Evidence map›Paper›PMID 34575533›Full record

ArticlePharmaceutics2021

Enhancement of Skin Delivery of Drugs Using Proposome Depends on Drug Lipophilicity.

Himanshu Kathuria, Harish K Handral, Saera Cha, Diep T P Nguyen, Junyu Cai, Tong Cao, Chunyong Wu, Lifeng Kang

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

13 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  6. Unveiling the Potential ofPharmaceuticals (Basel, Switzerland) · 2024
    Review
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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 4 institutions in 3 countries.

Himanshu KathuriaDepartment of Pharmacy, National University of Singapore, Singapore 117543, Singapore.ORCID 0000-0002-9502-2901
Harish K HandralStem Cell Bioprocessing, Bioprocessing Technology Institute, A*STAR, Singapore 138668, Singapore.
Saera ChaDepartment of Pharmacy, National University of Singapore, Singapore 117543, Singapore.
Diep T P NguyenDepartment of Pharmacy, National University of Singapore, Singapore 117543, Singapore.
Junyu CaiSchool of Pharmacy, Faculty of Medicine and Health, University of Sydney, Sydney, NSW 2006, Australia.
Tong CaoFaculty of Dentistry, National University of Singapore, Singapore 119085, Singapore.ORCID 0000-0002-7994-9627
Chunyong WuKey Laboratory of Drug Quality Control and Pharmacovigilance, China Pharmaceutical University, Nanjing 210009, China.
Lifeng KangSchool of Pharmacy, Faculty of Medicine and Health, University of Sydney, Sydney, NSW 2006, Australia.ORCID 0000-0002-1676-7607
National University of Singapore · SGThe University of Sydney · AUAgency for Science, Technology and Research · SGChina Pharmaceutical University · CN

Funding

National Natural Science Foundation of China 82074128National University of Singapore n/aUniversity of Sydney n/a
6 · The paper itself

Abstract

The study aims to investigate the propylene glycol-based liposomes named 'proposomes' in enhancing skin permeation of drugs with different physicochemical properties. Ibuprofen, tofacitinib citrate, rhodamine B, and lidocaine were loaded into proposomes. These drug formulations were analyzed for particle size, zeta potential, polydispersity index, entrapment efficiency, and in vitro skin permeation. The confocal laser scanning microscopy was performed on skin treated with calcein and rhodamine B laden proposomes. The transdermal delivery relative to physicochemical properties of drugs such as logP, melting point, molecular weight, solubility, etc., were analyzed. We tested the safety of the proposomes using reconstructed human skin tissue equivalents, which were fabricated in-house. We also used human cadaver skin samples as a control. The proposomes had an average diameter of 128 to 148 nm. The drug's entrapment efficiencies were in the range of 42.9-52.7%, translating into the significant enhancement of drug permeation through the skin. The enhancement ratio was 1.4 to 4.0, and linearly correlated to logP, molecular weight, and melting point. Confocal imaging also showed higher skin permeation of calcein and rhodamine B in proposome than in solution. The proposome was found safe for skin application. The enhancement of skin delivery of drugs through proposomes was dependent on the lipophilicity of the drug. The entrapment efficiency was positively correlated with logP of the drug, which led to high drug absorption.

Indexed as

ibuprofenlidocaineproposomerhodaminetofacitinibtransdermal delivery

Identifiers

PMID34575533
PMCPMC8469902
OpenAlexW3199554032

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.