Evidence map›Paper›PMID 38774026›Full record

ArticleInternational journal of nanomedicine2024

Polyvinylpyrrolidone Assisted One-Pot Synthesis of Size-Tunable Cocktail Nanodrug for Multifunctional Combat of Cancer.

Cheng Wang, Jiaoyang Pan, Shaoqing Chen, Lin Qiu, Huaanzi Hu, Li Ji, Jianhao Wang, Wenjia Liu, Xinye Ni

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2024. 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
–field-weighted citation impact
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.

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

9 authors.

Cheng Wang *School of Pharmacy, Changzhou University, Changzhou, Jiangsu Province, People's Republic of China.ORCID 0000-0003-3873-7350
Jiaoyang Pan *School of Pharmacy, Changzhou University, Changzhou, Jiangsu Province, People's Republic of China.
Shaoqing ChenDepartment of Radiology, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, Changzhou, Jiangsu Province, People's Republic of China.
Lin QiuSchool of Pharmacy, Changzhou University, Changzhou, Jiangsu Province, People's Republic of China.
Huaanzi HuSchool of Pharmacy, Changzhou University, Changzhou, Jiangsu Province, People's Republic of China.
Li JiDepartment of Otorhinolaryngology, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, Nanjing, Jiangsu Province, People's Republic of China.
Jianhao WangSchool of Pharmacy, Changzhou University, Changzhou, Jiangsu Province, People's Republic of China.
Wenjia LiuDepartment of Gastroenterology, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, Changzhou, Jiangsu Province, People's Republic of China.
Xinye NiDepartment of Radiology, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, Changzhou, Jiangsu Province, People's Republic of China.ORCID 0000-0002-2402-9719

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The in vivo barriers and multidrug resistance (MDR) are well recognized as great challenges for the fulfillment of antitumor effects of current drugs, which calls for the development of novel therapeutic agents and innovative drug delivery strategies. Nanodrug (ND) combining multiple drugs with distinct modes of action holes the potential to circumvent these challenges, while the introduction of photothermal therapy (PTT) can give further significantly enhanced efficacy in cancer therapy. However, facile preparation of ND which contains dual drugs and photothermal capability with effective cancer treatment ability has rarely been reported. Methods: In this study, we selected curcumin (Cur) and doxorubicin (Dox) as two model drugs for the creation of a cocktail ND (Cur-Dox ND). We utilized polyvinylpyrrolidone (PVP) as a stabilizer and regulator to prepare Cur-Dox ND in a straightforward one-pot method. Results: The size of the resulting Cur-Dox ND can be easily adjusted by tuning the charged ratios. It was noted that both loaded drugs in Cur-Dox ND can realize their functions in the same target cell. Especially, the P-glycoprotein inhibition effect of Cur can synergistically cooperate with Dox, leading to enhanced inhibition of 4T1 cancer cells. Furthermore, Cur-Dox ND exhibited pH-responsive dissociation of loaded drugs and a robust photothermal translation capacity to realize multifunctional combat of cancer for photothermal enhanced anticancer performance. We further demonstrated that this effect can also be realized in 3D multicellular model, which possibly attributed to its superior drug penetration as well as photothermal-enhanced cellular uptake and drug release. Conclusion: In summary, Cur-Dox ND might be a promising ND for better cancer therapy.

Indexed as

CurcuminDoxorubicinPovidoneAnimalsAntineoplastic AgentsATP Binding Cassette Transporter, Subfamily B, Member 1Cell Line, TumorCell SurvivalDrug CarriersDrug LiberationHumansMiceNanoparticlesNeoplasmsParticle SizePhotothermal TherapyAntineoplastic AgentsATP Binding Cassette Transporter, Subfamily B, Member 1CurcuminDoxorubicinDrug CarriersPovidonecancermultifunctionalone-pot synthesissize-tunable

Identifiers

PMID38774026
PMCPMC11107942

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.