Evidence map›Paper›PMID 35889427›Full record

ArticleMolecules (Basel, Switzerland)2022

Hyaluronic Acid Modified Nanostructured Lipid Carrier for Targeting Delivery of Kaempferol to NSCLC: Preparation, Optimization, Characterization, and Performance Evaluation In Vitro.

Yufei Ma, Jinli Liu, Xinyu Cui, Jiafu Hou, Fengbo Yu, Jinghua Wang, Xiaoxue Wang, Cong Chen, Lei Tong

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 26 citations in OpenAlex.

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  6. DualAntioxidants (Basel, Switzerland) · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Yufei MaDepartment of Pharmacy, Mudanjiang Medical University, Mudanjiang 157000, China.
Jinli LiuDepartment of Basic Medicine, Mudanjiang Medical University, Mudanjiang 157000, China.
Xinyu CuiDepartment of Public Health, Mudanjiang Medical University, Mudanjiang 157000, China.
Jiafu HouDepartment of Pharmacy, Mudanjiang Medical University, Mudanjiang 157000, China.
Fengbo YuDepartment of Pharmacy, Mudanjiang Medical University, Mudanjiang 157000, China.
Jinghua WangDepartment of Pharmacy, Mudanjiang Medical University, Mudanjiang 157000, China.
Xiaoxue WangDepartment of Pharmacy, Mudanjiang Medical University, Mudanjiang 157000, China.
Cong ChenDepartment of Pharmacy, Mudanjiang Medical University, Mudanjiang 157000, China.
Lei TongDepartment of Pharmacy, Mudanjiang Medical University, Mudanjiang 157000, China.
Mudanjiang Medical University · CN

Funding

Natural Science Foundation of Heilongjiang Province SS2021H004
6 · The paper itself

Abstract

Lung cancer seriously threatens the health of human beings, with non-small cell lung cancer (NSCLC) accounting for 80%. Nowadays, the potential position of nano-delivery in treating cancer has been the subject of continuous research. The present research aimed to prepare two molecular weight hyaluronic acid (HA)-modified kaempferol (KA)-loaded nanostructured lipid carriers (HA-KA-NLCs) by the method of melting ultrasonic and electrostatic adsorption, and to assess the antitumor effect of the preparations on A549 cells. The characterization and safety evaluation of the preparations illustrated that they are acceptable for drug delivery for cancer. Subsequently, differential scanning calorimetry (DSC) curve and transmission electron microscopy (TEM) images indicated that the drug was adequately incorporated in the carrier, and the particle appeared as a sphere. Moreover, HA-KA-NLC showed predominant in vitro antitumor effects, inhibiting proliferation, migration, and invasion, promoting apoptosis and increasing cellular uptake of A549 cells. Otherwise, the Western blot assay revealed that preparations could activate epithelial-mesenchymal transition (EMT)-related signaling pathways and modulate the expression of E-cadherin, N-cadherin, and Vimentin in A549 cells. Our present findings demonstrated that HA-KA-NLC could be considered as a secure and effective carrier for targeted tumor delivery and may have potential application prospects in future clinic therapy of NSCLC.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsNanostructuresDrug CarriersExcipientsHumansHyaluronic AcidKaempferolsLipidsParticle SizeDrug CarriersExcipientsHyaluronic AcidKaempferolsLipidskaempferolnanostructured lipid carriernon-small cell lung cancer

Identifiers

PMID35889427
PMCPMC9318624
OpenAlexW4285732213

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.