Evidence map›Paper›PMID 32158208›Full record

ArticleInternational journal of nanomedicine2020

Preparation, Characterization, and Pharmacokinetic Study of a Novel Long-Acting Targeted Paclitaxel Liposome with Antitumor Activity.

Bing Han, Yue Yang, Jinglin Chen, Huan Tang, Yuxin Sun, Zheng Zhang, Zeng Wang, Yan Li, Yao Li, Xue Luan and 8 more

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

25 citing papers in PubMed, 89 citations in OpenAlex.

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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

18 authors at 1 institution in 1 country.

Bing Han *Department of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, ChangChun, People's Republic of China.
Yue Yang *Department of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, ChangChun, People's Republic of China.
Jinglin ChenDepartment of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, ChangChun, People's Republic of China.
Huan TangDepartment of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, ChangChun, People's Republic of China.
Yuxin SunDepartment of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, ChangChun, People's Republic of China.
Zheng ZhangDepartment of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, ChangChun, People's Republic of China.
Zeng WangDepartment of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, ChangChun, People's Republic of China.
Yan LiDepartment of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, ChangChun, People's Republic of China.
Yao LiDepartment of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, ChangChun, People's Republic of China.
Xue LuanDepartment of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, ChangChun, People's Republic of China.
Qianwen LiDepartment of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, ChangChun, People's Republic of China.ORCID 0000-0002-6498-5887
Zhihui RenDepartment of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, ChangChun, People's Republic of China.ORCID 0000-0002-6213-6267
Xiaowei ZhouDepartment of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, ChangChun, People's Republic of China.
Dengli CongDepartment of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, ChangChun, People's Republic of China.
Zhiyi LiuDepartment of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, ChangChun, People's Republic of China.
Qin MengDepartment of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, ChangChun, People's Republic of China.
Fei SunDepartment of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, ChangChun, People's Republic of China.
Jin PeiDepartment of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, ChangChun, People's Republic of China.
Jilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBreast cancer is the leading cause of cancer death in women. Chemotherapy to inhibit the proliferation of cancer cells is considered to be the most important therapeutic strategy. The development of long-circulating PEG and targeting liposomes is a major advance in drug delivery. However, the techniques used in liposome preparation mainly involve conventional liposomes, which have a short half-life, high concentrations in the liver and spleen reticuloendothelial system, and no active targeting.

methodsFour kinds of paclitaxel liposomes were prepared and characterized by various analytical techniques. The long-term targeting effect of liposomes was verified by fluorescence detection methods in vivo and in vitro. Pharmacokinetic and acute toxicity tests were conducted in ICR mice to evaluate the safety of different paclitaxel preparations. The antitumor activity of ES-SSL-PTX was investigated in detail using in vitro and in vivo human breast cancer MCF-7 cell models.

resultsER-targeting liposomes had a particle size of 137.93±1.22 nm and an acceptable encapsulation efficiency of 88.07±1.25%. The liposome preparation is best stored at 4°C, and is stable for up to 48 hrs. Cytotoxicity test on MCF-7 cells demonstrated the stronger cytotoxic activity of liposomes in comparison to free paclitaxel. We used the near-infrared fluorescence imaging technique to confirm that ES-SSL-PTX was effectively targeted and could quickly and specifically identify the tumor site. Pharmacokinetics and acute toxicity in vivo experiments were carried out. The results showed that ES-SSL-PTX could significantly prolong the half-life of the drug, increase its circulation time in vivo, improve its bioavailability and reduce its toxicity and side effects. ES-SSL-PTX can significantly improve the pharmacokinetic properties of paclitaxel, avoid allergic reaction of the original solvent, increase antitumor efficacy and reduce drug toxicity and side effects.

conclusionES-SSL-PTX has great potential for improving the treatment of breast cancer, thereby improving patient prognosis and quality of life.

Indexed as

AnimalsAntineoplastic Agents, PhytogenicBreast NeoplasmsCell Line, TumorDrug Delivery SystemsFemaleHalf-LifeHumansLiposomesMCF-7 CellsMice, Inbred BALB CMice, Inbred ICRPaclitaxelToxicity Tests, AcuteXenograft Model Antitumor AssaysAntineoplastic Agents, PhytogenicLiposomesPaclitaxelbreast cancerestrogen receptorslong-acting liposomespaclitaxeltargeted drug delivery

Identifiers

PMID32158208
PMCPMC6986409
OpenAlexW3001431784

What OpenQuestion holds

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Registered trials

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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.