Evidence map›Paper›PMID 38424427›Full record

ArticleCurrent drug delivery2025

An Enzyme-responsive Porphyrin Metal-organic Framework Nanosystem for Targeted and Enhanced Synergistic Cancer Photo-chemo Therapy.

Mengqi Yi, Yangxin Lin, Yuyang Li, Bei Xiong, Yunhan Huang, Wei Guo, Bo Lu

Abstract read
PubMed Publisher
In one paragraph

Article in Current drug delivery, 2025. 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
0.4field-weighted citation impact, top 47% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

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

7 authors at 2 institutions in 1 country.

Mengqi YiSchool of Chemistry, Department of Chemical Engineering and Life Sciences, Wuhan University of Technology, Wuhan, 430070, China.
Yangxin LinSchool of Chemistry, Department of Chemical Engineering and Life Sciences, Wuhan University of Technology, Wuhan, 430070, China.
Yuyang LiSchool of Chemistry, Department of Chemical Engineering and Life Sciences, Wuhan University of Technology, Wuhan, 430070, China.
Bei XiongSchool of Chemistry, Department of Chemical Engineering and Life Sciences, Wuhan University of Technology, Wuhan, 430070, China.
Yunhan HuangSchool of Chemistry, Department of Chemical Engineering and Life Sciences, Wuhan University of Technology, Wuhan, 430070, China.
Wei GuoSchool of Chemistry, Department of Chemical Engineering and Life Sciences, Wuhan University of Technology, Wuhan, 430070, China.
Bo LuSchool of Chemistry, Department of Chemical Engineering and Life Sciences, Wuhan University of Technology, Wuhan, 430070, China.
Wuhan University · CNWuhan University of Technology · CN

Funding

National College Students' Innovation and Entrepreneurship Training Program, China S202310497123National Natural Science Foundation of China 51773162, 21204071
6 · The paper itself

Abstract

backgroundThe clinical efficiency of photodynamic therapy (PDT) in combination with chemotherapy has proven to be a promising strategy for tumor treatment, yet is restricted by the high glutathione (GSH) concentration at the tumor site and nonspecific drug targeting.

objectiveThe goal of the current research was to create a biocompatible GSH-depleting and tumor- targeting nanoparticle (denoted as DOX/CA@PCN-224@HA) for the combined photodynamic and chemo photo-chemo) therapy.

methodsThe nanoparticles were characterized by transmission electron microscopy (TEM). A UV-vis spectrophotometer was used to measure the drug loading efficiency (DE) and encapsulation efficiency (EE). The GSH-depleting ability was measured using Ellman's test. Confocal laser scan microscopy (CLSM) was used to assess the cellular uptake. MTT was adopted to evaluate the cytotoxicity of DOX/CA@PCN-224@HA against 4T1 cells.

resultsThe altered PCN-224 showed excellent monodispersing with a dimension of approximately 193 nm ± 2 nm in length and 79 nm ± 3 nm in width. The larger and spindle grid-like structure of PCN-224 obtains better dual-drug loading ability (DOX: 20.58% ± 2.60%, CA: 21.81% ± 1.98%) compared with other spherical PCN-224 nanoparticles. The ultimate cumulative drug release rates with hyaluronidase (HAase) were 74% ± 1% (DOX) and 45% ± 2% (CA) after 72 h. DOX/CA@PCN-224@HA showed GSH-consuming capability, which could improve the PDT effect. The drug-loaded nanoparticles could accurately target 4T1 cells through biological evaluations. Moreover, the released DOX and CA display cooperative effects on 4T1 cells

conclusionThis nanosystem displays great potential for tumor-targeted enhanced (photo-chemo) therapy.

Indexed as

Antibiotics, AntineoplasticDoxorubicinMetal-Organic FrameworksNanoparticlesPhotochemotherapyPhotosensitizing AgentsPorphyrinsAnimalsCell Line, TumorCell SurvivalDrug CarriersDrug LiberationFemaleGlutathioneHyaluronoglucosaminidaseMiceAntibiotics, AntineoplasticDoxorubicinDrug CarriersGlutathioneHyaluronoglucosaminidaseMetal-Organic FrameworksPhotosensitizing AgentsPorphyrinscombined therapeuticFBS.metal-organic frameworkPDTPhotodynamic therapytumor targeting

Identifiers

PMID38424427
OpenAlexW4392352554

What OpenQuestion holds

Textmetadata
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.