Evidence map›Paper›PMID 36176605›Full record

ArticleBioengineering & translational medicine2022

Photoresponsive prodrug-dye nanoassembly for in-situ monitorable cancer therapy.

Kaiqi Long, Yifan Wang, Wen Lv, Yang Yang, Shuting Xu, Changyou Zhan, Weiping Wang

Open access · goldAbstract read
In one paragraph

Article in Bioengineering & translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

12 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Light-Activated Anti-Vascular Combination Therapy against Choroidal Neovascularization.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Stimuli-Responsive Boron-Based Materials in Drug Delivery.International journal of molecular sciences · 2023
    Review
  11. Article
  12. Article
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 3 countries.

Kaiqi LongState Key Laboratory of Pharmaceutical Biotechnology The University of Hong Kong Hong Kong China.ORCID https://orcid.org/0000-0002-3582-2341
Yifan WangState Key Laboratory of Pharmaceutical Biotechnology The University of Hong Kong Hong Kong China.ORCID https://orcid.org/0000-0002-7887-9719
Wen LvState Key Laboratory of Pharmaceutical Biotechnology The University of Hong Kong Hong Kong China.
Yang YangDepartment of Pharmacology, School of Basic Medical Sciences & State Key Laboratory of Molecular Engineering of Polymers Fudan University Shanghai China.
Shuting XuState Key Laboratory of Pharmaceutical Biotechnology The University of Hong Kong Hong Kong China.
Changyou ZhanDepartment of Pharmacology, School of Basic Medical Sciences & State Key Laboratory of Molecular Engineering of Polymers Fudan University Shanghai China.
Weiping WangState Key Laboratory of Pharmaceutical Biotechnology The University of Hong Kong Hong Kong China.ORCID https://orcid.org/0000-0001-7511-3497
University of Hong Kong · HKFudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Photocleavable prodrugs enable controllable drug delivery to target sites modulated by light irradiation. However, the in vivo utility is usually hindered by their insolubility and inefficient delivery. In this study, we report a simple strategy of co-assembling boron-dipyrromethene-chlorambucil prodrug and near-infrared dye IR783 to fabricate photoresponsive nanoassemblies, which achieved both high prodrug loading capacity (~99%) and efficient light-triggered prodrug activation. The incorporated IR783 dye not only stabilized the nanoparticles and contributed tumor targeting as usual, but also exhibited degradation after light irradiation and in-situ monitoring of nanoparticle dissociation by fluorescent imaging. Systemic administration of the nanoparticles and localized light irradiation at tumor sites enabled monitorable and efficient drug release in vivo. Our results demonstrate that such prodrug-dye co-assembled nanomedicine is a promising formulation for photoresponsive drug delivery, which would advance the translation of photoresponsive nanomedicines.

Indexed as

drug deliveryin‐situ monitoringIR783 dyenanomedicinephotocleavable prodrugphotopharmacologyself‐assembly

Identifiers

PMID36176605
PMCPMC9472000
OpenAlexW4220666246

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.