Evidence map›Paper›PMID 32420382›Full record

ArticleBioMed research international2020

Aptamer-Conjugated Multifunctional Polymeric Nanoparticles as Cancer-Targeted, MRI-Ultrasensitive Drug Delivery Systems for Treatment of Castration-Resistant Prostate Cancer.

Youqiang Fang, Shaoxiong Lin, Fei Yang, Jie Situ, Shudong Lin, Yun Luo

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

21 citing papers in PubMed, 48 citations in OpenAlex.

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  7. Biotechnology reports (Amsterdam, Netherlands) · 2024
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  15. Polymer-Based Nanosystems-A Versatile Delivery Approach.Materials (Basel, Switzerland) · 2021
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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

6 authors at 2 institutions in 1 country.

Youqiang FangDepartment of Urology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou 510630, China.ORCID https://orcid.org/0000-0001-7814-4889
Shaoxiong LinDepartment of Otorhinolaryngology, The First Affiliated Hospital of Shantou University Medical College, Shantou 515041, China.
Fei YangDepartment of Urology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou 510630, China.ORCID https://orcid.org/0000-0002-2768-5949
Jie SituDepartment of Urology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou 510630, China.
Shudong LinGuangzhou Institute of Chemistry, Chinese Academy of Sciences, Guangzhou 510650, China.ORCID https://orcid.org/0000-0002-3124-2905
Yun LuoDepartment of Urology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou 510630, China.ORCID https://orcid.org/0000-0003-3539-3310
Sun Yat-sen University · CNChinese Academy of Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nanoscopic therapeutic systems that incorporate therapeutic agents, molecular targeting, and imaging capabilities have gained momentum and exhibited significant therapeutic potential. In this study, multifunctional polymeric nanoparticles with controlled drug delivery, cancer-targeted capability, and efficient magnetic resonance imaging (MRI) contrast characteristics were formulated and applied in the treatment of castration-resistant prostate cancer (CRPC). The "core-shell" targeted nanoparticles (NPs) were synthesized by the self-assembly of a prefunctionalized amphiphilic triblock copolymer composed of poly(lactic-co-glycolic-acid) (PLGA), polyethylene glycol (PEG), and the Wy5a aptamer (Apt), which have been screened for targeting the CRPC cell line PC-3 by cell-SELEX technique as described in our previous study. Docetaxel (Dtxl) and a cluster of hydrophobic superparamagnetic iron oxide (SPIO) nanoparticles were simultaneously encapsulated into the targeted nanoparticles. The targeted NPs showed a controlled drug release and an increased contrast-enhanced MRI capability. The presence of Wy5a on the nanoparticle surface resulted in the cancer-targeted delivery to PC-3 cells

Indexed as

Aptamers, NucleotideContrast MediaDocetaxelDrug CarriersMagnetic Resonance ImagingNanoparticlesProstatic Neoplasms, Castration-ResistantDelayed-Action PreparationsHumansMalePC-3 CellsAptamers, NucleotideContrast MediaDelayed-Action PreparationsDocetaxelDrug Carriers

Identifiers

PMID32420382
PMCPMC7201588
OpenAlexW3018771613

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.