Evidence map›Paper›PMID 40547705›Full record

ReviewACS omega2025

Lipid-Based Nanocarriers for Topical Therapy of Cutaneous Leishmaniasis: An Insight into the Mechanism of Action.

Amina Riaz, Muhammad Farhan Ali Khan, Aamir Jalil, Asim Ur Rehman, Naveed Ahmed, Zobia Mubarak, Maryam Parhizkar, Hira Muqaddas

Abstract readReview
In one paragraph

Review in ACS omega, 2025. 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
–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

2 citing papers in PubMed.

  1. Article
  2. Review
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.

Amina RiazDepartment of Pharmacy, The Women University Multan, Multan 6000, Pakistan.
Muhammad Farhan Ali KhanDepartment of Pharmacy, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad 45320, Pakistan.
Aamir JalilDepartment of Pharmaceutics, Faculty of Pharmacy, Bahauddin Zakariya University, Multan 60800, Pakistan.
Asim Ur RehmanDepartment of Pharmacy, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad 45320, Pakistan.ORCID https://orcid.org/0000-0003-4619-0359
Naveed AhmedDepartment of Pharmacy, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad 45320, Pakistan.ORCID https://orcid.org/0000-0002-4780-9945
Zobia MubarakPunjab University College of Pharmacy, University of the Punjab, Lahore 54000, Pakistan.
Maryam ParhizkarSchool of Pharmacy, University College London, London WC1N 1AX, United Kingdom.ORCID https://orcid.org/0000-0003-3679-7130
Hira MuqaddasDepartment of Zoology, The Women University Multan, Multan 6000, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cutaneous leishmaniasis (CL) is a parasitic infection caused by Leishmania species, affecting millions worldwide. The current treatment options for CL have several limitations, including low efficacy, inability to reach the target site, potential toxicity, and longer treatment duration, leading to poor patient compliance. Therefore, there is an urgent need for alternative treatments, especially topical ones, that are more effective, safe, and patient-friendly. Although numerous reviews have described the advantages of a wide range of nanoparticles in the treatment of CL, this review narrows its focus to the utilization of novel lipid-based nanocarriers for the topical treatment of CL, offering an in-depth analysis of the topical potential and mechanism of skin permeation of these lipidic nanocarriers. Lipid-based nanostructures such as liposomes, solid lipid nanoparticles, and nanostructured lipid carriers have been extensively studied for CL treatment, either alone or in combination with other drugs or therapies. These carriers can improve the bioavailability, stability, and efficacy of the drug, target the infected site, and reduce adverse effects on healthy tissues. Moreover, these can be easily formulated into different dosage forms, such as creams, gels, or ointments, for convenient topical application. Despite the many benefits of lipid-based carriers, there are still some challenges that need to be addressed, such as optimizing the formulation parameters, ensuring the reproducibility and scalability of the process, and evaluating the long-term safety and efficacy in clinical trials. This study aims to provide a comprehensive overview of the current state-of-the-art lipid-based nanocarriers for topical treatment of CL, covering the recent advances, limitations, clinical evidence, and prospects of this promising approach. In addition, the skin and macrophage targeting potential of various lipid-based nanocarriers is also discussed, which is especially helpful in treating the lesions of CL.

Identifiers

PMID40547705
PMCPMC12177655

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Registered trials

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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.