Evidence map›Paper›PMID 40006557›Full record

ReviewPharmaceutics2025

PEGylated Nanoliposomes Encapsulated with Anticancer Drugs for Breast and Prostate Cancer Therapy: An Update.

Sijongesonke Peter, Vuyolwethu Khwaza, Sibusiso Alven, Tobeka Naki, Blessing Atim Aderibigbe

Abstract readReview
In one paragraph

Review in Pharmaceutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Article
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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

5 authors.

Sijongesonke PeterDepartment of Chemistry, University of Fort Hare, Alice 5700, South Africa.ORCID 0000-0002-6935-905X
Vuyolwethu KhwazaDepartment of Chemistry, University of Fort Hare, Alice 5700, South Africa.ORCID 0000-0003-4875-1535
Sibusiso AlvenDepartment of Chemistry, University of Fort Hare, Alice 5700, South Africa.ORCID 0000-0001-7100-4007
Tobeka NakiDepartment of Chemistry, University of Fort Hare, Alice 5700, South Africa.ORCID 0000-0002-7934-9998
Blessing Atim AderibigbeDepartment of Chemistry, University of Fort Hare, Alice 5700, South Africa.ORCID 0000-0003-1157-7481

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There are different types of cancer treatments, including surgery, radiotherapy, and chemotherapy. However, the complexity of cancer has resulted in treatment challenges to medicinal scientists and a socio-economic burden to the public health system globally. The pharmacological limitations associated with the current conventional anticancer drugs include lack of specificity, poor bioavailability, toxicity, drug resistance, and poor delivery mechanisms, which make cancer treatment challenging. Thus, the number of cancer cases is escalating rapidly, especially breast and prostate cancer in women and men, respectively. The application of nanoformulations is gaining momentum for treating different cancer types. However, they also exhibit challenges that must be addressed for effective cancer treatment. Nanoliposomes are nanoformulations that are widely explored for cancer treatment with interesting therapeutic outcomes. They have been functionalized with PEG to further improve their therapeutic outcomes. Hence, this review provides an update on PEGylated nanoliposomes loaded with anticancer drugs for the treatment of breast and prostate cancer, focusing on pre-clinical studies published in the last decade (2015 to 2024) to reflect the recent advancements made in the design of PEGylation nanoliposomes. Highlights of the clinically and commercially available PEGylation nanoliposomes are also presented in this review.

Indexed as

anticancerbioavailabilitybreast cancerchemotherapeuticsdrug resistancenanoliposomesPEGprostate cancertoxicity

Identifiers

PMID40006557
PMCPMC11859135

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.