Evidence map›Paper›PMID 36564675›Full record

ArticleApplied biochemistry and biotechnology2023

Formulation of Aucklandiae Radix Extract-Loaded Nanoemulsions and Its Characterization and Evaluations In Vitro and In Vivo.

Meng Zhang, Huimin Li, Li Zhang, Jingyang Li, Xinrui Wang, Lifei Luo, Jingze Zhang, Dailin Liu

Abstract read
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In one paragraph

Article in Applied biochemistry and biotechnology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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

8 authors at 2 institutions in 1 country.

Meng Zhang *Tianjin University of Traditional Chinese Medicine, Tianjin, 301617, People's Republic of China.
Huimin Li *Department of Pharmaceutical Sciences, Beijing Institute of Radiation Medicine, Beijing, 100850, People's Republic of China.
Li ZhangDepartment of Pharmacy, Logistics College of Chinese People's Armed Police Forces, Tianjin, 300309, People's Republic of China.
Jingyang LiDepartment of Pharmacy, Logistics College of Chinese People's Armed Police Forces, Tianjin, 300309, People's Republic of China.
Xinrui WangTianjin University of Traditional Chinese Medicine, Tianjin, 301617, People's Republic of China.
Lifei LuoTianjin Modern Innovation Chinese Medicine Technology Co., Ltd, Tianjin, 300380, People's Republic of China.
Jingze ZhangTianjin University of Traditional Chinese Medicine, Tianjin, 301617, People's Republic of China.
Dailin LiuTianjin University of Traditional Chinese Medicine, Tianjin, 301617, People's Republic of China. dailinlch@163.com.
Tianjin University of Traditional Chinese Medicine · CNChinese People's Armed Police Force

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to screen, design, and evaluate an optimal nanoemulsion formulation for Aucklandiae Radix extraction (ARE). A simple lattice design (SLD) method was used to determine the preparation process of Aucklandiae Radix extract-nanoemulsions (ARE-NEs). After optimization, the average particle size of ARE-NEs was 14.1 ± 1.1 nm, polydispersity index was 0.2376, and pH was 6.92. In vitro penetration tests verified that the permeability ratios of costunolide (CE), dehydrocostus lactone (DE), and ARE-NEs were approximately 6.33 times and 8.20 times higher, respectively, than those of the control group. The results of the pharmacokinetic study indicated that after topical administration, the content of the index components of ARE-NEs increased in vivo, with a longer release time and higher bioavailability in vivo than in vitro. The index components were CE and DE, respectively. In addition, a skin irritation test was conducted on normal and skin-damaged rabbits, aided by HE staining and scanning electron microscopy, to reveal the transdermal mechanism of ARE-NEs and proved that NEs are safe for topical application. ARE-NEs energetically developed the properties of skin and penetration through the transdermal route, which were secure when applied via the transdermal delivery system .

Indexed as

SkinAdministration, CutaneousAnimalsEmulsionsRabbitsEmulsionsAucklandiae RadixCostunolideDehydrocostus lactoneNanoemulsionPenetration enhancerTransdermal drug delivery system

Identifiers

PMID36564675
OpenAlexW4312115555

What OpenQuestion holds

Textmetadata
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.