Evidence map›Paper›PMID 28194730›Full record

ArticleDrug delivery and translational research2017

Preparation and in-vitro/in-vivo characterization of trans-resveratrol nanocrystals for oral administration.

Sandeep K Singh, Vishal Makadia, Shweta Sharma, Mamunur Rashid, Sudhir Shahi, Prabhat R Mishra, Mohammed Wahajuddin, Jiaur R Gayen

Abstract read
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In one paragraph

Article in Drug delivery and translational research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  8. Focus on the Use of Resveratrol in Bladder Cancer.International journal of molecular sciences · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Sandeep K SinghPharmacokinetics and Metabolism Division, CSIR-Central Drug Research Institute, Sitapur Road, Lucknow, 226031, India.
Vishal MakadiaNational Institute of Pharmaceutical Education and Research, Raebareli, India.
Shweta SharmaPharmaceutics Division, CSIR-Central Drug Research Institute, Lucknow, 226031, India.
Mamunur RashidPharmacokinetics and Metabolism Division, CSIR-Central Drug Research Institute, Sitapur Road, Lucknow, 226031, India.
Sudhir ShahiPharmacokinetics and Metabolism Division, CSIR-Central Drug Research Institute, Sitapur Road, Lucknow, 226031, India.
Prabhat R MishraPharmaceutics Division, CSIR-Central Drug Research Institute, Lucknow, 226031, India.
Mohammed WahajuddinPharmacokinetics and Metabolism Division, CSIR-Central Drug Research Institute, Sitapur Road, Lucknow, 226031, India.
Jiaur R GayenPharmacokinetics and Metabolism Division, CSIR-Central Drug Research Institute, Sitapur Road, Lucknow, 226031, India. jr.gayen@cdri.res.in.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Trans -resveratrol (t-RES) is a natural polyphenolic compound with extensive therapeutic activities; however, its clinical application is circumscribed due to its poor solubility and low bioavailability. The purpose of this study was to prepare stable t-RES nanocrystals (t-RES-NCs) with different stabilizers to improve its oral bioavailability. t-RES-NCs were fabricated by the probe sonication method and optimized by particles size, poly dispersive index and zeta potential. The pharmaceutical characterization of t-RES-NCs was further performed systematically. The in vitro cellular efficacy and in vivo pharmacokinetics of t-RES-NCs were also evaluated. The optimized NCs were successfully accomplished in a sub-micron particle size (110.28 ± 12.55 nm) with high ζ-potential (-32.96 ± 3.85 mV) value. Scanning electron microscopy (SEM) image indicated that morphology of t-RES-NCs was regular and rod like in shape. Meanwhile, the result of in vitro cellular efficacy against MDA-MB-231 cells revealed that developed t-RES-NCs were more efficacious and potent (p < 0.05) than plain t-RES. Compared to plain t-RES, t-RES-NCs exhibited significant increase (p < 0.05) in AUC

Indexed as

Administration, OralAnimalsApoptosisCell CycleCell Line, TumorCell SurvivalDrug LiberationDrug StabilityHumansLecithinsMicroscopy, Electron, ScanningNanoparticlesParticle SizePoloxamerRats, Sprague-DawleyResveratrolLecithinsPoloxamerResveratrolStilbenestocophersolanVitamin EBioavailabilityChemotherapeuticsMDA-MB-231 cell linesNanocrystalsTrans-resveratrol

Identifiers

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.