Evidence map›Paper›PMID 39502637›Full record

ArticleInternational journal of nanomedicine2024

Penetration Enhancer-Free Mixed Micelles for Improving Eprinomectin Transdermal c Efficiency in Animal Parasitic Infections Therapy.

Yujuan Mao, Tianjiao Hao, Hongxiu Zhang, Xiaofei Gu, Jing Wang, Feifei Shi, Xiaolan Chen, Liuna Guo, Jie Gao, Yan Shen and 2 more

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

12 authors.

Yujuan Mao *Jiangsu Agri-Animal Husbandry Vocational College, Taizhou, Jiangsu, 225300, People's Republic of China.
Tianjiao Hao *Department of Pharmaceutics, China Pharmaceutical University, Nanjing, 210009, People's Republic of China.
Hongxiu Zhang *Department of Pharmaceutics, China Pharmaceutical University, Nanjing, 210009, People's Republic of China.
Xiaofei GuDepartment of Pharmaceutics, China Pharmaceutical University, Nanjing, 210009, People's Republic of China.
Jing WangJiangsu Agri-Animal Husbandry Vocational College, Taizhou, Jiangsu, 225300, People's Republic of China.
Feifei ShiJiangsu Agri-Animal Husbandry Vocational College, Taizhou, Jiangsu, 225300, People's Republic of China.
Xiaolan ChenJiangsu Agri-Animal Husbandry Vocational College, Taizhou, Jiangsu, 225300, People's Republic of China.
Liuna GuoJiangsu Agri-Animal Husbandry Vocational College, Taizhou, Jiangsu, 225300, People's Republic of China.
Jie GaoJiangsu Agri-Animal Husbandry Vocational College, Taizhou, Jiangsu, 225300, People's Republic of China.
Yan ShenDepartment of Pharmaceutics, China Pharmaceutical University, Nanjing, 210009, People's Republic of China.
JinLin ZhangJiangsu Institute for Food and Drug Control, Nanjing, Jiangsu Province, 210019, People's Republic of China.
Shenglan YuCollege of Animal Medicine, Jiangsu Agri-Animal Husbandry Vocational College, Taizhou, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Eprinomectin offers promise against parasitic infections. This study develops Eprinomectin (EPR) mixed micelles for transdermal delivery, aiming to enhance efficacy and convenience against endoparasites and ectoparasites. Physicochemical characterization and pharmacokinetic studies were conducted to assess its potential as an effective treatment for parasitic infections. Methods: Blank and EPR mixed micelles were prepared using PEG-40 Hydrogenated castor oil (RH-40) and Nonyl phenol polyoxyethylene ether 40 (NP-40). Critical micelle concentrations (CMC) determined using the pyrene fluorescence probe method. Particle size, EE, DL, in vitro release, permeation, and skin irritation were evaluated. In vivo pharmacokinetic studies were conducted in male Sprague-Dawley rats. Results: Results show that EPR mixed micelles present suitable stability, physicochemical properties, and safety. Moreover, the rapid release and high bioavailability of EPR mixed micelles have also been verified in the study. Pharmacokinetic experiments in vivo showed that an improvement in the transdermal absorption and bioavailability of EPR after encapsulation in mixed micelles formulations. Conclusion: The results proved that the novel mixed micelles are safe and effective and are expected to become a promising veterinary nano-delivery system.

Indexed as

Administration, CutaneousIvermectinMicellesRats, Sprague-DawleySkin AbsorptionAnimalsAntiparasitic AgentsBiological AvailabilityDrug CarriersMaleParticle SizePolyethylene GlycolsRatsSkinAntiparasitic AgentsDrug CarrierseprinomectinIvermectinMicellesPolyethylene Glycolseprinomectinmixed micellespharmacokineticstransdermal delivery

Identifiers

PMID39502637
PMCPMC11537163

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.