Evidence map›Paper›PMID 42429317›Full record

ReviewMacromolecular rapid communications2026

Research Progress of Platinum-Based Anticancer Drugs in Combination with Macrocyclic Drug Delivery System.

Li Yang, Pengmin Shi, Bo Yang, Jing Yang, Jian Zhao, Chuanzhu Gao

Abstract readReview
In one paragraph

Review in Macromolecular rapid communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Li YangFaculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, Yunnan, P. R. China.
Pengmin ShiSchool of Chemistry and Chemical Engineering, Southeast University, Nanjing, P. R. China.
Bo YangFaculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, Yunnan, P. R. China.
Jing YangFaculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, Yunnan, P. R. China.
Jian ZhaoSchool of Chemistry and Chemical Engineering, Southeast University, Nanjing, P. R. China.ORCID https://orcid.org/0000-0002-9365-7727
Chuanzhu GaoFaculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, Yunnan, P. R. China.

Funding

National Natural Science Foundation of China 22367016
6 · The paper itself

Abstract

Platinum-based anticancer drugs represent a cornerstone of clinical cancer chemotherapy, yet their clinical application is severely limited by inherent drug resistance and systemic toxic side effects. Macrocyclic compounds, such as cucurbiturils, cyclodextrins, crown ethers, calixarenes and pillararenes, possess unique cavity structures and excellent molecular recognition capabilities, offering promising strategies for optimizing the chemotherapeutic efficacy of platinum-based drugs. This review summarizes the latest research progress in supramolecular systems constructed from macrocyclic compounds and platinum-based drugs via host-guest interactions. It focuses on the roles of such supramolecular complexes in improving drug solubility, stability, tumor targeting, and controlled release performance, as well as their potential to overcome drug resistance and reduce toxicity. Furthermore, the applications of functionalized macrocyclic compounds in intelligent drug delivery and combination therapy are discussed, and future directions, including novel macrocyclic carriers, multifunctional nanoplatforms, and combination with immunotherapy and gene therapy, are prospected. This review aims to provide useful references for the development of precise and personalized applications of platinum-based drugs in cancer therapy.

Indexed as

Antineoplastic AgentsDrug Delivery SystemsMacrocyclic CompoundsNeoplasmsOrganoplatinum CompoundsPlatinumDrug CarriersHumansAntineoplastic AgentsDrug CarriersMacrocyclic CompoundsOrganoplatinum CompoundsPlatinumantitumordrug delivery systemmacrocyclic compoundsplatinum‐based anticancer drugstargeted delivery

Identifiers

PMID42429317
PMCPMC13489197

What OpenQuestion holds

Textmetadata
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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.