Evidence map›Paper›PMID 30957571›Full record

ArticleDrug delivery2019

Novel ultra-small micelles based on ginsenoside Rb1: a potential nanoplatform for ocular drug delivery.

Mengshuang Li, Jie Lan, Xuefei Li, Meng Xin, Hui Wang, Fan Zhang, Xiaohong Lu, Zengfang Zhuang, Xianggen Wu

Abstract read
In one paragraph

Article in Drug delivery, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–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

20 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Natural Products from Herbal Medicine Self-Assemble into Advanced Bioactive Materials.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Review
  11. Smart nanoparticles for cancer therapy.Signal transduction and targeted therapy · 2023
    Review
  12. Article
  13. Article
  14. Article
  15. Ubisol-QAntioxidants (Basel, Switzerland) · 2021
    Review
  16. Review
  17. The Effects of Ginsenosides on the Nrf2 Signaling Pathway.Advances in experimental medicine and biology · 2021
    Article
  18. Review
  19. Article
  20. Review
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

9 authors.

Mengshuang Lia Department of Pharmacy, College of Chemical Engineering , Qingdao University of Science and Technology , Qingdao , China.
Jie Lanc Qingdao Eye Hospital , Shandong Eye Institute, Shandong Academy of Medical Sciences , Qingdao , China.
Xuefei Lia Department of Pharmacy, College of Chemical Engineering , Qingdao University of Science and Technology , Qingdao , China.
Meng Xina Department of Pharmacy, College of Chemical Engineering , Qingdao University of Science and Technology , Qingdao , China.
Hui Wanga Department of Pharmacy, College of Chemical Engineering , Qingdao University of Science and Technology , Qingdao , China.
Fan Zhanga Department of Pharmacy, College of Chemical Engineering , Qingdao University of Science and Technology , Qingdao , China.
Xiaohong Lua Department of Pharmacy, College of Chemical Engineering , Qingdao University of Science and Technology , Qingdao , China.
Zengfang Zhuanga Department of Pharmacy, College of Chemical Engineering , Qingdao University of Science and Technology , Qingdao , China.
Xianggen Wua Department of Pharmacy, College of Chemical Engineering , Qingdao University of Science and Technology , Qingdao , China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesGinsenosides Rb1 (Rb1) could form micelles in aqueous solutions. Self-assembled Rb1 micelles could potentially be utilized as ocular drug delivery system, and it was postulated that the encapsulation of a medicine within Rb1 micelles might strengthen the drug's therapeutic action and reduce side effects.

methodsDiclofenac-loaded Rb1 micelles (Rb1-Dic micelles) were formulated, optimized, and then further evaluated for in vitro cytotoxicity/in vivo ocular irritation, in vivo corneal permeation, and in vivo anti-inflammatory efficacy.

resultsRb1 self-assembled into micelles with ultra-small particle size (<8 nm) in a homogeneous distribution state (polydispersity index [PDI] < 0.3). Diclofenac was highly encapsulated into the micelles according to the weight ratios of Rb1 to diclofenac. The ophthalmic solution of Rb1-Dic micelle was simple to prepare. Rb1 had good cellular tolerance, and it also improved the cellular tolerance of the encapsulated diclofenac. Rb1-Dic micelles also showed non-irritants to the rabbit eyes. The use of Rb1 micelles significantly improved the in vivo corneal permeation as well as the anti-inflammatory efficacy of diclofenac when compared to commercial diclofenac eye drops.

conclusionRb1 micelle formulations have great potential as a novel ocular drug delivery system to improve the bioavailability of drugs such as diclofenac.

Indexed as

AnimalsAnti-Inflammatory Agents, Non-SteroidalBiological AvailabilityCell LineCell SurvivalCorneaDiclofenacDrug CarriersEpithelial CellsGinsenosidesHumansMicellesNanoparticlesOphthalmic SolutionsParticle SizeRabbitsAnti-Inflammatory Agents, Non-SteroidalDiclofenacDrug Carriersginsenoside Rb1GinsenosidesMicellesOphthalmic SolutionsdiclofenacGinsenoside Rb1micelleocular drug delivery

Identifiers

PMID30957571
PMCPMC6461112

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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.