Evidence map›Paper›PMID 34577193›Full record

ArticleMolecules (Basel, Switzerland)2021

Co-Crystals of Resveratrol and Polydatin with L-Proline: Crystal Structures, Dissolution Properties, and In Vitro Cytotoxicities.

Yijie Lou, Kaxi Yu, Xiajun Wu, Zhaojun Wang, Yusheng Cui, Hanxiao Bao, Jianwei Wang, Xiurong Hu, Yunxi Ji, Guping Tang

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.9field-weighted citation impact, top 14% of its field
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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Advances for pharmacological activities ofPharmaceutical biology · 2023
    Review
  7. Article
  8. Article
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

10 authors at 2 institutions in 1 country.

Yijie LouFirst Clinical Medical College, Zhejiang Chinese Medical University, Hangzhou 310053, China.
Kaxi YuDepartment of Chemistry, Zhejiang University, Hangzhou 310028, China.
Xiajun WuFirst Clinical Medical College, Zhejiang Chinese Medical University, Hangzhou 310053, China.
Zhaojun WangFirst Clinical Medical College, Zhejiang Chinese Medical University, Hangzhou 310053, China.
Yusheng CuiFirst Clinical Medical College, Zhejiang Chinese Medical University, Hangzhou 310053, China.
Hanxiao BaoDepartment of Chemistry, Zhejiang University, Hangzhou 310028, China.
Jianwei WangDepartment of Chemistry, Zhejiang University, Hangzhou 310028, China.
Xiurong HuDepartment of Chemistry, Zhejiang University, Hangzhou 310028, China.
Yunxi JiFirst Clinical Medical College, Zhejiang Chinese Medical University, Hangzhou 310053, China.
Guping TangDepartment of Chemistry, Zhejiang University, Hangzhou 310028, China.
Zhejiang Chinese Medical University · CNZhejiang University · CN

Funding

National Natural Science Foundation of China 81873268
6 · The paper itself

Abstract

Resveratrol (RSV) and polydatin (PD) have been widely used to treat several chronic diseases, such as atherosclerosis, pulmonary fibrosis, and diabetes, among several others. However, their low solubility hinders their further applications. In this work, we show that the solubility of PD can be boosted via its co-crystallization with L-proline (L-Pro). Two different phases of co-crystals, namely the RSV-L-Pro (RSV:L-Pro = 1:2) and PD-L-Pro (PD:L-Pro = 1: 3), have been prepared and characterized. As compared to the pristine RSV and PD, the solubility and dissolution rates of PD-L-Pro in water (pH 7.0) exhibited a 15.8% increase, whereas those of RSV-L-Pro exhibited a 13.8% decrease. A 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay of pristine RSV, PD, RSV-L-Pro, and PD-L-Pro against lung cancer cell line A549 and human embryonic kidney cell line HEK-293 indicated that both compounds showed obvious cytotoxicity against A549, but significantly reduced cytotoxicity against HEK-293, with PD/PD-L-Pro further exhibiting better biological safety than that of RSV/RSV-L-Pro. This work demonstrated that the readily available and biocompatible L-Pro can be a promising adjuvant to optimize the physical and chemical properties of RSV and PD to improve their pharmacokinetics.

Indexed as

A549 CellsCell SurvivalCrystallizationDrug CompoundingGlucosidesHEK293 CellsHumansIn Vitro TechniquesMolecular ConformationProlineResveratrolSolubilityStilbenesGlucosidespolydatinProlineResveratrolStilbenescrystal structureL-prolinepharmaceutical co-crystalpolydatinresveratrolsolubility and dissolution rate

Identifiers

PMID34577193
PMCPMC8469398
OpenAlexW3199596180

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.