Evidence map›Paper›PMID 36131817›Full record

ArticleNanoscale advances2022

An esterase-activatable prodrug formulated liposome strategy: potentiating the anticancer therapeutic efficacy and drug safety.

Linlin Shi, Xinkai Wu, Tongyu Li, Yuan Wu, Liwei Song, Wei Zhang, Luxi Yin, Yuhui Wu, Weidong Han, Yunhai Yang

Open access · goldAbstract read
In one paragraph

Article in Nanoscale advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

12 citing papers in PubMed, 24 citations in OpenAlex.

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  7. Recent advances in drug delivery and targeting for the treatment of pancreatic cancer.Journal of controlled release : official journal of the Controlled Release Society · 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

10 authors at 3 institutions in 1 country.

Linlin ShiCancer Institute (Key Laboratory of Cancer Prevention and Intervention, China National Ministry of Education), 2nd Affiliated Hospital, School of Medicine, Zhejiang University Hangzhou Zhejiang PR China 310009.
Xinkai WuDepartment of Medical Oncology, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University Hangzhou PR China 310016 hanwd@zju.edu.cn.
Tongyu LiDepartment of Hematology, Ningbo First Hospital Ningbo Zhejiang PR China 315010.
Yuan WuDepartment of Respiratory Medicine, The Fourth Affiliated Hospital, College of Medicine, Zhejiang University Yiwu Zhejiang PR China 310014.
Liwei SongShanghai Pulmonary Tumor Medical Center, Shanghai Chest Hospital Affiliated to Shanghai Jiaotong University Shanghai PR China 200030 docyyh@163.com.
Wei ZhangDepartment of Medical Oncology, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University Hangzhou PR China 310016 hanwd@zju.edu.cn.
Luxi YinDepartment of Medical Oncology, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University Hangzhou PR China 310016 hanwd@zju.edu.cn.
Yuhui WuDepartment of Medical Oncology, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University Hangzhou PR China 310016 hanwd@zju.edu.cn.
Weidong HanCancer Institute (Key Laboratory of Cancer Prevention and Intervention, China National Ministry of Education), 2nd Affiliated Hospital, School of Medicine, Zhejiang University Hangzhou Zhejiang PR China 310009.ORCID https://orcid.org/0000-0001-7227-3671
Yunhai YangShanghai Pulmonary Tumor Medical Center, Shanghai Chest Hospital Affiliated to Shanghai Jiaotong University Shanghai PR China 200030 docyyh@163.com.
Sir Run Run Shaw Hospital · CNShanghai Chest Hospital · CNNingbo First Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Liposomal nanomedicine represents a common and versatile carrier for the delivery of both lipophilic and hydrophilic drugs. However, the direct formulation of many chemotherapeutics into a liposomal system remains an enormous challenge. Using the topoisomerase I inhibitor 7-ethyl-10-hydroxycamptothecin (SN38) as a model drug, we combined lipophilic prodrug construction with subsequent integration into an exogenous liposomal scaffold to assemble a prodrug-formulated liposome for systemic administration. Reconstructing SN38 with lipid cholesterol

Identifiers

PMID36131817
PMCPMC9418717
OpenAlexW4205691970

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.