Evidence map›Paper›PMID 31741089›Full record

ArticlePharmaceutical research2019

E-Jet 3D-Printed Scaffolds as Sustained Multi-Drug Delivery Vehicles in Breast Cancer Therapy.

Xiaoyin Qiao, Yikun Yang, Ruiying Huang, Xuelei Shi, Haoxiang Chen, Jian Wang, Yanxiang Chen, Yongjun Tan, Zhikai Tan

Abstract read
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In one paragraph

Article in Pharmaceutical research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Review
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  3. Article
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  6. Article
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  8. Review
  9. Article
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  11. 3D printing of pharmaceuticals for disease treatment.Frontiers in medical technology · 2022
    Review
  12. Article
  13. Review
  14. Review
  15. 3D printedTheranostics · 2020
    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

9 authors.

Xiaoyin QiaoCollege of Biology, Hunan University, Changsha, 410082, Hunan, China.
Yikun YangCollege of Biology, Hunan University, Changsha, 410082, Hunan, China.
Ruiying HuangCollege of Biology, Hunan University, Changsha, 410082, Hunan, China.
Xuelei ShiCollege of Biology, Hunan University, Changsha, 410082, Hunan, China.
Haoxiang ChenCollege of Biology, Hunan University, Changsha, 410082, Hunan, China.
Jian WangCollege of Biology, Hunan University, Changsha, 410082, Hunan, China.
Yanxiang ChenDepartment of Obstetrics and Gynecology, Renmin Hospital, Wuhan University, Wuhan, 430060, Hubei, China. ppfff365@163.com.
Yongjun TanCollege of Biology, Hunan University, Changsha, 410082, Hunan, China.
Zhikai TanCollege of Biology, Hunan University, Changsha, 410082, Hunan, China. tanzk@hnu.edu.cn.

Funding

Hunan University 53112102National Natural Science Foundation of China 31600782Natural Science Foundation of Hunan Province 2019JJ40018Shenzhen Science and Technology Innovation Commission JCYJ20170818112151323
6 · The paper itself

Abstract

purposeCombination chemotherapy is gradually receiving more attention because of its potential synergistic effect and reduced drug doses in clinical application. However, how to precisely control drug release dose and time using vehicles remains a challenge. This work developed an efficient drug delivery system to combat breast cancer, which can enhance drug effects despite reducing its concentration.

methodsControlled-release poly-lactic-co-glycolic acid (PLGA) scaffolds were fabricated by E-jet 3D printing to deliver doxorubicin (DOX) and cisplatin (CDDP) simultaneously.

resultsThis drug delivery system allowed the use of a reduced drug dosage resulting in a better effect on the human breast cancer cell apoptosis and inhibiting tumor growth, compared with the effect of each drug and the two drugs administrated without PLGA scaffolds. Our study suggested that DOX-CDDP-PLGA scaffolds could efficiently destroy MDA-MB-231 cells and restrain tumor growth.

conclusionsThe 3D printed PLGA scaffolds with their time-programmed drug release might be useful as a new multi-drug delivery vehicle in cancer therapy, which has a potential advantage in a long term tumor cure and prevention of tumor recurrence.

Indexed as

AnimalsAntineoplastic AgentsApoptosisBreast NeoplasmsCell Line, TumorCell Membrane PermeabilityCell SurvivalCisplatinDoxorubicinDrug CarriersDrug LiberationDrug Therapy, CombinationExcipientsFemaleHumansMiceAntineoplastic AgentsCisplatinDoxorubicinDrug CarriersExcipientsPolylactic Acid-Polyglycolic Acid Copolymercisplatincombination chemotherapycontrolled releasedoxorubicinE-jet 3D printing

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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.