Evidence map›Paper›PMID 25347456›Full record

ArticleMolecules (Basel, Switzerland)2014

Microemulsion system for topical delivery of thai mango seed kernel extract: development, physicochemical characterisation and ex vivo skin permeation studies.

Jiraporn Leanpolchareanchai, Karine Padois, Françoise Falson, Rapepol Bavovada, Pimolpan Pithayanukul

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2014. 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
–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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Exploring Anti-Aging Potential ofNanotechnology, science and applications · 2025
    Article
  5. Review
  6. Article
  7. Optimization ofPharmaceutics · 2020
    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

5 authors.

Jiraporn LeanpolchareanchaiDepartment of Pharmacy, Faculty of Pharmacy, Mahidol University, 447 Sri-Ayuthaya Road, Rajathevi, Bangkok 10400, Thailand. jiraporn.lea@mahidol.ac.th.
Karine PadoisEA 4169 "Fonctions Normales et Pathologiques de la Barrière Cutanée", Laboratoire de Recherche et Développement de Pharmacie Galénique Industrielle, ISPB-Faculté de Pharmacie, Université Claude Bernard Lyon-I, 8 Avenue Rockefeller, F-69373 Lyon Cedex 08, France. poretk@hotmail.com.
Françoise FalsonEA 4169 "Fonctions Normales et Pathologiques de la Barrière Cutanée", Laboratoire de Recherche et Développement de Pharmacie Galénique Industrielle, ISPB-Faculté de Pharmacie, Université Claude Bernard Lyon-I, 8 Avenue Rockefeller, F-69373 Lyon Cedex 08, France. francoise.falson@recherche.univ-lyon1.fr.
Rapepol BavovadaDepartment of Pharmacognosy and Pharmaceutical Botany, Faculty of Pharmaceutical Sciences, Chulalongkorn University, 254 Payathai Road, Pathumwan, Bangkok 10330, Thailand. rapepol1@hotmail.com.
Pimolpan PithayanukulDepartment of Pharmacy, Faculty of Pharmacy, Mahidol University, 447 Sri-Ayuthaya Road, Rajathevi, Bangkok 10400, Thailand. pimolpan.pit@mahidol.ac.th.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A microemulsion system containing Thai mango seed kernel extract (MSKE, cultivar "Fahlun") was developed and characterised for the purpose of topical skin delivery. The MSKE-loaded microemulsions were prepared by using the spontaneous emulsification method. Isopropyl myristate (IPM) was selected as the oil phase. A polyoxyethylene sorbitan monooleate and sorbitan monododecanoate (1:1, w/w) system was used as the surfactant phase; an aqueous mixture of different cosurfactants (absolute ethanol, 96.3% v/v ethanol, 1-propanol, 2-propanol or 1,2-propanediol) at a weight ratio of 1:1 was used as the aqueous phase. Among the cosurfactants studied, the 1-propanol aqueous mixture had the largest microemulsion region (48.93%) in the pseudo-ternary phase diagram. Microemulsions containing 1% MSKE demonstrated good physicochemical stability during a six-month study period at 25 ± 2 °C/60% ± 5% RH. The ex vivo skin permeation study demonstrated that the microemulsions exhibited a potent skin enhancement effect allowing MSKE to penetrate skin layers up to 60-fold higher compared with the control. Neither skin irritation nor skin corrosion was observed in ex vivo studies. The present study revealed that IPM-based microemulsion systems may be promising carriers to enhance skin penetration and delivering MSKE for topical treatment.

Indexed as

1-PropanolCells, CulturedDrug Delivery SystemsEmulsionsFibroblastsHumansMangiferaMyristatesPermeabilityPlant ExtractsSeedsSkinSkin AbsorptionSurface-Active Agents1-PropanolEmulsionsisopropyl myristateMyristatesPlant ExtractsSurface-Active Agents

Identifiers

PMID25347456
PMCPMC6271960

What OpenQuestion holds

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LicenceCC BY
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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.