Evidence map›Paper›PMID 33469196›Full record

ArticleActa pharmacologica Sinica2021

Chitosan oligosaccharide modified liposomes enhance lung cancer delivery of paclitaxel.

Yun-Qiu Miao, Ming-Shu Chen, Xin Zhou, Lin-Miao Guo, Jing-Jing Zhu, Rui Wang, Xin-Xin Zhang, Yong Gan

Open access · bronzeAbstract read
In one paragraph

Article in Acta pharmacologica Sinica, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.2field-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

23 citing papers in PubMed, 70 citations in OpenAlex.

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  2. Developing Biomaterial-Based mRNA Delivery System for Lung Disease Treatment.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
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  14. A new strain ofFrontiers in microbiology · 2024
    Article
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  16. Review
  17. Article
  18. Review
  19. Review
  20. Nanocarriers for anticancer drugs: Challenges and perspectives.Saudi journal of biological sciences · 2022
    Review
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

8 authors at 4 institutions in 1 country.

Yun-Qiu MiaoSchool of Pharmacy, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China.
Ming-Shu ChenSchool of Pharmacy, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China.
Xin ZhouShanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.
Lin-Miao GuoShanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.
Jing-Jing ZhuShanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.
Rui WangSchool of Pharmacy, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China. ellewang@163.com.
Xin-Xin ZhangShanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China. xinxinzhang@simm.ac.cn.
Yong GanShanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China. ygan@simm.ac.cn.
Shanghai Institute of Materia Medica · CNChinese Academy of Sciences · CNShanghai University of Traditional Chinese Medicine · CNUniversity of Chinese Academy of Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer is one of the leading causes of cancer-related death worldwide. Various therapeutic failed in the effective treatment of the lung cancer due to their limited accumulation and exposure in tumors. In order to promote the chemotherapeutics delivery to lung tumor, we introduced chitosan oligosaccharide (CSO) modification on the liposomes. CSO conjugated Pluronic P123 polymers with different CSO grafting amounts, called as CP50 and CP20, were synthesized and used to prepare CSO modified liposomes (CP50-LSs and CP20-LSs). CP50-LSs and CP20-LSs displayed significantly enhanced cellular uptake in A549 cells in vitro as well as superior tumor accumulation in vivo compared with non-CSO modified liposomes (P-LSs). This phenomenon was related to the increased affinity between CSO modified liposomes and tumor cells following massive adsorption of collagen, which was highly expressed in lung tumors. In the A549 tumor-bearing mouse model, intravenous injection of paclitaxel (PTX)-loaded CP50-LSs every 3 days for 21 days resulted in optimal antitumor therapeutic performance with an inhibition rate of 86.4%. These results reveal that CSO modification provides promising applicability for nanomedicine design in the lung cancer treatment.

Indexed as

A549 CellsAnimalsAntineoplastic AgentsChitosanDrug CarriersDrug LiberationHumansLiposomesLungLung NeoplasmsMaleMiceMice, Inbred BALB CMice, NudeOligosaccharidesPaclitaxelAntineoplastic AgentsChitosanDrug CarriersLiposomesOligosaccharidesPaclitaxelantitumorchitosan oligosaccharidedrug deliveryliposomeslung cancernanomedicinepaclitaxel

Identifiers

PMID33469196
PMCPMC8463567
OpenAlexW3125953498

What OpenQuestion holds

Textmetadata
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.