Evidence map›Paper›PMID 31238562›Full record

ArticleMolecules (Basel, Switzerland)2019

Niosomal Nanocarriers for Enhanced Skin Delivery of Quercetin with Functions of Anti-Tyrosinase and Antioxidant.

Banyi Lu, Yanting Huang, Zhongyun Chen, Jingyi Ye, Hongyu Xu, Wenrong Chen, Xiaoying Long

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing 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

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

  1. Pooled it
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  3. Niosomal Encapsulation ofPharmaceutics · 2026
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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

7 authors.

Banyi LuSchool of Traditional Chinese Medicine, Guangdong Pharmaceutical University, Guangzhou 510006, China.
Yanting HuangSchool of Traditional Chinese Medicine, Guangdong Pharmaceutical University, Guangzhou 510006, China.
Zhongyun ChenDepartment of Pharmaceutics, School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou 510006, China.
Jingyi YeDepartment of Pharmaceutics, School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou 510006, China. small.yjy@163.com.
Hongyu XuSchool of Traditional Chinese Medicine, Guangdong Pharmaceutical University, Guangzhou 510006, China. hongyx0663@163.com.
Wenrong ChenResearch and Development Center, Sirio Pharma Co., Ltd, Shantou 515041, China. cwr@sirio.cn.
Xiaoying LongSchool of Traditional Chinese Medicine, Guangdong Pharmaceutical University, Guangzhou 510006, China. longxy3156@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to screen an effective flavonoid with promising whitening and antioxidant capacities, and design flavonoid-loaded niosomes to improve its solubility, stability, and penetration. In vitro anti-tyrosinase and 1,1-diphenyl-2-picrylhydrazyl (DPPH) free radical scavenging experiments were conducted to investigate the whitening and antioxidant capacities of several flavonoids, including quercetin, morin, festin, myricetin, rutin, and breviscapine. The conductivity, viscosity, and particle size of Span60-RH40-based formulation of nonionic surfactant vesicles (niosomes) with different mass ratios were studied to determine the most appropriate formulation. Drug-loaded niosomes were characterized for size, zeta potential, morphology, and entrapment efficiency. The photostability, solubility, release behavior, ex vivo drug penetration, and skin retention were also studied. The results showed that quercetin has considerable whitening and antioxidant capacities and Span60-RH40 at a mass ratio of 9:11 forms spherical or oval niosomes of 97.6 ± 3.1 nm with a zeta potential range of 31.1 ± 0.9 mV, and drug entrapment efficiency as high as 87.3 ± 1.6%. Niosomes remarkably improved the solubility and photostability of quercetin. Furthermore, compared to quercetin solution, quercetin-niosomes had the advantages of sustained release and improved transdermal penetration, with skin retention 2.95 times higher than quercetin solution.

Indexed as

Drug CarriersLiposomesNanoparticlesAdministration, CutaneousAnimalsAntioxidantsChemistry, PharmaceuticalDose-Response Relationship, DrugDrug Delivery SystemsDrug LiberationDrug StabilityFlavonoidsMolecular StructureMonophenol MonooxygenaseProtease InhibitorsQuercetinAntioxidantsDrug CarriersFlavonoidsLiposomesMonophenol MonooxygenaseProtease InhibitorsQuercetinantioxidantanti-tyrosinaseniosomesphotostabilitytransdermal delivery

Identifiers

PMID31238562
PMCPMC6632015

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Registered trials

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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.