Evidence map›Paper›PMID 31692522›Full record

ArticleInternational journal of nanomedicine2019

Tumor-targeting photodynamic therapy based on folate-modified polydopamine nanoparticles.

Shufeng Yan, Qingqing Huang, Jincan Chen, Xiaorong Song, Zhuo Chen, Mingdong Huang, Peng Xu, Juncheng Zhang

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

17 citing papers in PubMed, 45 citations in OpenAlex.

  1. Phototherapy in cancer treatment: strategies and challenges.Signal transduction and targeted therapy · 2025
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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 2 countries.

Shufeng YanMedical Plant Exploitation and Utilization Engineering Research Center, Sanming University, Sanming, Fujian 365004, People's Republic of China.
Qingqing HuangMedical Plant Exploitation and Utilization Engineering Research Center, Sanming University, Sanming, Fujian 365004, People's Republic of China.
Jincan ChenState Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002, People's Republic of China.
Xiaorong SongState Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002, People's Republic of China.
Zhuo ChenState Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002, People's Republic of China.
Mingdong HuangCollege of Chemistry, Fuzhou University, Fuzhou, Fujian 350116, People's Republic of China.
Peng XuInstitute of Molecular and Cell Biology, ASTAR (Agency for Science, Technology and Research), Singapore 138673, Singapore.
Juncheng ZhangMedical Plant Exploitation and Utilization Engineering Research Center, Sanming University, Sanming, Fujian 365004, People's Republic of China.
Chinese Academy of Sciences · CNSanming University · CNAgency for Science, Technology and Research · SGFuzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPhotodynamic therapy (PDT), a clinical anticancer therapeutic modality, has a long history in clinical cancer treatments since the 1970s. However, PDT has not been widely used largely because of metabolic problems and off-target phototoxicities of the current clinical photosensitizers. PURPOSE: The objective of the study is to develop a high-efficiency and high-specificity carrier to precisely deliver photosensitizers to tumor sites, aiming at addressing metabolic problems, as well as the systemic damages current clinical photosensitizers are known to cause.

methodsWe synthesized a polydopamine (PDA)-based carrier with the modification of folic acid (FA), which is to target the overexpressed folate receptors on tumor surfaces. We used this carrier to load a cationic phthalocyanine-type photosensitizer (Pc) and generated a PDA-FA-Pc nanomedicine. We determined the antitumor effects and the specificity to tumor cell lines in vitro. In addition, we established human cancer-xenografted mice models to evaluate the tumor-targeting property and anticancer efficacies in vivo.

resultsOur PDA-FA-Pc nanomedicine demonstrated a high stability in normal physiological conditions, however, could specifically release photosensitizers in acidic conditions, eg, tumor microenvironment and lysosomes in cancer cells. Additionally, PDA-FA-Pc nanomedicine demonstrated a much higher cellular uptake and phototoxicity in cancer cell lines than in healthy cell lines. Moreover, the in vivo imaging data indicated excellent tumor-targeting properties of PDA-FA-Pc nanomedicine in human cancer-xenografted mice. Lastly, PDA-FA-Pc nanomedicine was found to significantly suppress tumor growth within two human cancer-xenografted mice models.

conclusionOur current study not only demonstrates PDA-FA-Pc nanomedicine as a highly potent and specific anticancer agent, but also suggests a strategy to address the metabolic and specificity problems of clinical photosensitizers.

Indexed as

AnimalsCell Line, TumorDrug CarriersDrug StabilityFemaleFolic AcidHeLa CellsHumansIndolesIsoindolesMCF-7 CellsMiceNanomedicineNanoparticlesOrganometallic CompoundsPhotochemotherapyDrug CarriersFolic AcidIndolesIsoindolesOrganometallic CompoundsPhotosensitizing AgentspolydopaminePolymersZinc CompoundsZn(II)-phthalocyanineanticancer specificityfolate receptorsphotodynamic therapypolydopamine nanoparticlestumor-targeting

Identifiers

PMID31692522
PMCPMC6711554
OpenAlexW2969351019

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.