Evidence map›Paper›PMID 38164268›Full record

ArticleInternational journal of nanomedicine2023

Zeolitic Imidazolate Framework (ZIF-8) Decorated Iron Oxide Nanoparticles Loaded Doxorubicin Hydrochloride for Osteosarcoma Treatment - in vitro and in vivo Preclinical Studies.

Wenbo Wu, Xiaoli Yu, Jiaxiang Sun, Yuanyuan Han, Yuanye Ma, Guoqing Zhang, Qingming Ma, Qiang Li, Hongfei Xiang

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

14 citing papers in PubMed, 27 citations in OpenAlex.

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  13. PMA-Zeolite: Chemistry and Diverse Medical Applications.Journal of functional biomaterials · 2024
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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

9 authors at 1 institution in 1 country.

Wenbo Wu *Department of Orthopedics, the Affiliated Hospital of Qingdao University, Qingdao, 266003, People's Republic of China.ORCID 0009-0000-2336-3275
Xiaoli Yu *Department of Anesthesiology, the Affiliated Hospital of Qingdao University, Qingdao, 266100, People's Republic of China.ORCID 0009-0004-6439-4202
Jiaxiang SunCollege of Physics, Center for Marine Observation and Communications, Qingdao University, Qingdao, 266021, People's Republic of China.
Yuanyuan HanCollege of Physics, Center for Marine Observation and Communications, Qingdao University, Qingdao, 266021, People's Republic of China.
Yuanye MaDepartment of Orthopedics, the Affiliated Hospital of Qingdao University, Qingdao, 266003, People's Republic of China.
Guoqing ZhangDepartment of Orthopedics, the Affiliated Hospital of Qingdao University, Qingdao, 266003, People's Republic of China.
Qingming MaDepartment of Pharmaceutics, School of Pharmacy, Qingdao University, Qingdao, 266021, People's Republic of China.
Qiang LiCollege of Physics, Center for Marine Observation and Communications, Qingdao University, Qingdao, 266021, People's Republic of China.
Hongfei XiangDepartment of Orthopedics, the Affiliated Hospital of Qingdao University, Qingdao, 266003, People's Republic of China.
Qingdao University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: As a broad-spectrum antitumorigenic agent, doxorubicin (DOX) is commonly used as a chemotherapeutic drug for treating osteosarcoma (OS). Still, it is associated with significant cell toxicity and ineffective drug delivery, whereas the zeolite imidazolate framework is extensively applied in the biomedical field as a carrier owing to its favorable biocompatibility, high porosity, and pH-responsiveness. Therefore, we need to develop a drug delivery platform that can effectively increase the antitumorigenic effect of the loaded drug and concurrently minimize drug toxicity. Methods: In this study, a Fe Results: DFZ nanoparticles possessed have a size of ~110 nm, with an encapsulation rate of 21% and pH responsiveness. DFZ exerted a superior cytostatic effect and apoptosis rate on K7M2 cells in vitro compared to DOX(p<0.01). In animal experiments, DFZ offers up to 67% tumor inhibition and has shown a superior ability to induce apoptosis than DOX alone in TUNEL results(p<0.01). Tumor-targeting experiments have validated that DFZ can be effectively accumulated in the tumor tissue and enhance anticancer performance. Conclusion: In summary, the DFZ nano-delivery system exhibited a more substantial anti-tumorigenic effect as well as superior active tumor targeting of DOX- Fe

Indexed as

Bone NeoplasmsMetal-Organic FrameworksNanoparticlesOsteosarcomaZeolitesAnimalsDoxorubicinDrug CarriersDrug Delivery SystemsMagnetic Iron Oxide NanoparticlesMiceDoxorubicinDrug CarriersMetal-Organic FrameworksZeolitesnanocarriersosteosarcoma chemotherapyPH-responsivetumor targetingzeolite imidazolate framework

Identifiers

PMID38164268
PMCPMC10758197
OpenAlexW4390297425

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.