Bipin D Lade

Dr. Bipin D Lade

The National Center for Earth and Environmental Nanotechnology Infrastructure, Virginia Tech, Blacksburg, Virginia, USA
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Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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26 November 2020
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Book Chapter
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Bipin D LadeBipin D Lade
Bipin D Lade
ASArti S. Shanware
Arti S. Shanware
The greener way of producing silver nanoparticles is the easiest, cheapest and most efficient way of producing large-scale nanoparticles that have no adverse effect on the environment. The nanosynthesis using various methodologies and the biological synthesis of silver nanoparticles have been discussed in detail. Plant extracts have been known to be competent for the extracellular biosynthesis of silver nanoparticles suggested by the various publications. Further, effects of various sources and methods on nanoparticle synthesis have been examined. Additionally, the impact of conditions such as dark, light, heating, boiling, sonication, autoclave on the size and shape of colloidal nanoparticles has been analyzed. Moreover, effects of specific parameters such as leaf extract concentration, AgNO3, reaction temperature, pH, light and stirring time for nanoparticle synthesis are discussed, and the impact of silver nanoparticles on plant physiology has examined.

1 January 2019
Verified
Book Chapter
Closed access
Bipin D LadeBipin D Lade
Bipin D Lade
DGDayanand P. Gogle
Dayanand P. Gogle
DLDiksha B. Lade
Diksha B. Lade
GMGautam M. Moon
Gautam M. Moon
SNSukhdev B. Nandeshwar
Sukhdev B. Nandeshwar
SKShravan D. Kumbhare
Shravan D. Kumbhare

26 October 2017
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Journal Article
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Bipin D LadeBipin D Lade
Bipin D Lade
DGDayanand P Gogle
Dayanand P Gogle
SNSukhdev B Nandeshwar
Sukhdev B Nandeshwar

1 April 2017 in Applied Nanoscience
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Journal Article
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Bipin D LadeBipin D Lade
Bipin D Lade
APAnita S. Patil
Anita S. Patil
The main purpose of the experiment is to develop a greener low cost SNP fabrication steps using factories of secondary metabolites from Passiflora leaf extract. Here, the leaf extraction process is omitted, and instead a leaf disc was used for stable SNP fabricated by optimizing parameters such as a circular leaf disc of 2 cm (1, 2, 3, 4, 5) instead of leaf extract and grade of pH (7, 8, 9, 11). The SNP synthesis reaction is tried under room temperature, sun, UV and dark condition. The leaf disc preparation steps are also discussed in details. The SNP obtained using (1 mM: 100 ml AgNO3+ singular leaf disc: pH 9, 11) is applied against featured room temperature and sun condition. The UV spectroscopic analysis confirms that sun rays synthesized SNP yields stable nano particles. The FTIR analysis confirms a large number of functional groups such as alkanes, alkyne, amines, aliphatic amine, carboxylic acid; nitro-compound, alcohol, saturated aldehyde and phenols involved in reduction of silver salt to zero valent ions. The leaf disc mediated synthesis of silver nanoparticles, minimizes leaf extract preparation step and eligible for stable SNP synthesis. The methods sun and room temperature based nano particles synthesized within 10 min would be use certainly for antimicrobial activity.

23 August 2014 in SpringerPlus
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Bipin D LadeBipin D Lade
Bipin D Lade
APAnita Surendra Patil
Anita Surendra Patil
HPHariprassad Madhukarrao Paikrao
Hariprassad Madhukarrao Paikrao
In Present work, the main objective is to develop less time consuming protocol for genomic DNA isolation from leaves of Passiflora foetida. Optimized protocol is cost effective, as it avoided use of expensive liquid nitrogen. The important parameters of CTAB buffer composition such as Polyvinylpyrrolidone PVP40000 (without PVP, 1%, 2%, 3.5%, 4.0%, 4.5%, 5.0%), CTAB (w, 1%, 2%, 3%, 4%, 5%), water bath temperature (30°C to 70°C) and duration on water bath for half hr and one and half hr has been optimized. CTAB (2%), PVP (1%), water bath temperature (70%), duration on water bath (1 hr) has efficiently yielded DNA quality of 200-1782 μg/0.5gm from leaf, stem, root, tendril and flower. However, 168 μg - 1782 μg of DNA has been obtained from 0.5 g of leaf of Passiflora foetida. Polyphenol contamination has been overcome using 5M NaCl and PVP. Acetate has been used for obtaining double-stranded DNA in stabilized form. Current DNA extraction protocol takes maximum of four hours for completion, which is many time savings. RAPD-PCR reaction parameters such as DNA concentration (100ng), Primer concentration (2 μM), Dream Taq polymerase (2 U), annealing temperature (29°C) and number of cycles for amplification of DNA has been optimized. Primer fragment Akansha 7 shows high polymorphism of 7 fragments ranges from 200bp – 2500 bp. Current optimized protocol of DNA isolation is specifically for Passiflora foetida, which can be used for downstream molecular techniques.

5 October 2019
Verified
Book Chapter
Closed access
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Bipin D LadeBipin D Lade
Bipin D Lade
DGDayanand P. Gogle
Dayanand P. Gogle