Pratima Yadav

Pratima Yadav

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Pratima Yadav

Department of Chemistry, Institute of Chemical Technology, Mumbai

Research Focus & Metrics

Academic Career Length

6Years (2021-Present)

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

Representative Publications

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2 April 2024 in Journal of Materials Chemistry C
Verified
Journal Article
Closed access
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PYPratima Yadav
Pratima Yadav
SMSunil Madagyal
Sunil Madagyal
ACAniket Chaudhari
Aniket Chaudhari
GGGokul Ganesan
Gokul Ganesan
GSGuan-Yu Su
Guan-Yu Su
ACAtul Chaskar
Atul Chaskar
Colour tunable TADF emitters with strong AIE characteristics exhibited EQEs above 20%.

1 October 2021 in Journal of Clinical and Diagnostic Research
Verified
Journal Article
Open access
PSPreetilata Singh
Preetilata Singh
PYPratima Yadav
Pratima Yadav
GTGayatri Tanwar
Gayatri Tanwar
SUShobha Ujwal
Shobha Ujwal
Introduction: Intravenous (i.v.) paracetamol is considered as an effective and safe analgesic agent in labouring women, but its effect on patients already receiving epidural analgesia is not well documented. Aim: To know whether i.v. paracetamol reduces epidural local anaesthetic opioid combination consumption in labour by virtue of its analgesic effects. Materials and Methods: The present double blind, randomised clinical study was conducted on 88 singleton term pregnant women in active labour. Half of these women (n=44, Group P) received 1000 mg (100 mL) i.v. paracetamol and rest (n=44, Group C) received 100 mL normal saline as placebo (n=44). Thirty minutes later all women received 10 mL of ropivacaine 0.125% with 2 μg/mL fentanyl through epidural catheter, followed by continuous background epidural infusion of 5 mL/h with a provision of patient controlled bolus 5 mL of same drug with a lock-out interval of 15 minutes. The primary outcome was hourly mean consumption of epidural drug in mL. Results: The hourly mean drug consumption in the paracetamol group was significantly lower as compared to control group (7.75±0.93 mL/hr vs. 8.23±0.99 mL/hr; p=0.022). The mean number of boluses needed by parturient were also significantly less in the paracetamol group (0.58±0.66 vs. 1.02±0.82; p=0.005). Pain relief after epidural placement was adequate in both groups with similar Visual Analogue Scale (VAS) values without significant intergroup differences. Conclusion: It can be concluded that 1000 mg i.v. paracetamol is a safe and effective adjunct to Patient Controlled Epidural Analgesia (PCEA).

4 January 2026 in Organic Communications
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Journal Article
Closed access
VBVikas Borge
Vikas Borge
PYPratima Yadav
Pratima Yadav
BPBhushan Popatkar
Bhushan Popatkar
SMSatish Manjare
Satish Manjare
PKPragati Kharpade
Pragati Kharpade
PDPreeti Dwivedi
Preeti Dwivedi
Quinoline is one of the most widely studied scaffold due to its high biological activities like antimalarial, antitubercular, antitumor, anti-inflammatory, antifungal, antiprotozoal, etc. this compound also has corrosion resistant, fluorescent properties, which make it industrially also important. There are various conventional methods to synthesize this scaffold, but these have several drawbacks like harsh conditions, susceptible functional group get affected. These drawbacks can be overcome by the use of green methods. These methods include Tandem/domino methods, cascade synthesis, cyclization/annulation by C-C, C-N bond formation, use of microwave, ultrasonication, ionic liquids, recyclable nano-catalyst, solid phase synthesis, solvent free synthesis, water as solvent, ball milling, use of cheap, easily available metal catalyst etc. Nowadays various naturally occurring biomass as raw material are also utilized as one of the reactant. These green methods reduce hazards to human as well as environment. This review provides an overview of recent discoveries in green synthetic methods of quinoline scaffold, and various applications of quinoline scaffold in medicine and other industrial applications.

25 April 2023 in International Journal of Research in Ayurveda and Pharmacy
Verified
Journal Article
Open access
PYPratima Yadav
Pratima Yadav
AKAjay Kumar
Ajay Kumar