Evidence map›Paper›PMID 25756651›Full record

ArticleMolecules (Basel, Switzerland)2015

Bioavailability enhancement of paclitaxel via a novel oral drug delivery system: paclitaxel-loaded glycyrrhizic acid micelles.

Fu-Heng Yang, Qing Zhang, Qian-Ying Liang, Sheng-Qi Wang, Bo-Xin Zhao, Ya-Tian Wang, Yun Cai, Guo-Feng Li

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
8.0field-weighted citation impact, top 3% 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

48 citing papers in PubMed, 121 citations in OpenAlex.

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  13. Natural Products from Herbal Medicine Self-Assemble into Advanced Bioactive Materials.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
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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

8 authors at 2 institutions in 1 country.

Fu-Heng YangDepartment of Pharmacy, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China. fhyang2011@126.com.
Qing ZhangDepartment of Pharmacy, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China. zq1699@126.com.
Qian-Ying LiangDepartment of Pharmacy, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China. qianyinglny@163.com.
Sheng-Qi WangDepartment of Pharmacy, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China. wsq2011@126.com.
Bo-Xin ZhaoDepartment of Pharmacy, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China. zhaobx@smu.edu.cn.
Ya-Tian WangDepartment of Pharmacy, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China. alicemagic@126.com.
Yun CaiDepartment of Pharmacy, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China. cayun2@126.com.
Guo-Feng LiDepartment of Pharmacy, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China. liguofeng_2010@126.com.
Southern Medical University · CNNanfang Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Paclitaxel (PTX, taxol), a classical antitumor drug against a wide range of tumors, shows poor oral bioavailability. In order to improve the oral bioavailability of PTX, glycyrrhizic acid (GA) was used as the carrier in this study. This was the first report on the preparation, characterization and the pharmacokinetic study in rats of PTX-loaded GA micelles The PTX-loaded micelles, prepared with ultrasonic dispersion method, displayed small particle sizes and spherical shapes. Differential scanning calorimeter (DSC) thermograms indicated that PTX was entrapped in the GA micelles and existed as an amorphous state. The encapsulation efficiency was about 90%, and the drug loading rate could reach up to 7.90%. PTX-loaded GA micelles displayed a delayed drug release compared to Taxol in the in vitro release experiment. In pharmacokinetic study via oral administration, the area under the plasma concentration-time curve (AUC0→24 h) of PTX-loaded GA micelles was about six times higher than that of Taxol (p < 0.05). The significant oral absorption enhancement of PTX from PTX-loaded GA micelles could be largely due to the increased absorption in jejunum and colon intestine. All these results suggested that GA would be a promising carrier for the oral delivery of PTX.

Indexed as

Drug CarriersDrug Delivery SystemsAdministration, OralAnimalsAnti-Inflammatory AgentsAntineoplastic Agents, PhytogenicBiological AvailabilityDrug LiberationGlycyrrhizic AcidIntestinal AbsorptionIntestinal MucosaJejunumMaleMicellesPaclitaxelRatsAnti-Inflammatory AgentsAntineoplastic Agents, PhytogenicDrug CarriersGlycyrrhizic AcidMicellesPaclitaxel

Identifiers

PMID25756651
PMCPMC6272134
OpenAlexW2030607193

What OpenQuestion holds

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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.