified with human Transferrin (TR) to improve the drug delivery. The particle size, zeta potential, and PDI of the TR-modified NLCs were 185.29±6.7nm, -28.68±3.37 mV, and 0.247±0.06, respectively. The in vitro release of IDV molecules from the NPs was best fitted to the Weibull model indicating hybrid diffusion/erosion behavior. Conclusion: As the major in vivo findings, compared to the free drug, the NLCs and TR-NLCs displayed significantly higher and augmented concentrations in the brain. In this case, NLC and TR-NLC were 6.5- and 32.75-fold in their values of the brain uptake clearance compared to free drug.

scholarly journals Preclinical study of Doxorubicine-loaded liposomal drug delivery for the treatment of head and neck cancer: Optimization by Box-Behnken statistical design

2020 ◽  
Author(s):  
Baihui Yang
Keyword(s):  
Drug Delivery ◽  
Particle Size ◽  
Head And Neck Cancer ◽  
Head And Neck ◽  
Neck Cancer ◽  
Average Particle Size ◽  
Statistical Design ◽  
Liposomal Formulation ◽  
Average Particle

The present investigation aimed at developing Doxorubicin (DOX)-loaded liposome-mediated drug delivery system for head and neck cancer. The liposomes were prepared by film hydration technique using egg phosphatidylcholine and cholesterol using Box-Behnken statistical design. The prepared liposomes were evaluated for the percentage encapsulation efficiency, particle size and in vitro release. The average particle size of the DOX-encapsulating liposomes formulated by thin-film hydration technique was between 150.5 nm and 200 nm with an average particle size of 165.80 nm. The PDI (Polydispersity index) was found to be 0.315 which indicated that particles were monodispersed and narrow-dispersed. In vitro drug release of DOX-loaded liposomes and DOX-loaded peptide-conjugated liposomes was performed in phosphate buffered saline (pH 7.4) and both formulations showed sustained release behavior over the period of 40 hours. The optimized liposomal formulation was conjugated to a peptide and subsequently radiolabeled with 186Re-perrhenate solution and BMEDA-glucoheptonate-stannous chloride solution. Comparative cytotoxicity assay of DOX, DOX-liposomes and DOX-liposomes-peptide on SCC9 cells was performed and it was found that liposomal formulation was not cytotoxic. The antitumor efficacy of 186Re-liposomes, unlabelled liposomes, 186Re-perrhenate solution and 186Re-BMEDA solution was determined in SCC cell lines injected into BALB/c-nu/nu athymic nude rats. The efficacy of antitumor activity was found to be in the following order: peptide-conjugated DOX-loaded liposomes>unlabelled liposomes>186Re-perrhenate solution>186Re-BMEDA solution. The present investigation showed that peptide-conjugated DOX-loaded liposomes significantly suppress the tumor growth in the nude rat model. These results suggest the significant potential of liposomes as carriers for clinical applications in head and neck cancer.

scholarly journals Smart Magnetically Responsive Hydrogel Nanoparticles Prepared by a Novel Aerosol-Assisted Method for Biomedical and Drug Delivery Applications

2011 ◽  
Vol 2011 ◽  
pp. 1-13 ◽  
Author(s):  
Ibrahim M. El-Sherbiny ◽  
Hugh D. C. Smyth
Keyword(s):  
Drug Delivery ◽  
Particle Size ◽  
Low Cost ◽  
Average Particle Size ◽  
Average Particle ◽  
Partial Acid Hydrolysis ◽  
Hydrogel Nanoparticles ◽  
Air Jet ◽  
Magnetic Hydrogel ◽  
Drug Delivery Applications

We have developed a novel spray gelation-based method to synthesize a new series of magnetically responsive hydrogel nanoparticles for biomedical and drug delivery applications. The method is based on the production of hydrogel nanoparticles from sprayed polymeric microdroplets obtained by an air-jet nebulization process that is immediately followed by gelation in a crosslinking fluid. Oligoguluronate (G-blocks) was prepared through the partial acid hydrolysis of sodium alginate. PEG-grafted chitosan was also synthesized and characterized (FTIR, EA, and DSC). Then, magnetically responsive hydrogel nanoparticles based on alginate and alginate/G-blocks were synthesized via aerosolization followed by either ionotropic gelation or both ionotropic and polyelectrolyte complexation using CaCl2or PEG-g-chitosan/CaCl2as crosslinking agents, respectively. Particle size and dynamic swelling were determined using dynamic light scattering (DLS) and microscopy. Surface morphology of the nanoparticles was examined using SEM. The distribution of magnetic cores within the hydrogels nanoparticles was also examined using TEM. In addition, the iron and calcium contents of the particles were estimated using EDS. Spherical magnetic hydrogel nanoparticles with average particle size of 811 ± 162 to 941 ± 2 nm were obtained. This study showed that the developed method is promising for the manufacture of hydrogel nanoparticles, and it represents a relatively simple and potential low-cost system.

Determination of grinding parameters of fenugreek seed

1970 ◽  
Vol 26 (1) ◽  
pp. 16 ◽  
Author(s):  
S Balasubramanian ◽  
Rajkumar Rajkumar ◽  
K K Singh
Keyword(s):  
Particle Size ◽  
Energy Consumption ◽  
Moisture Content ◽  
Specific Energy ◽  
Feed Rate ◽  
Average Particle Size ◽  
Specific Energy Consumption ◽  
Average Particle ◽  
Fenugreek Seeds ◽  
Fenugreek Seed

Experiment to identify ambient grinding conditions and energy consumed was conducted for fenugreek. Fenugreek seeds at three moisture content (5.1%, 11.5% and 17.3%, d.b.) were ground using a micro pulverizer hammer mill with different grinding screen openings (0.5, 1.0 and 1.5 mm) and feed rate (8, 16 and 24 kg h-1) at 3000 rpm. Physical properties of fenugreek seeds were also determined. Specific energy consumptions were found to decrease from 204.67 to 23.09 kJ kg-1 for increasing levels of feed rate and grinder screen openings. On the other hand specific energy consumption increased with increasing moisture content. The highest specific energy consumption was recorded for 17.3% moisture content and 8 kg h-1 feed rate with 0.5 mm screen opening. Average particle size decreased from 1.06 to 0.39 mm with increase of moisture content and grinder screen opening. It has been observed that the average particle size was minimum at 0.5 mm screen opening and 8 kg h-1 feed rate at lower moisture content. Bond’s work index and Kick’s constant were found to increase from 8.97 to 950.92 kWh kg-1 and 0.932 to 78.851 kWh kg-1 with the increase of moisture content, feed rate and grinder screen opening, respectively. Size reduction ratio and grinding effectiveness of fenugreek seed were found to decrease from 4.11 to 1.61 and 0.0118 to 0.0018 with the increase of moisture content, feed rate and grinder screen opening, respectively. The loose and compact bulk densities varied from 219.2 to 719.4 kg m-3 and 137.3 to 736.2 kg m-3, respectively.  

Azithromycin nanosuspension preparation using evaporative precipitation into aqueous solution (EPAS) method and its comparative dissolution study

2020 ◽  
Vol 17 ◽  
Author(s):  
Mohammad Hossain Shariare ◽  
Tonmoy Kumar Mondal ◽  
Hani Alothaid ◽  
Md. Didaruzzaman Sohel ◽  
MD Wadud ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Particle Size ◽  
Dissolution Rate ◽  
Average Particle Size ◽  
Scale Up ◽  
Average Particle ◽  
Total Drug ◽  
Residual Solvent ◽  
Dissolution Study ◽  
Drug Content

Aim: EPAS (evaporative precipitation into aqueous solution) was used in the current studies to prepare azithromycin nanosuspensions and investigate the physicochemical characteristics for the nanosuspension batches with the aim of enhancing the dissolution rate of the nanopreparation to improve bioavailability. Methods: EPAS method used in this study for preparing azithromycin nanosuspension was achieved through developing an in-house instrumentation method. Particle size distribution was measured using Zetasizer Nano S without sample dilution. Dissolved azithromycin nanosuspensions were also compared with raw azithromycin powder and commercially available products. Total drug content of nanosuspension batches were measured using an Ultra-Performance Liquid Chromatography (UPLC) system with Photodiode Array (PDA) detector while residual solvent was measured using gas chromatography (GC). Results: The average particle size of azithromycin nanosuspension was 447.2 nm and total drug content was measured to be 97.81% upon recovery. Dissolution study data showed significant increase in dissolution rate for nanosuspension batch when compared to raw azithromycin and commercial version (microsuspension). The residual solvent found for azithromycin nanosuspension is 0.000098023 mg/ mL or 98.023 ppb. Conclusion: EPAS was successfully used to prepare azithromycin nanoparticles that exhibited significantly enhanced dissolution rate. Further studies are required to scale up the process and determine long term stability of the nanoparticles.

scholarly journals Evaluation of the Effects of Filler Fineness on the Properties of an Epoxy Asphalt Mixture

Materials ◽  
2021 ◽  
Vol 14 (8) ◽  
pp. 2003
Author(s):  
Wei Xu ◽  
Jintao Wei ◽  
Zhengxiong Chen ◽  
Feng Wang ◽  
Jian Zhao
Keyword(s):  
Particle Size ◽  
Average Particle Size ◽  
Asphalt Mixture ◽  
Average Particle ◽  
Fine Dust ◽  
Bonding Structure ◽  
Epoxy Asphalt ◽  
Mineral Powder ◽  
Marshall Stability ◽  
Mixture Sample

The type and fineness of a filler significantly affect the performance of an asphalt mixture. There is a lack of specific research on the effects of filler fineness and dust from aggregates on the properties of epoxy asphalt (EA) mixtures. The effects of aggregate dust and mineral powder on the properties of an EA mixture were evaluated. These filler were tested to determine their fineness, specific surface area and mineral composition. The effects of these fillers on the EA mastic sample and mixture were evaluated. The morphology of the EA mastic samples was analyzed using scanning electron microscopy (SEM). The effects of the fillers on the Marshall stability, tensile strength and fatigue performance of the EA mixture were evaluated. The dust from the aggregates exhibited an even particle size distribution, and its average particle size was approximately 20% of that of the mineral powder. The SEM microanalysis showed that the EA mastic sample containing relatively fine dust formed a tight and dense interfacial bonding structure with the aggregate. The EA mixture sample containing filler composed of dust from aggregate had a significantly higher strength and longer fatigue life than that of the EA sample containing filler composed of mineral powder.

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